As you were listing the 'not normal symptons' I was wondering who the hell would be able to do things like sports, have regular bowel movements on your period, and be able to live your normal life. I didn't even really know that was possible
I have endometriosis, thoracic specifically. It is such a difficult situation. It took me nearly 5 years to get a diagnosis. I am on year 11 now. Thanks for sharing this information with the world. Lots of women are suffering silently.
Yea I had a doctor tell me it was pretty much nothing gave my hormones and pain told me to move on but something didn't feel right I went to other doctors come to find out I had this I'm on year 3
I’m pretty damn sure I have endometriosis, I’ve been stabbed before and the feeling is almost completely the same! The pain is so intense it caused me to throw up when I was younger (I’ve trained myself to not anymore) and when I rest I’ll stay asleep for almost 24 hours. I really don’t want surgery for just for someone to confirm it because everyone in my life has seen me breakdown from pain at least once. They freak out and want me to go to the ER and I have to explain to them I’m not actually dying this is just the way my period is.
I went to the ER a couple days ago because of my period pain. I almost passed out on the bathroom floor because of it. I actually I had an organ rupture. There was a moment of "oh my god, I'm going to die". That's what it finally took for my doctor to even be okay with doing an ultrasound on me. It's so, so frustrating.
Get the surgery to clean out the endometriosis if possible. You get a few years without pain afterwards. Or start the anti inflammatory diet. Fasting, exercise...all the other things to help the pain be tolerable.
This is really off-topic, but I legit thought you were Reese Witherspoon, and I was excited that she was raising awareness about endometriosis. You're still lovely, and I appreciate you discussing this!
I'm 16 and I have extreme period cramps where I take 4-6 ibuprofen pills to help with pain(2-3 at a time until pain comes back), I have diarrhea and I throw up. I end up not eating the first few days of my period because of the pain, if I eat I throw up. My periods also normally last 12-14 days. My last period lasted 16 days. My mom says that some people are like that and not to worry. This has been going on since a year or 2 after I got my first period around 10 yrs old.
It's definitely not normal. It may be her normal because there seems to be familial similarities and cramps and issues can be common, but it doesn't make it normal. I'm so sorry you aren't being heard when you're suffering. See if you can provide your mom videos that you find to educate her so that you can advocate for yourself. Work on her to get her to take you to a Dr to begin the process of getting treatment that can help. I'm 43 & wish I had advocated for myself sooner. Luckily for me the likely fertility issues weren't a problem since I've never tried having kids, but at your age you really don't know how that journey for a future family will go so you don't want damage in case you choose to have kids one day. Per my research, EXPERT surgical excision is definitely the gold standard treatment. For me, birth control has never been helpful to significantly help symptoms and caused side effects of its own. I wish I had known sooner to advocate for myself.
I have the exact same symptoms as you except for the heavy bleeding mine usually last for 5-6 days and i have medium flow, but the cramps are unbearable, I barely eat anything when im on my period like 1 meal a day and that too in small portions. I am afraid of vomitting and making the cramps worse.
I had an investigstion last year into the problems I have with excessive pain and mood swings, I usually have a day or two off work each month because the pain gets too much. I get lower back pain, hip and leg pain, migraines, cramps and spasms, and I get an excruciating sharp pain in the lower left of my abdomen. I nearly called an ambulance the first time I felt it. And the mood swings, well, I feel like a different person. I ususlly isolate myself if I can, because I become so nasty and erratic. I saw a 'specislist' about it last year, was told my ovaries are 'enlarged' but there was nothing to worry about and until I decide I want children they won't do anything. Didn't care in the slightest that my life self destructs every month, I miss work, and feel pain that literally puts me on the floor. I left that appointment feeling invisible. Like I don't matter. Unless of course I want to reproduce, then I matter a bit more. But until then I have basically been told to suffer in silence.
You aren't invisible. I see you. Endometriosis is a fully reversible condition. It is mostly caused by a high-carbohydrate diet. Carbs = inflamation + insulin = hormone disruption = endometriosis Fastest and safest way to completely reverse endometriosis is to stop eating carbs. In other words, try the carnivore (or keto) diet for three months. I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days. Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility. You don't need to be on birth control. You don't need surgery. You don't need to live with that pain and suffering. Change your diet and in 90 days you'll feel like you have a completely different body.
Hello love, Please continue to look for a better obgyn doctor. Look for reviews and (if you are comfortable) ask on your local fb women's group what obgyn they recommend and WHY ... For example, valley women for women in AZ were great when i went there several years back. Your wellbeing is worth putting in the effort to keep trying. ❤
The pain is one thing, but the mood swings. The bloody mood swings have caused more destruction in my life than I can imagine. Every month, the entirety of my energy is spent in fear of the next round of horrible mood swings that'll ruin more of my relationships with others. There is absolutely no grip. I feel so bad for myself and anyone who has to interact with me during the mood swings. Isolation has become the only way to save my ties with the people I care about. My parents and long-time friends have an understanding, but people who I have newer relationships with are most affected. I don't understand what I should be doing.
I was diagnosed at 17 in 1980. At the time endometriosis was thought to occur only in women near 35 or older. This was actually the second surgery I had for it. In total I had 9 surgeries including my hysterectomy. Five surgeries were open and four were scopes. I'm so glad that doctors have a better understanding of how this condition effects younger women and teens.
I went for a hysterectomy today due to pre cancerous cervical cells. I’ve had really bad pelvic pain, period pain and pain during intercourse for a few years now. That’s what made me go get a pap in the first place. Glad I did or I wouldn’t have caught cervical dysplasia. But after my hysterectomy they said they discovered I had started getting endometriosis. THAT would explain the pain I’ve been having. I killed two birds with one stone today. SO glad I had the surgery!
Hello, I went yesterday to have a full hysterectomy to only find out I have endometriosis and still have all my reproduction parts except 1 tube, I got referred to a Dr that specializes in endo to see what the next steps are. Hope you are recovering wonderful!
I just had a hysterectomy and Dr also told me I have endometriosis. Great 😓. What advice can you give? Have you started taken a daily progesterone? Dr advised me I can take that. To suppress the “pain” But a side defect is weight gain (as w everything 🤦🏽♀️) and bleeding. I don’t want to bleed that’s why I had a hysterectomy. Ugh. Idk what to do.
@@sglover3664thank you! Recovery went really well and now I don’t have anymore pain. I feel normal again so I am really happy with my decision. Hope your recovery went well too and doing great :)
@@amorales015hope your recovery is going good so far. Luckily for me they got rid of all the endometriosis so I don’t need to take anything now. I had a total hysterectomy. Is that what you had?
This video almost made my cry. I was never diagnosed with this. But everything you explain about painful periods, minus vomiting that was me. I never had a problem getting pregnant and my symptoms seemed to have changed once I had children. It is interesting to me that you mention this is autoimmune. I also believe my mom had this situation. So this could be given to me through 2 factors genetically and or because it is autoimmune. I started the carnivore diet and within my first cycle I had expirenced really my first time ever of 0 pain in a period. I felt like a period was a beautiful thing, not something to be dreaded.
I used to experience horrible breast pain to the extent that wearing bra and showering were huge struggles. The breast pain always hit me -especially my right breast - at least 2 weeks before menstruation. Symptoms: breast tenderness, lumpy, and formation of cysts and fibroids. This right one has a number of cysts and fibroids than the left. All in all, the discomfort was such a nightmare that i often worried that i had cancer 😢😭 Recently i underwent laparoscopy to remove this culprit from my right ovary after discovering that it had grown bigger to 5cm from an ultrasound. M so glad that i had it done as i am free from breast pain today! 5 days to menstruation and i am happy ~ say bye bye to mood swing 😊🥳 Just that i have to be on medication permanently and my gynae suggestsd birth control pill to prevent the return of endometriosis. Another proposed solution is to get pregnant which hopefully will help in hormonal changes 😂 but i am not going for it.
Just got diagnosed today with 90% certainty stage 3 endometriosis and 2 cysts. The doctor said she was confused how no one had diagnosed me with it before. I will be having an operation next week and medication to suppress it from there, hopefully to avoid a major surgery. Thank you for the informative video! ❤
Endometriosis is a fully reversible condition. It is mostly caused by a high-carbohydrate diet. Carbs = inflamation + insulin = hormone disruption = endometriosis Fastest and safest way to completely reverse endometriosis is to stop eating carbs. In other words, try the carnivore (or keto) diet for three months. I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days. Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility. You don't need to be on birth control. You don't need surgery. You don't need to live with that pain and suffering. Change your diet and in 90 days you'll feel like you have a completely different body.
@@LC-sp9ox she first diagnosed me based on history and ultrasound but to remove the cysts, she did sclerotherapy and took a biopsy. The diagnosis was confirmed based on the biopsy. Sadly i have no insight into how severe the condition is because sclerotherapy doesnt allow the doctor to have an actual look inside, its ultrasound-guided.
I just turned 40 last week. I was diagnosed with endometriosis (through laparoscopy) when I was 16. I went through depo lupron and provera back then. I wish my Dr had discussed fertility with my family and I back then. Anyway, I've never been pregnant and today after binge watching a few of your videos I feel inspired to see if I still have a shot at motherhood.
@@henrythecat3094 Not yet. I've spent the last few years working on ovulation naturally. I'm going to see my ob/gyn Dr in May so plan to have my fertility discussion then.
