A Cambridge scientist is getting close to finding a cure for MS. 2.3 million American’s would love to see that happen. Read about this woman’s discovery about how to stop the immune system from attacking it’s own body.
Read this thought provoking article about studies being done about motion and movement in people with MS. How exercise is so worth doing, even though you would think it would add to your fatigue, it actually helps with it.
Read this great blog about finding out you have MS
Your essay really hit home for me, as it expressed exactly how i felt waiting for the dr to tell me the news. As i was walking into the doctors, there was a long hall to get to his door and i thought to myself, “when i walk out this door my life will be changed forever” and it did. But like you said, it doesn’t define me, thinking the worst is only a first response, since i had progressive kind i thought my life was over. After the initial shock of it all, was over, i developed into a calm state where i began the first day of the rest of my life. My MS stabilized and hasn’t progressed in 10 years, . One day when i was cleaning out my closets, i found my journals from the early days when i first moved to Oregon, when i worked as a timber inventory forester in the Wallowa Mts in eastern OR. As i read them, i started to chuckle and thought, these would make a good book, so i wrote three fictionalized memoirs, i never would have found the time to write, if it wasn’t because of MS. I worked 35 years in service to people with disabilities, who better to know, life can be just as good even if you use a walker or are in a wheelchair. My profession taught me how to access grants, durable medical equipment so i knew the ropes. So without MS i never would have published my three books. “The Eve Chronicles” by Diane DeVillers, check it out on amazon. Life changes, we adapt, and then finally we accept. Your story transported me back to the early days when i found out that yes MS can be a monster, but i am no longer afraid of my dragon, who waits for me, who someday will consume me, but i fight it, i do my best to adapt and move forward to what ever my path will be.
I went years before i found out that I had MS. at first they thought i had sympathetic nerve dystrophy in my foot, I spend loads of money on PT and alternative medicine. It wasn’t until 6 years later that i was sent to a neurologist that i finally found out i had MS. It was a relief to finally find out what the heck was going on with my body.
I had balance problems, my foot dropped causing me to twist my ankle and wrench my upper leg muscles more than a few times. I found out that i had progressive MS, the kind that can keep steadily worsening. My right leg is partially paralyzed, i walk with a walker and sometimes need to use a wheelchair. I have severe back pain, which i can now get relief from massage. During the summer, i have to make sure i don’t get too warm, as people with MS don’t process heat correctly and it can cause me to get vertigo.
The fatigue that comes with MS is a constant companion. I have to ration out my energy so i don’t hit a wall and run out of energy. But its bearable, all of it, i still have a quality of life i have always longed for. I became a writer and published three books in a paperback book called “The Eve Chronicles”.
This is my entry to the WorldPulse site for the world’s women to unify. They asked for us to submit our stories to show the world how we survive and thrive.
After moving to Oregon and experiencing some of the darkest winters ever, I found out I have extremly low levels. It may have been part of the reasons why i developed Multiple Sclerosis. That and the fact i was exposed to a virus or toxin by the age of 15, mine being Mono.
Research shows that perhaps higher levels of Vitamin D like 10,000 IU could slow the progression of the disease by deflating the immune system.