Good morning beloved ms family. I hope everybody is as well as can be expected and it continues for "YOU"
As we all know I am a HUGE believer in Disease-Modifying Therapy (DMT)), It is strong medicine, there might be side effects. Learn to cope and avoid them. This is a serious long term illness. There is NO KNOWN cause or cure. "YOU" are encouraged to look, and if "YOU" find one please let me know. In my 20+ years, I have never, not taken a DMT. I have switched 3 times, because I dislike intensely needles, and because Interferon Beta 1 B is different from 1A and 1A does not like me.
I take Tecfidera now and write this standing at my desk. As best as I can tell, I still have Relapsing-remitting ms(RRMS). I have injection site scars on my skinny buttocks and often feel the hard injection site scarring lumps. BUT I still walk to the mailbox and walk to the bathroom after all these years.
ms is PROGRESSIVE, it is CHRONIC, DMT or not "YOU" will get worse, that is the nature of this illness. With DMT "YOU" are supposed to get worse slower. DMT keeps "YOU standing and walking longer. Nobody can say exactly how long longer is, but not taking something leaves "YOU" completely open to the possible ravages of this disease.
"YOU" make the choice to walk or possibly not. The odds were against me getting ms, yet I got it. I am now willing to make another bet against not taking a DMT. I do not feel lucky enough to win. What about "YOU"? It is your choice in the long run.
Royce (your ms writer and Brother)
there are services out there to help you finance iasl, and we are here to help emtionslly, do what is best for you