Endometriosis is a fully reversible condition. It is mostly caused by a high-carbohydrate diet. Carbs = inflamation + insulin = hormone disruption = endometriosis Fastest and safest way to completely reverse endometriosis is to stop eating carbs. In other words, try the carnivore (or keto) diet for three months. I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days. Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility. You don't need to be on birth control. You don't need surgery. You don't need to live with that pain and suffering. Change your diet and in 90 days you'll feel like you have a completely different body.
Yes I have endo and I found out about a decade too late , wa wa , if my gynecologists ever talked to me like you , I might have been able to save my eggs before it was too late . Thank you for sharing such important reproductive health information!
I have endo and just got a BFP pregnancy test on 8/7/23 hoping and praying my little bean implanted in my uterus and not my tube again. I had an ectopic in January 2018 and lost half of my right tube. Thought I was infertile. God said yes! When I said No ❤️❤️
@@K.DeVille my dear girl, be strong, now is the time to get as much rest as possible and get your body into a state of relaxation. You need to create an internal environment that your little bean is going to be comfortable in. Please consider doing some vagus nerve breathing exercises for relaxation and also listening to calming music with frequencies that support love. And of course pray. I pray that you and little bean will have safe passage in your journey together. Please remember to feel joy for the life that you are carrying so that little bean knows he/she is already loved. Be blessed.
@@bash4374 I really needed this. ❤️ As a woman you feel like a failure when you can’t carry life for your spouse… like you’re defective or something… but I will take your advice. I appreciate these kind words.
@@K.DeVille it's hard to understand the trials of life sometimes, yours truly are amongst the most devastating but remember, do all the things you can do and ask God to take care of the rest. Call both your and little bean's angels, guardians and guides to support you and clear the path to safe delivery. You are surrounded by the team of loving and supportive angels that God has given charge over you and your baby, don't be shy, tell them what you need right now. You are braver and stronger than you know even when it doesn't feel like it. Sending you a cyber hug
I have endometriosis and got diagnosed at 18. It's definitely been a rough journey only a couple months into it. I got diagnosed with a 3cm endometrioma on my left ovary. I definitely agree that it should be talked about and spread more! It's a very under talked about disease.
Endometriosis is a fully reversible condition. It is mostly caused by a high-carbohydrate diet. Carbs = inflamation + insulin = hormone disruption = endometriosis Fastest and safest way to completely reverse endometriosis is to stop eating carbs. In other words, try the carnivore (or keto) diet for three months. I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days. Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility. You don't need to be on birth control. You don't need surgery. You don't need to live with that pain and suffering. Change your diet and in 90 days you'll feel like you have a completely different body.
Thank you for this video! After many years of undiagnosed endo, finally had a laparoscopy in 2021. This month we are finally starting IVF after conceiving naturally post surgery but unfortunately that resulted in miscarriage. Looking forward to your next video! ❤️
This is what I needed today. My doctor refuses to even look into it when I’m pretty sure I have it. I had painful periods growing up, dark spotting before my period now, pain gets worse during intercourse, and I’m infertile right now. How can I advocate when my doctor laughs when I bring it up? I’m so frustrated with this whole process.
@@CBNX7 Problem is here in Canada you have to be referred or spend money on private clinics for $150 a generic visit. All the good doctors aren’t taking patients.
Much needed video Ma'am. I have been suffering from last 14 years... Every other doctor told me its just a bad period and hormonal imbalance. Or don't over exaggerate the pain. Got diagnosed this year. Excruciating pain and heavy bleeding feels like I am in a blood pool. Thanks for this video as now I know that I am not alone.
I am 15 years old and every time I experience cramps, I end up vomiting quite severely, and no painkillers are helping me. My mother and grandmother both have endometriosis, so I’m thinking I have it. The problem is, I’ve been to the hospital multiple times, but I don’t think anyone fully understands the severity of the pain I’m experiencing, and they usually just send me home and tell me to take painkillers (which don’t work) when I use heat, it just brings on nausea and usually causes me to vomit. More people need to raise awareness for this illness so doctors take it more seriously. I’m in so much pain.
This is such a fine line, I just turned 39. I have been diagnosed they called it cyst on the ovaries at age 30, and that I voluntarily asked for the ultrasound,and when asked to remove it surgically, the gynecologist told me if your ovary bursts , we will have to remove it, since that day I have been traumatized and never went to see that gyno again. And since then , I have been just getting ultrasounds left and right to monitor the size of those cysts, they call it chocolate cysts. Been trying to conceive for 5 years and been to 2 infertility specialists, and that’s when the first infertility specialists said I have endometriosis on my both of my ovaries , and they are size 3cm on both of my ovaries, and requested straight to do ivf, I wanted to try less invasive and less expensive options first and that insurance covers. Tried clomid , and nothing ,when I found the 2nd infertility specialist this year I have been on letrozole , clomid for the past 6 months and failed iui , nothing . And now that I want to consider a surgery, infertility specialist recommended not to as it can compromise the egg reserve, but endometriosis already compromised my egg reserve for the past 9 years almost a decade that I knew I had cysts on my ovaries. And I am at that stage of life to just go for the surgery with a endometriosis specialist surgeon ? Or forget about the surgery and go straight to IVF? My heart goes out to all the women who have been diagnosed with endometriosis and have infertility issues. Please get ultrasounds even in your 20s and dont take endometriosis or cysts on the ovaries lightly. It’s sad there are gynecologists out there that does not take endometriosis serious and just say keep trying or take birth control , which I believe can be the cause of getting endo in the first place. But I am not a doctor , however I do educate myself and I wish I educated myself way earlier in my 20s . Good luck to all the women who on a roller coaster and hardship trying to conceive.
I have endometriosis. I didn't take birth control until after I was diagnosed, and it's been an absolute lifesaver. I don't believe it causes endometriosis.
Same have you had a lapriscopy yet? I know it's only been 6 months but I hope you're hanging in there. Just got out of a psychiatric stay for it because I thought I was going insane
@@GloomyStrawberries I haven’t even done anything tbh im scared of doctor visits hospital visits etc😥😭 also my period is a few days late it was supposed to start last night and never did
My mom had this and was treated like a freak because she was super hormonal and had excessive weight gain. But she found a great doctor who properly diagnosed her, and had a hysterectomy when I was young because it was very bad. But she felt significantly better after that and later on in life.
Very informative. Im having pain and several issues that have lasted for almost 2 months, but the obgyn i went to is not testing, not imaging, not helping. Hoping to find a new one. Grateful for the relief that's coming.
I have had inflammation markers on my blood work for years, sent to multiple specialists. This is the first time I have heard it could be related to Endo. After 9 years I finally had a doctor go "your symptoms sound like Endo would you like to have the surgery to check it out?" I went in to have a discussion on a hysterectomy since the pain has been debilitating; this was the first time Endo ever got brought up for me. Scared and excited to see if this is actually what is going on and that it can be managed.
Thank you so much ❤. I am 38 years and I probably have 2 huge (10x8cm) miomas, and will schedule an OP to get it out. I was looking for information from a reliable source and I’m so glad I found you!
Thank you for such an informative video. I was diagnosed with endometriosis in 2017 and had a chocolate cyst on my right ovary. I had surgery to remove it and have had almost no pain during my period since then. My doctor told me I have stage 2 endo and my husband and I are currently trying to conceive for the past 6 months. Can you please address TTC naturally with endo? Thank you again💕
I’m on progesterone and it was literally the only thing that improved my pain, aka made it manageable(I’ve had the painful periods since I was 12) so yeah pretty sure I have it..
Endometriosis is a fully reversible condition. It is mostly caused by a high-carbohydrate diet. Carbs = inflamation + insulin = hormone disruption = endometriosis Fastest and safest way to completely reverse endometriosis is to stop eating carbs. In other words, try the carnivore (or keto) diet for three months. I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days. Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility. You don't need to be on birth control. You don't need surgery. You don't need to live with that pain and suffering. Change your diet and in 90 days you'll feel like you have a completely different body.
I've been suspecting I have endo for years, but my doctor said I don't because my cramps go away with two liquigel advils, but if I don't take them on time, I'm bent over in pain and feel like crying. It's so bad. I talked to a friend last night who had a hysterectomy because of bad endo and I described what I was going through (bloating, bad cramps, pelvic discomfort between period, painful sex and bleeding after sex, insanely heavy flow (I have to change my cup four times a day because it literally overflows. Not leaks, overflows.), huge clots in my period, etc.) and she said it was exactly the same symptoms as hers.
Can you do a video or podcast on low estrogen? I’m struggling to find good, trustworthy information on it in regards to ttc. Upcoming appointment with a doctor and I just want to be self education to ask good questions and understand them. Thank you!
I was diagnosed with stage 4 endo about 8 weeks ago at age 24. My husband also has mild MFI. I have had 2 periods since surgery, and my plan is to proceed with IVF in the near future. I’m wondering how long after surgery you would recommend waiting before proceeding with IVF? What is your typical recommendation for your patients? Thank you for all you do! I’m a PA in internal medicine and frequently refer patients to your videos!
Natalie! Thank you so much for your videos. You always make me feel so seen and at ease. I need to find a doctor who advocates like you do where I live!
Thank you for this video! I have a follow-up question. Is there such a thing as "normal" amount of pain during period and ovulation? I've been suspecting that I may have Endo for years, but most gynecologists I've met say it's normal to have some pain and indigestion around period and ovulation. So I just want to understand how much discomfort and GI symptoms are the "norm" and at which point I should seek a GYN who is known for treating or managing endometriosis.
I’ve ready many papers and it’s noted that it’s not endometrial lining , it’s SIMILAR to endometrial lining, it’s not the exact same tissue. What are your thoughts?
