The blood sugar makes sense - where do you recommend people to start if they eat no carbs / no sugar, but are still navigating all the roving symptoms? Thanks for your time.
@@SpectrumOfChange Hi there, thanks for watching. We'd love to share more info. You can chat with the team here for resources m.me/maggieyumd?ref=w14110934
As an scientist specialized in autoimmunity, and as someone who has healed my own 7 autoimmune diseases and has helped thousands of others, we always test the root causes underneath the antibodies. Autoimmunity is always caused by a combination genetics, cellular deficiencies, toxins (both chemical and biologicals) and stress. All of this can be corrected and it’s so doable. The newer scientific root cause testing finds the deeper causes in about 3 weeks. Once found, it’s not difficult to correct root causes. ❤ 😊 ❤ You can feel better.
You're right that you absolutely can feel better! Autoimmunity is not talked about enough in conventional medicine. Dr. Maggie takes on the root cause approach and has developed a 5 pillar protocol for autoimmunity! You can watch her video on he 5 pillar protocol here ruclips.net/video/tINaOsutOPI/видео.html
I cannot thank you enough for this video. My symptoms started as a teenager which became more and more debilitating as I got older and raised a family. I’m 49 and was only diagnosed in 2019. Since I was 20, I’ve been on anti anxiety medication because they thought it was anxiety related. I’m on meds to lower my pulse, but am now mainly bedridden. My life has been completely upended. Thank you for giving me hope.
We appreciate you watching this Angela and for sharing your issues. To learn more about how to work with us, you can start a chat with us here m.me/maggieyumd?ref=w14110934
Ha! This was like reading my story. Except I think my symptoms probably started at birth. I'm 50 currently. I was on beta blockers (I only had anger management issues) for the high heart rate for years in my late twenties and thirties. In my thirties I went to the doctors, when I was considering starting a family, because I knew I just could not cope with it because of the constant fatigue. The doctor said I was fine (as they always said), but I still chose not to have children. Ten years later I was vomiting and bed ridden. Been like that for 7 years now. My experience: beta blockers and calcium channel blockers are contra-indicative. The problems is not the heart rate or the blood pressure spikes. The problem is why the body needs them. I got really in a bad state with the beta blockers in the end. My body would fight against the disease plus against the beta blockers and exhausted itself to the point that I had like pseudo-Addison's disease with skin tone changes and autoimmune symptoms until I stopped the beta blockers. I knew to stop the calcium blockers after a couple years because they just ended up increasing my heart rate even at rest (got them for muscle tremours and gastric pain - the one caused by lack of blood supply to the gut). My advice: try reducing the beta blockers and try reducing carbs.
@Sam Hartford how was your heart rate coming off the beta blockers? I'm terrified of ever coming off of mine because I don't want my tachycardia to get worse than it already is.
@@kerrysue9280 I had to do it over a 10-month period for the first time because I was on a really high dose. But I was in a place in my life then when I did not need to move as much and was not under as much stress as before. Now my heart rate is typically around 95-110 when sitting. It gets into 140-150 only if I do something physically active like go shopping etc. The problem really was that I needed a higher heart rate in order to have any energy and not lactic acid in my muscles. But you need to go with what your body needs. My experience was that my heart rate was not that much lower on beta blockers, although it limited the spikes. It's just that the beta blockers made my body work harder to function normally.
Oh God . I feel the same... Currently on beta blockers. They dont really lower my HR but just stop the spikes. I am afraid to come off of them as I have really bad spikes in my BP and HR. It makes me totally bed ridden😢
I’m seeing this was posted a year ago. Have 3 autoimmunes, been functioning. Had Covid in February, turned my life upside down. I have felt bad since, nausea, I eat to stay alive, no energy. 2 weeks ago went to ER. Blood pressure 60/40, vomiting, dizzy. Just functioning, everybody looks at me like I’m crazy! Praying I can find answers here.
Absolutely, we're glad you found your way to the channel! We have another great resource for you, a community on Facebook filled with other people going through the same thing as you! We invite you to join us ❤️facebook.com/groups/transformautoimmune/
Ibs, adrenal fatigue, high heart rate, estrogen dominate. I have every symptom. I stopped eating sugar, corn and gluten, a relaxed ketogenic diet. Now taking COQ10, vitamin B1( organic nutritional yeast), electrolytes, vit c, fermented foods, pre and pre biotic, parsley, clove,magnesium, vitamin D, castor-oil-packs on my liver, thyroid and kidneys and adrenals, tapping, dry brushing, lymphatic massage and drainage, deep breathing, hitt workout 💪 After 5 months of my protocol I am 85% better, I'm not and won't go to a Dr. I literally asked God what to do.
I don't get car sick never have, but do have shakiness in legs and arms its my nervous system, then feel hot and cold or sweaty, feel off balance but my inner ear issue in sacculus
The same here I think Adrenal fatigue is one of the most problems...I visit Cardiologist...Gastrointestinal and ya nothing wrong...Vitamin B5 for adrenal fatigue help me alot...My headache imrpove and heart rate imrpove...But it takes long time to improve
The first time I experienced my “dizzy spells” was 2003. I fell and hit my head. Over the years I’ve seen multiple cardiologists and psychologists. I’ve been diagnosed with Hashimoto’s, Lupus, and Sjogrens. I recently wore a 30 day heart monitor and I recording over 100 incidents of dizziness. But they told me I didn’t have POTS and wouldn’t give me a table tilt test. It was such a waste of time. I’ve given up on being diagnosed with anything many times because I always get my hopes up and I’m always let down with “we don’t know what’s wrong”.
We hear you Hannah and you are not alone! It is crucial for you to have a root cause based approach process and system to turn around all this. We'd love to share more info about this and know how we can help. Send us a message here m.me/maggieyumd?ref=w14110934
Try finding a teaching hospital near you and schedule an appointment with a resident. There is a lot more passion about their career at that point. Everything they do is reviewed by more experienced doctors. Finding out what's wrong with you is a matter of getting put in front of the right group of specialists. You need to find a doctor who cares and won't dismiss you.
I was at a club, I passed out in the bathroom after only having three drinks 😩 I’ve never passed out before and I’ve had up to 9 drinks and I was fine. After that, it all went downhill and I noticed my coffee addiction made it even worse.
"If they don't know how to treat it, it doesn't really exist." That's the key phrase there. ME/CFS and a POTS comorbidity. I'm actually surprised that I wasn't diagnosed with IBS because my guts are messed up. And, yeah, I get horribly motion sick, sometimes just by seeing too much motion.
Thank you for watching Amber. We'd love to get to know you more and see how we can help. Send us a message here to learn more: m.me/maggieyumd?ref=w14110934
This is the first time I’ve seen POTS related to autoimmunity and I’ve been researching the tar out of it for several months now. I’ve had Long Covid for 21 months now and my symptoms are all Dysautonomia/POTS related. I have Hashimoto’s so this is resonating with me for sure. Thank you so much for this education!
Thank you for watching and sharing some of your journey with us Laurel! To learn more about how to work with us, you can start a chat with us here m.me/maggieyumd?ref=w14110934
@@siobhancunningham2923 We have a Facebook group that you can join for free where you can see tons of trainings and resources and support from the community. And we also have a paid program. You can send us a message to learn more m.me/maggieyumd?ref=w14110934
I was not diagnosed by my cardiologist, but by a neurologist I was sent to! My BP was 60/40 the first time I saw the neurologist, and he immediately knew!!
i am a therapist thought i had ms. vegas nerve affected. felt like i was in earthquake and no earthquake happened. i have 4 pts now. who are told they have ms its long covid. a
Are you experiencing dizziness, vertigo, fatigue, brain fog, low blood pressure, and fast heart rate? Did you know that you have POTS? Start a chat with our team and tell us more about you, so that we can send over additional resources m.me/maggieyumd?ref=w14110934
I am bedridden with POTS. I develpoed POTS at the beginning of 2019. My guess is maybe chronic stress and long term mold exposure has brought this on. My body has crashed recently and i am so scared. I am on a beta blocker and thats not controlling my heart rate anymore. Unlike most, my blood pressure is higher rather than lower and my resting heart rate is higher too. My heart increases 50+ beats when i stand. Its difficult to see a doctor because my POTS keeps me from working. This video is inspiring and gives me hope that maybe one day i can have a life again. Just have to find a way to make that happen.
There is definitely hope Kerry! You need to address the root cause to have a sustainable recovery. To learn more about how to work with us, you can start a chat with us here m.me/maggieyumd?ref=w14110934
I'm 70 years old and was just diagnosed with POTS yesterday. I have been struggling with irregualar heart beat for several years. I had no idea that it was related to auto immune issues. That is very interesting to me. I have been falling, being dizzy etc. I've been on metoprolol and the issues getting worse. I'm glad there are these other solutions.
I hear you.... glad to see you are finally starting to see what's happening-- definitely autoimmune! You can live chat our team at 503-647-4568 for more information on our programs, we would love to help you address this :)
Hey all! We are inviting you to Dr. Maggie’s FREE live virtual event. Get a chance to meet and work with her in this workshop. Happening this Thursday, Nov 9th 4pm PST/7pm EST. Register here to join and for more info: drmaggieyu.respond.ontraport.net/nov-live-event
One year later and Dr. Maggie has completely described my experience with the medical field. Lost our entire savings and still unable to work trying to find a dx. Jumping thru stupid red hoops and fire for insurance. Choosing to pay out of pocket to expedite things only to become more frustrated. Losing precious time with my IVF baby who is now 4 and I have been barely able to function for the past 3 of those 4. The alone was enough to destroy my mental health and nearly make me think about giving up to find relief. Now, finding social media and videos such as these …. I have fought harder than ever, been more direct than ever, and shed more tears than ever to get someone to believe me and know what the hell I am trying to describe and be patient with me while Itell my entire tale or AT LEAST read my symptom journal and research correlations. I’m not seeking drugs, I don’t even ask for pain relievers and just suffer so they take me more seriously. I’m so tired but want to truly LIVE my life.
This is why channels like this are so important alongside doing your best to compare info from various, verified sources…. I’ve become pretty decent at reading medical academic papers and studies lol using my elem ed study practices and a dictionary helps hahaha
And people like you, working so hard dealing with all these symptoms, are exactly why we're here. We'd love to see how we can support you, please get in contact directly with our team by texting 503-647-4568 with your name and symptoms!
So sorry I can completely relate for me it’s been since as young as I can remember 4 years old, I have was admitted to hospital and just got out 2 days ago after a week. I actually developed seizures because of it. Battening the medical bureaucracy is a nightmare. I even asked for an ambulance report several years ago as I was treated so poorly and they actually put hypochondria!
@@pinapple60 That sounds incredibly tough to deal with. It must be frustrating to encounter such dismissive attitudes from medical professionals. How are you feeling now after your recent hospital stay? We are here to help! Speak to us live via text at (503) 647-4568
I have 2 young daughters with it. One was diagnosed by a Neurologist & Nuclear Physio Cardiologist, the other by a Pediatric Cardiologist. Neither of their primary doctors knew what was wrong. Both of their Cardiologists diagnosed them & they both did it right away. And yes it’s so frustrating when doctors don’t believe them. I was diagnosed with long haul Covid 3 years ago & told it’s a form of Pots. It’s been on the rise since covid & vax.
Yes we so hear you! We have worked with tons of those who struggled with the same issues. We'd love to share info and know how we can help. Do chat with our team here m.me/maggieyumd?ref=w14110934
Yes I agree, I’m a coeliac and symptoms started after the first and second vaccine. It was sporadic at first but I was told to write it down every time I had a flare up to try and figure out what was going on. Then it finally clicked when the doctors asked last week was I sick or anything that happened around that date? I wasn’t sick and I’ve never had Covid but yes I’d had the vaccine. The doctor I saw last week thinks it’s Pots. It was sporadic at first and now daily. It’s so debilitating
13:45 "Autoimmunity: antibody attacks enzyme in brainstem responsible for creating chemical for balance. " 26:15 Blood - Mineral - Vitamin: Ferritin, Iron and Vitamin B12 28:35 Digestion - Low stomach acid 31:55 Foodmapping - allergies
WOW WOW WOW YOU CAN'T IMAGINE WHAT THIS VIDEO MEANS TO ME. I KNEW I WAS NOT CRAZY EVERY TIME I ASKED DOCTORS TO CHECK MY SUGAR, BECAUSE I WAS SURE THERE WAS A CONNECTION TO MY SYMPTOMS. AFTER BEING TAKING MEDS THAT DON'T WORK AND ARE MAKING ME MORE SICK. I HAVE BEING DEPRESSED AND OUT OF WORK NOT EVEN ABLE TO DRIVE AND STILL WAITING FOR ANSWERS. I WAS WOW ALSO WHEN YOU MENTIONED THE CAR SICKNESS. MY TEANEAGE DAUGHTER IS ALWAYS SICK AND COMPLAINING ABOUT THAT. I COULD KEEP GOING , BUT ONE MORE THING I WANT TO SAY IS : THANK YOU, THANK YOU, THANK YOU. 😊
I’m curious to see how to “end” my POTS… How ridiculous is Na when POTS is shown to affect RAAS and lowers Na+ reuptake? If we’re losing it, why is it wrong to treat with salt tablets or electrolyte drinks? I almost want to cry hearing the other people explaining their symptoms. I went 12 years undiagnosed, called hypochondriac, cardiologist said I was too young to have anything wrong but couldn’t explain my idiopathic tachycardia, and lived in fear of strenuous exercise because of my heart and losing my eyesight because of the (silent) migraines that made my optometrist think my retina was detaching. It’s thinning, but it’s still kicking. I didn’t have pain so the fact that my flashing twinkling lights were migraines was lost on us. The head pounding was the hardest to explain, and went ignored because my resting BP was normal range. It’s so relieving to hear someone else experienced it. I’m not alone 😢 ECG, EKG, eCat monitor, Labetalol, every eye test possible, MRI, MRA, blood tests, and nothing. The god-sent angel of a Neurologist knew what it was the moment he walked into the room when I was referred. Autoimmune disorders run in my family. It’s interesting to learn all of this. THANK YOU
We appreciate you sharing this! We have worked with tons of those who struggled with laundry list of POTS symptoms. Please send us a message here to learn more. We'd love to know how we can help m.me/maggieyumd?ref=w14110934
I’m there!!!!! I’ve seen all the specialists you listed and you described EXACTLY how I’ve been treated. No one I know understands me because I “look healthy” but EVERY SINGLE DAY IS A STRUGGLE within. I wish I could see you but I’m in California. Do you have colleagues here you could recommend.
