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What are the best treatments for Multiple Sclerosis?
Treatments for Multiple Sclerosis: what real patients say works for them, alongside a medically reviewed overview citing sources like NIH GARD and Orphanet.
That's a conversation for you and your specialist. There are many options available today. There are DMD drugs and special diets such as gluten free, dairy free plans.
Because MS symptoms are often triggered by inflammation it's a good idea to try to avoid goods that trigger an inflammatory response.
Physiotherapist is often helpful as well.
Because MS symptoms are often triggered by inflammation it's a good idea to try to avoid goods that trigger an inflammatory response.
Physiotherapist is often helpful as well.
Posted Apr 27, 2017 by Tess 811
Although placed under the MS umbrella this diesease is as invidivual as the people it affects. Everyone experiences different symptoms and struggles as a result. Therefore, it's unrealistic to suggest only one treatment works. What has worked for me will not necessarily work for someone else. However if you're interested in my personal experience, here it is. I was placed on copaxone and tecfidera, unfortunately I relapsed on both of these medications and was placed on Tysabri. After reading the book "Overcoming Multiple Sclerosis" by Prof George Jelinek I became more mindful of my diet and excercise regime. I do yoga, frequent meditation and cardio as well as weights occasionally.
Posted May 31, 2017 by Letty 700
Personally, I never bought into the idea of the pharmaceutical treatments available. I was diagnosed in June 2012, started Copaxone (which turns out I was allergic to) and quickly was taken off of it. Then I started on Rebif, leaving me bedridden with a high fever, aches, and flu-like symptoms every other day while trying to keep my 40-60 hour/week job in Human Resources. I couldn’t only stand to give Rebif about a month of my life before I told my doctor that I was done with the DMDs - or Disease Modification Drugs. In 2014, I applied to Northwestern Memorial to be considered for Dr. Burt’s HSCT (Hematopoietic Stem Cell Transplant) trial. I was contacted for an interview less than 12 hours later. After my evaluation in Chicago, Dr. Burt accepted me for HSCT and my insurance approved it at 90%. I had the transplant on July 28, 2015, and have been in remission since. No new activity in what was once a VERY aggressive MS brain! I can’t recommend it enough.
Posted Jan 10, 2018 by Brandi 300
Master Kong which is a nerves specialist, i followed his treatment for 3 years already. From fully paralyzed 3 years back then till now, im able to walk around.
Posted Feb 8, 2019 by Jessica 800
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The treatment that I'm wearing is Tecfidera, I will be well in time..take Fampyra and I don't gave a result
Posted Feb 28, 2017 by Belén 1111
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COPAXONE, TYSABRI, LEMTRADA
Posted Mar 1, 2017 by Jose 1140
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Acetato de glatiramer
Posted May 4, 2017 by Antonio 1050
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Acetato de glatiramer,gilenya, betaferon, etc
Posted May 4, 2017 by Bely 1000
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The IN has treatments with medications of high technology but there are some protocols that are often used as the vitamin D.
Posted May 11, 2017 by Thais Sivieri Tauil 1000
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I took 3 but what is controlling is the Gylenia Fingolimod
Posted May 11, 2017 by Tatiane 1000
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The neurologist will know best which medications to use in each case. But complement it with physical therapy is always a good solution.
Posted May 13, 2017 by Rui Rodrigues 2650
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Interferon, pregabalin and fluoxetine.
Posted May 27, 2017 by Laurentina 600
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Acetato de Glatiramer
Posted May 31, 2017 by Laura 2000
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In my opinion the best treatments for ms are, physical therapy, psychological treatment, exercise, aquatics, administration of the appropriate drug to each patient, which in my case would be Tysabri.
Posted Jun 1, 2017 by Ezequiel 2100
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I have not yet found
Posted Jun 1, 2017 by Damien 780
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A must see, with several neurologists
Posted Aug 16, 2017 by johnny 1000
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gilenya
tysabri
copaxone
tysabri
copaxone
Posted Aug 16, 2017 by Boucheron 1125
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Each patient is a different one. I after trying 4 different, I started with Lemtrada and for me it is the best.
Posted Aug 31, 2017 by Javi 200
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I've only known the tysabri or natalyzumad and from 5 years ago is who I slows down those dreaded outbreaks.
Posted Sep 2, 2017 by Gines 400
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I used first the interferon but with the time I could not bear the pain on the skin, I changed to an oral medication the tecfidera.
Posted Sep 14, 2017 by Cristy 700
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The intellectual activity, the life of the family
Posted Oct 2, 2017 by Joseph Alaimo 1000
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Aubagio, with the least side effects, in my case.
Posted Oct 6, 2017 by Maria Manuela 1020
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Colecalciferol. Protocol Coimbra.
Posted Oct 22, 2017 by Maria 200
