Heat making Fibromyalgia worse? - Fibromyalgia Acti...

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Heat making Fibromyalgia worse?

Seascapes31 profile image
41 Replies

Hi all, just wanted to ask if this heat affects anyone's Fibromyalgia symptoms as in increasing pain levels?It seems to make my pain levels worse! I unfortunately for some years now cannot withstand the heat and it actually makes me feel so poorly (on top of my fibromyalgia symptoms so not helpful obviously!

I was born in September so that's my ideal temperature warm and sunny but below the 70s Fahrenheit

with a lovely sea breeze (I live near the beach).....once it tips over that I immediately feel so unwell and have felt this way for years.

Any other lovely members experiences would be really helpful to hear.

Thank you

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Seascapes31 profile image
Seascapes31
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41 Replies
CheetieCat profile image
CheetieCat

Yes, I'm afraid it's the same for me. I overheat and can't cool down and the sweating is awful. Pain levels definitely increase and extra pain relief doesn't seem to make one bit of difference.

I think my ideal temperature is pretty cold, but even then I still overheat. If I was a boiler I would be condemned for a dodgy thermostat 😳

"What doesn't kill us makes us stronger?"

Well, whoever said that has obviously never met fibromyalgia because right now I feel about as weak as dishwater 😔

Hang in there Seascapes this heat won't last much longer - Surely ☔🌧️☔🙏

Nothing_but_books profile image
Nothing_but_books in reply toCheetieCat

Dodgy thermostat! Yes, exactly! Me too. Can't tolerate cold. Can't tolerate hot, that's even worse, down I go, smash on the floor.

CheetieCat profile image
CheetieCat in reply toNothing_but_books

Aw no! Just when you think it can't get any worse 😔

So far I've been lucky, I've remained upright but I've had that horrible feeling like you're going to pass out and then the gadzy sicky feeling is just an absolute joy! 🤮

Nothing_but_books profile image
Nothing_but_books in reply toCheetieCat

Sorry to hear it's you too. Me, I don't exactly pass out, I just slide down the wall. Oh, ya. Joy's the word.

AJ8824 profile image
AJ8824

yes, I also have increased pain and stiffness. If I get too warm I’m actually physically sick too

Nothing_but_books profile image
Nothing_but_books in reply toAJ8824

If I get too warm I’m physically sick -- I thought it was just me.

Furry profile image
Furry

Hi there, yes I’m exactly the same, much worse during the warm weather. I much prefer the cooler months .

Cat00 profile image
Cat00

I always preferred "What doesn't kill you makes you wish it had"...

CheetieCat profile image
CheetieCat in reply toCat00

🤣🤣 much better

Cat00 profile image
Cat00 in reply toCheetieCat

Bizarrely it was a Jehovahs Witness on my doorstep who said that to me !!

Seascapes31 profile image
Seascapes31 in reply toCat00

That's made me chuckle x

Wobblygirl profile image
Wobblygirl in reply toCheetieCat

What a hoot!Thank you for that intervention xxx

Chancechance profile image
Chancechance

I'm the same can't cope with the heat, the pain feels worse and the stiffness, try to stay as cool as you can. Hopefully it will ease soon.

Seascapes31 profile image
Seascapes31 in reply toChancechance

And youFingers crossed for pain free (ish) days ahead.......x

Oscarlola profile image
Oscarlola in reply toChancechance

I'm glad I'm not the only one I'm so sore today I can hardly walk it just hurts everywhere I wish we could just enjoy the heat like everyone else 😣

Seascapes31 profile image
Seascapes31 in reply toOscarlola

So with you on that! My sciatica has also decided to flare up to add to the mix :(Sending hugs x

PurpleTranmere profile image
PurpleTranmere

I’m definitely the same. I really struggle in the heat. I find I can cope and stay on top largely of my pain and chronic migraines when it’s cooler add hot temperatures and I really feel overwhelmed.

Seascapes31 profile image
Seascapes31 in reply toPurpleTranmere

I agree, I feel more able to get past the pain when I'm cooler if that makes sense?

DoubleMalibu profile image
DoubleMalibu

Wow… how lucky are you Seascapes31 living near the beach with a sea breeze!

heat intolerance is common in fibromyalgia sufferers, as is cold sensitivity unfortunately.

Both exacerbate my M.E & fibromyalgia symptoms hugely. Throw in severe menopause with flushes & it’s a complete mare of a time🥵😝

Guess we all just have to struggle through, finding our own way of dealing with it.

Chillmax pillows are good for cooling the body down, got all the family them last year when the heatwave was in the 30’s😅

Don’t forget plenty of ice lollies in the freezer too😁 🍡🍦

Seascapes31 profile image
Seascapes31 in reply toDoubleMalibu

The pillows sound good, yes I do love the sea breeze, I will keep my feet in paddling pool in garden :)) x

Lia06 profile image
Lia06

hi there like me also born in September I can’t say I noticed the heat making it worse because my pain is same all year around but it’s getting worse generally as time goes by, it’s hard to believe it can get any worse, fibromyalgia is really crippling for some people It has drastically changed and taken over my life, my life can’t do any of the things I normally did pain pain pain and pain that’s all my life has been for years now, I’m a full time carer for my elderly bed bound mum so you can imagine how hard that is anyway I hope things become easy for you and all my fellow fibromyalgia sufferers

Seascapes31 profile image
Seascapes31 in reply toLia06

Thank you for taking the time to reply, sending hugs x

Madewrong profile image
Madewrong

I'm right there with you,I hate to moan but this heat is killing me😞

My pain levels are through the roof, I cannot cool down, it's making me vomit and dizzy.🥵🤢

I'm literally sat in the house as it's very cool in there and can't go out,

The down side of my house is I can't stand the cold either 🙄🥶 and also have excruciating pain then and my bungalow is so hard to heat, I was definitely made wrong🙃

Seascapes31 profile image
Seascapes31 in reply toMadewrong

Sending hugs and hope you have better days ahead x

Wobblygirl profile image
Wobblygirl in reply toMadewrong

Feeling exactly the same...My house is so cold for months! Only felt warm enough these last 5days to rid my bed of high tog. duvet...

