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…
Archives for September 2019
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…
Writing an Appeal
I am looking for advice. Some of you know that my insurance denied any assistance with acquiring the Walk Aide L300; mostly on the basis of a lack of clinical evidence that that the device is not necessary to the diagnosis of MS. I am now filing an appeal and am looking for suggestions/advice/prior experience in the…
Is it possible to live disease free?
The following information is the original content of livediseasefree.com. …when I was diagnosed with MS 29 years ago, I was told there was no hope for me, and no cure.The experts told me there was nothing I could do to change the course of the disease, and they assured me I would end up in…