Honestly, an ultrasound technician told me to request an MRI referral from the OBGYN. The gynecologist may ask you to elaborate, but if your insurance covers it, you should push for it regardless of what your doctor is saying. I’ve been trying to find answers for almost a decade now, and unfortunately having to advocate for yourself assertively seems like the only way to get answers when it comes to reproductive healthcare… :(
2:45 I have three direct family members who has had endometriosis and I was still pushed to the side when asking doctors to check. 😢 “Not enough evidence” shameful practice. “Youre too young” 11:31 my story .. pain eventually stopped on its own. But can’t get pregnant
Thank You for this video. I am 20 and really think I have endometriosis. I have mentioned to a few doctors that I have been to about my symptoms and they have put me off and didn't take me seriously. I have no idea what to do but really want answers, struggling a lot. Is there a way to talk to you doctor about my symptoms? I am in Chicago and can't find a good doctor here.
Does lasting damage to nerves ever occur with endometriosis that causes sciatica or nerve pain? Or does endometriosis only cyclically compress the nerves or spinal cord?
A high carb diet contributes to nerve pain and fertility issues. Endometriosis is a fully reversible condition. It is mostly caused by a high-carbohydrate diet. Carbs = inflamation + insulin = hormone disruption = endometriosis Fastest and safest way to completely reverse endometriosis is to stop eating carbs. In other words, try the carnivore (or keto) diet for three months. I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days. Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility. You don't need to be on birth control. You don't need surgery. You don't need to live with that pain and suffering. Change your diet and in 90 days you'll feel like you have a completely different body.
Hi Natalie, Thank you for this video! You mentioned hormonal treatment - is the combined pill with both estrogen & progestin recommended? Or progestin only? Thank you!
If inflammation is such a huge factor for fertility and miscarriage, is it such a risk to take neproxen or advil while pregnant? Or is the bigger risk taking those inflammatories?
Excellent video you’re so clear and empathetic. Do you know of any reason for anovulation after a miscarriage. I had a missed miscarriage and required a D&C months ago and my ovulation hasn’t returned. In the past I was worried about PCOS but we didn’t really investigate it. I’m booked to see a specialist but wait times are long. Has this happened to other woman? I get my menstrual cycle but low LH and doesn’t look like I’m ovulating. I know it can take time to return after a late term miscarriage or live birth so I’m hoping it’s just that. Anything else which people recommend getting checked when I have the appointment? Feeling anxious
I've always used Piroxicam or Mefenamic acid for period cramps cos other NSAIDs didn't work. As of 5months ago, both drugs aren't effective (only relieves 20% of pain). Also, I started experiencing bad pelvic & low back pain with bloating & diarrhea from Day 12 (different from the one-sided ovulation pain). Shortly after it subsides, PMS takes over with similar symptoms from Day 22. I've been worried lately cos of I'm in med sch (3rd yr) which is super demanding so I plan to see an ObGyn in January. Just wondering if anyone has a very similar experience too.
It all started at the age of 13, one son painful child delivery and didn't get diagnosed until 36 during hysterectomy.... Crazy how women are not being heard. We are many times dismissed 😵💫
How to get pregnant and stay pregnant. Got pregnant naturally after surgery 1 1/2 years ago, ended in miscarriage at 8 weeks. Did IVF. First transfer in September didn’t work. 2nd transfer in October implanted but HCG didn’t go up at 4 weeks. What would you do differently?
I suspect that I might have endometriosis, and I was diagnosed with IBS many years ago. I’m starting to wonder this myself, maybe I don’t even have IBS and instead, I just have endometriosis and everything would be fixed if I could take care of it.
Yes; it's all related to overeating carbs/sugar. Endometriosis is a fully reversible condition. It is mostly caused by a high-carbohydrate diet. Carbs = inflamation + insulin = hormone disruption = endometriosis Fastest and safest way to completely reverse endometriosis is to stop eating carbs. In other words, try the carnivore (or keto) diet for three months. I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days. Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility. You don't need to be on birth control. You don't need surgery. You don't need to live with that pain and suffering. Change your diet and in 90 days you'll feel like you have a completely different body.
Thanks for this video! Would love if you could talk about endo & IVF. Does endo affect the stim/retrieval phase, or just (possibly) the transfer/implanting phase?
45 no kids, history of fibroids had myomectomy, ultrasounds been clear. I got off the pill to get bloodwork to check if HRT is needed. Gyno is saying I need to be back on pill until I reach 55 since my symptoms are back. What is this going to do w Testosterone levels in long run?
Once my period is over, im gonna go get myself checked up. The pain is unbearable, i suffer a lot during my period. I take Naproxen 550mg 2 days before my period starts (estimate with a period tracker) and i take it thru out my period but it doesn't seem to work at all. I tried drinking ginger tea twice a day for a whole month and that did not work. I feel like someone is stabbing my lower stomach over and over again. Once my period is over, im already in so much stress waiting for the next period. There are days i hope im dead before the next period
Endometriosis is a fully reversible condition. It is mostly caused by a high-carbohydrate diet. Carbs = inflamation + insulin = hormone disruption = endometriosis Fastest and safest way to completely reverse endometriosis is to stop eating carbs. In other words, try the carnivore (or keto) diet for three months. I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days. Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility. You don't need to be on birth control. You don't need surgery. You don't need to live with that pain and suffering. Change your diet and in 90 days you'll feel like you have a completely different body.
I’m 24 years old and I have such an irregular period ( I’ll completely miss a period or sometimes I’ll randomly bleed for just one day),pain during intercourse sometimes. I don’t have access to any kind of insurance, what should I do?
I am almost turning 17 and I have been having horrible period cramps for about 3 years. the pain is so bad that I can't stand straight, can't walk, and feel nausea and bloating. last week, I had to leave the exam room because I couldn't bear the pain. I don't know yet if it's endometriosis but I really would like 2 know what's the cause of this severe pain I experience.
(Wife here!) I had a laparoscopic bilateral salpingectomy almost a year ago and I believe I developed post-salpingectomy endometriosis (will be seeing my doc about it). I would love to see some videos geared towards childfree healthcare/ lifestyle options! Your videos are so helpful and informative, but women trying to conceive aren’t the only ones that require reproductive healthcare 🖤 thank you for educating people about these topics. It’s not talked about enough, imo!
I'm only 16 and Im going to the gynecologist next month as my primary doctor referred to one. I'm not sure if it could be endometriosis but i have alot of the same symptoms. I get very very very bad pain in my back stomach and sides. The back pain is sometimes more severe then it is on my stomach. I get it randomly through the month but it's so much worse on my period. Ibuprofen does nothing heat does nothing. Also idk if this is weird but sometimes when I'm walking while not on my period I get this slight cramping feeling on my left side near my hip bone. I also have irregular bleeding. I also get alot of blood clots. But while on my period it will like stop and start. Like day 1 I have a very heavy period but then day 2 it completely disappeares but then I still am getting cramps during my periods "disappearing" moments. The cramps will get so bad that I will be like shaking sometimes. My cramps also get worse when I use the bathroom. I also feel very fatigued and sometimes dizzy and nauseous when I'm on my period. Also embarrassing enough I get diarrhea only on my period,,,. Could this be signs of endometriosis??? I'm scared it could be but I'm also scared I'm just being dramatic
Hi! I just turned 20 last week but I’ve been feeling how you feel since I was about 14. Im considering myself if I should see a gynecologist. I started bc five months ago and it’s helped with my periods being SO heavy, the nauseous faint dizzy feelings, and the shaking which I used to get when using the bathroom. But I still get the slight cramps before my period, the lower back pain, but im also feeling pain run down my legs and my stomach feels so tight and bloated. How did your appointment go? Also, hope your feeling better ❤
@@acupajo sorry you've had those symptoms for so long. My appointment also went pretty well and the gynecologist listened to me and I'm getting an ultrasound done on the 11th. Sadly my symptoms have not changed much 😞
HI! Please never feel like you are "being dramatic"! What you are describing here are horrible symptoms and I hope you find a doctor who takes you seriously and helps you. I wish you all the best and hope your symptoms get much much better. xxx
@@helloooo0617 hi there 💕 I’m so sorry to hear about what you are going through. I’m having similar issues with the pain, nausea, bowel changes, etc on my period. Are the wanting to check for endo??
My fear is shaking me terribly, I have left ovarian cyst and endometriosis, bleeding for over 35 days with intervals of 8_10 days after taking primolute N,,, I see no changes
Endometriosis is a fully reversible condition. It is mostly caused by a high-carbohydrate diet. Carbs = inflamation + insulin = hormone disruption = endometriosis Fastest and safest way to completely reverse endometriosis is to stop eating carbs. In other words, try the carnivore (or keto) diet for three months. I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days. Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility. You don't need to be on birth control. You don't need surgery. You don't need to live with that pain and suffering. Change your diet and in 90 days you'll feel like you have a completely different body.
I’ve been trying to get a diagnosis since I was 15 I’m now 26 still on a waiting list! I’ve been off work many times as well as yesterday was the worst pain It lasted 21 hours felt like labour. Sweating sore to breathe leg pain , felt like I my stomach and back was being stabbed plus I was throwing up!! This needs to end
I just had endometriosis removed from my pelvis, bladder, intestine and ovaries, I have no idea what "stage" I have/had.. I got so little information after the surgery. Was just told that I should start up on birth control, as soon as possible.. I just had my first period after the surgery, and it's still very painful, had to take codeine to be able to go to work.. I've had these issues for 20 years, I honestly thought it was normal.
