does anyone get the same symptoms
Posted , 9 users are following.
I just wondered if other people were the same. Some days I feel like I have nothing wrong with me but this week I can hardly move and in agony.I'm
Still struggling to go to work because haven't been able to claim anything.
Really struggling to know what to do
0 likes, 49 replies
tiswas24537 ingrid19972
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nitropilot tiswas24537
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arual2014 ingrid19972
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nitropilot arual2014
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Check out info on the HPA Axis, Chronic Fatigue, Fibromyalgia, etc. They all have a common theme. Biochemical imbalances that affect the nervous system. Hormones. They control every process in our body. One jacked up producer or receptor and everything else on down through the processes is doomed. Sounds catastrophic but its just biology, the endocrine system.
Taking care of yourself is the best thing you can do. And don't stress the blank out when you don't meet your own expectations of how you should be!
brenda59210 ingrid19972
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I certainly experience times when the pain level changes to some extent but am convinced that there is an element of allergic reaction, e.g. I am usually much worse in cold weather, like now; in england anyway, but apart from cold and damp making arthritic pain worse in general there seems to be a link to something connected with the weather change like, possibly, some additive in the gas supply. I have had 25 yrs to weighit all up and something causing extra sensitivity seems definitely to be a part of it.
Just try to think if there is anything different going on when you have the pain at it's worst. I am trying to collect info on this. How about food and/or water?
I can only hope that things improve for you. More is gradually being learned about fibromyalgia so hope is never gone.
Brenda
Tigs brenda59210
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tiswas24537 Tigs
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the past summer nearly killed me it was so hot and humid i was house bound, now its cooled down and gone damp so its just as bad. give me dry heat .or crisp frosts and i am fine but humidty and damp kill me. we dont realise how weather sensistive we are . glad you had a nice holiday.
Tigs tiswas24537
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nitropilot tiswas24537
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nitropilot Tigs
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I was thinking of rearranging slash redecorating often to make things feel different in my room. Where the suffering is most prominent. IDK.
Glad you had such a great trip & I'm sorry you don't have the support. My family took eight years to understand how severe FM is!
tiswas24537 nitropilot
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Angel51 ingrid19972
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Yes I am the same, absolutely! I think its when I have rested for a few days and the pains have subsided slightly that I start to think either A its gone or B I never really had it in the first place, lol. Its just so unpredictable, dont you think? And then when you have a bad day it can bring me crashing back to reality, leaving me upset and angry. I take my hat off to you for working, I really dont know how you do it, well done. I gave up work gradually as I was getting more and more fatigued and never had a clue what was wrong....got my diagnosis this September. I am sad at needing to leave though. Also you should try claiming again, send as much evidence as you can and dont give up trying. All the best Ingrid and let us know how you get on. Regards Angie x
tiswas24537 Angel51
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although i am going to within the next few weeks .iv always inteneded to beat this and get well and this is the only chance that i can see at present of doing it. take alook it cant do any harm listening and looking at the info.
ingrid19972 Angel51
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jackie20702 ingrid19972
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