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@angieH 

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angieH

TN

Hi, I was wondering if anyone has had trigeminal neuralgia present as teeth pain! I have had sinuses the made my teeth hurt before but not this pulsating, shocking kind of pain along the upper row of teeth on left side. I thought tn was more like head/face pain? At first I thought it was sensitiv...

@Thorpee 

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Thorpee

UK car insurance..

Hello everyone, a thought came to me in the dead of last night. Has a diagnosis of MS dramatically affected anyone's car insurance? I presume it has to be declared? Weak legs and twitching eyes are one thing, but if this affects my pocket as well I'll be very unhappy. My car insurance is currently c...

MS moms & opinion poll

Years ago I needed to change my life completely. Why? That was not my choice but my health conditions. I was diagnosed with MS and it felt heavy to carry with me. I was afraid to dream about the future or even live a day with love, care, and understanding to myself. I felt guilty when I wanted to ...

@Lonnie_Warren 

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Lonnie_Warren

Symptoms

Hi all hope we’re all good have a weird one , well for me any way laying in bed last nite not getting to sleep as ever , and I had my eyes closed but it felt like my eyes were darting all over the place but I’m sure there weren’t actually moving . Not like when your drunk and room spins but farting ...

New PPE for the Mind episode

How would you describe your emotion in this moment? Calm? 🙂 Sad? 😢 Angry? 😡 Anxious? 😨 Happy? 😄 - In episode 6 of 'PPE for the Mind' episode, Jo asks us to observe our bodies, noticing any areas of discomfort or emotions 💆‍♀️ To get the most out of the episodes, grab a cuppa ☕️, take a ...

@Aiga_Akmentina 

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Aiga_Akmentina

What`s your well-being story

Hi! I<code>m not usually the one to write and ask, but there come moments like this when it</code>s just a natural action. So to the point...I understand your questions, life challenges, your ups, and down days. I`m an MS mom and have the disease for 17 years now. So the first time I met MS as a dia...

@kbuda 

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kbuda

Friends

New here and not sure how to find friends. Is this like FB for MS?

@angieH 

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angieH

RRMS to SPMS?

I have read that rrms always eventually becomes spms. Is this so? I have a neuro who says that usually by my age (53 and diagnosed at 29), ms has established the pattern it is going to be. One sounds promising and one not so much. What would clue me in that it’s becoming spms? I have more difficu...

@tiffscriv 

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tiffscriv

Extreme shivering/chills with Brabio

Hi, It’s currently just gone 1am here in the UK after the hottest day this year and I am wrapped up in my duvet and I cannot stop shivering. I’m aware this is a common side effect when using Brabio/Copaxone but was wondering if anyone else has experienced similar and how long does it generally last...

@Claire_Juliet_Woon 

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Claire_Juliet_Woon

Advise on Exercise

Hi I have RRMS, diagnosed September last year and been on Tec since May this year. Anyway to cut long story short started weight training again after a period of not doing anything, the issue I have is after lifting weights I have had NO arm/muscle ache at all the day after, it is like I have not ...