Endometriosis is a fully reversible condition. It is mostly caused by a high-carbohydrate diet. Carbs = inflamation + insulin = hormone disruption = endometriosis Fastest and safest way to completely reverse endometriosis is to stop eating carbs. In other words, try the carnivore (or keto) diet for three months. I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days. Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility. You don't need to be on birth control. You don't need surgery. You don't need to live with that pain and suffering. Change your diet and in 90 days you'll feel like you have a completely different body.
31 year old NEWBIE TO "officially" TTC 🙋♀ I have questioned my fertility over the years but my GYN said all was "good". Two years ago, I was diagnosed with endometriosis and PCOS via excision surgery. i have a schedule appointment with my first RE. Is there a recommended line of testing you suggest with these conditions?
Is adenomysis also an endometriosis? I always have very painful period since my period started at age 11. I have to take painkillers bec the pain is making me faint. It was only diagnosed in my 40s when I had endometrial hyperplasia with atypia. Through numerous ultrasound it was found out. I’m still experiencing painful pelvic now that I’m menopause. Is that normal? My gynecologist said it’s atrophy.
What I'm having a hard time with is Sciatica pain and i can't get anyone to tell me what it stems from. I do have firbroids but they're confused because the fibroids are not to them of significant size. And i have pain even when I'm not on my period
The pain is so bad every month and I would consider mine mild. I'm thankful though I will never have children, possibly a daughter I could pass this down to. Life with this is so not worth it to me. I'm also glad I can deal with this pain without being a wife or mother and that I can schedule things around it without being punished.
I wish you were my doctor. I’ve been trying to find a cause to my symptoms for years but every doctor I’ve spoken to just brushes it off as period pain
Should I do an HSG and then if tubes are blocked do a laparoscopy? I suspected Endometriosis or prior PID since 7 years ago but no Gyno has ever wanted to ck me for it
i have had a LOT of these signs, my mom has had it worse but i don’t remember what she was diagnosed with. i’m on a hormonal birth control and that genuinely seemed to get rid of a lot of the pain after about 3 months of daily use. i believe it’s a synthetic estrogen and something else. the pain has slowly been coming back though. is it possible for hormonal birth control to work and then stop working for something like this?
Endometriosis is a fully reversible condition. It is mostly caused by a high-carbohydrate diet. Carbs = inflamation + insulin = hormone disruption = endometriosis Fastest and safest way to completely reverse endometriosis is to stop eating carbs. In other words, try the carnivore (or keto) diet for three months. I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days. Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility. You don't need to be on birth control. You don't need surgery. You don't need to live with that pain and suffering. Change your diet and in 90 days you'll feel like you have a completely different body.
Hi mam is any chance to conceive in endometriosis plz help me I try all the method I become totally helpless and hopeless I am very alone no one understanding my pain
I have endometriomas on both ovaries which confirma I have endometriosis. I get bad pain in pelvic during periods and sometimes ovulation. I also have fibroids.
I am 34 have recently been diagnosed with stage 4 endometriosis(through ultrasound) with bowel involvement and kissing ovaries, endometriomas on both ovaries and moderate adenomyosis. Im in Australia have been waiting for surgery for 6+ months already. Have been trying to conceive for 12 months with multiple miscarriages at 6 weeks. AMH and all bloodwork are good. Doctor just says keep trying while waiting for surgery. I have changed my whole lifestyle and diet. What else can I do treatment wise to help my chances of carrying a baby naturally?
You could try TCM (Traditional Chinese Herbs) and acupuncture as an adjunct to the lifestyle and dietary changes. My mother spent about 6 months having this after multiple miscarriages and being told by doctors she'd never carry to full term; she went on to give birth to 5 more children. Additionally research has shown that acupuncture has been found to increase rates of clinical pregnancy when acupuncture was done during IVF.
I e always had horrible lower back pain with mine. I was in debilitating pain 24-7 for 10 years until I got a full hysterectomy at 33. I truly believe getting an IUD caused mine. I got endo 6 months after my first IUD. I know have inter cystial cystitis which is also horribly painful. I constantly have blood in my urine. I have a mass in my peritoneum, diverticulosis and IBD. I'm a mess with constant cramping and abdominal pain. Endo is miserable.
Hi Dr. Nathalie, I had a failed a IUI & IVF. Been trying to get pregnant for 5 years and was diagnosed with right endometriotic cyst and with dilatation of distal right tube. There were only 6 eggs retrieved to me, 4 matured, and 2 were transfered, but to no luck. My Dr. said to do the IVF again after 2 months. Do you think it is the right protocol for my case? Thanks in advance 🙏🏻
Is there a connection between this and arthritis? I'm just curious because you mentioned auto immune diseases, and i was diagnosed with early onset arthritis at 26 and have ALWAYS had 7-14 day painful periods... usually, i am laying in bed the first 2-4 days (it can vary). Incl other symptoms. Also, i was onlynable to get pregnant twice at 19 and 21... im 35 and haven't been able to conceive since. There has been no prevention for pregnancy since i was 24/25. I have been with my husband for 18 years. I have made my peace with it, but it is VITAL that YOU, Younger ladies seek treatment ! Idgaf if you have to obgyn shop, find a doc who will TAKE YOU SERIOUS! ❤ Best of luck.
I've been dealing with horrible painful periods for 2 years now. I'm in bed for 4 days with heating pad and a lot of ibuprofen and Tylenol and it don't really help then usually add another 4 days of pain but it's tolerable. Ive been to doctors and I still feel like I'm being misdiagnosed. All of my pain is in my left pelvic low abdomen and sometimes low left side of back. I've been told it was my sciatica nerve. I went to ER yesterday they did x-ray said it was bursitis but I'm still not convinced that's what's wrong. I feel like nobody cares what I tell them and they just keep pushing me off to doctor after doctor. I'm so frustrated and aggravated
Endometriosis is a fully reversible condition. It is mostly caused by a high-carbohydrate diet. Carbs = inflamation + insulin = hormone disruption = endometriosis Fastest and safest way to completely reverse endometriosis is to stop eating carbs. In other words, try the carnivore (or keto) diet for three months. I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days. Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility. You don't need to be on birth control. You don't need surgery. You don't need to live with that pain and suffering. Change your diet and in 90 days you'll feel like you have a completely different body.
Thanks for the excellent video, I have had period pain for many many years, basically when my period started and now I am 36 and finally after been to many doctors they are going to do a camera and take tissue for testing under general anesthesia, not the laparoscopy but still hoping they find out if its endometriosis after all the years of vomiting, heavy bleeding, bloating and now more bleeding between cycles and very short cycles. I sometimes vomit up to thirteen times a month due to pain. Would anybody know if this testing can still show up endometriosis? Thanks for your help here .
I just gaslighted myself throughout this entire video until you said 'pain when you were a teenager.' Sold.
As you were listing the 'not normal symptons' I was wondering who the hell would be able to do things like sports, have regular bowel movements on your period, and be able to live your normal life. I didn't even really know that was possible
No bc same. Every time my period comes around I know I have to pause my life or else ):
I have endometriosis, thoracic specifically. It is such a difficult situation. It took me nearly 5 years to get a diagnosis. I am on year 11 now. Thanks for sharing this information with the world. Lots of women are suffering silently.
You need to do surgery ASAP 😘
I am so sorry and thankful you got the diagnosis
Yea I had a doctor tell me it was pretty much nothing gave my hormones and pain told me to move on but something didn't feel right I went to other doctors come to find out I had this I'm on year 3
I’m pretty damn sure I have endometriosis, I’ve been stabbed before and the feeling is almost completely the same! The pain is so intense it caused me to throw up when I was younger (I’ve trained myself to not anymore) and when I rest I’ll stay asleep for almost 24 hours. I really don’t want surgery for just for someone to confirm it because everyone in my life has seen me breakdown from pain at least once. They freak out and want me to go to the ER and I have to explain to them I’m not actually dying this is just the way my period is.
This is literally me. Minus having been stabbed but i imagine that it feel similar to being stabbed.
I went to the ER a couple days ago because of my period pain. I almost passed out on the bathroom floor because of it. I actually I had an organ rupture. There was a moment of "oh my god, I'm going to die". That's what it finally took for my doctor to even be okay with doing an ultrasound on me. It's so, so frustrating.
Get the surgery to clean out the endometriosis if possible. You get a few years without pain afterwards.
Or start the anti inflammatory diet. Fasting, exercise...all the other things to help the pain be tolerable.
That’s so scary. Especially bc the way I always explain it to my husband is that it feels like someone is stabbing me. Never knew I was spot on..
This is really off-topic, but I legit thought you were Reese Witherspoon, and I was excited that she was raising awareness about endometriosis. You're still lovely, and I appreciate you discussing this!
Mee too!!!😂😂
I'm 16 and I have extreme period cramps where I take 4-6 ibuprofen pills to help with pain(2-3 at a time until pain comes back), I have diarrhea and I throw up. I end up not eating the first few days of my period because of the pain, if I eat I throw up. My periods also normally last 12-14 days. My last period lasted 16 days. My mom says that some people are like that and not to worry. This has been going on since a year or 2 after I got my first period around 10 yrs old.
That doesn’t sound normal
I go through the same procedure. So happy that I'm not alone in this.