Yes!! This is so common for people struggling with autoimmunity-- oftentimes there are "invisible" symptoms so from an outward perspective you might appear to be fine. All of our programs are online so we can actually help you worldwide! You can live chat with our team at (503) 647-4568 for more information and to get started with us :))
My daughter was a competitive dancer and top of her class. She's 17 and been in bed mostly since 13. She got Covid and got worse. We're been to 9 states trying to get help. She has EDS and Mast cell activation syndrome. She has a PFO too. After Covid she received the monoclonal antibodies and got her life back for 3 months. Then back down after the antibodies wore off. I've talked to FDA and Regeneron pharmaceuticals company that says they are no longer available because they were given on an emergency basis. My daughter is homebound due to car sickness.
Thank you for sharing this Kim. I'm sure this hasn't been an easy journey for you and your daughter. We'd love to know how we can help. Please chat with our team here: m.me/maggieyumd?ref=w14110934
I am so glad I found this video. I have psoriasis, became lactose intolerant in my late 30's, became hypertensive at 38, i am 44 now. I also developed IBS. About two yeas ago I started experiencing the symptoms of POTs, the dizziness, high pulse rate, headaches, brain fog. Was diagnosed with BPPV a Neurologist and was placed on beta blockers and vertigo drugs. The symptoms disappeared the whole of last year only to return this year with a bang. Its all so frustrating. I find that taking sea salt helps with the symptoms.
We so hear you! And you are not alone. We'd love to share more info about ending POTS naturally and know how we can help. Do send us a message here m.me/maggieyumd?ref=w14110934
@mary-annosuide942 Wow this is also my case! I have both Psoriasis and POTs. I have been diagnosed with POTs very recently even though Inhad symptoms for years! Starting medications beta blockers also now. Does the POT symptoms really come back suddenly like that?
@@miriamarajaoalisoa7294 Getting to the root cause is the key to have a long term and sustainable recovery with POTS and psoriasis! We'd love to know how we can help you, send us a message here m.me/maggieyumd?ref=w14110934
Told my Doctor I was pretty sure my issues were happening because I have IBS… she said “no that’s not how it works” Brought it up to my chiro who does holistic medicine. To which her policy is “everything starts with the gut”
We hear you Amber! Most conventional doctors often know nothing about these issues. We'd love to share invaluable resources. Chat with our team here for more info: m.me/maggieyumd?ref=w14110934
What are your top 3 POTS symptoms and challenges now Victoria? Addressing the root cause of the symptoms is the key, it is so crucial. That is what our 5 pillars protocol is about. If you're interested to learn more, send us a chat here m.me/maggieyumd?ref=w14110934
Since I was a child I experience vertigo, car sickness and severe sea-sickness. I’ve been lactose intolerant since I was 9. Tinnitus appeared in 2014, alopecia areata in 2014 too, IBS in 2017 and vulvodynia in 2018. Since 2-3 years I have vertigo when standing. Three months ago after a virus I have POTS symptoms and my HR goes up to 120 when standing. I have fasciculations. Even my resting HR is higher then before (85-90 bpm when seated in the morning). At the end of this month I will have my Tilt Table Test done. :( . Thank you so much for this HUGE explanation!
Thank you for sharing this and for watching Clara! We'd love to know how we can help. We have worked with tons of those who had the same issues. Send us a message here if you haven't yet for more info m.me/maggieyumd?ref=w14110934
We all have so much to learn-- its great when we can learn and share with our loved ones. We would love to help you and your husband address these conditions, text us at (503) 647-4568 to get started with us!
My autoimmune journey started with digestive issues. It took 15 years to get my Celiac diagnosis (after removal of my gallbladder didn’t help). It took 6 years to FINALLY get a POTS diagnosis.
Thanks for sharing! Most of the symptoms you have with digestive issues, Celiac and POTS are connected. The key is to get to the root cause of them and the good news is a diagnosis doesn't matter! We'd love to share with you more info and see how we can best help. Let's connect, chat with us here m.me/maggieyumd?ref=w14110934
2 and half years ago I had Covid I never recovered many of the symptoms yall mentioned have been a daily fight. It has kept me from returning to work. Iv been dealing with my heart racing sometimes when I’m doing nothing ,low oxygen ,worst brain fog imaginable.
It really can be an ongoing fight when your symptoms aren't being treated properly. If you want to get to the root cause of your symptoms text our team here at (503) 647-4568, we can absolutely help you address this so you can go back to living!
You hit the nail on the head for me , for years l have been suffering from symptoms, number 1 when l wake up l feel like l have the flu , my voice changed about 10 years ago l was 65 years old l had nerve damage in my left ear oh when l was a child l would get terrible car sickness, especially in the back seat , l have pain problems everywhere, they have diagnosed me with fibromyalgia and chronic fatigue syndrome, l have fluctuations in my blood pressure on high doses of meds l have type 2 diabetes, hypothyroidism , it’s getting worse as l age , l stay sick at my stomach, my mother constantly was taking me to Doctors as a child ,,diagnosed me with a nervous stomach finally at 75 they are giving me a MRI , had a nerve conduction and EMG test that shows carpal tunnel syndrome and pinched nerves , l have numbness throughout my body l am suffering
Oh wow, appreciate you sharing this and you are not alone! We have worked with tons of those who struggled with the same issues. So crucial for you to address the root cause of your symptoms. We'd love to share info and know how we can help. Do send us a message here m.me/maggieyumd?ref=w14110934
Yes!! Sent to cardiologist. He said it’s normal! It’s been hell. Well after collapsing and hospitalized I finally got attention. It was the allergist who correctly diagnosed it!
Medical gaslighting is hell. Being told it's "normal" whilst dealing with debilitating symptoms is unacceptable. Text our team at 503-647-4568, we would love to offer you some *actual* help with this!
I was diagnosed with Primary Sjogren's Syndrome in August of 2023, but I seriously believe I have undiagnosed POTS along with Sjögren’s being that I've either almost passed out or completely passed out several times this past year. Each time it happened I was standing up only a few minutes, and the area I was standing in whether it was inside a building or outside each was of a comfortable tempature and all I was doing was standing for a few minutes. My doctor's keep referring me to a cardiologist but by my own research I know its POTS. I feel like no one is really listening to me but I know something is wrong because two years ago I could stand up for several hours and be fine, but all of a sudden a year ago I started fainting, or feeling weak, dizzy and nauseous with just standing. I feel defeated, my family label me at lazy but the only time I don't feel sick is when I'm sitting or laying down. It sucks when you know something is off with your body but no one is LISTENING. And its at the point where its getting dangerous, the last time it happened I was at work standing while working and I had to be rushed to the hospital, where I was told I had a mild concussion, apparently when I fainted I hit the back of my head.
And you are not alone! Do you realize that Sjogrens and POTS symptoms are connected. Appreciate you watching and sharing your issues. Chat our team to learn more how to address and get rid of your symptoms m.me/maggieyumd?ref=w14110934
Try see if a chiropractor can help, there is a thing called cervical pots, where the neck being out can cause it too, also get your thyroid checked and get checked for hashimotos!! My daughter has POTS real bad, and her thyroid is so slow, they are testing her for hashimotos now! Poor thing can just sit all day😢 only 21 yrs old😮❤
@FeralFairyRae Wow thank you for your comment!! My thyroid and cervix were both recently checked, and came back normal. I hope your daughter is feeling better while fighting this battle of illness.
@PrettyHazelEyedMLS Thankyou xx glad you got normal results, yes my poor girl, and in Australia they don't test for lymes or treat it, as they don't believe it exists here!!!
I’m in California. Just diagnosed with MCAS and maybe POTs. Hospitalized for collapsing. BP was 67/44. I have high blood pressure and medicated. Doctors told me the light headedness when getting was normal. It’s not. Love your videos. Thank you.
My 24 year son just got diagnosed with this and is going through the workup with cardiologist. We did echo, stress test, and have a heart monitor for 2 weeks.
Glad to hear that you are finding answers for what your son is going through. We have a full POTS training series that you can access here, hopefully it helps in you journey :) drmaggieyu.respond.ontraport.net/training-pots
Thanks for sharing this Martin and for watching. We have resources about MS and POTS, we have worked with tons of those who struggled with these issues. We'd love to know how we can help. Send us a message m.me/maggieyumd?ref=w14110934
I remember complaining to my doctor about all of the issues I was struggling with and they just kept brushing me aside telling me I was just sleep deprived from technology and have low iron because I’m female. Turns out it’s neither of those, I displayed iron deficiency symptoms from blood pooling and after sitting on iron supplements for quiet some time my symptoms are still prevalent though not drastically. Still not too sure as to what I have but it’s a starting point knowing my illness is an autoimmune problem and not an iron deficiency
Thank you for sharing this. So common to have a novel of symptoms and still get little to no help from doctors. Addressing the root cause is crucial in turning these symptoms around and preventing new symptoms from continuing to pop up! To learn more about how to work with us, you can start a chat with us here m.me/maggieyumd?ref=w14110934
Thank you for all this information. My daughter has been so sick. It sounds like this. She is so dizzy, blind head aches, nauseous, weakness, brain fog, It hit really hard about 2 years ago. She is gluten free. She had to quit working the dizziness was a big problem at her job. She has gone to to ENT, Physical Therapy, Chiropractor, they have her schedule for Cardiologist, and Nuerologist. She had her do the MRI months ago. But doesn't get to see Nuerologist until May. It is terribly scary to watch her go through this. They can't figure out what is wrong. She is streeed from this illness.
I gave the info to my pulmonologist and she seemed almost irritated at me for trying to figure out what’s wrong with myself. I have Multiple Sclerosis, I have long Covid almost didn’t make it in 2021, it’s so scary to not be able to catch your breath I’m scared to be alone.
Oh wow, thanks for sharing this. Must have been tough. We'd love to know how we can help. We have worked with those who had similar issues. Do send us a message here m.me/maggieyumd?ref=w14110934
I been diagnosed with pots I feel like the older I get the worse it gets and I just had a episode last week and it was bad I passed out. At work and i was taken to the hospital I’m having brain frog and my vision is not good and I can’t sit up without and getting dizzy
Thank you so much for this. I finally after many many years finally had Dr do tilt test and got diagnosis of orthostatic hypotension with probable pots. I also have diastolic heart failure and pacemaker for heart block
It’s crazy this video I have just come upon was a lightbulb moment! 4 months ago I went to the ER after getting dizzy and neauseous and car and boat sick on a Holyday, after non being boat or car sick.. all my tests turned out normal.. 4 months later I’ve had a recurrence for the past week when I’m standing too long I’m fatigued dizzy lightheaded.. when I eat I feel sick.. when I’m exerting myself I feel dizzy.. all my tests from GP come back normal.. in my deep dive into my symptoms nothing was 100% then on a video my Dr. Axe talking about IBS Potts was mentioned in passing and a big flag went to I started researching pottts and it literally fit into all my symptoms, except the last time this happened I had the car sickness and boat sickness and then watching this video you mentioned it as one of the warning signs and boom 💥 it all fits together!
Glad you found this video and thank you for sharing this! We'd love to share more info and resources about POTS. Chat with our team here to learn more m.me/maggieyumd?ref=w14110934 It is really crucial for you to address the root cause of the symptoms naturally
My 20 year-old was diagnosed with POTS. Symptoms are SO SEVERE. Tilt table test: passed out and systolic number of blood pressure was 60! Immediately given meds but she was only ok after saline IV at hospital. She was great day one. She is back to incredibly weak. My first child, age 27 ALSO has POTS, but was not diagnosed. She was diagnosed with RA. I have hypothyroidism and had a SCAD heart attack last year (at age 57).
Thank you for sharing that with us Chris and we hear you. It is crucial to get to the root cause to really understand what is going on. You can start a chat with us here for more info: m.me/maggieyumd?ref=w14110934
Ive passed 2 stress tests lol My cardiologist told me I have anxiety and I need antidepressants. I've seen ears and throat doctors. I get car sickness. I don't deal with motion well anymore. Nausea is a big problem right now and dizziness along with heart rate skyrocket after standing.
Must have been challenging, thanks for sharing. Meds and pills are not a long term solution and only make the symptoms worse. We'd love to share more info and know how we can help. Send us a message here m.me/maggieyumd?ref=w14110934
Yes, I have had these symptoms. Vestibular migraines and Meniere's. My heartrate can go up when I am standing a while. I get carsick. Very dry eyes. My ANA was negative,
Must have been challenging and you are not alone! Thanks for sharing. We'd love to share more info about turning these symptoms around and know how we can help. Chat with our team m.me/maggieyumd?ref=w14110934
Thank you SO much for this video! I’m only 3 minutes in ( 3:24 ) and already feel so validated. I’ve been working with a ophthalmologist and he’s the one who very strongly thinks I may have POTS. My next step is to see a rheumatologist, but I’m just researching in the meantime. Thanks for this ❤
I'm glad you enjoyed it :) Half of the battle is feeling seen and finding hope. I'm glad to see that you're taking your health into your own hands and taking steps to learn more. You can always live chat with our team at (503) 647-4568, we would love to redirect you to more resources!
