I'm Pamela, I was diagnosed with Multiple Sclerosis on November 15, 2002. I was on Copaxone from November 2004 till May of 2013 and have since been on Tefidera. I hope my blog can help benefit others!
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Pamela, I work with a company, Good Days from Chronic Disease Fund, and it is our mission to help chronic disease patients get the medical care they need, at an affordable price. Visit our website to learn how to support our cause http://www.gooddaysfromcdf.org/
I had coordination problems and had difficulty walking. I would get "real tired and my speech was like I had had a stroke" then it would get better. I will be pretty good and then have a part of me that gets very touchy. I sometimes could burn myself and not even feel it. I had a nerve test for a possible pinched nerve and they did the test 4 times. They said I had only 60% of my nerves functioning and called me superwoman, because I walked into their office, upright and reasonably normal. The test put me in a weakened condition but I did walk out the office without much help. I can't be around many insecticides because they bring on the symptoms and can put me down. I was down once for 8 months. We figured I probably had this since age 13 or so, but now I am 65 and still going. Good vitamins help a lot. And Limu gives me energy, so I can go even when the symptoms are there. Doctors were killing me, so I sought alternative medicine.
I’m not that much of a online reader to be honest but your site provides so much valuable information, keep it up! I’ll go ahead and bookmark your site to come back in the future. All the best!
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