It's definitely not normal. It may be her normal because there seems to be familial similarities and cramps and issues can be common, but it doesn't make it normal. I'm so sorry you aren't being heard when you're suffering. See if you can provide your mom videos that you find to educate her so that you can advocate for yourself. Work on her to get her to take you to a Dr to begin the process of getting treatment that can help. I'm 43 & wish I had advocated for myself sooner. Luckily for me the likely fertility issues weren't a problem since I've never tried having kids, but at your age you really don't know how that journey for a future family will go so you don't want damage in case you choose to have kids one day. Per my research, EXPERT surgical excision is definitely the gold standard treatment. For me, birth control has never been helpful to significantly help symptoms and caused side effects of its own. I wish I had known sooner to advocate for myself.
I have the exact same symptoms as you except for the heavy bleeding mine usually last for 5-6 days and i have medium flow, but the cramps are unbearable, I barely eat anything when im on my period like 1 meal a day and that too in small portions. I am afraid of vomitting and making the cramps worse.
I have same symptoms too, every month the periods come i feel like wanna die like that 😢
I had an investigstion last year into the problems I have with excessive pain and mood swings, I usually have a day or two off work each month because the pain gets too much. I get lower back pain, hip and leg pain, migraines, cramps and spasms, and I get an excruciating sharp pain in the lower left of my abdomen. I nearly called an ambulance the first time I felt it. And the mood swings, well, I feel like a different person. I ususlly isolate myself if I can, because I become so nasty and erratic.
I saw a 'specislist' about it last year, was told my ovaries are 'enlarged' but there was nothing to worry about and until I decide I want children they won't do anything. Didn't care in the slightest that my life self destructs every month, I miss work, and feel pain that literally puts me on the floor.
I left that appointment feeling invisible. Like I don't matter. Unless of course I want to reproduce, then I matter a bit more. But until then I have basically been told to suffer in silence.
You aren't invisible.
I see you.
Endometriosis is a fully reversible condition.
It is mostly caused by a high-carbohydrate diet.
Carbs = inflamation + insulin = hormone disruption = endometriosis
Fastest and safest way to completely reverse endometriosis is to stop eating carbs.
In other words, try the carnivore (or keto) diet for three months.
I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days.
Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility.
You don't need to be on birth control.
You don't need surgery.
You don't need to live with that pain and suffering.
Change your diet and in 90 days you'll feel like you have a completely different body.
Hello love,
Please continue to look for a better obgyn doctor. Look for reviews and (if you are comfortable) ask on your local fb women's group what obgyn they recommend and WHY ...
For example, valley women for women in AZ were great when i went there several years back.
Your wellbeing is worth putting in the effort to keep trying. ❤
That is awful I am so sorry this happened to you I hope things are better for you now
The pain is one thing, but the mood swings. The bloody mood swings have caused more destruction in my life than I can imagine. Every month, the entirety of my energy is spent in fear of the next round of horrible mood swings that'll ruin more of my relationships with others. There is absolutely no grip. I feel so bad for myself and anyone who has to interact with me during the mood swings. Isolation has become the only way to save my ties with the people I care about. My parents and long-time friends have an understanding, but people who I have newer relationships with are most affected. I don't understand what I should be doing.
I was diagnosed at 17 in 1980. At the time endometriosis was thought to occur only in women near 35 or older. This was actually the second surgery I had for it. In total I had 9 surgeries including my hysterectomy. Five surgeries were open and four were scopes. I'm so glad that doctors have a better understanding of how this condition effects younger women and teens.
I went for a hysterectomy today due to pre cancerous cervical cells. I’ve had really bad pelvic pain, period pain and pain during intercourse for a few years now. That’s what made me go get a pap in the first place. Glad I did or I wouldn’t have caught cervical dysplasia. But after my hysterectomy they said they discovered I had started getting endometriosis. THAT would explain the pain I’ve been having. I killed two birds with one stone today. SO glad I had the surgery!
I was diagnosed with endometriosis and it was a big disturb to me until I came across Doctor eromon herbal channel. his medication cured me.
Hello, I went yesterday to have a full hysterectomy to only find out I have endometriosis and still have all my reproduction parts except 1 tube, I got referred to a Dr that specializes in endo to see what the next steps are. Hope you are recovering wonderful!
I just had a hysterectomy and Dr also told me I have endometriosis. Great 😓. What advice can you give? Have you started taken a daily progesterone? Dr advised me I can take that. To suppress the “pain” But a side defect is weight gain (as w everything 🤦🏽♀️) and bleeding. I don’t want to bleed that’s why I had a hysterectomy. Ugh. Idk what to do.
@@sglover3664thank you! Recovery went really well and now I don’t have anymore pain. I feel normal again so I am really happy with my decision. Hope your recovery went well too and doing great :)
@@amorales015hope your recovery is going good so far. Luckily for me they got rid of all the endometriosis so I don’t need to take anything now. I had a total hysterectomy. Is that what you had?
This video almost made my cry. I was never diagnosed with this. But everything you explain about painful periods, minus vomiting that was me. I never had a problem getting pregnant and my symptoms seemed to have changed once I had children. It is interesting to me that you mention this is autoimmune. I also believe my mom had this situation. So this could be given to me through 2 factors genetically and or because it is autoimmune. I started the carnivore diet and within my first cycle I had expirenced really my first time ever of 0 pain in a period. I felt like a period was a beautiful thing, not something to be dreaded.
I used to experience horrible breast pain to the extent that wearing bra and showering were huge struggles. The breast pain always hit me -especially my right breast - at least 2 weeks before menstruation. Symptoms: breast tenderness, lumpy, and formation of cysts and fibroids. This right one has a number of cysts and fibroids than the left. All in all, the discomfort was such a nightmare that i often worried that i had cancer 😢😭
Recently i underwent laparoscopy to remove this culprit from my right ovary after discovering that it had grown bigger to 5cm from an ultrasound.
M so glad that i had it done as i am free from breast pain today! 5 days to menstruation and i am happy ~ say bye bye to mood swing 😊🥳
Just that i have to be on medication permanently and my gynae suggestsd birth control pill to prevent the return of endometriosis.
Another proposed solution is to get pregnant which hopefully will help in hormonal changes 😂 but i am not going for it.
Just got diagnosed today with 90% certainty stage 3 endometriosis and 2 cysts. The doctor said she was confused how no one had diagnosed me with it before. I will be having an operation next week and medication to suppress it from there, hopefully to avoid a major surgery. Thank you for the informative video! ❤
Endometriosis is a fully reversible condition.
It is mostly caused by a high-carbohydrate diet.
Carbs = inflamation + insulin = hormone disruption = endometriosis
Fastest and safest way to completely reverse endometriosis is to stop eating carbs.
In other words, try the carnivore (or keto) diet for three months.
I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days.
Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility.
You don't need to be on birth control.
You don't need surgery.
You don't need to live with that pain and suffering.
Change your diet and in 90 days you'll feel like you have a completely different body.
How was it diagnosed? MRI?
@@LC-sp9ox she first diagnosed me based on history and ultrasound but to remove the cysts, she did sclerotherapy and took a biopsy. The diagnosis was confirmed based on the biopsy. Sadly i have no insight into how severe the condition is because sclerotherapy doesnt allow the doctor to have an actual look inside, its ultrasound-guided.
What type of doctor diagnosed you?
@@GodIsWithinHer. an obgyn!
I just turned 40 last week. I was diagnosed with endometriosis (through laparoscopy) when I was 16. I went through depo lupron and provera back then. I wish my Dr had discussed fertility with my family and I back then. Anyway, I've never been pregnant and today after binge watching a few of your videos I feel inspired to see if I still have a shot at motherhood.
Have you try ivf?
@@henrythecat3094 Not yet. I've spent the last few years working on ovulation naturally. I'm going to see my ob/gyn Dr in May so plan to have my fertility discussion then.
@@sheabutta5425 I hope the best for you!
Endometriosis is a fully reversible condition.
It is mostly caused by a high-carbohydrate diet.
Carbs = inflamation + insulin = hormone disruption = endometriosis
Fastest and safest way to completely reverse endometriosis is to stop eating carbs.
In other words, try the carnivore (or keto) diet for three months.
I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days.
Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility.
You don't need to be on birth control.
You don't need surgery.
You don't need to live with that pain and suffering.
Change your diet and in 90 days you'll feel like you have a completely different body.
Yes I have endo and I found out about a decade too late , wa wa , if my gynecologists ever talked to me like you , I might have been able to save my eggs before it was too late . Thank you for sharing such important reproductive health information!
I have endo and just got a BFP pregnancy test on 8/7/23 hoping and praying my little bean implanted in my uterus and not my tube again. I had an ectopic in January 2018 and lost half of my right tube. Thought I was infertile. God said yes! When I said No ❤️❤️
Good luck, I hope everything goes well for you.
@@bash4374 thank you so much. I’m so worried I’m not even sleeping
@@K.DeVille my dear girl, be strong, now is the time to get as much rest as possible and get your body into a state of relaxation. You need to create an internal environment that your little bean is going to be comfortable in. Please consider doing some vagus nerve breathing exercises for relaxation and also listening to calming music with frequencies that support love. And of course pray. I pray that you and little bean will have safe passage in your journey together. Please remember to feel joy for the life that you are carrying so that little bean knows he/she is already loved. Be blessed.
@@bash4374 I really needed this. ❤️ As a woman you feel like a failure when you can’t carry life for your spouse… like you’re defective or something… but I will take your advice. I appreciate these kind words.
@@K.DeVille it's hard to understand the trials of life sometimes, yours truly are amongst the most devastating but remember, do all the things you can do and ask God to take care of the rest. Call both your and little bean's angels, guardians and guides to support you and clear the path to safe delivery. You are surrounded by the team of loving and supportive angels that God has given charge over you and your baby, don't be shy, tell them what you need right now. You are braver and stronger than you know even when it doesn't feel like it. Sending you a cyber hug
I have endometriosis and got diagnosed at 18. It's definitely been a rough journey only a couple months into it. I got diagnosed with a 3cm endometrioma on my left ovary. I definitely agree that it should be talked about and spread more! It's a very under talked about disease.
