These people seem to be living without any palliative care. I have had a progressing form of FMD/CFID/ME since I was 9ish. It has been like this--with spasms, seizures and an inability to talk for only a few of 50 years. But it never felt good, though in adolescence and through my twenties it was no more than a bother and there was question whether I could graduate from high school. because I was out sick so much. I had trouble sleeping, trigger points, was easily injured. There was pain.
Another excellent report on ME and poor Sophia.
rosybunny100 1 year ago
These people seem to be living without any palliative care. I have had a progressing form of FMD/CFID/ME since I was 9ish. It has been like this--with spasms, seizures and an inability to talk for only a few of 50 years. But it never felt good, though in adolescence and through my twenties it was no more than a bother and there was question whether I could graduate from high school. because I was out sick so much. I had trouble sleeping, trigger points, was easily injured. There was pain.
DadsBlueAngel 1 year ago
Met ME/CVS sta je alleen.
Lijden in stilte.
Schandalig medische wereld, ik wens jullie allemaal ME/CVS toe. Stelletje ongelovige, niet onderzoekende lui.
xliefertjj 3 years ago
Sophia's tragic story has never reached the national media. Why? There seems to be a huge cover up.
Bluebottle83 3 years ago 5