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MS Medications

11/19/2014

1 Comment

 
When I was diagnosed 23yrs ago with MS. My neurologist told me there was no cure at that time, no MS drugs to take (but they were in works) and not to take flu shots.

A couple years later the first MS drug had come out and I went to my first seminar about the new drug. The representative passed out the brochure’s and began the meeting. She told us what the drug would not do, what it would do and about the side effects. Plus it was very expensive and so we should check with our insurance carrier to see if it was covered. Depending on the person it would not be for everyone. One had to discuss this with one’s doctor and get a prescription. If you could not afford the cost and you met the requirements the drug manufacture may be able to help.

Then she opened the floor for questions and there were lots. I learned a lot as did everyone else. At my next MS support meeting that was the topic all evening. As time went by people starting taking the drug and would share with others how it was going and how they managed it all.

Well the years went by and many other MS drugs became available to the point they are today with many choices. Still no cure or how we get it but now we have more help with it. Also there is more medical help available for symptoms of the disease. Some years back the MS Society gave the go ahead to get the flu shots for people with MS. This really helped me since each year I got so ill with the flu and now I don’t.

Bottom line, become very knowledgeable about all MS medications you take.  Every person with MS is unique so what works for one may not work for someone else. Remember to treat your body with utmost care and respect for it will help with your MS journey a lot!

-Holly

1 Comment
Tracey Robinson
12/3/2020 08:54:35 am

I was diagnosed in 2006 with MS.Since then I have taken a few drugs for it namely Avonex(did very little for me), then Tysabri which used to work extremely well but for the last 2 years doesn't seem to do much. I was diagnosed with RRMS . Could it have progressed to a different form my neurologist has recommended a new drug called Mayzent for me just waiting to get more info about it. How long do I have to be off Tysabri for before I can start taking this new drug. I have been on Tysabri for 9 years.

Thanks for the help
Tracey

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  • About Us
  • Home
  • Virtual MS Center
    • Q & A for Virtual MS Center
    • Read About Our Virtual MS Center Staff
  • News & Resources
  • Seminar Registration
  • Health & Wellness
  • Blogs
    • Physician Blog >
      • Healthcare Provider Blog
    • Physical Therapy Blog
    • Patient Blog
    • Caregiver Blog
    • Research Blogs >
      • "Ask Dr. Debbie" Research Blog
      • Multiple Perspectives In Multiple Sclerosis Research Blog
  • About MS
    • What is MS?
    • Diagnosis
    • Treatment
    • MS Tips
  • Symptoms
    • Balance and Walking Issues
    • Breathing/Respiratory
    • Bowel Dysfunction
    • Cognitive Dysfunction
    • Crying/Laughing Uncontrollably (PBA)
    • Depression and Anxiety
    • Dizziness/Vertigo
    • Dysphagia
    • Fatigue
    • Foot Drop
    • Hearing or Smell or Taste Changes
    • Heat Sensitivity
    • Leg Weakness
    • Loss of Hand Dexterity and Coordination
    • Memory and Mutliple Sclerosis
    • Migraines
    • Numbness/Tingling/Altered Sensation
    • Nystagmus and Oscillopsia
    • Pain
    • Sexual Dysfunction
    • Sleep Issues
    • Spasticity/Spasms/Cramps
    • Speech/Swallowing
    • Urination/Bowel Problems
    • Vision
  • MS Clinics
  • MS Topics
    • Pregnancy and Infertility
    • Caregivers and Family Members
    • Employment and MS
    • Medical Costs and Insurance
    • Pediatric Multiple Sclerosis
  • Register With Us
  • Terms of Use/Privacy/HIPAA
  • MS HealthCare Journey