Multiple Sclerosis Symptoms
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- Опубликовано: 6 окт 2024
- Multiple Sclerosis Symptoms #Shorts
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NOTE: Make sure to talk to your provider before ANY treatment decision. We hope to educate, empower and energize those impacted by Multiple Sclerosis. This channel consists of a collection of formal lectures and informal video clips about MS (and in this case Multiple Sclerosis Symptoms) to help education others. These videos do not provide medical advice and are for informational/educational purposes only. The videos are not intended to be a substitute for professional medical advice, diagnosis or treatment. Always seek the advice of a qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read or seen in any of our videos. They are just to help educate you about the condition guys!
Heat intolerance is the one that I have more problems with when trying to explain.
That really really sucks! I did also until I learned to live in a cooking vest. Especially my first 4 years after Lemtrada, I couldn’t function if it was over 70-72. Forget 85 or 90. My mobility disappeared. Think about getting a quality cooking vest. The MS Society gives them away to us so that’s good. And try and he other advice Boster gave. Drink ice water. Not just really cold with a little ice. But tons of ice. He was right. It changed things slowly for me. Take care and I hope your HEat Intolerance improves soon!
@@ScottyRosencrance304I’m assuming you mean cooling vest?
@@KristinaLeeJonesYes, I'm sure that's what he meant. I can't imagine being in a "cooking" vest when I'm experiencing heat intolerance! 🥵🤣😂
YES..thank you for sharing this list. The tremor, numbness, pain, fatigue, falling is me right now. And people keep saying I'm "looking really well", meaning well and not getting it.
Thanks for sharing!!
Faking being energized when in fact I was super fatigued was the most annoying thing. Until the covid pandemic, when everyone has to work from home. Long live the quarantine, I no longer have to fake anything!
Thats how to look at it!!
Living with Ms and not trying to focus on it, this actually made me feel better! I go through just about all these symptoms, dreading each day.... It's good to see a clip, that says "YES" This is Ms 🙂
Thank you for this Aaron, feeling like I disappeared after years of having to say "me, yeah I am good, you?"
You know how to brighten someone's day! Lol. I also tell the uninformed "it damages your brain...what does your brain control?......."
This is absolutely true. I was diagnosed with MS I’m 2012 and I can tell you that everyday is different. Everyday there’s another pain or another stiffness or you just cannot get up because you’re so exhausted. It’s such a horrible and painful disease. I’m only 34 and I think I’m gonna need a walking cane soon because it’s so hard to even walk sometimes and go up and down stairs.
You gotta lot of heart dude .M.S. family here Schmids are 🙏praying 📿 for you
That covers it pretty well, and thinking I have them all ! But still fighting 8 day to overcome each pain, each commorbidity that . me !
In Portugal there's a saying:" I catch all the rocks in my path to build a castle !! " what doesn't kill you makes you stronger !!
Thank you Dr. Boster! I wish more people knew about these symptoms but I am so glad you listed some of them.
Hip hop Aaron Boster, I love the way you get the information out to us. Don't mind me,between the voice and the music I almost fell out of my chair laughing. Thankyou for brightening my day friend.
My numbness starts around my belly button and progreses up to the shoulders and down to the feet all around my body. The most annoying part is not the numbness, it is the feeling of this huuuge and heavy body.
Wow ❤❤❤
It's hard to explain my symptoms to family members bc they think I'm lying, or just being lazy. Most of the time, I try to stay in my room bc they get impatient with my questions or if they have to repeat themselves.
Family turns judgmental quicker than than we can pronounce sclerosis. I think most of us with MS were loners long before our actual diagnosis. Being called lazy my whole life taught me a lot about justice.
Same here. My husband of 26 years thinks that I'm faking a lot. I was diagnosed Dec 2008. I've had to push myself harder to prove that this isn't the way I want to be. I would love to have my life before MS but this is what I have to deal with now. I isolate myself in front of our basement walkout to not bother him.
Thanks for this as I sit here unable to feel face and legs not been working lately. Go to work and walk around like a drunk and people judging.
My day in a nut shell.. 😁Thank you for your video's ❤️
You are so welcome!
Thank you for sharing this list! I deal with a lot of symptoms daily, sometimes I get used to them and can mask it well, other days I can't pretend I'm fine even if it makes others uncomfortable.
