Something that has helped me
Posted , 7 users are following.
After reading a post from airyfairy85 about advances in FM, It says that pain is caused by the blood capillaries reducing the blood flow especially when it is cold.
I have for the first time in my life started to wear thick pyjamas and thermal sock at night. So far I have managed to go 1 week pain free at night. I have now bought some thermal tops and long johns to help during the day as I have noticed that when I feel the coldI get pain.
I will also say that since I have been doing this my pain has reduce that much that I don't need to to pain killers.
This may all be a coincidence, I am not sure but at the moment I am a lot happier and pain free..
2 likes, 10 replies
Lucyred ianstokes66
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ianstokes66 Lucyred
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Lucyred ianstokes66
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tiswas24537 ianstokes66
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joy47826 ianstokes66
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I was at the right place at the right time with grape seed ex info.....Joy
sarah-jane57 ianstokes66
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I saw a new neurologist last friday who said that the brain works differently when you have fibromyalgia. You feel pain when people who do not have fibromyalgia simply feel cold. I feel cold all the time to the touch - inside I feel as though I have freezing cold water under my skin. People stare at me I've often been called a poor cow because I am wearing hats gloves scarf and thick cardigan or jacket even in summer. The circulation has been rewired somehow with Fibromyalgia.
I have tried every alternative therapy there is and every alternate medication or herbal remedy there is. Devils claw worked in the beginning and Arnica is useful when you've had a fall and suffered bruising or after surgery. I had a `mild' Heart attack 3 weeks ago and now I am in one of the worst flare ups I've ever had. My thoughts are this when I start thinking why me : there is always someone worse off than yourself. My son has told me that as I look well (fibro unfortunately gives you a glowing healthy appearance when you feel as if you are dying inside) and has said that as I look well it must be all in my mind and that I cannot see my grandchild until I stop being ill! He's not a stroppy teenager he's nearly 40 and should be ashamed but he's not. That has broken my heart but not my spirit I say to everyone who has fibromyalgia - We are not being neurotic we are being very brave and are coping the best way we can - I will continue to look after myself and will continue to wear my thermals, flannelette pyjamas and welly socks in bed and longjohns, long sleeved thermal vests, hats, ear muffs, and mittens when I'm up and about .... Knitting keeps me sane Hand knitted socks anyone
joy47826 sarah-jane57
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tiswas24537 sarah-jane57
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anne90395 sarah-jane57
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How upsetting that must have been from your son. My children try their best to understand this, but I know they don't, truly, when they ask me to babysit at a moments notice! I will keep on trying to educate them! As for the keeping warm, I can totally relate to that. Strangely, my left foot is always cold, rarely warms up, even with socks thermals etc.
Take care, Anne
nitropilot ianstokes66
Posted
So were you normally cold at night or do you think wearing tighter clothing helped, like full body compression stockings?