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Cold weather and fibro
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juju71
juju71
Last activity on 28/05/2019 at 17:14
Joined in 2014
33 comments posted | 24 in the Fibromyalgia Forum
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Sometimes I wonder what a soak in the Bath would be like. But having been diagnosed Epileptic before my Fibro came on I cant have baths. Just had a wet room fitted and my bath removed. God send as I only used my bath to try and climb into to take a shower. Hardly practical and safe really. A bit disappointed with the length of the body in my new long sleeved thermal top, short, but it kept my arms warm and chest. Would recommend!
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Juju
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@juju71 Sorry to hear you can't have baths! That's a real shame. Awesome to have a wet room though, that's a bit different, must be fun :)
juju71
juju71
Last activity on 28/05/2019 at 17:14
Joined in 2014
33 comments posted | 24 in the Fibromyalgia Forum
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@GlionbarB Yes just so much better this whole wet room idea. Have a adapted shower unit (just a larger handle to change temp and a on and off switch that's all to use) and a handle on wall for steadiness. A chair
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Juju
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Hello everyone,
It's starting to be cold outside - do you experience more symptoms when it is cold? And how do you manage it?
Please feel free to share your stories and your advice here.
All the best,
Marina