Endometriosis is a fully reversible condition.
It is mostly caused by a high-carbohydrate diet.
Carbs = inflamation + insulin = hormone disruption = endometriosis
Fastest and safest way to completely reverse endometriosis is to stop eating carbs.
In other words, try the carnivore (or keto) diet for three months.
I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days.
Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility.
You don't need to be on birth control.
You don't need surgery.
You don't need to live with that pain and suffering.
Change your diet and in 90 days you'll feel like you have a completely different body.
Hi ❤ do u have any sharp pain in left abdominal
This video is perfectly put together and incredibly informative. Thank you for making it so easy for us to understand this disease.
Thank you for this video! After many years of undiagnosed endo, finally had a laparoscopy in 2021. This month we are finally starting IVF after conceiving naturally post surgery but unfortunately that resulted in miscarriage. Looking forward to your next video! ❤️
So sorry for your loss! Hugs!
This is what I needed today. My doctor refuses to even look into it when I’m pretty sure I have it. I had painful periods growing up, dark spotting before my period now, pain gets worse during intercourse, and I’m infertile right now. How can I advocate when my doctor laughs when I bring it up? I’m so frustrated with this whole process.
See a reproductive endocrinologist. They will take you seriously.
@@CBNX7 Problem is here in Canada you have to be referred or spend money on private clinics for $150 a generic visit. All the good doctors aren’t taking patients.
@@juliebranton1730 Canadian doctors are horrible here.
Also try to find a doctor who is very knowledgable about endometriosis.
Did the doctor tell you hard to get pregnant?
Much needed video Ma'am. I have been suffering from last 14 years... Every other doctor told me its just a bad period and hormonal imbalance. Or don't over exaggerate the pain. Got diagnosed this year. Excruciating pain and heavy bleeding feels like I am in a blood pool. Thanks for this video as now I know that I am not alone.
I am 15 years old and every time I experience cramps, I end up vomiting quite severely, and no painkillers are helping me. My mother and grandmother both have endometriosis, so I’m thinking I have it. The problem is, I’ve been to the hospital multiple times, but I don’t think anyone fully understands the severity of the pain I’m experiencing, and they usually just send me home and tell me to take painkillers (which don’t work) when I use heat, it just brings on nausea and usually causes me to vomit. More people need to raise awareness for this illness so doctors take it more seriously. I’m in so much pain.
This is such a fine line, I just turned 39. I have been diagnosed they called it cyst on the ovaries at age 30, and that I voluntarily asked for the ultrasound,and when asked to remove it surgically, the gynecologist told me if your ovary bursts , we will have to remove it, since that day I have been traumatized and never went to see that gyno again. And since then , I have been just getting ultrasounds left and right to monitor the size of those cysts, they call it chocolate cysts. Been trying to conceive for 5 years and been to 2 infertility specialists, and that’s when the first infertility specialists said I have endometriosis on my both of my ovaries , and they are size 3cm on both of my ovaries, and requested straight to do ivf, I wanted to try less invasive and less expensive options first and that insurance covers. Tried clomid , and nothing ,when I found the 2nd infertility specialist this year I have been on letrozole , clomid for the past 6 months and failed iui , nothing . And now that I want to consider a surgery, infertility specialist recommended not to as it can compromise the egg reserve, but endometriosis already compromised my egg reserve for the past 9 years almost a decade that I knew I had cysts on my ovaries. And I am at that stage of life to just go for the surgery with a endometriosis specialist surgeon ? Or forget about the surgery and go straight to IVF? My heart goes out to all the women who have been diagnosed with endometriosis and have infertility issues. Please get ultrasounds even in your 20s and dont take endometriosis or cysts on the ovaries lightly. It’s sad there are gynecologists out there that does not take endometriosis serious and just say keep trying or take birth control , which I believe can be the cause of getting endo in the first place. But I am not a doctor , however I do educate myself and I wish I educated myself way earlier in my 20s . Good luck to all the women who on a roller coaster and hardship trying to conceive.
I have endometriosis. I didn't take birth control until after I was diagnosed, and it's been an absolute lifesaver. I don't believe it causes endometriosis.
@@kp361ru conceived?
I hope I don’t have endometriosis but I’m scared though I’m in pain constantly😥
Same have you had a lapriscopy yet? I know it's only been 6 months but I hope you're hanging in there. Just got out of a psychiatric stay for it because I thought I was going insane
@@GloomyStrawberries I haven’t even done anything tbh im scared of doctor visits hospital visits etc😥😭 also my period is a few days late it was supposed to start last night and never did
Same
@@jessicalinbarnettany updates??
Me too
My mom had this and was treated like a freak because she was super hormonal and had excessive weight gain. But she found a great doctor who properly diagnosed her, and had a hysterectomy when I was young because it was very bad. But she felt significantly better after that and later on in life.
Very informative. Im having pain and several issues that have lasted for almost 2 months, but the obgyn i went to is not testing, not imaging, not helping. Hoping to find a new one. Grateful for the relief that's coming.
I have had inflammation markers on my blood work for years, sent to multiple specialists. This is the first time I have heard it could be related to Endo. After 9 years I finally had a doctor go "your symptoms sound like Endo would you like to have the surgery to check it out?" I went in to have a discussion on a hysterectomy since the pain has been debilitating; this was the first time Endo ever got brought up for me. Scared and excited to see if this is actually what is going on and that it can be managed.
Thank you so much ❤. I am 38 years and I probably have 2 huge (10x8cm) miomas, and will schedule an OP to get it out. I was looking for information from a reliable source and I’m so glad I found you!
Im 16 and newly diagnosed with endo! Thank you for this
Thank you for such an informative video. I was diagnosed with endometriosis in 2017 and had a chocolate cyst on my right ovary. I had surgery to remove it and have had almost no pain during my period since then. My doctor told me I have stage 2 endo and my husband and I are currently trying to conceive for the past 6 months. Can you please address TTC naturally with endo? Thank you again💕
How did u got diagnosed with endometriosis . And do u have any symptoms.
I’m on progesterone and it was literally the only thing that improved my pain, aka made it manageable(I’ve had the painful periods since I was 12) so yeah pretty sure I have it..
Endometriosis is a fully reversible condition.
It is mostly caused by a high-carbohydrate diet.
Carbs = inflamation + insulin = hormone disruption = endometriosis
Fastest and safest way to completely reverse endometriosis is to stop eating carbs.
In other words, try the carnivore (or keto) diet for three months.
I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days.
Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility.
You don't need to be on birth control.
You don't need surgery.
You don't need to live with that pain and suffering.
Change your diet and in 90 days you'll feel like you have a completely different body.
Yup i have endo didn't find out until I was going in for my iud
I have had painful periods since I first started when I was 13 years old
I've been suspecting I have endo for years, but my doctor said I don't because my cramps go away with two liquigel advils, but if I don't take them on time, I'm bent over in pain and feel like crying. It's so bad. I talked to a friend last night who had a hysterectomy because of bad endo and I described what I was going through (bloating, bad cramps, pelvic discomfort between period, painful sex and bleeding after sex, insanely heavy flow (I have to change my cup four times a day because it literally overflows. Not leaks, overflows.), huge clots in my period, etc.) and she said it was exactly the same symptoms as hers.
Can you do a video or podcast on low estrogen? I’m struggling to find good, trustworthy information on it in regards to ttc. Upcoming appointment with a doctor and I just want to be self education to ask good questions and understand them. Thank you!
Does really painful ovulation with rectal pain be a sign of endometriosis?
Thank you for the informative videos you upload! I’d love to see a video and hear your thoughts on endometritis and polyps!
Can you make a video on laparoscopy and infertility specifically?
I was diagnosed with stage 4 endo about 8 weeks ago at age 24. My husband also has mild MFI. I have had 2 periods since surgery, and my plan is to proceed with IVF in the near future. I’m wondering how long after surgery you would recommend waiting before proceeding with IVF? What is your typical recommendation for your patients? Thank you for all you do! I’m a PA in internal medicine and frequently refer patients to your videos!
Natalie! Thank you so much for your videos. You always make me feel so seen and at ease. I need to find a doctor who advocates like you do where I live!
I'm so glad! :)
I have endometriosis and it's giving me a big problem
Thank you for this video! I have a follow-up question. Is there such a thing as "normal" amount of pain during period and ovulation? I've been suspecting that I may have Endo for years, but most gynecologists I've met say it's normal to have some pain and indigestion around period and ovulation. So I just want to understand how much discomfort and GI symptoms are the "norm" and at which point I should seek a GYN who is known for treating or managing endometriosis.
Very informative video, looking forward for the next one.
Which ivf protocol would you recommend for endo patients?
will be doing an endo Q&A and will add this Q to this list!
I’ve ready many papers and it’s noted that it’s not endometrial lining , it’s SIMILAR to endometrial lining, it’s not the exact same tissue. What are your thoughts?
Natalie, what type of specialist should I see to begin test for this? I’ve only ever seen gynecologists and it was a dead end EVERY SINGLE TIME.
