Would you like to know why I with a diagnosis of CFS/ME could:
- Enjoy a normal (not business or premier) long haul flight and arrive happy and with energy?
- Go walking with the dogs in the tropical heat, up and down dale without feeling coma-tosed exhausted?
- Muster up the determination to cope with the terror of going into the big, wide, ocean with the turtles despite not being able to swim or float?
- Not get ill after copious amounts of alcohol while we were celebrating?
Are these things something you would like to do, or are you like I was a few months ago saying: No way, I can only cope with where I am because that is the only thing that works for me now?
My life from diagnosis has changed, and to all intents and purposes most who know me well would say I am recovered.
I am writing a book about my life with CFS/ME and probable fibromyalgia.
If this interests you, please let me know!
Hi my names Kate.I went to school with Jonathan and suffered with M.E for 13 years from 17-30 until I became pregnant, it went into remission for a number of years through the pregnancy and while I was extended feeding but has been back with a vengance for over a year now worse than before.To the point where I am virtually housebound.I would be very interesed in purchasing your book and extremely grateful for any advice you may have to help me get my life back.
How lovely to hear from you.
I am so sorry you have this illness.
I will contact you via your email address for a more private chat.
My Tone and Stretch DVD may help in the first instance.
Watch out for an email from me, it may land in your spam folder.