Skip to Accessibility Tools Skip to Content Skip to Footer

Matt’s Story with MS

Hi my name is Matthew. I was born in Michigan. I have a nickname up their and it is Mutty down in lower Michigan. It’s Mattie so thats the nickname I use. I found out I had MS in 2001 it was relapsing remitting. It was painful my nerves hurt bad, but I could still work my job.

Then got a job down in Virginia. I was helping build a ship for Northtup Grumman. I helped build CVN 78 for the military. I truly liked the job but got laid off. While I was still there, my MS changed to SPMS. I had to find out how to keep on going so I could live my independent lifestyle.

So, I now do a exercise with 5 to 10 pound rubber band weights. Keep the muscles moving. My neurologist says if you don’t move it, you are going to lose it. So I exercise everyday safely. I also eat a lot healthier now. I take my prescription meds and my OTC vitamins and meds for helping my body fight against my SPMS to do my best to slow the progression down. I try to keep using my muscles that I use all the time. I don’t want to lose my ability to be independent.

This article represents the opinions, thoughts, and experiences of the author; none of this content has been paid for by any advertiser. The MultipleSclerosis.net team does not recommend or endorse any products or treatments discussed herein. Learn more about how we maintain editorial integrity here.

Comments

  • HeatherH
    11 months ago

    Thanks for sharing your story!

  • Carol
    1 year ago

    Mattie,

    What are you doing now since being laid off from Northrup Grumman? I know you have been eating healthier, taking your meds, and exercising, but are you able to still work? I pray that you are still able to do so because it is so very upsetting when the realization comes that you can no longer work.

  • H Parks
    1 year ago

    Love the nickname variation! My family (Parks) is originally from Long Island, NY. My Dad had the nickname, “Pax”, which I never understood until I heard someone from the East coast pronounce it! To someone in Kansas City it made no sense; until now!

  • Erin Rush moderator
    1 year ago

    Hi matthew76mattie! Thank you for sharing a part of your MS story with the MultipleSclerosis.net community! It sounds like you have created some great ways to maintain your health and I think that is wonderful. I hope you are able to maintain your health and independence for as long as you would like! Thank you again for sharing! Best, Erin, MultipleSclerosis.net Team Member.

  • Poll