I've had Hashimotos for 22 years and my bizarre symptoms have increased dramatically in the last two years (I just turned 48.) I am just learning I have POTS (I think I've had it for years and just didn't know) through a conversation with my functional doctor about how I "have issues with my salt" and "I'm just so dizzy and my heart pounds." I had NO idea. Now...I'm ravaging information to help me. This is 100% debilitating and I am SICK of having to "be in bed." I am angry and I want to get better.
Thank you for sharing that with us Belinda. Addressing the root cause is crucial in turning these symptoms around and preventing new symptoms from continuing to pop up! We'd love to know how we can help her! Please send us a message here to learn more to get started m.me/maggieyumd?ref=w14110934
I have POTS as do my kids. My 17 year old son has been terribly suffering with debilitating exhaustion since puberty. We have been to SO many specialists. No one put the POTS to the exhaustion. I have been pushing 2 liters of water and Electrolyte pills for a few days, HUGE difference with just that. I have made a huge dent in my autoimmune with figuring out trigger foods, grains, legumes, sugar (including maple or honey), nightshade, lactose, eggs, onions, etc, and healing my gut and eating to keep my blood sugar balanced.
Thanks for sharing some of your journey with us. Unfortunately, most conventional doctors often know nothing about these issues. Addressing the root cause is crucial in turning these symptoms around. We'd love to share more info and helpful resources. Chat with our team here to learn more: m.me/maggieyumd?ref=w14110934
I’m in the uk, I found this hugely interesting, thank you. Luckily I was referred to a specialist in POTS from my cardiologist. My specialist has told me about trying a wheat free diet as my daughter is wheat intolerant and my other daughter is lactose intolerant. I’m going to start keeping a diary.
Thank you for watching Carol! It is so crucial to address the root cause no matter what your diagnosis is. We'd love to share more info with you. Chat with our team to learn more: m.me/maggieyumd?ref=w14110934
Omg...i need to book a call...this maybe what my youngest has- constantly dizzy, car sicknesses, cluster headaches, insominia, has to pace or lay down ...has over 12 specialists...he gets better than he gets worse
I'm truly sorry to hear about your youngest's health struggles-constant dizziness, car sickness, cluster headaches, insomnia, and the need to pace or lay down. It sounds incredibly challenging. If you're interested in learning more about how we can help address these symptoms, please start a chat with us here: m.me/maggieyumd?ref=w14110934. We're here to provide support and guidance.
Thanks for watching Vicky! If you're dealing with POTS symptoms and interested to learn more, you can send us a message here m.me/maggieyumd?ref=w14110934
POTS & hEDS for me. Ignored/dismissed by conventional medicine then finally diagnosed at age 45, after 3+ decades of suffering. Anyone else flattened for days by any form of moderate or intense exercise? If I do anything more than a short walk or a 10 min bike ride, I’m bedridden with a flare that includes full brain fog/shutdown. Weight toning completely out of the question (which is tough since we need to tone muscles for bone health). Please tell me I’m not alone on this front!
Appreciate you sharing some of your journey with us, Wendy. It is really challenging, but you are not alone. And what you need is to address the root cause. Dr. Maggie has worked with tons of those who struggled with these issues and they were able to get their life back. To learn more about how to work with us, you can start a chat with us here m.me/maggieyumd?ref=w14110934
My son was diagnosed (by 2 different doctors) with POTS. But I’m confused because labs show that he does not have an auto immune disorder……His worse symptoms are Insomnia, brain fog, a restless leg syndrome feeling all over his body, and heart racing.
It is crucial to address the root cause regardless of what the diagnosis is or if he doesn't have one. To learn more about turning around chronic symptoms naturally. Send us a message here m.me/maggieyumd?ref=w14110934
I am long c, long Lyme, celiac w gut dysbiosis, was pre med studied this 2 years.. it's possible to have an autoimmune+ be asymptomatic (no signs).. took 6yrs to dx me w celiac! Yr GUT IS yr health, may wish to get a blood celiac + an ana test to check subclass igg, igm, ige, .this Dr is spot on w gut /auto dx info🙏❤️
@@brendabrenner2891 It's great that you're proactive about your health. If you're interested in exploring ways to address autoimmune conditions and gut health, you can initiate a chat with us here: m.me/maggieyumd?ref=w14110934. We're here to provide more information and support based on your specific needs.
I have Ehlers Danlos and all of the symptoms of POTS. My cardiologist found that I had heart arrhythmia, but know one could explain the nauseous, weakness, and dizziness.
Thanks for watching Victoria! The problem is that the conventional way doesn’t properly address these issues. We'd love to share more info and see how we can help. Chat with our team to learn more: m.me/maggieyumd?ref=w14110934
That sounds like a lot to deal with :(( Chat with our team at (503) 647-4568, we can definitely help you address these! You should also check out our POTS training series here drmaggieyu.respond.ontraport.net/training-pots!
I went carnivore (with raw milk) and my life got exponentially better. Gave up all plant foods. Who knew? Seems to be helping quite a few people so maybe worth trying? Need to really make sure your nutrient deficiencies are addressed and the nervous system. Also doing coherent breathing (and light Buteyko breathing). Getting rid of toxins and poisons too. Good luck!
You have just told the story of my life for the last three years. Dr after Dr and a trip to Mayo and an outside cardiologist. Last visit to the cartiologist and a heart monitor. I knew I was having Tachycardia. The Dr confirmed that and told me something in my body is causing it and he did not know what was causing it. Sent me home with no diagnosis and no medicine. The next week my heart was doing something different. It was a different feeling. Got my cardia mobile out and I was in AFib. I couple days later passed out in the middle of the night in the kitchen. Drs are not willing to help people that have been Vaccine injured. I have given up on doctors.
You're NOT alone, so many people are struggling with the exact same thing. Send a text to 503-647-4568 with your name and what you're struggling with, we'll get you the help you need.
Thank you for watching Joni. We'd love to share more info and additional resources with you. Be sure to send our team a message here to learn more: m.me/maggieyumd?ref=w14110934
I have fluxuations in blood pressure that goes scary high like 240/169 and racing heart rate and after several ER visit been told im having an anxiety attack ! Soooo wrong !
And you are not alone in that experience! Most regular doctors often know nothing about finding out the root cause of these symptoms like POTS. We'd love to learn more about your everyday challenges. Chat with us here m.me/maggieyumd?ref=w14110934
This is me and it started for me after the birth of my twins. Thankfully I haven’t passed out but every time I bend over and stand back upright or get up from off the floor is when I get extremely dizzy. Scheduled to get a pots test finally after 9 years. I also get the vibrating sensations and when I first experienced right after the birth of my twins my Dr wanted to admit me. 😔 I also noticed it was related to my blood sugar based on various diets I’ve tried and how it would become worse with them.
Yes! Bloog Sugar balance is really crucial to this and also having the right food test just like Dr Maggie's Food mapping which is unique to the program. All of these aspects are crucial to turning around POTS and other health challenges We'd love to share more info and how we can help. Chat us here to learn more m.me/maggieyumd?ref=w14110934
I've been having symptoms of illness as long as I can remember but since Feb 2020 is when the severe dizziness, fatigue, and fainting. They diagnosed me with PoTS in Jan 2021.. I did the compression, I did the heart lowering meds, I did the salt and water.. nothing helped and the meds made me faint even more. Its been awful and I'm completely disabled (90% bedridden). It is super interesting to hear you say stuff about the adrenal gland (and others) because I ended up in the hospital recently my symptoms were so bad and my doctor there noticed some minor things off with my blood work that doctors have been missing since this all started. My cortisol is messed up (for those who dunno that is produced in the adrenal gland) and my hemoglobin is high (I'm trans so if I were still taking testosterone it would actually be a normal level but I haven't been on T since before I got sick so she was like other doctors should have noticed this if they'd actually just given a shit about you). It's a whirlwind but I feel like maybe I'm finally on the road towards getting better because of her.
Thankfully I am in Canada so it was not thousands and thousands of dollars but it does take months to see any specialist and then months to get any tests that are "more complicated" than blood work. I just want to be a normal functioning human being so that I can go swimming, biking, hiking, and rescue doggies.
Interesting I am gluten intolerant or celiac maybe but I also have an egg issue where I can have like potato salad or eggs baked into something but if I eat actual scrambled eggs I get sick too. I've never heard of anyone else having an issue with eggs!
@@beepboop27 Hey there, thank you for sharing this and for watching our video! You are not alone in this experience. And it can be really challenging to deal with POTS and other chronic symptoms. It is crucial to get to the root cause, address them naturally and properly. That is the key. If you want to learn more about this and have the knowledge to reverse your symptoms. Please send us a message here m.me/maggieyumd?ref=w14110934
After months of health centre visits, they kept saying "you're fine, its anxiety just take deep breaths'' We then went to general doctors, they did blood tests over and over. I saw a cardiologist, did an ecg and echo, he said I had a murmur, I need surgery maybe in 5 years. I was added to a cardiac clinic, the doctor ran an ecg, echo, ultrasound, then I was FINALLY diagnosed with POTS. Im only 15, at the time I was 14 and it was so bad, I missed school for weeks. I suffer with chest pain, motion sickness, dizziness, darkening vision, nausea, extreme fatigue, tachycardia, low blood pressure, I feel faintish if I stand for too long.
@@Renelle2007 Appreciate you sharing that with Renelle. So many suffer for years being told it's all in their heads and their labs are normal, all the while your symptoms are worsening. Our team would love to know how we can help. Start a chat with our team here for more info: m.me/maggieyumd?ref=w14110934
This just happened to me in my cardiologists office. they checked my bp in the sitting position (I was fine), then the nurse asked me to lay down on the exam table. Within 15 seconds I went into tachy at 180 bpm, bp shot up to 210/110, whole body went into a sympathetic state. Had to take every one of my emergency cardiac meds right there. The doctor said it was related to my mast cell activation, but never said a work about blood sugar dysregulation. Now after viewing a few of Dr. Maggie's videos on POT's, I realize that I have POTS and have no one has ever mentioned this issue as being a possible reason for my symptoms related to changes in my body position, especially when I lay down or get up too quickly.
It sounds like a very intense and scary situation. Based on your symptoms, it does seem like POTS could be playing a role, especially with the changes in your heart rate and blood pressure with position changes. It's great that you've found our videos helpful in identifying this. Speak to us live via text at (503) 647-4568
Hi! Thank you for watching. Most symptoms of Lyme, Hashimotos and POTS are connected and it is crucial to find out the root cause and address them. We have helped many people turn around these kinds of health challenges. If you're interested to learn more, chat with us here m.me/maggieyumd?ref=w14110934
What can you say are your top 3 symptoms and challenges now? We'd like to learn more about it and share specific resources. Send us a message so we can connect m.me/maggieyumd?ref=w14110934
Thank you for sharing. It's really challenging but you are not alone. We'd love to know how we can help. You can chat with the team here for more info: m.me/maggieyumd?ref=w14110934
Me too. All my symptoms including severe “MCAS” like anaphylactic reactions to foods that I was fine with only the day before…started 5mins after the first and only jab. Starting with pounding heart heat flush and left side paralysis. intermittent paralysis after certain foods or stress to the body of any kind continued, intermittent drooling and crazy dry mouth, breathing pattern completely turned to manual, had to concentrate on breathing or just suffocate and pass out. Racing heart panic attacks 8hrs at a time waking up in the middle of the night with adrenaline and heart at 200bpm, 200”doctors” and it “must be anxiety” 😂… one year housebound while living overseas unable to work too sick to get on a train let alone a plane. Embassy staff laughing at me not saying you’re crazy but the pandemic was just a stressful time for everyone… now go get your second shot! I didn’t have any signs of autoimmunity before the shot, so it would have been ideal for someone to stick me in a lab and study what the exact mechanism was to educate and help all the people suffering now and those who WILL suffer in the future and when it’s these uneducated lazy ass doctors’ kids or grandkids they’re gonna be PISSED they didn’t take me up on my offer to be thrown in a lab to get the hell out in front of this before it became THEIR life and their problem. I still only eat 5foods preparing every meal everyday while working 3jobs to try to pay back debt. The only reason I can walk or work is due to finding an acupuncturist who really understands the root cause. I don’t know how it works but it does!! Still many substances throw me into POTS and anaphylaxis that I never had before even perfume candles grass …but if I am careful to avoid potential triggers I can function and am truly grateful. Now I know the truth and will never have to be at the mercy of mainstream shitty “medicine.” Completely drug free 🎉
With tachycardia ended up at ER got admitted overnight extensive tests nothing wrong with the heart sent home and told+me follow the cardiologist. Now I’m taking digestive enzymes and not much episodes.
Must have been challenging. We got tons of resources about POTS and tachychardia in our Facebook group, you can join here www.drmaggieyu.com/transform you can also start a chat with the team here m.me/maggieyumd?ref=w14110934
Thank you ! You are very passionate for what you do Dr. Yu and I will transform my health with your help naturally I’m 77 yrs. Old and never been on any pharmaceutical drugs.
