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Has Anyone Found That Switching MS Meds Helped Them Get Back To Work?

Has Anyone Found That Switching MS Meds Helped Them Get Back To Work?

I've been on Copaxone for the past 3-4 years since my diagnosis. I have multiple new lesions and the neuro wants me to switch to Tecfidera. I have flare symptoms every couple of months and my spasticity has gotten so bad. Along with memory and speech issues. I'm hoping that a switch to Tec may help me get a true remission for a while.

posted almost 5 years ago
A MyMSTeam Member said:

From my personal experience....I started on Copaxone. In the next year I gained 5-6 new lesions. The next year I spent on Rebif, and it made me feel horrible. Finally I switched to Tecfidera. 4 and 1/2 years later, MRIs have been stable. I still have issues from time to time, but feeling the best I have on Tec. We can only hope that our treatments help slow things down! Hope this helps a little!

posted almost 5 years ago
A MyMSTeam Member said:

I, too, was on Copaxone for 20 years when an MRI showed it was no longer working. I was switched to Tecficera. My fatigue level is through the moon, but taking care of my 15-month-old granddaughter keeps me up and moving. I wish Tecfidera would help with my walking speed.

posted almost 5 years ago
A MyMSTeam Member said:

I have been on Tecfodera. 4. A. Year. Don’t seem 2. B. Helping

posted almost 5 years ago
A MyMSTeam Member said:

I am on Tecfidera. I have had minimal side effects. Prior meds included Copaxone, Rebif and Tysabri. All were O.K. The key is to make sure that you don't get taken off one without being placed on another. I was taken off of Copaxone due to a site infection by a prior doctor who did not put me on anything else. 4 months later I had a exasperation and ended up in a nursing home for 3 months. I had full functions (walking too) prior to the incident and now I am wheelchair bound and only able to use my left arm.

posted almost 5 years ago
A MyMSTeam Member said:

I get MRI on Saturday to see if I need to switch as well.. Hoping I don't need to.. I really like @copaxone... I've had worse spasticity too but I've been dealing with this diagnosis for 30 years

edited, originally posted almost 5 years ago
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