This is MY journey with MS! I give you my thoughts, feelings, hopes, and prayers. My wish that one day this disease will come to an end. That one day there will be a cure. For now, I hold on to possibility. I HOPE this will help and inspire not only myself but others.
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About Me
- Jaime
- I was diagnosed with MS in 2004, have been through all of the FDA approved treatments I qualify for and now am participating in the HALT MS Study. This is my story...my life with MS (among other things).
Do you have a MS Story to tell? Any suggestions, ideas to make my blog better?
I would love to hear from you. Please send me an Email.....
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MS Advocacy
MS Bloggers
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MS Links
- Accelerated Cure Project for MS
- Allison Shaddy: MS & Your Feelings!
- Consortium of MS Centers
- Cure MS Now Research Fund
- Face of MS
- Heuga Center
- International MS Support Foundation
- Maureen Manley: Spirit in Motion
- Montel Williams MS Foundation
- MS Active Source
- MS Association of America
- MS Complementary & Alternative Medicine
- MS Foundation
- MS International Federation
- MSplus Foundation
- MS Watch
- National MS Society
- Race to Erase MS
- Rocky Mountain MS Center
- Top 10 Sources (I'm #3)
2 comments:
Thanks for sharing all that info! I don't keep up with all the MS news like I should be...and because of your post I won't be missing Montel's show next month! Oh to be a child with MS!
I can't even imagine what it must be like to have this illness as a child. As difficult as this has been for me..to be diagnosed at the prime of my life...just finishing school, having a small child, etc. but to have your whole life to look forward to not knowing what will happen from one day to the next. I wish her and her family the best!
I am sure she is such an amazing child. I worked in Pediatric Nephrology (kidney disease for those of you who don't know what that is) and I was always amazed at the spirit and hope those children had...they were always willing to fight (some had never known anything different). They came each week for dialysis, prepared for transplant, etc. It sounds to me as if this girl is just as amazing. I look forward to hearing about her story next month on Montel and hope that she is well.
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