That's amazing to hear that you want to share your journey on your blog and podcast! Your openness can bring comfort and support to others going through similar experiences. If you need more information or have any questions, feel free to reach out to us at m.me/maggieyumd?ref=w14110934
Hey I'm 17 I get dizzy when I stand up I'm always very have very low energy and and extremely bad memory a focus and I'm I'm underweight. (I was also sent to a cardiologist and was told everything is fine)The doctor to my blood pressure laying down then sitting up then standing and said I have low blood pressure I think he said pots but I'm not sure. He told me to eat a lot of salt and maybe take vitamin d and that's about it! My life has been hell for a long time, I'm even out of school currently! I've takin b vitamins and iron but then my heart was racing and I didn't feel like it was really helping so I stopped. (idk if this has to do with anything but I went on a diet with a lot of meat fish eggs and that's when my memory was the worst) so if God was so kind to me to put this in front of your eyes plz tell me what I should do next be my family thinks I'm psychotic and Its all anxiety and I'm just a lazy fck. So if you can tell me who I should see/or do/or eat, or supplement with it's would be a life changer!
Thanks for sharing and for watching! It is crucial for you to address the root cause of your symptoms naturally. We'd love to share more info and know how we can help. Do send us a message m.me/maggieyumd?ref=w14110934
Your family sounds abusive. Abusive families cause health issues especially autoimmune, adhd, etc. It puts too much load on your body especially the nervous system. Search for Gabor Mate, Peter Levine, Teal Swan to help learn how to properly ground yourself and recover from abuse such as gaslighting that you mentioned. Best of luck.
Thank you for watching from Canada! We got tons of trainings and resources about this. Chat with us here, we'd love to know how we can help m.me/maggieyumd?ref=w14110934
I have Long Covid…had Covid 4 x in 16 months. 1st one had pneumonia and was the worst one. All were bad though. Developed POTS symptoms after the first one, only to be brushed off like I was exaggerating or it was anxiety. Last Covid was Dec 2022 and April 2023 ended up in the hospital for 5 days diagnosed with Dysautonomia and still waiting for neurologist appointment next month. Had another episode last week and hospitalized for 3 days. It’s soooooo frustrating!!!!
We so hear you! Thanks for sharing this and for watching the video. We have worked with those who had similar experiences and issues. We'd love to know how we can help. Start a chat with the team here m.me/maggieyumd?ref=w14110934
I was diagnosed with Primary Pulmonary hypertension at age 11 I am 52 now. Was on Coumadin, digoxin, procardia . In my 20’s I had a baby , at the time i was the only patient with my disease to live after having kids I had another child 5 years later. My heart doc thought I didn’t have PPH and messed with my meds. 3 weeks later I was barely hanging on. I’m. Now on Veletri, pump, tracleer during 2nd pregnancy tachycardia started. Then on Diltiazem. My heart guy doubled dig and Diltiazem. After covid my tachycardia changed. I have all the POTS symptoms. Went to special doc to discuss ablation. Took me off digoxin permanently. Im on heart monitor I’ve barely had full episodes to record. Still having PCV’s Going back on diltilazem after. Doc won’t discuss POTS until after meds change and ablation 🤷🏼♀️🤦♀️🤦♀️ I’m so frustrated. My current heart doc said my symptoms are long term covid. My heart is in normal range🤷🏼♀️ Also had emergency Gallbladder surgery and lost part of my colon because of complications. I’ve been losing 1 1/2 pounds a month for the past 6 months with half the activity 🤷🏼♀️
Oh wow, appreciate you sharing all this. Must have been challenging for sure. Many have experience POTS and worse symptoms after the virus! It is crucial for you to address the root cause properly. We'd love to learn more about you and know how we can help. Kindly send us a message here m.me/maggieyumd?ref=w14110934
I have been lightheaded/dizzy everyday for over 6 years and none of my drs have ever been able to figure it out. I’ve seen a family physician, cardiologist, neurologist, etc.. always told everything’s fine. I do have Graves. I passed the tilt table test.. I’m so lightheaded all the time and dizzy, migraines, weakness, fatigue, heart rate jumps frequently.. feel like I’m floating on a boat or a bobble head. So many things and I’m so exhausted of it all.
Yes, we do hear you! We have worked with tons of those who struggled with the same issues. We'd love to share info and know how we can help. Send us a message here at 503-647-4568 with your name.
I know POTS is often an ottoman a man thing, but it’s also related to Ehlers Danlos syndrome. I have POTS and EDS. I’m in Tucson AZ. I was diagnosed with POTS at like 25 and mostly it didn’t affect me too bad until I crashed into menopause at 37 HRT has helped but now in PT to help get back baseline
Thanks for sharing Amanda. It is crucial to address the root cause no matter your diagnosis. You can chat with the team here for more info and resources: m.me/maggieyumd?ref=w14110934
I’ve been suffering with dysautonomia since having Covid in November 21. Had hashimotos previously so this makes sense. Also always had car sickness. This is crazy to hear. The worst for me is the gastroparesis issues.
Hi! Unfortunately Dr. Yu does not do 1 on 1 calls, however the Transform Program does include group calls with her! I would also recommend you to join our facebook group, there is a lot of information and learning there :) facebook.com/groups/transformautoimmune/
Thanks for sharing Alice. Addressing the root cause is crucial in turning these symptoms around and preventing new symptoms from continuing to pop up! We'd love to share more info and see how we can help. Please chat with our team to learn more: m.me/maggieyumd?ref=w14110934
Thank you for watching and for sharing this Janet! What are your top 3 symptoms now? We'd love to know how we can help you. To learn more, you can send us a message here m.me/maggieyumd?ref=w14110934
I do I have several autoimmune. I did tilt test mine jumps 70-90. I have SFPN too but the sweating profusely is horrible. My cardiologist didn’t even think I had this before the tilt test. It’s auto immune. Oh the tilt test was horrible for me neuropathy hit, sweats, tried to keep from passing out so felt faint. I have a lot of allergies too. I was very flexible until my joints swelling and they said seronegative lupus and rheumatoid arthritis and osteoarthritis. I see neurologist, rheumatologist, ENT said blood labs show allergies so I get to see all these different doctors. I’m fully disabled
I hear you, the medical system can be so frustrating. I would love to refer you to this video ruclips.net/user/livedmJNUjnMO_Y on how Candi ended her pain from RA. I would also encourage you to text our team at 503-647-4568 to schedule a call for more help :)
I think you would also find our POTS training helpful drmaggieyu.respond.ontraport.net/training-pots :) How long have you been dealing with all of this?
Thank goodness for this video. I have autoimmune issues along with an Alpha-1 deficiency. I have tried all of these suggestions. In addition to all these symptoms, my biggest problem is methylation. My body holds on to all the toxins and I swell. The doctors said its bloating and I know its not! At this point I'm afraid of food. Doctors overlook the fact that I don't have a gall bladder. And I've had the stomach sphincter fixed. So frustrating!!
We hear you and you are not alone! Thanks for sharing. It is crucial for you to get to the root cause naturally, address it in the right order. We'd love to learn more about you and know how we can help. Do send us a message here m.me/maggieyumd?ref=w14110934
I have been from doctor to doctor these past 3 years on all kinds of medications and supplements. I finally was diagnosed with POTs in July all they did was put me on metoprolol and everyday is awful. Its affecting me as a mother and wife. I'm too tired to function. My heart is always all over the place. I get moments of random panicking and anxiety/adrenaline. They just put me on prozac to help the panicking moments and I can hardly eat anything from it. I just want to go back to normal and feel ok.
I understand, and I appreciate you sharing your experiences. Dealing with POTS and the associated challenges can be incredibly tough. If you're looking for more support and information, you're welcome to join our Facebook group at www.drmaggieyu.com/transform. Feel free to connect with our team for further details through this link: m.me/maggieyumd?ref=w14110934. We're here to assist you on your journey.
I have had all the symptoms, for at least the past 10 years. Mentioned to all my specialists and not one has ever mentioned POTS. I also have Lupus, arthritis, Sjögren’s and no thyroid 😢
Wow.... ridiculous!! Glad you've found our videos, conventional doctors really do not know how to handle autoimmunity. We would love to help you address these conditions further-- get started by live chatting with our team at (503) 647-4568 with your symptoms :)
I am currently being treated by an autonomic neurologist, one of the top pots specialists in the country. It’s definitely the best I felt in the 10 years I’ve had pots, but I’m still not 100% better. My pots began when I was diagnosed with chronic lyme disease and went through rigorous antibiotic treatment. I am also currently being treated for small fiber neuropathy. My Pots is So severe that I have convulsive syncope, which is when my blood pressure gets severely low, and my heart rate gets so high, causing me to collapse into a seizure like episode. I am starting to wonder if my oral contraceptive pill is making my symptoms worse. I am just starting your free training session, and I hope it gives me more insight into what I can do to live a normal life because I am so sick and tired of having to be dependent on others to function.
Hi Riley :) Appreciate you taking the time to share your story... dealing with POTS can be awful. We've had so many alumni who were able to beat it though. I know you're starting off with our free training, but if you would like to learn more about our different programs you are welcome to text us at 503-647-4568! We would love to learn more about you to see how we can further help
Omg! You are so good! My daughter was recently diagnosed with POTS and I never heard of this in my life, also she is going to see a Cardiologist in January 2025 that’s is when she can get in. I am going to forward this podcast to her, thank you! For putting this out there for people who are lost about this disease.
so glad you found this helpful! It's tough navigating a new diagnosis like POTS, especially when it's something unfamiliar. Speak to us live via text at (503) 647-4568
![Felix "Unfair" | [Stray Kids : SKZ-PLAYER]](http://i.ytimg.com/vi/Oswujxm2Ag0/mqdefault.jpg)
Want to learn about the Transform System for Reversing Chronic Disease? Click here: go.drmaggieyu.com/start-now
The blood sugar makes sense - where do you recommend people to start if they eat no carbs / no sugar, but are still navigating all the roving symptoms? Thanks for your time.
@@SpectrumOfChange Hi there, thanks for watching. We'd love to share more info. You can chat with the team here for resources m.me/maggieyumd?ref=w14110934
@@DrMaggieYu hi, thanks so much for the reply. Is there somewhere to chat other than FB/Meta?
@@SpectrumOfChange Yes, you can send us an email at support@drmaggieyu.net or directly book a call with us www.drmaggieyu.com/apply
@@DrMaggieYu thank you
As an scientist specialized in autoimmunity, and as someone who has healed my own 7 autoimmune diseases and has helped thousands of others, we always test the root causes underneath the antibodies. Autoimmunity is always caused by a combination genetics, cellular deficiencies, toxins (both chemical and biologicals) and stress. All of this can be corrected and it’s so doable. The newer scientific root cause testing finds the deeper causes in about 3 weeks. Once found, it’s not difficult to correct root causes. ❤ 😊 ❤ You can feel better.
You're right that you absolutely can feel better! Autoimmunity is not talked about enough in conventional medicine. Dr. Maggie takes on the root cause approach and has developed a 5 pillar protocol for autoimmunity! You can watch her video on he 5 pillar protocol here ruclips.net/video/tINaOsutOPI/видео.html
I cannot thank you enough for this video. My symptoms started as a teenager which became more and more debilitating as I got older and raised a family. I’m 49 and was only diagnosed in 2019. Since I was 20, I’ve been on anti anxiety medication because they thought it was anxiety related.
I’m on meds to lower my pulse, but am now mainly bedridden. My life has been completely upended. Thank you for giving me hope.
We appreciate you watching this Angela and for sharing your issues. To learn more about how to work with us, you can start a chat with us here m.me/maggieyumd?ref=w14110934
Ha! This was like reading my story. Except I think my symptoms probably started at birth. I'm 50 currently. I was on beta blockers (I only had anger management issues) for the high heart rate for years in my late twenties and thirties.
In my thirties I went to the doctors, when I was considering starting a family, because I knew I just could not cope with it because of the constant fatigue. The doctor said I was fine (as they always said), but I still chose not to have children. Ten years later I was vomiting and bed ridden. Been like that for 7 years now.
My experience: beta blockers and calcium channel blockers are contra-indicative. The problems is not the heart rate or the blood pressure spikes. The problem is why the body needs them.
I got really in a bad state with the beta blockers in the end. My body would fight against the disease plus against the beta blockers and exhausted itself to the point that I had like pseudo-Addison's disease with skin tone changes and autoimmune symptoms until I stopped the beta blockers. I knew to stop the calcium blockers after a couple years because they just ended up increasing my heart rate even at rest (got them for muscle tremours and gastric pain - the one caused by lack of blood supply to the gut).
My advice: try reducing the beta blockers and try reducing carbs.
@Sam Hartford how was your heart rate coming off the beta blockers? I'm terrified of ever coming off of mine because I don't want my tachycardia to get worse than it already is.
@@kerrysue9280 I had to do it over a 10-month period for the first time because I was on a really high dose. But I was in a place in my life then when I did not need to move as much and was not under as much stress as before.
Now my heart rate is typically around 95-110 when sitting. It gets into 140-150 only if I do something physically active like go shopping etc.
The problem really was that I needed a higher heart rate in order to have any energy and not lactic acid in my muscles.
But you need to go with what your body needs.
My experience was that my heart rate was not that much lower on beta blockers, although it limited the spikes. It's just that the beta blockers made my body work harder to function normally.
Oh God . I feel the same... Currently on beta blockers. They dont really lower my HR but just stop the spikes. I am afraid to come off of them as I have really bad spikes in my BP and HR. It makes me totally bed ridden😢
I’m seeing this was posted a year ago. Have 3 autoimmunes, been functioning. Had Covid in February, turned my life upside down. I have felt bad since, nausea, I eat to stay alive, no energy. 2 weeks ago went to ER. Blood pressure 60/40, vomiting, dizzy. Just functioning, everybody looks at me like I’m crazy! Praying I can find answers here.
