What Does The End Result Of Your Treatment Do For You?
May it be daily injections, prescriptions medication via liquid or pill, infusion treatments etc....what can you personally attest to it improving or effecting? Is it a general maintenance of your current condition, prevention of progression or an overall improvement of your symptoms? Please share if you’re inclined. 💫✨✌🏻🌟 Thank you.
This was a great Question @A MyMSTeam Member! I have no idea how to answer because i was diagnosed on. 4/30/19...i have had both beginner dosages of Ocrevus, completed 2 rounds of physical and occupational therapy, i take amitripline 50 mg, vitamin D 5000 mg daily, 1300 primrose, 5000 mg B-12. Im taking these meds because i have made huge improvements.
When i was on meds, copaxone then rebiff, took them with understanding that they would prevent or reduce severity of relapses. As mri’s attested, ms was active at that time and i believed the injections were necessary to prevent a terrible worsening. Eventually course of ms seemed to change, two consecutive mri’s showed no active lesions, and i made decision to come off dmds, and began to concentrate on removing inflammation, taking vitamin supplements, diet change, exercise. Thats where im at today, no relapses, but dealing with a few ever present symptoms; heat intolerance, leg weakness, balance and memory issues, but overall feel grateful and pretty good
Ocrevus has been a game changer for me. I have been on it since January, no new lesions, plus after my last infusion on August 1st I'm walking without a cane & my gait is better. I also have been taking supplements, calcium, magnesium, vitamin D & MCT oil powder.
So glad so many were willing to respond.
Am taking Tysabri, Dalframidie,,Muti-vitamin etc. Was wearing a foot brace due to foot drop. This actually helped,to where I don't need o wear right now.
Recently Finished My 2nd Year Of Mavenclad. Sadly, Being Anemic To Begin With, I Am Not Having A Good End Result. Legs Weaker Than Before.
Hi! Has Anyone Had Stem Cell Treatment For MS? If So, What Was/is Your Result And Where Did You Have It Done? Thanks!
Does Anyone Else Have Issues With Your Legs Hurting Almost All The Time. What Do You Do For It?
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