I live on the East Coast where it's bn freezing w NE wind battering our area!

My energy bills are so high as I can't bear being cold+stiff+in pain!!!

Only just taken my vest off!

And always need woollies at hand.

This is such a distressing condition?

Wx

Seascapes31 profile image
Seascapes31 in reply toWobblygirl

Sending hugs and love x

Madewrong profile image
Madewrong in reply toWobblygirl

Sending gentle hugs x

Yassytina profile image
YassytinaFMA UK Volunteer

Hello, we didn’t really have a Spring here in Suffolk and up until last Tuesday temperatures were fairly low, then at the weekend it went up too 29 degrees 🤣I do tend too slow up with the heat and feel more tired im sure a lot of us do and drink plenty of fluids and pace much more. Sorry to read it makes your pain levels a lot worse. Must be marvellous living near a beach I would be dipping my toes in for sure too cool down, take it easy xx

Seascapes31 profile image
Seascapes31 in reply toYassytina

Although the beach is close by I don't get down there often due to my pain levels and mobility, agree that toes in the water would be so refreshing for sure!

Yassytina profile image
YassytinaFMA UK Volunteer in reply toSeascapes31

Must be very hard for you and such a shame we miss out on things, it’s currently 27degrees where I live , i think my little grandboys will be very tired after school, my husband will get them and I save some energy for when they come Chilled drinks and ice pops I think they are 9 and 6 years old . Always lift me and take my mind off pain/fatigue whilst they are here 😀

Seascapes31 profile image
Seascapes31 in reply toYassytina

Bless you, I get so much joy from my grandchildren too, and I do feel sad that there's so much I can't do with them, and like you I have to conserve my energy for my time with them.

I do agree I feel I miss out on so much because of my fibromyalgia symptoms x

Bluebell999 profile image
Bluebell999

My mother who had fibro as well as RA always found summers worse, although she was a sunlover when she was younger.

By a process of elimination, we discovered that she was eating more "nightshade plants" in the summer as she had more salads. New potatoes, peppers and tomatoes were particuarly bothersome, which was a shame as they formed a good part of her diet.

If you google nightshade vegetables it will give you a full list.

The same was true with strawberries, although sometimes she used to say she would put up with the extra stiffness and pain just for the enjoyment of her "treat"

She would sit in the shade with her feet in a large bowl of cool water, which sometimes had to be replenished. This did help her with the sweating.

She was well into her late seventies before her "hot flushes" finally stabilised.

Seascapes31 profile image
Seascapes31 in reply toBluebell999

Thank youI will look into the nightshade list for sure

Meditationlover profile image
Meditationlover

Hiya seascapes, I find heat makes me feel much better, pain reduces considerably, when cold I use heated pillow, heated blanket, and weighted blanket all year round. But I am aware some people find heat doesn't help them

Seascapes31 profile image
Seascapes31 in reply toMeditationlover

I'm pleased to hear that someone has benefited from current heat :) x

Onedaymore1 profile image
Onedaymore1

I’m exactly the same as you, I’ve been feeling totally overwhelmed with the heatwave & I dare anyone 🫣in our household to open a single blind or curtain & let the heat in!

I no longer seem able to deal with high or low temperatures, this ‘lump’ of a useless body I drag around the best I can, cannot adapt to the change in weather anymore.

Like you I’d say Sept Oct & April May are my most comfortable months.

I’ve got a can of face cooling spray & it does help a bit especially, at night in bed.

Stay strong ! x

Seascapes31 profile image
Seascapes31 in reply toOnedaymore1

Oh I feel your pain! Glad I'm not the only one to appreciate those months you mentioned too, thank you, we will stay strong! Sending hugs x

Aka-Ice profile image
Aka-Ice

Unfortunately I have had a lot more stiffness and pain especially in my hands and feet so am staying in the shade keeping my feet elevated. I loved the sun but my body clearly doesn't. Feeling a lot more drained also. Went on holiday to Tunisia few months ago and was fine for most of it until my feet gave in and where in agony for the second half of the hol. Not experienced anything like it before. I used to look forward to summer and the sun. Now I have to hide from it. At least I managed to get a good tan before it all kicked in.

Seascapes31 profile image
Seascapes31 in reply toAka-Ice

It's so unfair what this illness has taken away from so many of us, sending hugs x

caninecrazy profile image
caninecrazy

me too! my best time of year is October to april as its cool or cold. Anything above 17c and i am struggling even more. My body thermostat is broken too , i have fibro & lupus so it is important i protect myself from the sunlight. i am also menopausal so hot flushes added to the mix, it feels like will combust the amount of heat i feel! lol. i have to laugh or i will never stop crying. But yes, the heat makes me sick, dizzy, confused......endless list. sending you a gentle hug x

Seascapes31 profile image
Seascapes31 in reply tocaninecrazy

I'm sending hugs to you and hope you have a better day xx

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