tag:blogger.com,1999:blog-2810036471450306171.post6215542329072043824..comments2023-06-29T09:43:48.273-04:00Comments on I'm an MS Activist: Society Volunteers Testify at Social Security Administration HearingMS Activisthttp://www.blogger.com/profile/01166485651419984213noreply@blogger.comBlogger3125tag:blogger.com,1999:blog-2810036471450306171.post-26850242937590889842011-06-01T17:27:11.583-04:002011-06-01T17:27:11.583-04:00I believe that research should go into the CCSVI p...I believe that research should go into the CCSVI procedure since it really does work. I'm living proof of this. Without proper blood flow going to the brain, how good could that be? Once your jugulars are clear, almost all symptoms are gone, especially fatigue, which many if not most of us with MS endure.Anonymousnoreply@blogger.comtag:blogger.com,1999:blog-2810036471450306171.post-57980025204953049882011-05-02T18:51:54.124-04:002011-05-02T18:51:54.124-04:00I think that is wonderful, as a person that it see...I think that is wonderful, as a person that it seemed like it took forever to obtain SSI and social security and having MS I hope they do pass this. I am now in a wheelchair and on oxygen so I qualify. Should are disease really have to go that far?Donetta Self (Oklahoma)noreply@blogger.comtag:blogger.com,1999:blog-2810036471450306171.post-81959937096792864552011-05-02T16:30:29.069-04:002011-05-02T16:30:29.069-04:00I was diagnosed 3 years ago with Ms. I think it is...I was diagnosed 3 years ago with Ms. I think it is wonderful what the society does for all of us with this disease. Being a dad and husband I try to do as much as can to raise awareness of Ms. I work hard everyday and I plan on doing so until I can't no longer my family needs that. Remember no one can take this disease back so don't ever stop living. My family and I have done the Ms walk here in Ma, every year since I was diagnosed, and I plan on doing it for the rest of my life. THANK YOUJeffhttps://www.blogger.com/profile/06726635545301945050noreply@blogger.com