I posted here about 10 days ago regarding my daughter and this therapy for her M.E.
She continues to feel good . Its school holidays so she away caravanning with her boys. Last year she spent the week sitting outside the caravan having 2 lie down rests a day and by day 3 she feel exhausted and miserable
This year, despite the rain everyday, she has only had a few times when she thought she would ' crash' but its passed.
Her aching joints have also improved . I'm only talking to her on the phone but my dear daughter seems to have returned to me. Positive and so much more full of life.
She has been warned that progress might not be even and she may have a relapse when she goes back to work. She works part time as a teacher, having had to drop her hours to half time. Without me and her husband she would not have been able to do even that amount.
I'll post again once she goes back to work or if there is some change.
Can we have a poll or info gathering on how we are treated as Fibro/ME patients in the UK?
Women's immune system