Absolutely, we're glad you found your way to the channel! We have another great resource for you, a community on Facebook filled with other people going through the same thing as you! We invite you to join us ❤️facebook.com/groups/transformautoimmune/
I never got better either. Now I have vasculitis on top of everything else.
Dnrs helped me in 2016 a lot., but any stress and BOOM 💣
Did you get vaccinated Beverly?
Get your f ing adrenals checked along with all your hormone levels
Ibs, adrenal fatigue, high heart rate, estrogen dominate. I have every symptom. I stopped eating sugar, corn and gluten, a relaxed ketogenic diet. Now taking COQ10, vitamin B1( organic nutritional yeast), electrolytes, vit c, fermented foods, pre and pre biotic, parsley, clove,magnesium, vitamin D, castor-oil-packs on my liver, thyroid and kidneys and adrenals, tapping, dry brushing, lymphatic massage and drainage, deep breathing, hitt workout 💪
After 5 months of my protocol I am 85% better, I'm not and won't go to a Dr. I literally asked God what to do.
❤
Really want to ask you about your symptoms. Was told Its NCD neural circuit dizziness, and adrenal fatigue, hot and cold, hot feet and cold,
I don't get car sick never have, but do have shakiness in legs and arms its my nervous system, then feel hot and cold or sweaty, feel off balance but my inner ear issue in sacculus
Sure ask away@@lisagonzalez3861
The same here I think Adrenal fatigue is one of the most problems...I visit Cardiologist...Gastrointestinal and ya nothing wrong...Vitamin B5 for adrenal fatigue help me alot...My headache imrpove and heart rate imrpove...But it takes long time to improve
The first time I experienced my “dizzy spells” was 2003. I fell and hit my head. Over the years I’ve seen multiple cardiologists and psychologists. I’ve been diagnosed with Hashimoto’s, Lupus, and Sjogrens. I recently wore a 30 day heart monitor and I recording over 100 incidents of dizziness. But they told me I didn’t have POTS and wouldn’t give me a table tilt test. It was such a waste of time. I’ve given up on being diagnosed with anything many times because I always get my hopes up and I’m always let down with “we don’t know what’s wrong”.
We hear you Hannah and you are not alone! It is crucial for you to have a root cause based approach process and system to turn around all this. We'd love to share more info about this and know how we can help. Send us a message here m.me/maggieyumd?ref=w14110934
I also suffer from this plz help me
Try finding a teaching hospital near you and schedule an appointment with a resident. There is a lot more passion about their career at that point. Everything they do is reviewed by more experienced doctors. Finding out what's wrong with you is a matter of getting put in front of the right group of specialists. You need to find a doctor who cares and won't dismiss you.
I was at a club, I passed out in the bathroom after only having three drinks 😩 I’ve never passed out before and I’ve had up to 9 drinks and I was fine. After that, it all went downhill and I noticed my coffee addiction made it even worse.
Even I'd you are diagnosed they can't treat it.
"If they don't know how to treat it, it doesn't really exist." That's the key phrase there. ME/CFS and a POTS comorbidity. I'm actually surprised that I wasn't diagnosed with IBS because my guts are messed up. And, yeah, I get horribly motion sick, sometimes just by seeing too much motion.
Thank you for watching Amber. We'd love to get to know you more and see how we can help. Send us a message here to learn more: m.me/maggieyumd?ref=w14110934
This is the first time I’ve seen POTS related to autoimmunity and I’ve been researching the tar out of it for several months now. I’ve had Long Covid for 21 months now and my symptoms are all Dysautonomia/POTS related. I have Hashimoto’s so this is resonating with me for sure. Thank you so much for this education!
Thank you for watching and sharing some of your journey with us Laurel! To learn more about how to work with us, you can start a chat with us here m.me/maggieyumd?ref=w14110934
I have a 14 year old daughter who is suffering with pots and we are based in saudi/England how can we contact you and work with you?
@@raushanali5733 We'd love to know how we can help her! Please send us a message here to learn more to get started m.me/maggieyumd?ref=w14110934
@@DrMaggieYudo we Need to pay for the program
@@siobhancunningham2923 We have a Facebook group that you can join for free where you can see tons of trainings and resources and support from the community. And we also have a paid program. You can send us a message to learn more m.me/maggieyumd?ref=w14110934
I was not diagnosed by my cardiologist, but by a neurologist I was sent to! My BP was 60/40 the first time I saw the neurologist, and he immediately knew!!
i am a therapist
thought i had ms. vegas nerve affected. felt like i was in earthquake and no earthquake happened.
i have 4 pts now. who are told they have ms
its long covid. a
they received ms treatment. it did not wirk
Are you experiencing dizziness, vertigo, fatigue, brain fog, low blood pressure, and fast heart rate? Did you know that you have POTS? Start a chat with our team and tell us more about you, so that we can send over additional resources m.me/maggieyumd?ref=w14110934
I am bedridden with POTS. I develpoed POTS at the beginning of 2019. My guess is maybe chronic stress and long term mold exposure has brought this on.
My body has crashed recently and i am so scared. I am on a beta blocker and thats not controlling my heart rate anymore. Unlike most, my blood pressure is higher rather than lower and my resting heart rate is higher too. My heart increases 50+ beats when i stand.
Its difficult to see a doctor because my POTS keeps me from working.
This video is inspiring and gives me hope that maybe one day i can have a life again. Just have to find a way to make that happen.
There is definitely hope Kerry! You need to address the root cause to have a sustainable recovery. To learn more about how to work with us, you can start a chat with us here m.me/maggieyumd?ref=w14110934
Sending you love and healing energy ✨️ ❤️
@@volvaheidrbores663 That's so kind, thank you so much. I can really use that ❤️
I have similar form of POTS with increase in BP. All signs of hyperadrenergic POTS.
Your comment is almost just like me, I’m now in bed 24/7, it’s terrible I’m on Beta Blocker and it helps my Heart Rate but nothing else
I'm 70 years old and was just diagnosed with POTS yesterday. I have been struggling with irregualar heart beat for several years. I had no idea that it was related to auto immune issues. That is very interesting to me. I have been falling, being dizzy etc. I've been on metoprolol and the issues getting worse. I'm glad there are these other solutions.
I hear you.... glad to see you are finally starting to see what's happening-- definitely autoimmune! You can live chat our team at 503-647-4568 for more information on our programs, we would love to help you address this :)
Hey all! We are inviting you to Dr. Maggie’s FREE live virtual event. Get a chance to meet and work with her in this workshop. Happening this Thursday, Nov 9th 4pm PST/7pm EST.
Register here to join and for more info:
drmaggieyu.respond.ontraport.net/nov-live-event
One year later and Dr. Maggie has completely described my experience with the medical field. Lost our entire savings and still unable to work trying to find a dx. Jumping thru stupid red hoops and fire for insurance. Choosing to pay out of pocket to expedite things only to become more frustrated. Losing precious time with my IVF baby who is now 4 and I have been barely able to function for the past 3 of those 4. The alone was enough to destroy my mental health and nearly make me think about giving up to find relief. Now, finding social media and videos such as these …. I have fought harder than ever, been more direct than ever, and shed more tears than ever to get someone to believe me and know what the hell I am trying to describe and be patient with me while Itell my entire tale or AT LEAST read my symptom journal and research correlations. I’m not seeking drugs, I don’t even ask for pain relievers and just suffer so they take me more seriously. I’m so tired but want to truly LIVE my life.
This is why channels like this are so important alongside doing your best to compare info from various, verified sources…. I’ve become pretty decent at reading medical academic papers and studies lol using my elem ed study practices and a dictionary helps hahaha
And people like you, working so hard dealing with all these symptoms, are exactly why we're here. We'd love to see how we can support you, please get in contact directly with our team by texting 503-647-4568 with your name and symptoms!
So sorry I can completely relate for me it’s been since as young as I can remember 4 years old,
I have was admitted to hospital and just got out 2 days ago after a week.
I actually developed seizures because of it.
Battening the medical bureaucracy is a nightmare.
I even asked for an ambulance report several years ago as I was treated so poorly and they actually put hypochondria!
@@pinapple60 That sounds incredibly tough to deal with. It must be frustrating to encounter such dismissive attitudes from medical professionals. How are you feeling now after your recent hospital stay? We are here to help! Speak to us live via text at (503) 647-4568
at least now you know
you're not alone, you're not crazy, and it's not all in your head!
Thank you all for sharing your stories I learned much more about pots but had to take notes cause of brain fogs
I have 2 young daughters with it. One was diagnosed by a Neurologist & Nuclear Physio Cardiologist, the other by a Pediatric Cardiologist. Neither of their primary doctors knew what was wrong.
Both of their Cardiologists diagnosed them & they both did it right away.
And yes it’s so frustrating when doctors don’t believe them.
I was diagnosed with long haul Covid 3 years ago & told it’s a form of Pots. It’s been on the rise since covid & vax.
Yes we so hear you! We have worked with tons of those who struggled with the same issues. We'd love to share info and know how we can help. Do chat with our team here m.me/maggieyumd?ref=w14110934
Yes I agree, I’m a coeliac and symptoms started after the first and second vaccine. It was sporadic at first but I was told to write it down every time I had a flare up to try and figure out what was going on. Then it finally clicked when the doctors asked last week was I sick or anything that happened around that date? I wasn’t sick and I’ve never had Covid but yes I’d had the vaccine. The doctor I saw last week thinks it’s Pots. It was sporadic at first and now daily. It’s so debilitating
13:45 "Autoimmunity: antibody attacks enzyme in brainstem responsible for creating chemical for balance. "
26:15 Blood - Mineral - Vitamin: Ferritin, Iron and Vitamin B12
28:35 Digestion - Low stomach acid
31:55 Foodmapping - allergies
WOW WOW WOW YOU CAN'T IMAGINE WHAT THIS VIDEO MEANS TO ME. I KNEW I WAS NOT CRAZY EVERY TIME I ASKED DOCTORS TO CHECK MY SUGAR, BECAUSE I WAS SURE THERE WAS A CONNECTION TO MY SYMPTOMS. AFTER BEING TAKING MEDS THAT DON'T WORK AND ARE MAKING ME MORE SICK. I HAVE BEING DEPRESSED AND OUT OF WORK NOT EVEN ABLE TO DRIVE AND STILL WAITING FOR ANSWERS. I WAS WOW ALSO WHEN YOU MENTIONED THE CAR SICKNESS. MY TEANEAGE DAUGHTER IS ALWAYS SICK AND COMPLAINING ABOUT THAT. I COULD KEEP GOING , BUT ONE MORE THING I WANT TO SAY IS : THANK YOU, THANK YOU, THANK YOU. 😊
I’m curious to see how to “end” my POTS…
How ridiculous is Na when POTS is shown to affect RAAS and lowers Na+ reuptake? If we’re losing it, why is it wrong to treat with salt tablets or electrolyte drinks?
I almost want to cry hearing the other people explaining their symptoms. I went 12 years undiagnosed, called hypochondriac, cardiologist said I was too young to have anything wrong but couldn’t explain my idiopathic tachycardia, and lived in fear of strenuous exercise because of my heart and losing my eyesight because of the (silent) migraines that made my optometrist think my retina was detaching. It’s thinning, but it’s still kicking. I didn’t have pain so the fact that my flashing twinkling lights were migraines was lost on us.
The head pounding was the hardest to explain, and went ignored because my resting BP was normal range. It’s so relieving to hear someone else experienced it. I’m not alone 😢
ECG, EKG, eCat monitor, Labetalol, every eye test possible, MRI, MRA, blood tests, and nothing.
The god-sent angel of a Neurologist knew what it was the moment he walked into the room when I was referred. Autoimmune disorders run in my family. It’s interesting to learn all of this.
THANK YOU
We appreciate you sharing this! We have worked with tons of those who struggled with laundry list of POTS symptoms. Please send us a message here to learn more. We'd love to know how we can help m.me/maggieyumd?ref=w14110934
What treatment did you end up using that has helped??
Benfotiamine 150mg for 4 weeks and Celtic salt. All the best 👍
@@superstardj999do you get that medicine OTC??
@@TannerAquatics iherb. Start out low and work way up. Try to cycle out after 6 weeks for a week and see how you feel.
I’m there!!!!! I’ve seen all the specialists you listed and you described EXACTLY how I’ve been treated. No one I know understands me because I “look healthy” but EVERY SINGLE DAY IS A STRUGGLE within. I wish I could see you but I’m in California. Do you have colleagues here you could recommend.
Yes!! This is so common for people struggling with autoimmunity-- oftentimes there are "invisible" symptoms so from an outward perspective you might appear to be fine. All of our programs are online so we can actually help you worldwide! You can live chat with our team at (503) 647-4568 for more information and to get started with us :))
My daughter was a competitive dancer and top of her class. She's 17 and been in bed mostly since 13. She got Covid and got worse. We're been to 9 states trying to get help. She has EDS and Mast cell activation syndrome. She has a PFO too. After Covid she received the monoclonal antibodies and got her life back for 3 months. Then back down after the antibodies wore off. I've talked to FDA and Regeneron pharmaceuticals company that says they are no longer available because they were given on an emergency basis. My daughter is homebound due to car sickness.
Thank you for sharing this Kim. I'm sure this hasn't been an easy journey for you and your daughter. We'd love to know how we can help. Please chat with our team here:
m.me/maggieyumd?ref=w14110934
how is she doing now.
hope she's feeling better or got some help
I am so glad I found this video. I have psoriasis, became lactose intolerant in my late 30's, became hypertensive at 38, i am 44 now. I also developed IBS. About two yeas ago I started experiencing the symptoms of POTs, the dizziness, high pulse rate, headaches, brain fog. Was diagnosed with BPPV a Neurologist and was placed on beta blockers and vertigo drugs. The symptoms disappeared the whole of last year only to return this year with a bang. Its all so frustrating. I find that taking sea salt helps with the symptoms.
