I'm so pleased to hear that, as you were having such a hard time with the side effects. Long may this continue. A new year, new hope :)
That is great news Candy. I'm so happy for you & hope it continues this way from now on. I've been on so many DMD's from a young age due to my RA & some of them had me with my head in a bucket with constant nausea. Now I have MS there has been a few comments from doctors suggesting I look into the possibility of having an injectable as well as my Rituximab.
I really don't want to have a truck load of side effects on top of what I already have though so I'm just waiting to see if my MRI next week is any different. If it is no different I'm thinking I should be OK with just being on the Rituximab. I also have to be careful with my past history of Neutropenia as well.
I want to say well done for sticking with it Candy. It's certainly not nice to have such bad side effects week after week.
Hugs......Karry.
Karry you are so right, and if they suggest a DMD for you, maybe try Copaxone, that one didn't really have awful side effects, it just left lumps under the skin, and after 1 1/2 years of it they decided I should try something else, hence the Avonex.
I did not mind the Copaxone, it was just an every day one drug, and Avonex is once a week, but since it seems to kick me well for 2 days, I am hoping that the luck I had this time, will persist.
Hoping that you will feel better, and that wtih the MRI they will come up with a plan for you.
((hugs)) to you,
Candy
thxs Ghost, I am stubborn, and am also hopeful, so between the both, I should be able to try this for a while anyways.
Hope you are doing ok ......
((hugs)) to you,
Candy
I'm happy to hear things are improving for you :-)
Kyle
Sweetie, I am beyond thrilled that this is getting better for you.
Gentle hugs,
Corrie
thxs guys ...... for all the support !!
Glad things are going alright for you (at least in this area).