Living with MS without any DMT
Good morning everyone, I have found myself in the last two years living without any DMT’s because I have became allergic to everything. I find that in this lifetime of mine that I have been born into M.S since 1997 that the only thing that is keeping me going is my faith in God and the strength he has granted me to have to live through this monster. Not only do I have MS but I also have Graves disease in which both of those diseases fight one another for control of my body, like they have an authority to do whatever they want to do and I’ve given them that will to do it. My question for all of you M.S’s out there. What do you do? Are you in the same boat? I am are we paddling at the same stream if so, let me know your thoughts about how you’re dealing with your disease or multiple diseases that don’t like each other and I just wanna fight and take control of your body like an alien😉The one thing I find that is helping me is to take back control of myself keep control of myself, try to take medication‘s. That can ease my tremors and my nerves because that’s what M.S does to me. I know M.S is not fun. It’s not glamorous. It’s not helpful. It’s not not not not not but I keep my faith. I believe in God I believe in his miracles and because of that I’m still here. I can still walk without a cane, I can still dance, I can still create art, I can still think for myself, I still have God‘s giving will within me to keep pushing me to do better for myself. In this country that we’re living in that has taken away all of our rights, are our privileges, are right to have a decent education, a decent Medical for our bodies for our health for our continuous growth as a person on this planet, we all must continue to fight. We all must continue to fight this disease, so can get better and improving our lives. Tell me how you feel and what are you doing? What is your pro action to make your life better living with M.S.?
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To try to fight back, I have taken part in a medical trial - the use of high dose statin to slow down SPMS. The trial finished but unfortunately showed that the statins didn't help. But at least I tried!