again i have had a painful night with my back playing up all night long, every time i moved in bed it resulted in agony running up and down the spine all the time. I suppose i have to be grateful that its not the head setting off every five minuets but i am sure it wont be that long before it starts all over again. I don’t know witch is worst at times the head or the back. They both seem to last just as long as each other and leave me in sweats and agony all the time.
Today i am lucky to have my social and benefits review and maybe i can ask them if there s anything i am entitled to for help with getting about as it is becoming ore and more painful each day. Sometimes i wake u and i am in tears where the pain is hurting constantly and there is nothing i can do to ease the pain and then there are other days where i feel fins and can run around the block with no sign of pain at all. Its very strange and to what is causing it all i am in the dark.
When i first started this blog over 2 years ago i never through i would get any readers or people following my story but bow was i wrong. I seem to have touched a few people and its nice to know that if i can’t make a difference at least i can educate that this condition exists and it isn’t all in the imagination like i as lead to believe for over5 years solid. Once i got my diagnosis it was as if a light has been switched on and finally i knew what it was that was slowly destroying my life. Thanks the Dr Pickersgill, my specialist, he has been a god send and with the injections he has supplied and other medication i am finally getting my life back al be it slowly but surely.
I don’ care how slowly it takes as long as i keep getting improvements and hope that i can finally get this beast under control. It’s amazing how much its takes out of you having to deal with attack after attack bt hopefully one day it will all be over.