Not Just Multiple Sclerosis

This page is for the support of those living with Multiple Sclerosis and family members/caregivers

02/05/2023

"MY NAME IS MULTIPLE SCLEROSIS

Hi, my name is MS and I'm an invisible chronic illness. I am now velcroed to you for life. Others around you can't see me or hear me, but YOUR body feels me. I can attack you anywhere and anyhow I please. I can cause severe pain, or, if I'm in a good mood, I can just cause you to ache all over.

Remember when you and Energy ran around together and had fun? I took Energy from you and gave you Exhaustion. Try to have fun now! I also took Good Sleep from you and in its place gave you Brain Fog. I can make you tremble internally, or make you feel cold or hot when everyone else feels normal. Oh yeah, I can make you feel anxious or depressed too. If you have something planned or are looking forward to a great day, I can take that away too. You didn't ask for me. I chose your for various reasons: that virus you had that you never recovered from, or that car accident, or maybe it was the years of abuse and trauma. Well, anyway, I'm here to stay!

I hear you're going to see a doctor who can get rid of me. I'm rolling on the floor laughing! Just try. You will have to go to many, many doctors until you find one who can help you effectively. You will be put on pain pills, sleeping pills, energy pills; told you are suffering from anxiety or depression, given a TENS unit, get massaged, told if you just sleep and exercise properly I will go away; told to think positively, poked, prodded, and MOST OF ALL, not taken as seriously as you feel when you cry to the doctor how dibilitating life is every day.

Your family, friends, and coworkers will all listen to you until they just get tired of hearing about how I make you feel, and that I'm a dibilitating disease. Some of them will say things like "Oh, you are just having a bad day" or "Well, I can't do the things I used to do 20 YEARS ago", not hearing that you said 20 DAYS ago. Some will just start talking behind your back, while you slowly feel that your are losing your dignity trying to make them understand, especially when your are in the middle of a conversation with a "Normal" person and can't remember what you were going to say next!

10/25/2022

I completed my infusion of the second half loading dose of Ocrevus today! Only took 2 1/2 hrs and all went well!

08/25/2022

Please watch to understand

08/25/2022
What You Need to Know About Ocrevus 08/18/2022

https://youtu.be/NJLDMwfma4A

What You Need to Know About Ocrevus This video was created in Summer 2017 and features Derrick Robertson, MD, Janice Maldonado, MD and Kathleen Costello, MSCN. Information is accurate as of the...

08/11/2022
08/10/2022

This event is in uniontown ohio in September . I also found a closer MS Clinic, also located in uniontown!!! Www.oakclinic.com

Jessica sent you a Pin! 08/10/2022

https://pin.it/4CFjTLW
Look at this... 👀

Jessica sent you a Pin! Discover even more ideas for you

Multiple Sclerosis Vlog: Must we treat MS? What about Mild MS? 08/07/2022

https://youtu.be/kKo5rPsGSNo

Multiple Sclerosis Vlog: Must we treat MS? What about Mild MS? In this video I answer a viewer's question about if it's ok to NOT treat mild MS, or if it's ok to stop treatment after 5 years. To hear my answer, start wat...

How I’m Living My Best Life with Multiple Sclerosis | Robin Brockelsby | TEDxUniversityofNevada 08/04/2022

https://youtu.be/BwfqBBeQSQ0

How I’m Living My Best Life with Multiple Sclerosis | Robin Brockelsby | TEDxUniversityofNevada Does being diagnosed with an incurable disease mean you’re fighting a losing battle? Not according to Robin Brockelsby, who after 46 years of perfect health...

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