Commentary on life with MS (Multiple Sclerosis). Education and resources for friends and family of MS patients. Ramblings on Midwest living, gardening, food and anything else I decide to write about.
Saturday, February 27, 2010
Walk MS Event April 17 at Ball State
I am participating in the Walk MS event on April 17 at Ball State University, as part of the Anderson Area Takin' Strides team. I would be thrilled to have additional walkers as a show of support, and any of my friends are encouraged to walk with me. I don't know the time yet, but I will post it later today. As part of the event I am soliciting pledges, which are used by the National MS Society to do all sorts of good things, including research funding as well as direct aid to MS patients for things like modifications to their cars or homes or other needs. Please, take a moment to show me some love on my first walk. I thank God every day I am still walking.
Thursday, February 18, 2010
Greater Risk of Osteoporosis with Multiple Sclerosis
I have been aware of the benefits of Vitamin D on the course of MS for awhile now, but an article in the latest issue of Neurology Now discusses the increased risk of Osteoporosis as well. I am already taking Vitamin D and Calcium supplements, but may increase my dosage based on this article.
MS "Walking Pill" Approved
Ampyra (fampridine-SR) was FDA approved for all forms of MS on January 22. You can read more about it at the National Multiple Sclerosis Society's website. Click the headline of this post to go there.
Labels:
Ampyra,
fampridne-SR,
Gait,
MS,
Multiple Sclerosis,
Walking
MS Support Group Meeting Tonight
There is an MS Support Group meeting tonight, Thursday, February 18, 2010 at 7 pm. The location is the dining room at Bennett Rehab, inside St. John's. It is open to all.
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About My Blog
This is my personal blog. It details my own personal experiences with MS, as well as other ramblings about my life. I am NOT a medical professional and cannot offer advice or opinions of a medical nature. If you need medical atention, please contact a physician or, in emergencies, your nearest hospital emergency room. MS has many faces, and every single patient has his or her own unique experiences and challenges.
The links I provide are things I think may be of interest to those with MS or their friends and family for further research, and does not constitute an endorsement.