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

MS News Items

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News items from recent months related to MS, via RSS. Read Only


If you wish to discuss an entry, please do so in the in the "Lounge" or "MS Discussion" sections.

558 topics in this forum

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  1. Learning from Parkinson's Disease

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    • 122 views
  2. Stem cell trial is Safe

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    • 114 views
  3. How using your legs keeps your brain healthy

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  4. Scar Wars: Battle of the Labs

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    • 120 views
  5. Survey Results: Treating PPMS

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  6. Microglial Control of Astrocytes

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    • 179 views
  7. The neurologists tool kit - Stornoway talk

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    • 129 views
  8. What is HSCT?

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  9. Have your say on the big NHS England MS debate?

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    • 135 views
  10. 2018 List of Best MS Blogs

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    • 128 views
  11. Your brain stiffens

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    • 128 views
  12. Depression to reduce MS

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  13. The Cost of MS is more than just your Health

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    • 120 views
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  14. The importance of weight in MS

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    • 132 views
  15. Guest Post- Animal Studies Enough Already

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    • 126 views
  16. Care Home vs. Independence

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    • 124 views
  17. Imaging the Rim

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  18. Not managing expectations in someone with PPMS

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    • 118 views
  19. Neuros on the take:-)

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    • 161 views
  20. Guest post: FES and the #ThinkHand campaign

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    • 126 views
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About Us

Founded in 2004, MS People UK is a non-profit 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 community 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.
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