We so hear you! And you are not alone. We'd love to share more info about ending POTS naturally and know how we can help. Do send us a message here m.me/maggieyumd?ref=w14110934
Even being hypertensive .sea salt?
@@sheelawal7616 What are your top chronic health issues now? You can chat with the team here for more info m.me/maggieyumd?ref=w14110934
@mary-annosuide942 Wow this is also my case! I have both Psoriasis and POTs. I have been diagnosed with POTs very recently even though Inhad symptoms for years! Starting medications beta blockers also now. Does the POT symptoms really come back suddenly like that?
@@miriamarajaoalisoa7294 Getting to the root cause is the key to have a long term and sustainable recovery with POTS and psoriasis! We'd love to know how we can help you, send us a message here m.me/maggieyumd?ref=w14110934
I've passed out three times. Once while I was driving a car. The paramedics took my BP with the car issue and it was 60/40
Told my Doctor I was pretty sure my issues were happening because I have IBS… she said “no that’s not how it works”
Brought it up to my chiro who does holistic medicine. To which her policy is “everything starts with the gut”
Thank you for watching Monique! You can chat with the team here for more info and resources m.me/maggieyumd?ref=w14110934
p.s. also, yes, the "pass around to the specialists who want you to fit into their narrow knowledge base" is so real.
We hear you Amber! Most conventional doctors often know nothing about these issues. We'd love to share invaluable resources. Chat with our team here for more info: m.me/maggieyumd?ref=w14110934
I have POTS misdiagnose as a panic disorder and now is so hard to get care because all the time they send me to a psychiatrist 😡
What are your top 3 POTS symptoms and challenges now Victoria? Addressing the root cause of the symptoms is the key, it is so crucial. That is what our 5 pillars protocol is about. If you're interested to learn more, send us a chat here m.me/maggieyumd?ref=w14110934
Go see a cardiologist!! And also get tested for hashimotos!!
Got diagnosed with POTS by a cardiologist. Have several other diseases and even more Drs! All of what you are saying makes sense!!!
Yes! Anyone else here needs help with POTS? Do chat with our team and we'd love to share some resources m.me/maggieyumd?ref=w14110934
Since I was a child I experience vertigo, car sickness and severe sea-sickness. I’ve been lactose intolerant since I was 9. Tinnitus appeared in 2014, alopecia areata in 2014 too, IBS in 2017 and vulvodynia in 2018. Since 2-3 years I have vertigo when standing. Three months ago after a virus I have POTS symptoms and my HR goes up to 120 when standing. I have fasciculations. Even my resting HR is higher then before (85-90 bpm when seated in the morning). At the end of this month I will have my Tilt Table Test done. :( . Thank you so much for this HUGE explanation!
Thank you for sharing this and for watching Clara! We'd love to know how we can help. We have worked with tons of those who had the same issues. Send us a message here if you haven't yet for more info m.me/maggieyumd?ref=w14110934
I think you’re me, ha ha
@@thelman4496 We'd love to share more resources! Chat with the team here m.me/maggieyumd?ref=w14110934
@@thelman4496 😅😂
@@claradelcore9405hey
have you got test done
do you have pots ?
Late to the party! Found this video because husband has POTS! But I have MS and now am sticking around to learn more!
We all have so much to learn-- its great when we can learn and share with our loved ones. We would love to help you and your husband address these conditions, text us at (503) 647-4568 to get started with us!
My autoimmune journey started with digestive issues. It took 15 years to get my Celiac diagnosis (after removal of my gallbladder didn’t help). It took 6 years to FINALLY get a POTS diagnosis.
Thanks for sharing! Most of the symptoms you have with digestive issues, Celiac and POTS are connected. The key is to get to the root cause of them and the good news is a diagnosis doesn't matter! We'd love to share with you more info and see how we can best help. Let's connect, chat with us here m.me/maggieyumd?ref=w14110934
Oh my God, i have now just heard about "POTS" and i have 5 of those symptoms, earliest being car sick, since i was a child.
2 and half years ago I had Covid I never recovered many of the symptoms yall mentioned have been a daily fight. It has kept me from returning to work.
Iv been dealing with my heart racing sometimes when I’m doing nothing ,low oxygen ,worst brain fog imaginable.
It really can be an ongoing fight when your symptoms aren't being treated properly. If you want to get to the root cause of your symptoms text our team here at (503) 647-4568, we can absolutely help you address this so you can go back to living!
You hit the nail on the head for me , for years l have been suffering from symptoms, number 1 when l wake up l feel like l have the flu , my voice changed about 10 years ago l was 65 years old l had nerve damage in my left ear oh when l was a child l would get terrible car sickness, especially in the back seat , l have pain problems everywhere, they have diagnosed me with fibromyalgia and chronic fatigue syndrome, l have fluctuations in my blood pressure on high doses of meds l have type 2 diabetes, hypothyroidism , it’s getting worse as l age , l stay sick at my stomach, my mother constantly was taking me to Doctors as a child ,,diagnosed me with a nervous stomach finally at 75 they are giving me a MRI , had a nerve conduction and EMG test that shows carpal tunnel syndrome and pinched nerves , l have numbness throughout my body l am suffering
Oh wow, appreciate you sharing this and you are not alone! We have worked with tons of those who struggled with the same issues. So crucial for you to address the root cause of your symptoms. We'd love to share info and know how we can help. Do send us a message here m.me/maggieyumd?ref=w14110934
Do you think mold toxicity could have something to do with your health issues ?
Nobody but you dr. Said my stomach was linked to it thank you wow
Yes!! Sent to cardiologist. He said it’s normal! It’s been hell. Well after collapsing and hospitalized I finally got attention. It was the allergist who correctly diagnosed it!
Medical gaslighting is hell. Being told it's "normal" whilst dealing with debilitating symptoms is unacceptable. Text our team at 503-647-4568, we would love to offer you some *actual* help with this!
I was diagnosed with Primary Sjogren's Syndrome in August of 2023, but I seriously believe I have undiagnosed POTS along with Sjögren’s being that I've either almost passed out or completely passed out several times this past year. Each time it happened I was standing up only a few minutes, and the area I was standing in whether it was inside a building or outside each was of a comfortable tempature and all I was doing was standing for a few minutes. My doctor's keep referring me to a cardiologist but by my own research I know its POTS. I feel like no one is really listening to me but I know something is wrong because two years ago I could stand up for several hours and be fine, but all of a sudden a year ago I started fainting, or feeling weak, dizzy and nauseous with just standing. I feel defeated, my family label me at lazy but the only time I don't feel sick is when I'm sitting or laying down. It sucks when you know something is off with your body but no one is LISTENING. And its at the point where its getting dangerous, the last time it happened I was at work standing while working and I had to be rushed to the hospital, where I was told I had a mild concussion, apparently when I fainted I hit the back of my head.
And you are not alone! Do you realize that Sjogrens and POTS symptoms are connected. Appreciate you watching and sharing your issues. Chat our team to learn more how to address and get rid of your symptoms m.me/maggieyumd?ref=w14110934
Try see if a chiropractor can help, there is a thing called cervical pots, where the neck being out can cause it too, also get your thyroid checked and get checked for hashimotos!! My daughter has POTS real bad, and her thyroid is so slow, they are testing her for hashimotos now! Poor thing can just sit all day😢 only 21 yrs old😮❤
@FeralFairyRae Wow thank you for your comment!! My thyroid and cervix were both recently checked, and came back normal. I hope your daughter is feeling better while fighting this battle of illness.
@PrettyHazelEyedMLS Thankyou xx glad you got normal results, yes my poor girl, and in Australia they don't test for lymes or treat it, as they don't believe it exists here!!!
@@RAE-homely-fairy-of-the-light WOW!!
I’m in California. Just diagnosed with MCAS and maybe POTs. Hospitalized for collapsing. BP was 67/44. I have high blood pressure and medicated. Doctors told me the light headedness when getting was normal. It’s not. Love your videos. Thank you.
My 24 year son just got diagnosed with this and is going through the workup with cardiologist. We did echo, stress test, and have a heart monitor for 2 weeks.
Glad to hear that you are finding answers for what your son is going through. We have a full POTS training series that you can access here, hopefully it helps in you journey :) drmaggieyu.respond.ontraport.net/training-pots
I live with MS and have lesions on my brain stem. I also now live with PoTS.
I used to get car sick a lot when I was younger too.
Thanks for sharing this Martin and for watching. We have resources about MS and POTS, we have worked with tons of those who struggled with these issues. We'd love to know how we can help. Send us a message m.me/maggieyumd?ref=w14110934
I remember complaining to my doctor about all of the issues I was struggling with and they just kept brushing me aside telling me I was just sleep deprived from technology and have low iron because I’m female. Turns out it’s neither of those, I displayed iron deficiency symptoms from blood pooling and after sitting on iron supplements for quiet some time my symptoms are still prevalent though not drastically. Still not too sure as to what I have but it’s a starting point knowing my illness is an autoimmune problem and not an iron deficiency
Thank you for sharing this. So common to have a novel of symptoms and still get little to no help from doctors. Addressing the root cause is crucial in turning these symptoms around and preventing new symptoms from continuing to pop up! To learn more about how to work with us, you can start a chat with us here m.me/maggieyumd?ref=w14110934
Thank you for all this information. My daughter has been so sick. It sounds like this. She is so dizzy, blind head aches, nauseous, weakness, brain fog, It hit really hard about 2 years ago. She is gluten free. She had to quit working the dizziness was a big problem at her job. She has gone to to ENT, Physical Therapy, Chiropractor, they have her schedule for Cardiologist, and Nuerologist. She had her do the MRI months ago. But doesn't get to see Nuerologist until May. It is terribly scary to watch her go through this. They can't figure out what is wrong. She is streeed from this illness.
Feel free to get in touch with our team at m.me/maggieyumd?ref=w14110934, let's see what we can do to help
I gave the info to my pulmonologist and she seemed almost irritated at me for trying to figure out what’s wrong with myself. I have Multiple Sclerosis, I have long Covid almost didn’t make it in 2021, it’s so scary to not be able to catch your breath I’m scared to be alone.
Oh wow, thanks for sharing this. Must have been tough. We'd love to know how we can help. We have worked with those who had similar issues. Do send us a message here m.me/maggieyumd?ref=w14110934
I been diagnosed with pots I feel like the older I get the worse it gets and I just had a episode last week and it was bad I passed out. At work and i was taken to the hospital I’m having brain frog and my vision is not good and I can’t sit up without and getting dizzy
What if it's mold ? Or lyme ? Both
Thank you so much for this. I finally after many many years finally had Dr do tilt test and got diagnosis of orthostatic hypotension with probable pots. I also have diastolic heart failure and pacemaker for heart block
I'm glad you finally figured out what's going on! Are you still dealing with symptoms from these conditions?
It’s crazy this video I have just come upon was a lightbulb moment! 4 months ago I went to the ER after getting dizzy and neauseous and car and boat sick on a Holyday, after non being boat or car sick.. all my tests turned out normal.. 4 months later I’ve had a recurrence for the past week when I’m standing too long I’m fatigued dizzy lightheaded.. when I eat I feel sick.. when I’m exerting myself I feel dizzy.. all my tests from GP come back normal.. in my deep dive into my symptoms nothing was 100% then on a video my Dr. Axe talking about IBS Potts was mentioned in passing and a big flag went to I started researching pottts and it literally fit into all my symptoms, except the last time this happened I had the car sickness and boat sickness and then watching this video you mentioned it as one of the warning signs and boom 💥 it all fits together!
Glad you found this video and thank you for sharing this! We'd love to share more info and resources about POTS. Chat with our team here to learn more m.me/maggieyumd?ref=w14110934 It is really crucial for you to address the root cause of the symptoms naturally
Wow this program is great
My 20 year-old was diagnosed with POTS. Symptoms are SO SEVERE. Tilt table test: passed out and systolic number of blood pressure was 60! Immediately given meds but she was only ok after saline IV at hospital. She was great day one. She is back to incredibly weak.
My first child, age 27 ALSO has POTS, but was not diagnosed. She was diagnosed with RA.
I have hypothyroidism and had a SCAD heart attack last year (at age 57).
Thank you for sharing that with us Chris and we hear you. It is crucial to get to the root cause to really understand what is going on. You can start a chat with us here for more info: m.me/maggieyumd?ref=w14110934
Ive passed 2 stress tests lol My cardiologist told me I have anxiety and I need antidepressants. I've seen ears and throat doctors. I get car sickness. I don't deal with motion well anymore. Nausea is a big problem right now and dizziness along with heart rate skyrocket after standing.
Must have been challenging, thanks for sharing. Meds and pills are not a long term solution and only make the symptoms worse. We'd love to share more info and know how we can help. Send us a message here m.me/maggieyumd?ref=w14110934
Yes, I have had these symptoms. Vestibular migraines and Meniere's. My heartrate can go up when I am standing a while. I get carsick. Very dry eyes. My ANA was negative,
Must have been challenging and you are not alone! Thanks for sharing. We'd love to share more info about turning these symptoms around and know how we can help. Chat with our team m.me/maggieyumd?ref=w14110934
@ Dr. Maggie Yu -----------
Excellent presentation. Thank you very much for sharing your thoughts, knowledge, experiences.
