The national registry may be alive! We may be able to finally be counted! The email I just received from the National MS Society's activism team is asking the MS community to write their congress-person and urge the passage of H.R. 1362,the National Neurological Diseases Surveillance System Act, which will take a count of those with MS and other neurological diseases.
To my mind this would be a great first-step, long overdue, and it may shed some real light on MS and those afflicted. I believe when the numbers start coming in there will be a renewed sense of urgency to helping the MS community.
I just emailed my congressman (Mike Pence,R.,Indiana). It was easy to do, right from the National MS Society's website. I urge everyone to take a few minutes to do this, as this bill is currently being worked this session!
Click the title of this posting above.
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.
Monday, September 27, 2010
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.