We with fibo should be able to have messages from nhs as it part of making use feel better i belive i not had one yet my wholebody just full of knots. Does anone agree
Fibox massages on nhs: We with fibo... - Fibromyalgia Acti...
Fibox massages on nhs
If you can tolerate your muscles being pressed and poked good luck and have a massage BUT if any touches mine I scream in pain!!
I never had a massage but some say it helps i have a lot of burning pain on my skin is well where no one can touch me x
Hi cathy1110 I think your predictive text means massages, I think they are one of the few things that really help me but you have to get someone that knows about Fibro. My lady uses a lot less pressure and a Very gentle warm, aromatherapy or hot stone massage is very beneficial. It does hurt to begin with but done regularly gets easier & gets rid of all the knots that tend to build up with Fibro. I think you can get help with payment & I'm sure my lady said, one of her clients got some kind of voucher or token from her GP, I'm seeing her tomorrow & I'll ask her.
Luv Jan xx
Hi there
This is a classic example of how people who suffer with Fibro find that different things help different people.
One thing for sure is that massages on the NHS aren't going to happen anytime soon!
I hope you are having a decent day.
Lu xx
Hi
Do you have a college near you students are always looking for clients to go in when they are training .Thiers no charge
Hi Cathy
The though of anyone touching me hurts, even a hug, so massages are not for me,a lot of people advise me to have a massage, but there is just no way I could tolerate being touched and the pain😢😢. I do like the relaxing candles and music tho 😀😀
Hi cathy1110
I agree with you completely. I have been for massages before and they have not agreed with me but certain other medical conditions qualify for the patient for free medical treatment so why not Fibro? I want to sincerely wish you all the best of luck and please take care of yourself my friend.
All my hopes and dreams for you
Ken