Im sooo scared to get droopy face. I have an anxiety attack when it feels like it bc i *dont want ppl to see it*
I can identify with most of these issues... Most common response I get from people walk normal.. I have my MRI scheduled for February 23rd. Hopefully I'll get some answers
youre a trip brother. I love these!! Thanks Dr B :)
More to come!
Truth.
I love it! The part you could keep going lol! Tell me about it and the list goes on and on. I’m a MS fighter!!!💪🏽👊🏽
You got this!
Looove this!!!!
Always on point, Dr. B!
Sometimes I can’t handle noise either!😂
Not just me then earplugs are my new "best friends" 🥴
Thank you for this
Yeah I’m pretty sure I have this
Nailed it!!
I absolutely love this!
Yes!!! I've heard that so many times. Thank you for this video!
Any time!
Ty
Thank you for posting these. It helps me explain to my family.
🫡. Way to explain Doc..
Big big like doctor 👍🏽👍🏽🤞🏽
Thanks for sharing this AWARENESS. 🙌
1Day@AX
I am tired of diagnoses. I don't know if I have MS and/or Parkinson's. I am a young stroke survivor with limited scleroderma, high blood pressure and other issues.
I think you should of keep going.
Love all your videos! Thank you!
You are so welcome!
Good morning Dr.!
Hello there!
Please mores shorts
So true 💕
Good music choice!!
Thank you, you listed seizures and have had the for 25 years m. I had one Doctor say they were Pseudo-seizures. That was a cruel slap in the face.
Lol nice Dr B!
I'm only coming up on 2 years being diagnosed and I've experienced a lot of these in this list sadly 😡🤦🏻♂️
Thanks Dr.B
Guess I have come to a stop...lockdowns...anxiety...the old double vision...pain.
Now agoraphobia!♡ Sigh!
Listen to alan watts and understand the more u relax the better it gets. Dont try to control or force. Thats impossible. But understand the joke and fun of it all. Its serious but never tragic
@@DarkoFitCoach or its tragic and funny... I've developed some dark humor. Lol
Yaaasssss 😊
i have what I think is mild ms for just about seven years and i do have most of these symptoms but i have a hard time saying its from ms like my balance going to the pisser blurry vision mostly when I get tired or close to being tired. I'm still learning my body yet and acceptance is the first thing I found to get a handle on.
No depression and anxiety here
Omg I’m so glad I found your channel, I had everything you listed except 3 ! Why do ppl think MS have to look sick ? Why do they think we faking? It’s just awful that’s what they think of us …. 😞
Even neurologists think that way about us. It's very depressing.
I think living alone is the only way I can keep any semblance of self esteem. Doubt in the eyes of family and friends tears me down.
My coworkers tell me this when I say I don’t feel good
I get it all the time 😕
When I get brain fog it's like I dissappear for a few minutes
Lol! Dr. Boster, are you getting paid by S. Pellegrino? If not, you definitely should be!
no sponsorships, no brand deals, no monetization of the channel. I just really like pellegrino ;)
💯
Hey Dr. Boster! I was just diagnosed with MS yesterday after MRI findings the past few months.. I have a few questions when you have time! // Why & how do hormones exasperate MS? Related to this, could taking thyroid meds affect hormones therefore throw MS out of whack? Are depression & anxiety symptoms from the lesions themselves (say if they’re located in frontal lobe) or are they residual from the complexity of living life with MS? The DSM lists OCD under anxiety, but is it possible that brain lesions can cause OCD directly or is OCD always rooted in anxiety? Thank you for all that you do! You’re such a blessing!!
Lmao you Crack me up Doc
My wife had all of these 😢😢
THAT SHIT IS NOOOORMALLLL
👍🏻
Besides these I also have stiff neck , very hard to turn my head , feels like skull and vertebra catch on top of me
What water are you drinking?
And on and on and on 🥴
I am clumsy , I am absent minded , I cant see. Oh yeah, I have m.s. so what have you been up to?
I love your spirit Elaine.
Absent minded clumsy drag yeah I have ms nailed it
I have ms & LUPUS!!! 😢
I always get told oh you look great!
Especially when I feel like crap.
It’s called smiling through the pain Karen 😂