,,,especially when looking for a restroom. Once the initial reaction(s) of being diagnosed with MS is over, we Warriors are left to fend for ourselves…forever. If you’re not living with the disease, it is no longer personal to many of those around you. While…
Archives for 2019
Letters to the MonSter
Dear MonSter, What would you say if I told you I think it’s time to kick you to the curb? You are no longer welcome in my life. You need to leave me alone, find a new host, because I am simply tired of your existence. You’ve become a parasite. You live off my pain….
letter of appeal x3
This week I will add (hopefully) one more support letter to my appeal to the insurance company in regard to their denying a request to aid in the payment of the L300 Go. After my PT evaluation on Monday, I fear it may be too late for this walking device to help in reactivating the muscle in…
L300 Go, go, go
Today’s the day. It couldn’t come any sooner. The MonSter has been kicking my buttocks (isn’t that a fun word?) lately. Today I will receive my physical therapy evaluation in order to receive a letter from Rebecaa, my friendly PT. I will add this documentation to my impressive (If I do say so myself.) file of wordage…
Monday, Monday…
Ya want to know what MS looks like? Well, here ya go. My head ache began Saturday afternoon (that’s two days ago, it you are reading this post publication) and it’s not only still hanging around, it’s worse. The sledge hammer imprint makes wonder if I walked into a wall and don’t remember. The area around…
Do something nice for yourself
No matter how long I live in the company of the MonSter, I never get used to it. I get tired of pushing through the day on legs that will not move and feet that cannot feel. After treating myself to a gentle yoga class this morning, I could barely move. I forced myself to…