And we appreciate you watching! Glad you found this helpful. You can always chat with our team here to learn more m.me/maggieyumd?ref=w14110934
Everything you said is hitting home
Thank you SO much for this video! I’m only 3 minutes in ( 3:24 ) and already feel so validated. I’ve been working with a ophthalmologist and he’s the one who very strongly thinks I may have POTS. My next step is to see a rheumatologist, but I’m just researching in the meantime. Thanks for this ❤
I'm glad you enjoyed it :) Half of the battle is feeling seen and finding hope. I'm glad to see that you're taking your health into your own hands and taking steps to learn more. You can always live chat with our team at (503) 647-4568, we would love to redirect you to more resources!
I've had Hashimotos for 22 years and my bizarre symptoms have increased dramatically in the last two years (I just turned 48.) I am just learning I have POTS (I think I've had it for years and just didn't know) through a conversation with my functional doctor about how I "have issues with my salt" and "I'm just so dizzy and my heart pounds." I had NO idea. Now...I'm ravaging information to help me. This is 100% debilitating and I am SICK of having to "be in bed." I am angry and I want to get better.
Thank you for sharing that with us Belinda. Addressing the root cause is crucial in turning these symptoms around and preventing new symptoms from continuing to pop up! We'd love to know how we can help her! Please send us a message here to learn more to get started m.me/maggieyumd?ref=w14110934
Hope you're feeling better
I have POTS as do my kids. My 17 year old son has been terribly suffering with debilitating exhaustion since puberty. We have been to SO many specialists. No one put the POTS to the exhaustion. I have been pushing 2 liters of water and Electrolyte pills for a few days, HUGE difference with just that. I have made a huge dent in my autoimmune with figuring out trigger foods, grains, legumes, sugar (including maple or honey), nightshade, lactose, eggs, onions, etc, and healing my gut and eating to keep my blood sugar balanced.
Thanks for sharing some of your journey with us. Unfortunately, most conventional doctors often know nothing about these issues. Addressing the root cause is crucial in turning these symptoms around. We'd love to share more info and helpful resources. Chat with our team here to learn more:
m.me/maggieyumd?ref=w14110934
I’m in the uk, I found this hugely interesting, thank you. Luckily I was referred to a specialist in POTS from my cardiologist. My specialist has told me about trying a wheat free diet as my daughter is wheat intolerant and my other daughter is lactose intolerant. I’m going to start keeping a diary.
Thank you for watching Carol! It is so crucial to address the root cause no matter what your diagnosis is. We'd love to share more info with you. Chat with our team to learn more: m.me/maggieyumd?ref=w14110934
Omg...i need to book a call...this maybe what my youngest has- constantly dizzy, car sicknesses, cluster headaches, insominia, has to pace or lay down ...has over 12 specialists...he gets better than he gets worse
Hi, have you tried the program?
I'm truly sorry to hear about your youngest's health struggles-constant dizziness, car sickness, cluster headaches, insomnia, and the need to pace or lay down. It sounds incredibly challenging. If you're interested in learning more about how we can help address these symptoms, please start a chat with us here: m.me/maggieyumd?ref=w14110934.
We're here to provide support and guidance.
@cheyrider2Chey not yet. I just watched this video so I need to reach out to them.
Great to hear that you've watched the videos! We're here to provide support and insights tailored to your specific needs.@@profmj7630
Finally a great doctor, thank you! I’ve found healing in Acupunture - if you’re unable to get to any helpful doctor then it may be an option for you.
Thanks for watching Stephanie! If you want to learn more, you can chat with us here m.me/maggieyumd?ref=w14110934
Wow you are spot on with the experience 👏Never connected gut issues or blood sugar issues-wow
Thanks for watching Vicky! If you're dealing with POTS symptoms and interested to learn more, you can send us a message here m.me/maggieyumd?ref=w14110934
@@DrMaggieYu Indeed I am- Hope to connect soon! Thank you!!!
@@vickydittfield9822 We're looking forward to it!
trying to get a diagnosis, this is sooo true
We'd love to share info and know how we can help you. Send us a message here m.me/maggieyumd?ref=w14110934
Yes
I was diagnosed with pots and have Rheumatoid arthritis . Was told to go to a cardiologist.
We'd love to share info about ending POTS and RA and how they are connected. Send us a message here m.me/maggieyumd?ref=w14110934
POTS & hEDS for me. Ignored/dismissed by conventional medicine then finally diagnosed at age 45, after 3+ decades of suffering. Anyone else flattened for days by any form of moderate or intense exercise? If I do anything more than a short walk or a 10 min bike ride, I’m bedridden with a flare that includes full brain fog/shutdown. Weight toning completely out of the question (which is tough since we need to tone muscles for bone health). Please tell me I’m not alone on this front!
Appreciate you sharing some of your journey with us, Wendy. It is really challenging, but you are not alone. And what you need is to address the root cause. Dr. Maggie has worked with tons of those who struggled with these issues and they were able to get their life back. To learn more about how to work with us, you can start a chat with us here m.me/maggieyumd?ref=w14110934
My son was diagnosed (by 2 different doctors) with POTS. But I’m confused because labs show that he does not have an auto immune disorder……His worse symptoms are Insomnia, brain fog, a restless leg syndrome feeling all over his body, and heart racing.
It is crucial to address the root cause regardless of what the diagnosis is or if he doesn't have one. To learn more about turning around chronic symptoms naturally. Send us a message here m.me/maggieyumd?ref=w14110934
I am long c, long Lyme, celiac w gut dysbiosis, was pre med studied this 2 years.. it's possible to have an autoimmune+ be asymptomatic (no signs).. took 6yrs to dx me w celiac! Yr GUT IS yr health, may wish to get a blood celiac + an ana test to check subclass igg, igm, ige,
.this Dr is spot on w gut /auto dx info🙏❤️
@@brendabrenner2891 It's great that you're proactive about your health. If you're interested in exploring ways to address autoimmune conditions and gut health, you can initiate a chat with us here: m.me/maggieyumd?ref=w14110934.
We're here to provide more information and support based on your specific needs.
I have Ehlers Danlos and all of the symptoms of POTS. My cardiologist found that I had heart arrhythmia, but know one could explain the nauseous, weakness, and dizziness.
Thanks for watching Victoria! The problem is that the conventional way doesn’t properly address these issues. We'd love to share more info and see how we can help. Chat with our team to learn more: m.me/maggieyumd?ref=w14110934
I had low blood sugar as a teenager. Later Post vaccines fibromyalgia. Then POTS. I am lactose intolerant. CFS, Migraines, chronic fatigue....
That sounds like a lot to deal with :(( Chat with our team at (503) 647-4568, we can definitely help you address these! You should also check out our POTS training series here drmaggieyu.respond.ontraport.net/training-pots!
What are the supplements ladies??
I went carnivore (with raw milk) and my life got exponentially better. Gave up all plant foods. Who knew? Seems to be helping quite a few people so maybe worth trying? Need to really make sure your nutrient deficiencies are addressed and the nervous system. Also doing coherent breathing (and light Buteyko breathing). Getting rid of toxins and poisons too. Good luck!
@@lr1732 That's great 👍 👌 meat is wonderful!!!♡♡♡
You have just told the story of my life for the last three years. Dr after Dr and a trip to Mayo and an outside cardiologist. Last visit to the cartiologist and a heart monitor. I knew I was having Tachycardia.
The Dr confirmed that and told me something in my body is causing it and he did not know what was causing it. Sent me home with no diagnosis and no medicine. The next week my heart was doing something different. It was a different feeling. Got my cardia mobile out and I was in AFib. I couple days later passed out in the middle of the night in the kitchen. Drs are not willing to help people that have been Vaccine injured. I have given up on doctors.
You're NOT alone, so many people are struggling with the exact same thing. Send a text to 503-647-4568 with your name and what you're struggling with, we'll get you the help you need.
this is phenomenal info! thank you ♡
Thank you for watching Joni. We'd love to share more info and additional resources with you. Be sure to send our team a message here to learn more: m.me/maggieyumd?ref=w14110934
@@DrMaggieYu help me🙏🏻 I live in Guatemala, my daugther has POTS , diagnose 2 weeks ago, by a cardiólogo, his 1 patient
The Dr gave her antidepresion pills and pills for blod presure
I have fluxuations in blood pressure that goes scary high like 240/169 and racing heart rate and after several ER visit been told im having an anxiety attack ! Soooo wrong !
And you are not alone in that experience! Most regular doctors often know nothing about finding out the root cause of these symptoms like POTS. We'd love to learn more about your everyday challenges. Chat with us here m.me/maggieyumd?ref=w14110934
Same! You are not alone.
That is a very high BP. I have white coat hypertension but never have had that high. Hope you can get it under control
This is me and it started for me after the birth of my twins. Thankfully I haven’t passed out but every time I bend over and stand back upright or get up from off the floor is when I get extremely dizzy. Scheduled to get a pots test finally after 9 years. I also get the vibrating sensations and when I first experienced right after the birth of my twins my Dr wanted to admit me. 😔
I also noticed it was related to my blood sugar based on various diets I’ve tried and how it would become worse with them.
Yes! Bloog Sugar balance is really crucial to this and also having the right food test just like Dr Maggie's Food mapping which is unique to the program. All of these aspects are crucial to turning around POTS and other health challenges We'd love to share more info and how we can help. Chat us here to learn more m.me/maggieyumd?ref=w14110934
I've been having symptoms of illness as long as I can remember but since Feb 2020 is when the severe dizziness, fatigue, and fainting. They diagnosed me with PoTS in Jan 2021.. I did the compression, I did the heart lowering meds, I did the salt and water.. nothing helped and the meds made me faint even more. Its been awful and I'm completely disabled (90% bedridden). It is super interesting to hear you say stuff about the adrenal gland (and others) because I ended up in the hospital recently my symptoms were so bad and my doctor there noticed some minor things off with my blood work that doctors have been missing since this all started. My cortisol is messed up (for those who dunno that is produced in the adrenal gland) and my hemoglobin is high (I'm trans so if I were still taking testosterone it would actually be a normal level but I haven't been on T since before I got sick so she was like other doctors should have noticed this if they'd actually just given a shit about you). It's a whirlwind but I feel like maybe I'm finally on the road towards getting better because of her.
Thankfully I am in Canada so it was not thousands and thousands of dollars but it does take months to see any specialist and then months to get any tests that are "more complicated" than blood work. I just want to be a normal functioning human being so that I can go swimming, biking, hiking, and rescue doggies.
Interesting I am gluten intolerant or celiac maybe but I also have an egg issue where I can have like potato salad or eggs baked into something but if I eat actual scrambled eggs I get sick too. I've never heard of anyone else having an issue with eggs!
@@beepboop27 Hey there, thank you for sharing this and for watching our video! You are not alone in this experience. And it can be really challenging to deal with POTS and other chronic symptoms. It is crucial to get to the root cause, address them naturally and properly. That is the key. If you want to learn more about this and have the knowledge to reverse your symptoms. Please send us a message here m.me/maggieyumd?ref=w14110934
After months of health centre visits, they kept saying "you're fine, its anxiety just take deep breaths'' We then went to general doctors, they did blood tests over and over. I saw a cardiologist, did an ecg and echo, he said I had a murmur, I need surgery maybe in 5 years. I was added to a cardiac clinic, the doctor ran an ecg, echo, ultrasound, then I was FINALLY diagnosed with POTS. Im only 15, at the time I was 14 and it was so bad, I missed school for weeks. I suffer with chest pain, motion sickness, dizziness, darkening vision, nausea, extreme fatigue, tachycardia, low blood pressure, I feel faintish if I stand for too long.
Brain fog, so bad sometimes I forget what I did and ate in the morning. Numbness in my hands and feet sometimes, abdominal cramps. Headaches
@@Renelle2007 Appreciate you sharing that with Renelle. So many suffer for years being told it's all in their heads and their labs are normal, all the while your symptoms are worsening. Our team would love to know how we can help. Start a chat with our team here for more info: m.me/maggieyumd?ref=w14110934
Same for me! Did it get any better?
This just happened to me in my cardiologists office. they checked my bp in the sitting position (I was fine), then the nurse asked me to lay down on the exam table. Within 15 seconds I went into tachy at 180 bpm, bp shot up to 210/110, whole body went into a sympathetic state. Had to take every one of my emergency cardiac meds right there. The doctor said it was related to my mast cell activation, but never said a work about blood sugar dysregulation. Now after viewing a few of Dr. Maggie's videos on POT's, I realize that I have POTS and have no one has ever mentioned this issue as being a possible reason for my symptoms related to changes in my body position, especially when I lay down or get up too quickly.
It sounds like a very intense and scary situation. Based on your symptoms, it does seem like POTS could be playing a role, especially with the changes in your heart rate and blood pressure with position changes. It's great that you've found our videos helpful in identifying this. Speak to us live via text at (503) 647-4568
Massachusetts. Lyme, Hashimoto, and now POTS
Hi! Thank you for watching. Most symptoms of Lyme, Hashimotos and POTS are connected and it is crucial to find out the root cause and address them. We have helped many people turn around these kinds of health challenges. If you're interested to learn more, chat with us here m.me/maggieyumd?ref=w14110934
I was diagnosed with it. Two days ago. I was so sick they took 3 months to find out.
What can you say are your top 3 symptoms and challenges now? We'd like to learn more about it and share specific resources. Send us a message so we can connect m.me/maggieyumd?ref=w14110934
your a LEGEND Dr Maggie
Thank you for watching! You can chat with our team here to learn how to work with us m.me/maggieyumd?ref=w14110934
I got POTS after my Covid vaccine. Also developed GPCR autoantibodies. So it’s definitely autoimmune.
