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For People Newly Diagnosed
If you or someone close to you has recently been given a diagnosis of multiple sclerosis, you probably have a lot of questions and concerns. Or, you may be feeling so overwhelmed by the diagnosis that you aren’t sure what kinds of questions to ask. The National MS Society has developed programs to give you the information and support you need to live comfortably and confidently with this change in your life.
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An Introduction to MS |
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Living with MS
Addresses questions frequently asked after diagnosis of MS is received-from possible causes to advice on coping |
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Disclosure—The Basic Facts
Discusses whom, when, and how to tell in both personal and work situations; includes personal vignettes |
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"But You Look So Good!"
Coping with invisible MS symptoms |
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Someone You Know Has MS: A Book for Families
For children ages 6 to 12 who have a parent with MS. Provides facts and explores children's fears and concerns |
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F.A.Q. About Society-Funded MS Research
Frequently asked questions about Society-funded MS research, including funding, approach, philosphy, and progress |
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Treatments
Various treatments are available to help reduce future disease activity and/or manage symptoms. Talk to your doctor about what's right for you. |
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National MS Society Disease Management Consensus Statement
Early treatment recommendations regarding use of the current MS disease-modifying drugs |
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The Disease-Modifying Drugs
Information on the disease-modifying drugs (Betaseron, Avonex, Copaxone, Novantrone, Rebif, and Tysabri). Includes how each is taken, side effects, benefits, and available help |
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Visit our Treatments section for more on medications, symptom management, alternative therapies, and treating exacerbations (relapses) |
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Choosing the Right Health-Care ProviderMS Care Treatment TeamTreatment Locations |
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| Employment |
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MS and Employment
These programs and materials will assist you in making informed career decisions |
 "I started telling people close to me that I had MS. This was a huge weight off my shoulders." Meet Mike Zimits
 When Sharon Dodge was diagnosed, she and her family joined the fight against MS. Meet Sharon
| Magazines |
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Momentum (formerly InsideMS)
The magazine of the National MS Society |
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For Kids
Keep S'myelin—our newsletter for children | |
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Meruka Gupta—"I thought MS was an immediate sentence to a wheelchair, and having been very athletic all of my life, this terrified me. However, I very quickly realized that this was not the case. I was just beginning my life, and I was not going to allow MS to end it." Meet Meruka
Researchers need YOU!
People newly diagnosed with MS during 2007 are urgently needed for participation in a study of MS and quality of life. Early results from this study have increased our knowledge of MS, helping researchers understand the many factors that affect disease course. Get more information on how to join (PDF)
Read more about the Sonya Slifka Longitudinal MS Study
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Support |
Connect with others whose lives are affected by MS
There are over 1,800 National MS Society-affiliated self-help groups across the nation representing people with MS, family members, and friends. Contact your chapter to find out more.
1-800-344-4867
MSWorld offers the official National MS Society chat rooms and message boards with a hosted chat on Wed. at 8:00 pm EST specifically to answer questions and concerns for those just learning about MS.
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