Multiple Sclerosis Community
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198419 tn?1360242356

DMD Users: Past and Present Lists

While reading through the forum, I notice the med lists are not used so much any more.
In the past, these lists provided members a go-to person with some user experience. Hope you'll add yourselves to the list if you haven't done so already.

Below are the links


The search feature is a beautiful thing - If you do not want to copy the links individually, just type "past and present" in the search feature - it will bring them all up for you.

2 Responses
667078 tn?1316000935
I did Copaxone for a year. Now I am on chemo and can't take a DMD. My MS has not progressed while on chemo.

Glad to hear that - how much longer on treatment for you?
667078 tn?1316000935
They no longer talk about remissions. I will be on chemo the rest of my life. I am still riding and walking the dogs. The next chemo I go on in February is going to be rough and once a week. I will lose my hair again. I have liked having hair. People can't tell I am sick. I am hoping for five years. It will be four in May.

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