Thank you for sharing. It's really challenging but you are not alone. We'd love to know how we can help. You can chat with the team here for more info: m.me/maggieyumd?ref=w14110934
Me too. All my symptoms including severe “MCAS” like anaphylactic reactions to foods that I was fine with only the day before…started 5mins after the first and only jab. Starting with pounding heart heat flush and left side paralysis. intermittent paralysis after certain foods or stress to the body of any kind continued, intermittent drooling and crazy dry mouth, breathing pattern completely turned to manual, had to concentrate on breathing or just suffocate and pass out. Racing heart panic attacks 8hrs at a time waking up in the middle of the night with adrenaline and heart at 200bpm, 200”doctors” and it “must be anxiety” 😂… one year housebound while living overseas unable to work too sick to get on a train let alone a plane. Embassy staff laughing at me not saying you’re crazy but the pandemic was just a stressful time for everyone… now go get your second shot! I didn’t have any signs of autoimmunity before the shot, so it would have been ideal for someone to stick me in a lab and study what the exact mechanism was to educate and help all the people suffering now and those who WILL suffer in the future and when it’s these uneducated lazy ass doctors’ kids or grandkids they’re gonna be PISSED they didn’t take me up on my offer to be thrown in a lab to get the hell out in front of this before it became THEIR life and their problem. I still only eat 5foods preparing every meal everyday while working 3jobs to try to pay back debt. The only reason I can walk or work is due to finding an acupuncturist who really understands the root cause. I don’t know how it works but it does!! Still many substances throw me into POTS and anaphylaxis that I never had before even perfume candles grass …but if I am careful to avoid potential triggers I can function and am truly grateful. Now I know the truth and will never have to be at the mercy of mainstream shitty “medicine.” Completely drug free 🎉
My friend did too. It has completely upended her life. Crimes against humanity.
That happened to me! I had T cell mediated cytokinestorm after covid vaccine. Developed POTS and have antibodies to g protein cuppled receptor too.
I pray Dr. Yu will help me 🙏
Speak to us live via text at (503) 647-4568
With tachycardia ended up at ER got admitted overnight extensive tests nothing wrong with the heart sent home and told+me follow the cardiologist. Now I’m taking digestive enzymes and not much episodes.
Must have been challenging. We got tons of resources about POTS and tachychardia in our Facebook group, you can join here www.drmaggieyu.com/transform you can also start a chat with the team here m.me/maggieyumd?ref=w14110934
Thank you ! You are very passionate for what you do Dr. Yu and I will transform my health with your help naturally I’m 77 yrs. Old and never been on any pharmaceutical drugs.
@@vartvartan7492 Glad you found this video! :)
I’ve just been diagnosed and I’m going to make you my first stop. I want to blog this in my podcast too.
That's amazing to hear that you want to share your journey on your blog and podcast! Your openness can bring comfort and support to others going through similar experiences.
If you need more information or have any questions, feel free to reach out to us at m.me/maggieyumd?ref=w14110934
Hey I'm 17 I get dizzy when I stand up I'm always very have very low energy and and extremely bad memory a focus and I'm I'm underweight.
(I was also sent to a cardiologist and was told everything is fine)The doctor to my blood pressure laying down then sitting up then standing and said I have low blood pressure I think he said pots but I'm not sure. He told me to eat a lot of salt and maybe take vitamin d and that's about it! My life has been hell for a long time, I'm even out of school currently! I've takin b vitamins and iron but then my heart was racing and I didn't feel like it was really helping so I stopped. (idk if this has to do with anything but I went on a diet with a lot of meat fish eggs and that's when my memory was the worst)
so if God was so kind to me to put this in front of your eyes plz tell me what I should do next be my family thinks I'm psychotic and Its all anxiety and I'm just a lazy fck.
So if you can tell me who I should see/or do/or eat, or supplement with it's would be a life changer!
Thanks for sharing and for watching! It is crucial for you to address the root cause of your symptoms naturally. We'd love to share more info and know how we can help. Do send us a message m.me/maggieyumd?ref=w14110934
Your family sounds abusive. Abusive families cause health issues especially autoimmune, adhd, etc. It puts too much load on your body especially the nervous system. Search for Gabor Mate, Peter Levine, Teal Swan to help learn how to properly ground yourself and recover from abuse such as gaslighting that you mentioned. Best of luck.
I messaged you because I am READY to get some actual answers to my POTS. 🙏🏻
POTS and MCAS living in Canada Toronto
Thank you for watching from Canada! We got tons of trainings and resources about this. Chat with us here, we'd love to know how we can help m.me/maggieyumd?ref=w14110934
I have Long Covid…had Covid 4 x in 16 months. 1st one had pneumonia and was the worst one. All were bad though. Developed POTS symptoms after the first one, only to be brushed off like I was exaggerating or it was anxiety. Last Covid was Dec 2022 and April 2023 ended up in the hospital for 5 days diagnosed with Dysautonomia and still waiting for neurologist appointment next month. Had another episode last week and hospitalized for 3 days. It’s soooooo frustrating!!!!
We so hear you! Thanks for sharing this and for watching the video. We have worked with those who had similar experiences and issues. We'd love to know how we can help. Start a chat with the team here m.me/maggieyumd?ref=w14110934
I was diagnosed with Primary Pulmonary hypertension at age 11 I am 52 now. Was on Coumadin, digoxin, procardia . In my 20’s I had a baby , at the time i was the only patient with my disease to live after having kids I had another child 5 years later. My heart doc thought I didn’t have PPH and messed with my meds. 3 weeks later I was barely hanging on. I’m. Now on Veletri, pump, tracleer during 2nd pregnancy tachycardia started. Then on Diltiazem. My heart guy doubled dig and Diltiazem. After covid my tachycardia changed. I have all the POTS symptoms. Went to special doc to discuss ablation. Took me off digoxin permanently. Im on heart monitor I’ve barely had full episodes to record. Still having PCV’s Going back on diltilazem after. Doc won’t discuss POTS until after meds change and ablation 🤷🏼♀️🤦♀️🤦♀️ I’m so frustrated. My current heart doc said my symptoms are long term covid. My heart is in normal range🤷🏼♀️ Also had emergency Gallbladder surgery and lost part of my colon because of complications. I’ve been losing 1 1/2 pounds a month for the past 6 months with half the activity 🤷🏼♀️
Oh wow, appreciate you sharing all this. Must have been challenging for sure. Many have experience POTS and worse symptoms after the virus! It is crucial for you to address the root cause properly. We'd love to learn more about you and know how we can help. Kindly send us a message here m.me/maggieyumd?ref=w14110934
I have been lightheaded/dizzy everyday for over 6 years and none of my drs have ever been able to figure it out. I’ve seen a family physician, cardiologist, neurologist, etc.. always told everything’s fine. I do have Graves. I passed the tilt table test.. I’m so lightheaded all the time and dizzy, migraines, weakness, fatigue, heart rate jumps frequently.. feel like I’m floating on a boat or a bobble head. So many things and I’m so exhausted of it all.
Yes, we do hear you! We have worked with tons of those who struggled with the same issues. We'd love to share info and know how we can help. Send us a message here at 503-647-4568 with your name.
I know POTS is often an ottoman a man thing, but it’s also related to Ehlers Danlos syndrome. I have POTS and EDS. I’m in Tucson AZ. I was diagnosed with POTS at like 25 and mostly it didn’t affect me too bad until I crashed into menopause at 37 HRT has helped but now in PT to help get back baseline
Thanks for sharing Amanda. It is crucial to address the root cause no matter your diagnosis. You can chat with the team here for more info and resources: m.me/maggieyumd?ref=w14110934
I akso suffer from this plz help me
@@SAURABHSINGH-rm5xf Send us a message here so we know how we can help m.me/maggieyumd?ref=w14110934
Says msg link is broken.. have android phone.. agree w u ioo ❤
@@brendabrenner2891 If you're on Facebook, do join our group and community to see tons of resources and trainings www.drmaggieyu.com/transform
I’ve been suffering with dysautonomia since having Covid in November 21. Had hashimotos previously so this makes sense. Also always had car sickness. This is crazy to hear. The worst for me is the gastroparesis issues.
Can we see you as a doc via video. I’m desperate for help. I’ve been to 26 specialists since my long Covid diagnosis of dysautonomia.
I’m on disability and highly suicidal from this. It’s been 33 months and I can’t function. Please please help me.
Hi! Unfortunately Dr. Yu does not do 1 on 1 calls, however the Transform Program does include group calls with her! I would also recommend you to join our facebook group, there is a lot of information and learning there :) facebook.com/groups/transformautoimmune/
Would also like to refer you to this video ruclips.net/user/liveozwl-iUgT1U?si=xQyxLqGAYNSCtHjK
I have many symptoms was diagnosed by heart dr but recommends a special dr for it
Thanks for sharing Alice. Addressing the root cause is crucial in turning these symptoms around and preventing new symptoms from continuing to pop up! We'd love to share more info and see how we can help. Please chat with our team to learn more: m.me/maggieyumd?ref=w14110934
I went to several Dr.’s and had several tests before being diagnosed.
Thank you for watching and for sharing this Janet! What are your top 3 symptoms now? We'd love to know how we can help you. To learn more, you can send us a message here m.me/maggieyumd?ref=w14110934
Grateful granny appreciate information 🙏 ❤️ hugs from Az
Thank you for watching Laura! To learn more about Dr. Maggie's root cause approach, start a chat with our team here: m.me/maggieyumd?ref=w14110934
I do I have several autoimmune. I did tilt test mine jumps 70-90. I have SFPN too but the sweating profusely is horrible. My cardiologist didn’t even think I had this before the tilt test. It’s auto immune. Oh the tilt test was horrible for me neuropathy hit, sweats, tried to keep from passing out so felt faint. I have a lot of allergies too. I was very flexible until my joints swelling and they said seronegative lupus and rheumatoid arthritis and osteoarthritis. I see neurologist, rheumatologist, ENT said blood labs show allergies so I get to see all these different doctors. I’m fully disabled
I hear you, the medical system can be so frustrating. I would love to refer you to this video ruclips.net/user/livedmJNUjnMO_Y on how Candi ended her pain from RA. I would also encourage you to text our team at 503-647-4568 to schedule a call for more help :)
Midodrine is helpful for the fainting, or the blackening vision and muted hearing that happens 3 seconds after we stand up.
I think you would also find our POTS training helpful drmaggieyu.respond.ontraport.net/training-pots :) How long have you been dealing with all of this?
Tell us how to deal with it
We'd love to know how we can help! Speak to us live via text at (503) 647-4568
Thank goodness for this video. I have autoimmune issues along with an Alpha-1 deficiency. I have tried all of these suggestions. In addition to all these symptoms, my biggest problem is methylation. My body holds on to all the toxins and I swell. The doctors said its bloating and I know its not! At this point I'm afraid of food. Doctors overlook the fact that I don't have a gall bladder. And I've had the stomach sphincter fixed. So frustrating!!
We hear you and you are not alone! Thanks for sharing. It is crucial for you to get to the root cause naturally, address it in the right order. We'd love to learn more about you and know how we can help. Do send us a message here m.me/maggieyumd?ref=w14110934
I have been from doctor to doctor these past 3 years on all kinds of medications and supplements. I finally was diagnosed with POTs in July all they did was put me on metoprolol and everyday is awful. Its affecting me as a mother and wife. I'm too tired to function. My heart is always all over the place. I get moments of random panicking and anxiety/adrenaline. They just put me on prozac to help the panicking moments and I can hardly eat anything from it. I just want to go back to normal and feel ok.
I understand, and I appreciate you sharing your experiences. Dealing with POTS and the associated challenges can be incredibly tough. If you're looking for more support and information, you're welcome to join our Facebook group at www.drmaggieyu.com/transform. Feel free to connect with our team for further details through this link: m.me/maggieyumd?ref=w14110934. We're here to assist you on your journey.
Who should you see
I have had all the symptoms, for at least the past 10 years. Mentioned to all my specialists and not one has ever mentioned POTS. I also have Lupus, arthritis, Sjögren’s and no thyroid 😢
Wow.... ridiculous!! Glad you've found our videos, conventional doctors really do not know how to handle autoimmunity. We would love to help you address these conditions further-- get started by live chatting with our team at (503) 647-4568 with your symptoms :)
I am currently being treated by an autonomic neurologist, one of the top pots specialists in the country. It’s definitely the best I felt in the 10 years I’ve had pots, but I’m still not 100% better. My pots began when I was diagnosed with chronic lyme disease and went through rigorous antibiotic treatment. I am also currently being treated for small fiber neuropathy. My Pots is So severe that I have convulsive syncope, which is when my blood pressure gets severely low, and my heart rate gets so high, causing me to collapse into a seizure like episode. I am starting to wonder if my oral contraceptive pill is making my symptoms worse. I am just starting your free training session, and I hope it gives me more insight into what I can do to live a normal life because I am so sick and tired of having to be dependent on others to function.
Hi Riley :) Appreciate you taking the time to share your story... dealing with POTS can be awful. We've had so many alumni who were able to beat it though. I know you're starting off with our free training, but if you would like to learn more about our different programs you are welcome to text us at 503-647-4568! We would love to learn more about you to see how we can further help
POTS is like a gift that keeps on giving for big pharma.
There’s not any drugs that work work well for POTS
Omg! You are so good! My daughter was recently diagnosed with POTS and I never heard of this in my life, also she is going to see a Cardiologist in January 2025 that’s is when she can get in. I am going to forward this podcast to her, thank you! For putting this out there for people who are lost about this disease.
so glad you found this helpful! It's tough navigating a new diagnosis like POTS, especially when it's something unfamiliar. Speak to us live via text at (503) 647-4568