Honestly, an ultrasound technician told me to request an MRI referral from the OBGYN. The gynecologist may ask you to elaborate, but if your insurance covers it, you should push for it regardless of what your doctor is saying. I’ve been trying to find answers for almost a decade now, and unfortunately having to advocate for yourself assertively seems like the only way to get answers when it comes to reproductive healthcare… :(
2:45 I have three direct family members who has had endometriosis and I was still pushed to the side when asking doctors to check. 😢
“Not enough evidence” shameful practice. “Youre too young”
11:31 my story .. pain eventually stopped on its own. But can’t get pregnant
Thank You for this video. I am 20 and really think I have endometriosis. I have mentioned to a few doctors that I have been to about my symptoms and they have put me off and didn't take me seriously. I have no idea what to do but really want answers, struggling a lot. Is there a way to talk to you doctor about my symptoms? I am in Chicago and can't find a good doctor here.
Currently going through extreme period cramp and all of my symptoms match this.
Does lasting damage to nerves ever occur with endometriosis that causes sciatica or nerve pain? Or does endometriosis only cyclically compress the nerves or spinal cord?
A high carb diet contributes to nerve pain and fertility issues.
Endometriosis is a fully reversible condition.
It is mostly caused by a high-carbohydrate diet.
Carbs = inflamation + insulin = hormone disruption = endometriosis
Fastest and safest way to completely reverse endometriosis is to stop eating carbs.
In other words, try the carnivore (or keto) diet for three months.
I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days.
Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility.
You don't need to be on birth control.
You don't need surgery.
You don't need to live with that pain and suffering.
Change your diet and in 90 days you'll feel like you have a completely different body.
Same question pls answer
I want to know the same
Hi pls answer
Hi Natalie,
Thank you for this video!
You mentioned hormonal treatment - is the combined pill with both estrogen & progestin recommended? Or progestin only? Thank you!
Please can you discuss treatment and trying to conceive
If inflammation is such a huge factor for fertility and miscarriage, is it such a risk to take neproxen or advil while pregnant? Or is the bigger risk taking those inflammatories?
Excellent video you’re so clear and empathetic.
Do you know of any reason for anovulation after a miscarriage. I had a missed miscarriage and required a D&C months ago and my ovulation hasn’t returned.
In the past I was worried about PCOS but we didn’t really investigate it.
I’m booked to see a specialist but wait times are long. Has this happened to other woman? I get my menstrual cycle but low LH and doesn’t look like I’m ovulating. I know it can take time to return after a late term miscarriage or live birth so I’m hoping it’s just that. Anything else which people recommend getting checked when I have the appointment? Feeling anxious
I've always used Piroxicam or Mefenamic acid for period cramps cos other NSAIDs didn't work. As of 5months ago, both drugs aren't effective (only relieves 20% of pain).
Also, I started experiencing bad pelvic & low back pain with bloating & diarrhea from Day 12 (different from the one-sided ovulation pain).
Shortly after it subsides, PMS takes over with similar symptoms from Day 22.
I've been worried lately cos of I'm in med sch (3rd yr) which is super demanding so I plan to see an ObGyn in January.
Just wondering if anyone has a very similar experience too.
It all started at the age of 13, one son painful child delivery and didn't get diagnosed until 36 during hysterectomy.... Crazy how women are not being heard. We are many times dismissed 😵💫
If you’ve been trying to get pregnant for almost a year but have a regular period and ovulate on a regularly monthly basis are those good signs?
I had a intestinal adhesion caused by endometriosis, it never came up but I was diagnosed with dysmenorrhoea. My mums turned into uterine cancer also
How to get pregnant and stay pregnant. Got pregnant naturally after surgery 1 1/2 years ago, ended in miscarriage at 8 weeks. Did IVF. First transfer in September didn’t work. 2nd transfer in October implanted but HCG didn’t go up at 4 weeks. What would you do differently?
What are my options/treatments for conceiving with endometriosis?
it depends - natural, ovulation induction, IVF, surgery, IUI - recommend a full workup to see where you are
Can you get diagnosed with endometriosis after having kids or before and just been lucky?
I know someone who was diagnosed with endometriosis and had a child after diagnosis.
I wanted to know if you find gassy stomach, and sensitivity to foods (gluten, dairy, etc) to also be a common symptom.
I suspect that I might have endometriosis, and I was diagnosed with IBS many years ago. I’m starting to wonder this myself, maybe I don’t even have IBS and instead, I just have endometriosis and everything would be fixed if I could take care of it.
I have to take hyosycamine for my stomach pain related to my gas/IBS
Yes; it's all related to overeating carbs/sugar.
Endometriosis is a fully reversible condition.
It is mostly caused by a high-carbohydrate diet.
Carbs = inflamation + insulin = hormone disruption = endometriosis
Fastest and safest way to completely reverse endometriosis is to stop eating carbs.
In other words, try the carnivore (or keto) diet for three months.
I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days.
Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility.
You don't need to be on birth control.
You don't need surgery.
You don't need to live with that pain and suffering.
Change your diet and in 90 days you'll feel like you have a completely different body.
Thanks for this video! Would love if you could talk about endo & IVF. Does endo affect the stim/retrieval phase, or just (possibly) the transfer/implanting phase?
45 no kids, history of fibroids had myomectomy, ultrasounds been clear. I got off the pill to get bloodwork to check if HRT is needed. Gyno is saying I need to be back on pill until I reach 55 since my symptoms are back. What is this going to do w Testosterone levels in long run?
I feel pinching in my vulva when I have my period. Could this be a sign of Endo?
Once my period is over, im gonna go get myself checked up. The pain is unbearable, i suffer a lot during my period. I take Naproxen 550mg 2 days before my period starts (estimate with a period tracker) and i take it thru out my period but it doesn't seem to work at all. I tried drinking ginger tea twice a day for a whole month and that did not work. I feel like someone is stabbing my lower stomach over and over again. Once my period is over, im already in so much stress waiting for the next period. There are days i hope im dead before the next period
Endometriosis is a fully reversible condition.
It is mostly caused by a high-carbohydrate diet.
Carbs = inflamation + insulin = hormone disruption = endometriosis
Fastest and safest way to completely reverse endometriosis is to stop eating carbs.
In other words, try the carnivore (or keto) diet for three months.
I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days.
Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility.
You don't need to be on birth control.
You don't need surgery.
You don't need to live with that pain and suffering.
Change your diet and in 90 days you'll feel like you have a completely different body.
You can also detect endometriosis by MRI which is non-invasive and pretty accurate
I’m 24 years old and I have such an irregular period ( I’ll completely miss a period or sometimes I’ll randomly bleed for just one day),pain during intercourse sometimes. I don’t have access to any kind of insurance, what should I do?
I am almost turning 17 and I have been having horrible period cramps for about 3 years. the pain is so bad that I can't stand straight, can't walk, and feel nausea and bloating. last week, I had to leave the exam room because I couldn't bear the pain.
I don't know yet if it's endometriosis but I really would like 2 know what's the cause of this severe pain I experience.
same here
Hi im janet i have endometriosis i diagnosed last 2021 i have suffer this every month of my period .
Can a persistent cyst (years) be an indication of endometriosis even if it doesn’t have the typical characteristic as a “chocolate” cyst?
Hi Dr. Can you talk about Chronic Endometritis, was just diagnosed after recurrent miscarriages. Been TTC for over 2 years. Thank you!
(Wife here!) I had a laparoscopic bilateral salpingectomy almost a year ago and I believe I developed post-salpingectomy endometriosis (will be seeing my doc about it). I would love to see some videos geared towards childfree healthcare/ lifestyle options! Your videos are so helpful and informative, but women trying to conceive aren’t the only ones that require reproductive healthcare 🖤 thank you for educating people about these topics. It’s not talked about enough, imo!
I'm only 16 and Im going to the gynecologist next month as my primary doctor referred to one. I'm not sure if it could be endometriosis but i have alot of the same symptoms. I get very very very bad pain in my back stomach and sides. The back pain is sometimes more severe then it is on my stomach. I get it randomly through the month but it's so much worse on my period. Ibuprofen does nothing heat does nothing. Also idk if this is weird but sometimes when I'm walking while not on my period I get this slight cramping feeling on my left side near my hip bone. I also have irregular bleeding. I also get alot of blood clots. But while on my period it will like stop and start. Like day 1 I have a very heavy period but then day 2 it completely disappeares but then I still am getting cramps during my periods "disappearing" moments. The cramps will get so bad that I will be like shaking sometimes. My cramps also get worse when I use the bathroom. I also feel very fatigued and sometimes dizzy and nauseous when I'm on my period. Also embarrassing enough I get diarrhea only on my period,,,. Could this be signs of endometriosis??? I'm scared it could be but I'm also scared I'm just being dramatic
Hi! I just turned 20 last week but I’ve been feeling how you feel since I was about 14. Im considering myself if I should see a gynecologist. I started bc five months ago and it’s helped with my periods being SO heavy, the nauseous faint dizzy feelings, and the shaking which I used to get when using the bathroom. But I still get the slight cramps before my period, the lower back pain, but im also feeling pain run down my legs and my stomach feels so tight and bloated. How did your appointment go? Also, hope your feeling better ❤
@@acupajo sorry you've had those symptoms for so long. My appointment also went pretty well and the gynecologist listened to me and I'm getting an ultrasound done on the 11th. Sadly my symptoms have not changed much 😞
HI! Please never feel like you are "being dramatic"! What you are describing here are horrible symptoms and I hope you find a doctor who takes you seriously and helps you. I wish you all the best and hope your symptoms get much much better. xxx
@@acupajo found out today I have a 7cm ovarian cyst that's all I know so far
@@helloooo0617 hi there 💕 I’m so sorry to hear about what you are going through. I’m having similar issues with the pain, nausea, bowel changes, etc on my period. Are the wanting to check for endo??
