on 23-08-2014 09:58 PM
on 26-08-2014 02:25 PM
http://www.webmd.com/fibromyalgia/guide/what-is-fibromyalgia
That does sound nasty, Kilroy. I hope they manage to find some relief for you.
on 26-08-2014 02:31 PM
on 26-08-2014 02:56 PM
on 26-08-2014 03:14 PM
on 26-08-2014 03:16 PM
Keerp a positive attitude and try to not let it limit you too much.
My attitude is that if I don't do it, or I do do it, I am going to hurt, so what the heck just do it.
Sleep deprivation is not exactly fun though, nor is the broken thermostat (hot cold sensitivity)
I also have Auto immune induced chronic active hepastitis (cactussed liver) so I can't take pain killers and other meds, well I hadn't been until a few weeks ago and now I take one panadol osteo in the morning so I can get through the domestics easier lol. It takes the edge off. I am on weekly blood tests to make sure the meds aren't damaging the liver.
If you have had it a long time you would have been on pain management I would assume. Even without diagnosis I assume you have been taking pain relief.
It is far better to know than not to know, because now when the brain fog happens you can just deal with it and not think you are losing it.
on 26-08-2014 03:26 PM
Yeah it is a bit ordinary isn't it. Just don't let it rule you, and don't let it get you mentally down
Also don't assume everything is just the fibromyalgia as you progress through the years. It is too easy to let something worsen because you assume it is just the fibro, and then you get to be up the proverbial creek without paddle.
I know, I know don't be bossy channys_mum
on 26-08-2014 04:15 PM
on 26-08-2014 04:20 PM
on 26-08-2014 04:33 PM
oh..my dear...i'm so sorry...i have friends here who are dealing with fibro...so many people don't realize that what you look like isn't what you feel...i can ask for links to give you,if you want to see them? maybe you've read them already,...but maybe not?
on 26-08-2014 04:37 PM