Unusual MS Symptoms Part 1
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- เผยแพร่เมื่อ 28 มิ.ย. 2024
- Multiple Sclerosis (MS) can affect the entire central nervous system so there can be a lot of unusual symptoms. In this video I share some of these unusual or uncommon symptoms such as cog fog, MS hugs, Lhermitte’s sign, Pseudobulbar Affect, and dysesthetic itching. I also share my thoughts on how to deal with some of these symptoms.
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Do you experience any of these symptoms? And how do you manage them?
It’s me again. Just checking out your videos. 😊
Thanks for watching!
I get the electric shocks all the time. But I don’t have to lean my head forward to get them. A lot of times it just happens. It started all this happening only on the left side but now it happens in multiple places sometimes up my spine, sometimes in my throat and in my tongue, which wakes me up at night.
Oh no, that sounds annoying. Perhaps there is something the doctors can recommend to settle it down?
I have this shocking, too! The dr gave me pregabalin. It doesn't get rid of it, but it helps a lot!
Thank you for your informative videos. I have MS and your videos are excellent teaching tools to family and friends. 🙏🙏
Thanks Siena! I am glad you find them helpful!
Thanks for your excellent videos spreading important and useful information on MS.
You are most welcome! Thanks for watching!
I have had a few MS hugs especially in the night and electric shocks I have those all my life especially in the upper spine / neck it’s rather scary just comes and goes. Thank you for your great video xxx
Hi Margaret. Thanks for watching. Ugh, the hug at night must be terrible. We need our sleep.
@@EvenSoItIsWell yes indeed and the first time it was very scary as if somebody was trying to strangle me but it was around the rib cage which took away my breath and I could not move.
@@margaretpeelen3968 oh I am sorry it was so scary. I often think fear is our worst symptom.
Lesions will cause many symptoms depending upon where they are Our nerves have neuroplasticity and can change, help, or remove these symptoms by creating better pathways Being self aware 24/7 is a good start to ridding cognition issues Focus on YOU FIRST and your brain won’t be so cluttered Your body will follow close behind
I have terrible sleep!!! Nothing I do gives me good sleep
Me too!
Ladies have you tried Tumeric , in hot milk at night before bed, remember to add a touch of black pepper.
Keep lifted
Me too! I’m exhausted but can’t sleep that’s MS .
I have classic symptoms.
Absolutely 💯 ❣️ As always I completely agree 💕and also staying consistent meaning a little bit of every tip you gave at the end - every day! It adds up and I have seen the great results!! I have also experienced back tracking when I don't keep my regiment up of Meditation,Healthy eating,sleeping enough hours without waking up all hours of the night& Excersise! ect... Glad to see you😍 You look great Ms. Vicky💕
Thank you Ms Vicky! I hope you are doing well!!
I have cog fog, I have the crazy itching, I have difficulty swallowing.
I am sorry you are having all those. It is amazing how varied the symptoms can be, isn't it?
I have difficulty swallowing and the right vocal cord paralyzed, too!!
Oh interesting. I have not heard of paralyzed vocal cords before but it makes sense. MS can affect any part of us.
Thank you Vickie, always find your videos so reassuring and informative. Jane x
Thanks Jane! It is good to see you again. I hope you are well!
Thanks Vickie doing well thank you 😊 6 weekly Tysabri seems to be doing the job! More plant based foods and less diary too! Still haven’t quite managed to quit the coffee habit!
@@lemonpeelangelfish so glad the Tysabri is working well for you. And good on you for making changes to your diet! Giving up coffee? Can I ask why? I still drink my half caffeine in the morning.
Yes, yes, yes!
Thanks so much for watching!
I have had MS since I was 19 but only diagnosed when I was 52. But I had always known I had Ms as everything I read applied to me. I have Lerhmittes and for a lot of years I made investigations into what was causing it. Know one knew. I am just happy when I found out it was in fact apart of my ‘journey’. Hahahahaha
Wow! That is the longest diagnosis journey I have heard! How are you doing now?
@@EvenSoItIsWell hi I am doing well I am 87 next month just have a little bother walking use a walker which helps. But I spent a lot of years thinking I was a bit nuts. Hahahaha. Hope you keep well. I don’t take any medication as I figure I have lasted all this time without. Hope you have good health.
@@MatidaJane so glad you are doing well!
Im getting checked for MS. Nobody mentions the inability to talk. Seeing an actress with speech problems and then having some kind of surgery to make so many symptoms disappear, im hoping to hear more about that. .The MS hug is what grabbed my attention. I suffer from that every morning. Im checking to see if because of bad back or MS. Also numbness with left side, hands and arms and a slight numbness in left leg.
Thanks for watching. Good luck with the doctor’s appointments. I hope you find answers.
Hello there. I commented in one of your videos a couple months ago about my own ms suspicion. Yesterday I had an mri done and although there were signs of ms, I am now being referred to a neurologist to investigate further. I just want to know and the waiting is difficult. I guess I thought the mri would give more conclusive results. 😢
Hang in there. Diagnosing autoimmune conditions can be difficult and long. Hoping you get answers soon!