Also can endometriosis cause fibroids
Can I go for a BC pill? I have endo and adeno..painful.period.I just.take Nsaid monthly..
My fear is shaking me terribly, I have left ovarian cyst and endometriosis, bleeding for over 35 days with intervals of 8_10 days after taking primolute N,,, I see no changes
Endometriosis is a fully reversible condition.
It is mostly caused by a high-carbohydrate diet.
Carbs = inflamation + insulin = hormone disruption = endometriosis
Fastest and safest way to completely reverse endometriosis is to stop eating carbs.
In other words, try the carnivore (or keto) diet for three months.
I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days.
Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility.
You don't need to be on birth control.
You don't need surgery.
You don't need to live with that pain and suffering.
Change your diet and in 90 days you'll feel like you have a completely different body.
I’ve been trying to get a diagnosis since I was 15 I’m now 26 still on a waiting list! I’ve been off work many times as well as yesterday was the worst pain It lasted 21 hours felt like labour. Sweating sore to breathe leg pain , felt like I my stomach and back was being stabbed plus I was throwing up!! This needs to end
I'm uncertain whether my severe pain during the first 1-2 days of my period is due to endometriosis or my retroverted uterus.
I just had endometriosis removed from my pelvis, bladder, intestine and ovaries, I have no idea what "stage" I have/had.. I got so little information after the surgery. Was just told that I should start up on birth control, as soon as possible.. I just had my first period after the surgery, and it's still very painful, had to take codeine to be able to go to work.. I've had these issues for 20 years, I honestly thought it was normal.
On endo medication to treat the pain, it's been a few days, my OB put me on new birth control and now I have a consult for surgery 😰
Endometriosis is a fully reversible condition.
It is mostly caused by a high-carbohydrate diet.
Carbs = inflamation + insulin = hormone disruption = endometriosis
Fastest and safest way to completely reverse endometriosis is to stop eating carbs.
In other words, try the carnivore (or keto) diet for three months.
I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days.
Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility.
You don't need to be on birth control.
You don't need surgery.
You don't need to live with that pain and suffering.
Change your diet and in 90 days you'll feel like you have a completely different body.
31 year old NEWBIE TO "officially" TTC 🙋♀ I have questioned my fertility over the years but my GYN said all was "good". Two years ago, I was diagnosed with endometriosis and PCOS via excision surgery. i have a schedule appointment with my first RE. Is there a recommended line of testing you suggest with these conditions?
Based on my carrier status, we are being told to do IVF. Both my husband and I are carriers for cystic fibrosis.
Is adenomysis also an endometriosis? I always have very painful period since my period started at age 11. I have to take painkillers bec the pain is making me faint. It was only diagnosed in my 40s when I had endometrial hyperplasia with atypia. Through numerous ultrasound it was found out. I’m still experiencing painful pelvic now that I’m menopause. Is that normal? My gynecologist said it’s atrophy.
What I'm having a hard time with is Sciatica pain and i can't get anyone to tell me what it stems from. I do have firbroids but they're confused because the fibroids are not to them of significant size. And i have pain even when I'm not on my period
Laparo is soooo expensive! I was given an estimate of over $4,000 with my insurance. I am stuck now what to do :(
The pain is so bad every month and I would consider mine mild. I'm thankful though I will never have children, possibly a daughter I could pass this down to. Life with this is so not worth it to me. I'm also glad I can deal with this pain without being a wife or mother and that I can schedule things around it without being punished.
I think I'm late on my period? I have no symptoms. Is that possible? But my back has been hurting.
Sorry for yelling at the screen lol , but paps are awful for me , and I had endometriosis before i had 10lb cyst on my fallopian tube
I wish you were my doctor. I’ve been trying to find a cause to my symptoms for years but every doctor I’ve spoken to just brushes it off as period pain
I am a hypochondriac, so I’m just convinced I have endometriosis
Should I do an HSG and then if tubes are blocked do a laparoscopy? I suspected Endometriosis or prior PID since 7 years ago but no Gyno has ever wanted to ck me for it
i have had a LOT of these signs, my mom has had it worse but i don’t remember what she was diagnosed with.
i’m on a hormonal birth control and that genuinely seemed to get rid of a lot of the pain after about 3 months of daily use. i believe it’s a synthetic estrogen and something else. the pain has slowly been coming back though. is it possible for hormonal birth control to work and then stop working for something like this?
I have endometriosis for past 10 years I'm trying to conceive but isn't working please what are the treatment I'm 38 year please
Endometriosis is a fully reversible condition.
It is mostly caused by a high-carbohydrate diet.
Carbs = inflamation + insulin = hormone disruption = endometriosis
Fastest and safest way to completely reverse endometriosis is to stop eating carbs.
In other words, try the carnivore (or keto) diet for three months.
I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days.
Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility.
You don't need to be on birth control.
You don't need surgery.
You don't need to live with that pain and suffering.
Change your diet and in 90 days you'll feel like you have a completely different body.
Hi mam is any chance to conceive in endometriosis plz help me I try all the method I become totally helpless and hopeless I am very alone no one understanding my pain
So doing estrogen cream can make it worse?
I have endometriomas on both ovaries which confirma I have endometriosis. I get bad pain in pelvic during periods and sometimes ovulation. I also have fibroids.
Is endometrial stripe endometriosis?
I am 34 have recently been diagnosed with stage 4 endometriosis(through ultrasound) with bowel involvement and kissing ovaries, endometriomas on both ovaries and moderate adenomyosis. Im in Australia have been waiting for surgery for 6+ months already. Have been trying to conceive for 12 months with multiple miscarriages at 6 weeks. AMH and all bloodwork are good. Doctor just says keep trying while waiting for surgery. I have changed my whole lifestyle and diet. What else can I do treatment wise to help my chances of carrying a baby naturally?
How are you now ?? Surgery done ?
You could try TCM (Traditional Chinese Herbs) and acupuncture as an adjunct to the lifestyle and dietary changes. My mother spent about 6 months having this after multiple miscarriages and being told by doctors she'd never carry to full term; she went on to give birth to 5 more children. Additionally research has shown that acupuncture has been found to increase rates of clinical pregnancy when acupuncture was done during IVF.
Can endometriosis cause back pain?
I e always had horrible lower back pain with mine. I was in debilitating pain 24-7 for 10 years until I got a full hysterectomy at 33. I truly believe getting an IUD caused mine. I got endo 6 months after my first IUD. I know have inter cystial cystitis which is also horribly painful. I constantly have blood in my urine. I have a mass in my peritoneum, diverticulosis and IBD. I'm a mess with constant cramping and abdominal pain. Endo is miserable.
Yes... horrific back pain...not normal at all...
Hi Dr. Nathalie,
I had a failed a IUI & IVF. Been trying to get pregnant for 5 years and was diagnosed with right endometriotic cyst and with dilatation of distal right tube.
There were only 6 eggs retrieved to me, 4 matured, and 2 were transfered, but to no luck. My Dr. said to do the IVF again after 2 months. Do you think it is the right protocol for my case? Thanks in advance 🙏🏻
Best of luck to you hon , I hear you!
Please make a video on adenomyosis and fertility/miscarriage!
Is there a connection between this and arthritis? I'm just curious because you mentioned auto immune diseases, and i was diagnosed with early onset arthritis at 26 and have ALWAYS had 7-14 day painful periods... usually, i am laying in bed the first 2-4 days (it can vary). Incl other symptoms.
Also, i was onlynable to get pregnant twice at 19 and 21... im 35 and haven't been able to conceive since. There has been no prevention for pregnancy since i was 24/25. I have been with my husband for 18 years.
I have made my peace with it, but it is VITAL that YOU, Younger ladies seek treatment ! Idgaf if you have to obgyn shop, find a doc who will TAKE YOU SERIOUS! ❤ Best of luck.
I've been dealing with horrible painful periods for 2 years now. I'm in bed for 4 days with heating pad and a lot of ibuprofen and Tylenol and it don't really help then usually add another 4 days of pain but it's tolerable. Ive been to doctors and I still feel like I'm being misdiagnosed. All of my pain is in my left pelvic low abdomen and sometimes low left side of back. I've been told it was my sciatica nerve. I went to ER yesterday they did x-ray said it was bursitis but I'm still not convinced that's what's wrong. I feel like nobody cares what I tell them and they just keep pushing me off to doctor after doctor. I'm so frustrated and aggravated
Endometriosis is a fully reversible condition.
It is mostly caused by a high-carbohydrate diet.
Carbs = inflamation + insulin = hormone disruption = endometriosis
Fastest and safest way to completely reverse endometriosis is to stop eating carbs.
In other words, try the carnivore (or keto) diet for three months.
I guarantee you that your life will be completely changed for the better if you do carnivore for just 90 days.
Look up Dr. Kiltz. He is a fertility doc that combines cutting edge western medicine with diet to recover fertility.
You don't need to be on birth control.
You don't need surgery.
You don't need to live with that pain and suffering.
Change your diet and in 90 days you'll feel like you have a completely different body.
Hi what happened next pls reply
Thanks for the excellent video, I have had period pain for many many years, basically when my period started and now I am 36 and finally after been to many doctors they are going to do a camera and take tissue for testing under general anesthesia, not the laparoscopy but still hoping they find out if its endometriosis after all the years of vomiting, heavy bleeding, bloating and now more bleeding between cycles and very short cycles. I sometimes vomit up to thirteen times a month due to pain. Would anybody know if this testing can still show up endometriosis? Thanks for your help here .