What medication, therapy, or alt. treatment that helped the most?

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Lee__R

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07/23/2019 at 5:57 AM

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Lee__R

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There are various types of medications, therapies, or alternative treatments that are said to control or reduce multiple sclerosis symptoms.

Which have you found that has helped the most? What benefits have you seen?

Share and discuss with others and help share advice and support.

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msslady

09/21/2019 at 11:52 PM

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msslady

Last activity on 05/26/2020 at 7:09 PM

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I am taking Copaxone. I had also taken rituximab for RMS.

I have minimal side effects from the treatment... lots of fatigue and shortness of breath. But the doctor says it is working in slowing the progression. So I am hopeful it continues to do so.

What medication, therapy, or alt. treatment that helped the most? https://www.carenity.us/forum/other-discussions/your-opinion-on-multiple-sclerosis-treatments/what-medication-therapy-or-alt-treatment-that-1189 2019-09-21 23:52:07

MS_283

09/23/2019 at 2:32 AM

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MS_283

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I am also on Copaxone and have not had shortness of breath as a side effect but definitely fatigue. I'm hopeful for the same@msslady

Cgonlag

03/06/2020 at 7:58 PM

Cgonlag

Last activity on 04/21/2020 at 7:34 AM

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Has anyone taken Ocrevus or Gilenya? I am currently on Tysabri but I tested positive for the JC Virus so I have to switch meds.

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Carrie

Monkey

03/07/2020 at 3:51 PM

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@Cgonlag I do take ocrevus and it does work. but it tends to wear off at the end of 6 months. Plus when u start it fatigue is a side affect. Just makes most people sleepy

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Marcus

Cgonlag

03/17/2020 at 4:26 AM

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Thank you! Had you tried any of the pill options? (If you dont mind me asking).

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Carrie

DCircular

05/09/2020 at 6:49 PM

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I'm currently taking Ocrevus, but I've had difficulty walking for a year now. What helps with that?

pksouth514

05/13/2020 at 1:48 PM

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I am an MS fighter of 30 years now. I have been on:

Copaxone - did fine, hated the injections

Once oral meds became available, I jumped on that opportunity

Tecfidera - had a severe allergic reaction. My face swelled up - I looked like Will Smith in the movie Hitch

Aubagio - I have been on Aubagio for about 5 years now. I love it. MRI's are showing no new lesions and RRMS has been stable.

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PKSouthgate

DCircular

05/14/2020 at 5:11 PM

DCircular

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I've had difficulty walking for a year now. I was diagnosed 2 years ago, and a pretty good, and established pool player. I'd just like to walk better again. Suggestions?

1988MS

05/25/2020 at 7:17 PM

1988MS

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@DCircular I have a friend from my MS group who takes Ampyra which I think is meant for walking. I'll have to ask her more about it. I don't have any experience with it myself but maybe you can ask your doctor about if it'd be a good option for you?

DCircular

05/25/2020 at 10:58 PM

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I've taken Ampyra for some time. It initially helped me with balance, but nothing more. Walking is still a difficulty.

What medication, therapy, or alt. treatment that helped the most?

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