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@fuzzy9 

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fuzzy9

PPMS

Hello! I was recently diagnosed with PPMS. Ever since I have had usually heartburn and swallowing issues. I visited gastroenterologist some months ago and according his review I had no visible problems when swallowing. The question is that can MS cause problems with swallowing? Whenever I try to sw...

30th Aug Sunday Meeting

This coming Sunday at the Holiday Inn, Kidderminster Road, Bromsgrove B61 9AB is a MS meeting, all welcome, free parking, good coffee and hopefully an interesting meet up. www.wholesorts.com take a read of my blogs as I am sure you will enjoy

@Jo_Perpetual 

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Jo_Perpetual

MS in Africa

Is any one here from an African country? I'd like to not be the only one i know

@Ralee 

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Ralee

Whats everyones feelings on the future?

As the title suggests, whats everyones gut feeling on the future advancements of MS? Are you optimistic or unsure? The world of MS recently discussed. Fasting, along with 2 known diabetes drugs. Some proteins that can aid recover and maybe half progression. I think, a cashew molecule was looking ...

@Aaron_Holden 

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Aaron_Holden

Recent diagnosis

Hello everyone. I just wanted to say hello and maybe get any useful info from anyone who may have had similar experiences. Firstly I want to point out that I am not suffering badly and am well aware that I am more fortunate than many so really don't want any sympathy, just thought my story might be ...

@MJSCRUGGS@8374 

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MJSCRUGGS@8374

Brain leisons

Are headaches common with brain leisons in MS?

@DesN 

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DesN

Sleep.... I really miss you!

Hi all...... I had a really good friend once called sleep... however since MS came along we seem to have grown apart! Share your miracle cures to get us back together again! Pleeeease...... I really miss him

@Shannon_Simons 

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Shannon_Simons

Multiple auto immune disorders

Hi everyone I just joined I was wondering if any of you have multiple auto immune disorders? I found out I was diabetic (type 1) when I was 20 and recently at 36 diagnosed with MS last year. Now knowing that a lot of what I was experiencing for years had to do with the MS it explains a lot. I actual...

@Paul_Hennessy 

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Paul_Hennessy

What a great Platform ☸

Has anyone never had a days rest?. Always something with my MS spasms pain bladder optic nerve inflammation in the nerve so on so forth never-ending since I was diagnosed I was wondering is this common with MS