DMD Users: Past and Present Lists

[sllowe]

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

http://www.medhelp.org/posts/Multiple-Sclerosis/Gilenya-Users-Past-and-Present/show/1469412
http://www.medhelp.org/posts/Multiple-Sclerosis/Copaxone-users---past-and-present/show/643683
http://www.medhelp.org/posts/Multiple-Sclerosis/Tysabri-Users---Past-and-Present/show/1569374
http://www.medhelp.org/posts/Multiple-Sclerosis/Aubagio-Users-Past-and-Present/show/1946899
http://www.medhelp.org/posts/Multiple-Sclerosis/Our-Tysabri-Users---Past-and-Present/show/658918
http://www.medhelp.org/posts/Multiple-Sclerosis/DMD-Users-Past--Present---Copaxone--Rebif--Avonex--Betaseron--Tysabri--other/show/1193746

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.

~shell

[HVAC]

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.

Alex

[HVAC]

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.

Alex

[sllowe]

Glad to hear that - how much longer on treatment for you?