Jump to content
The MS PEOPLE UK Forum
Support, help, advice and information for Multiple Sclerosis. Ask questions and share experiences with people affected by MS.
Jamesmatheson

Body temperature

3 posts in this topic Last Reply

Recommended Posts

Jamesmatheson

Hello friends

I am a student and i believe i have found a treatment i hope we can ask the medical board to allow.

I believe that adjusting body temperature will help in treating MS.

Just like when a person goes outside when its cold.

They forget about what they were thinking and focus on the cold.

The reason is their veins get more narrow which stores more oxygen and makes them focus.

I am having made a needle that adjusts blood temperature so veins are more narrow and stores more oxygen. The needle also heats up the blood and releases oxygen.

It makes a person warm when its cold outside and cold when its warm.

Theres no drugs.

Its only a needle that heats and cools blood.

I only ask for advocates to ask the medical board to allow the device to be used.

I promise it will help a lot.

Please reply 

I hope you like what I share

James

Share this post


Link to post
Procrastinating
Stumbler

@Jamesmatheson , heat (and cold) sensitivity are known symptoms of MS that can cause issues, so a device to regulate our core body temperature seems like an obvious solution.

However, this Forum is specifically for UK Msers, so I'm not sure how we can help with your development in Canada. Although, I wish you well with it.

 

:moonieman:


John aka Stumbler (as I do fall over!)

Illegitimi non carborundum

 

"Life is not a journey to the grave with the intention of arriving safely in a pretty and well-preserved body, but rather to skid in broadside, thoroughly used up, totally worn out, and loudly proclaiming... "Wow! What a ride!"

Share this post


Link to post
Balanced
Happymama

I'm a redhead so we have odd issues.  Core temp - changes too easily - give me a hot drink and I'm boiling.  Cold drinks - freezing.  I hate cold drinks, bar  white wine (lol) and prefer water at room temp.  I love hot baths though.  Helps the sore back ... a legacy issue.  And also any spasmed muscles!  Oh, YES.  

 

Also, heat and cold pain, is a thing with redheads. We really are a different phenotype. We even smell differently.  Our skin is more acidic and different bugs grow on us.  But we can't half handle chilli.  No one knows why. But GIVE US CHILLI!   We also need 25% more anaesthetic and there's not a redhead in my family that's not woken under it.  Me included, a dental anaesthesia.  

 

I have also been diagnosed with skinny veins that roll, so they run away from the needle.  The only people I have confidence in to get bloods from me are midwives.  They do LOTS of blood takes.  A consultant once when I was PG with twins had to resort to the back of my hand and went right through to the other side and I was close to punching her.  When I was in the RAF, in a fast jet, the negative G used to make the pilot pass out and I'd be there in the back (for purposes of fault Dx) , with those bands squeezing my legs, wide awake and hands ON.  What FUN!

 

 


Edited by Happymama

Share this post


Link to post

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Similar Topics

    • Moving your body!

      I have lived with MS  14 years ( now SPMS), I’m housebound but I’m not in wheelchair! I walk and balance a bit dodgy !! I try to exercise so I don’t seize up and I teach other warriors exercises too !! It’s great mentally & physically! It increases fitness, endurance, strength, flexibility, gait, posture, balance, coordination and mood ! Decreasing spasisity, pain, weight, fatigue!! If you have MS like me ... If your balance is not good... If your walking is dodgy... If your body is seizing up... If your symptoms are exacerbating... DO THIS, SEATED, STANDING, LYING ONLY: “Multiple Sclerosis Fitness with Jayne MSer & Warrior “: YouTube U.K. Try if you are able to 💋Big hug 💋 Encouragement, inspiration and help is all I want to give!!!!!    

      in General Discussion about MS

    • Body temperature

      Hi everyone, I've been sitting in the lovely warm sun this morning, reading my Kindle, sunglasses & hat on when I decided it was time to move around. Well! I felt really unwell & was glad to take a proffered strong hand. Feeling much better now in the cool of the sitting room and after a long drink. Just made me wonder if ms can make you lose your temperature awareness & control. This would also explain my sudden sneezing fits! Any views out there? Jill x

      in General Discussion about MS

    • body temperature ?

      does ms play a part in body temperature ? I have no cold or flu symptons always feeling the cold,ive got the heating on full ,and family are moaning its too hot !!,and stripped of to the bare minium !! tc guys xx

      in General Discussion about MS

    • weird sensation over body when drying hair

      Hi, I don't know why but I've just noticed that when I'm drying my hair (quite vigourosly) I'm getting weird tingly sensations all over my body. I can replicate whenever I rub my scalp.   Has anyone else ever experienced this ?   Steve

      in General Discussion about MS

    • Temperature control

      Hello everyone, it's a very long time since I've been on here but I've got a curious question to ask you.   I seem to be having trouble controlling my temperature. I get very cold and my fingers go prune like, but then I suddenly go hot and sometimes sweat. It doesn't always come over me in a wave so I am not sure about putting it down to menopause, it can be quite sudden. Then I can go cold again.   Does anyone else suffer from this and do you know if it is MS related.   Thanks.   Jill.

      in General Discussion about MS

About Us

Founded in 2004, MS People UK is a community website and discussion forum by and for people with Multiple Sclerosis as well as for friends, families, supporters and those interested in this disabling condition.

If you’re newly diagnosed or want to ask about possible first symptoms, or if you’ve had Relapse Remit, Secondary or Primary Progressive MS for some time, a welcoming group of fellow MS sufferers is here to chat with you about MS symptoms, diagnosis and treatments.

The atmosphere is friendly whilst being compassionate, supportive and caring. Members also post about a variety of subjects not related to MS, as well as share jokes, talk about their hobbies, have fun, and more.


The MS People Forum is not responsible for advice or information supplied by members. We suggest you seek medical advice before trying anything.
×