Cold weather
ClaireSaul
Community member Posts: 92 Empowering
Hi all,
many apologies for not being about over the weekend - had a pain flare, Ehlers Danlos symptoms worse, passed out and dislocated both shoulders!! But I am catching up with chats and comments, I promise!
I just wondered how everyone is coping in this cold weather as for me it is one of the worst things for my nerve and joint pain? Do you have any fab tips to share with the rest of us?
I am about to brave the cold now, so look forward to catching up with your tips later!
Claire
many apologies for not being about over the weekend - had a pain flare, Ehlers Danlos symptoms worse, passed out and dislocated both shoulders!! But I am catching up with chats and comments, I promise!
I just wondered how everyone is coping in this cold weather as for me it is one of the worst things for my nerve and joint pain? Do you have any fab tips to share with the rest of us?
I am about to brave the cold now, so look forward to catching up with your tips later!
Claire
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Comments
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It makes my arthritis so much worse but being a 23 year old stubborn male I persevere and pay for it later on in the day.
I find that wearing extra layers rather than one thick layer helps greatly. Not sitting immobile for too long, eating hot meals, drinking hot drinks etc
All the usual.
Although I wish I could afford to stay at home all day in bed with the heating on!! Seems like the greatest cure.
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I’m new on here.im only 54 and got severe rheumatoid arthritis as well as oesteoarthritis and raynaurds.The cold weather makes my joint pain terrible,I have a deformed hand which is constantly in a ball,can’t straigjten or hardly use it,So I can’t wear gloves or mittens which makes my raynaurds terrible to deal with.The snow here is quite thick,I’ve cancelled a appointment,because of all my pain,hope you all are not suffering too bad because of the cold weather.Im a very quiet person but I’ve been listening to some of your chats.1
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@gillian29,hello and welcome to you and all the other members who suffer from the cold. Myself like many other MS suffers we don't like it to hot or to cold even taking a shower can be a problem getting the temperature just right.2
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@wilko,hi it’s no joke when most temperatures don’t suit you.I forgot to say I have lupus as well,and I can’t be out in the sun for long,and certain types. Of light can trigger a massive flair up,can’t say roll on summer lol.Im like you it will be about impossible to get a temperature what will suit all of us1
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Me too
Too jot tpp cold. Big problems2 -
gillian29 said:I’m new on here.im only 54 and got severe rheumatoid arthritis as well as oesteoarthritis and raynaurds.The cold weather makes my joint pain terrible,I have a deformed hand which is constantly in a ball,can’t straigjten or hardly use it,So I can’t wear gloves or mittens which makes my raynaurds terrible to deal with.The snow here is quite thick,I’ve cancelled a appointment,because of all my pain,hope you all are not suffering too bad because of the cold weather.Im a very quiet person but I’ve been listening to some of your chats.0
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@gillian29, hello again don't worry about being shy , I tell it as it is or how I understand it to be. Some times I get it wrong or my posts are written to play devils advocate, somtimes its starts a string of posts high lighting many faults and failing of the benefits system mainly PIP hope you are well and staying warm.
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