Is fibro heredatory?
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First off i am sitting here thinking the only part of my body that doesnt ache is my head , then I thought ahhh what would it be like to be pain free, even when i am in bed i have to keep switching sides because of pain. Then I looked over at my daughter and thought please god she doesnt suffer like this or my son. My dads ( who died at 43 brain tumour) half sister ( same mum) has Fibro and her daughter ( my cousin). I asked the doctor but he didnt know . For me I feel there has to be more to fibro than just specialists saying its a trauma or depresion. I am hearing more and more people talk about fibro. Why would we all be in so much pain just because somthing once happend to us, and why would doctors prescibe pain relief if they think its just in your head?. the pain is very real and pain relief can help ease it, I dont know about you but every day i wake up thinking I hope i have a pain free day , if thats not positive thinking i dont know what is.. Any way just wondering if anyone else has family members suffering the same. night night have a good nights sleep. Ha ha had alot of questions.
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christine26761 hazel70459
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bluesman hazel70459
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Carinaeta hazel70459
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wendy22970 hazel70459
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JulieBadger hazel70459
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At least I know that I will be sympathitic to them and try to help them achieving their dreams whilst still coping with Fibro or ME/CFS if they do get it. Which will emotionally help them a lot I think. x
hazel70459 JulieBadger
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bluesman hazel70459
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hazel70459 bluesman
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