Does rainy, humid weather affect pain?: I feel like... - LUPUS UK

LUPUS UK

32,249 members28,608 posts

Does rainy, humid weather affect pain?

Natura profile image
27 Replies

I feel like connective tissue bad on rainy, or cloudy, humid days. Anyone else notice this?

Written by
Natura profile image
Natura
To view profiles and participate in discussions please or .
27 Replies
Shadows-walker profile image
Shadows-walker

Yes I do I am totally washed out ,on days like that , I am in awrful pain in the winter , but this year I was so looking forward to warmer weather but as this illness progresses , so my ability to adept to the inviroment is getting worse ,I get headaches if the sun is shining , as well so I feel I can't win and I am turning into a bit of a hermit I hope I am ok in the autum that's my favourite time of the year , this past 12 months has been quite a learning curve .

Natura profile image
Natura in reply toShadows-walker

Shadows.....little concerned. My kidney dr (who knows nothing about lupus) made a comment that low end sufferers generally stay low end. I noticed since being diagnosed 4 months ago new symptoms seem to arise. Does lupus get worse and why? I know winter is tough with me. Even gloves can't keep the tips of my fingers warm. Well, warm weather is here! Yeah! Hope u r feeling better. And autumn is my favorite too!

esky profile image
esky

Hi Natura

I have really bad pain on rainy days. It might sound weird but I seem to know that it is going to rain before it does because of the increase in pain. I know exactly what u mean. I think alot of people with our conditions are affected by damp weather.

Hugs esky x

Natura profile image
Natura in reply toesky

Thanks hugs...weather cleared up and so did pain. I think I need to move to Arizona. But, it's really hot there. My ideal life would be summer in Montana and winter in Arizona. Oh well....I live in NY...go figure...

BrownChocolate profile image
BrownChocolate

Natura ,

Do you know the saying I can feel it in my bones. I too can tell when the weather is going to change as I too can feel it , especially in my ankles which makes walking very difficult.

But it seems like we all try and get on with it.

.

Cann profile image
Cann in reply toBrownChocolate

I am always ill when it is going to thunder. My mother said I took after my grandmother who was just the same and they could always tell when it was going to thunder by my grandmother's state.

Natura profile image
Natura in reply toCann

Interesting Cann....I was very ill when I was pregnant with my first daughter when it was very hot and humid one day....terrible

Cann profile image
Cann in reply toNatura

Yes, we are very sensitive people for some reason!

misty14 profile image
misty14

Hi Natura

I find my joints are stiffer and ache more in humidity making walking very difficult. Where do you live in New York?. I've got an American pen friend who lives in Suffern.

Hope your as well as can be.X

Natura profile image
Natura in reply tomisty14

misty... I wish I lived in Suffern. I live on Long Island. Wish I could live in the country. Not my choice living here.

GEISHAGAL profile image
GEISHAGAL in reply toNatura

I live on Long Island also. Our weather this past year has been questionable. Severe winter, cold and rainy spring. We haven't had any summer at all here. I hate hot weather, but can't do anything about that, just use an Emergency Weather email with a 10 day forecast so I can prepare for those bad days. Glad to know that other LI-ers are here.

Natura profile image
Natura in reply toGEISHAGAL

Giesha....I didn't know u were from LI. It seems as though no one knows what lupus is.

GEISHAGAL profile image
GEISHAGAL in reply toNatura

Natura, I've had nothing but a wagon full of crap from the doctors here. I was diagnosed by 3 different doctors in Texas, 20 years ago, doctors that had no connection to one another, because I wanted to be sure. ANAtest, blah, blah, blah, forward to now, here, they say no, don't have it. Had both knees replaced, even my surgeon said that my knees were the worst he's ever seen and if I don't have Lupus, what do I have. He even questioned the other doctors, I'm disgusted, my pain is at a level that I can't even explain. Just hope I don't snap, I know the human psyche is fragile, I'm at a loss. Keep putting me on antidepressants, I'm not depressed, I'm in effing pain! What does it take to get them to listen, to help? My Rheumy recently put me in crap that made me hurt more and sick. Any suggestions on a decent doctor? The docs here never requested my past records. Don't understand-

Natura profile image
Natura in reply toGEISHAGAL

Geisha....I don't know any good doctors yet. I have been trying to deal with this on my own. I am finally seeing a rheumatologist at end of July, Dr. Bernstein is his name. Affiliated with Mather and st. Charles hospitals. He is 3 months to an appt, so I am assuming he is good. Will see. I have had terrible experiences with drs. My entire life. I had one call me bipolar because I was crying in his office crying for help. He wanted to put me on Zoloft. What a jerk! I was exhausted and at home all day with two small children. Hope you can find the right help...keep looking. There are bad doctors out there, but in the same token good ones.

bevjane74 profile image
bevjane74

Wow so it's not just me that feels like this, any changes to weather as in its going to get really hot or really cold and I'm riddled with aches and pains I've only very recently been diagnosed with sle and hughs, amongst other things, I used to always think it was arthritis until my diagnosis

Natura profile image
Natura in reply tobevjane74

bev...that's what I though it was too, arthritis. I am finally going to a rheumy at end of July. Just frustrating. Hard to feel pain and not moan.

farmerfester profile image
farmerfester

hi natura not so much in summer but cold rainy or even just damp days are a real pain and hear in Scotland we get plenty of cold damp days

as far as the sun goes I stay in side middle of day and go out eary and later in the day athough sn doesent affect me as bad as it used to g

Natura profile image
Natura in reply tofarmerfester

farmerfester...Wow! Scotland. It is cold and rainy there! My daughter wants to go there to see the castles...just wonder for me, if its worth considering to move.

GEISHAGAL profile image
GEISHAGAL

Yes, it does reek havoc on my system. I believe the barometric pressure is responsible for most of these problems. We can't do anything to control the weather, just try to help ourselves. Stay on top of the weather forecast with a ten day plan. This way you could be one step ahead on what you need to do for yourself. Hope it helps.

Natura profile image
Natura in reply toGEISHAGAL

Thanks geisha....rainy today but the pain is minimal. It depends on whether I have symptoms or not I guess. Thanks for the advice.

farmerfester profile image
farmerfester

Natural at the moment it is wall to wall sun shine for the last few days but in the last few weeks three has been very heavy fain at times

We can have all four seasons in one day g

Natura profile image
Natura in reply tofarmerfester

Cool farmer fester....always fascinated by how others live ...I was an Anthropology major in college. Never finished, but feel like I am still studying cultures. Love it...

Jo883 profile image
Jo883

Hi Natura

Yes me too, totally and today is one of those days here! I also can tell if it's going to rain or not. I'm ill pretty much all winter - I do definitely feel better in dryer weather. Today the fatigue has hit me like a bus and knocked me for 6 to the point where moving is an effort!! Well wishes xx

Natura profile image
Natura in reply toJo883

Jo...rainy here today...low energy and moving slow myself. Hate that....I did too many chores and errands yesterday, and was feeling real tired by the evening. I don't know how to relay this to my family. They still think I am fine because I look ok on the outside.

Jo883 profile image
Jo883 in reply toNatura

Yesterday it was sunny here and I'd been stuck inside for 2 days as had builders in and packages being delivered, so like you I crammed and had a busy one - I'm still in a state of limbo with diagnosis as I'm sero negative. Despite all the symptoms, malar rashes, levido reticularis, joint pain, and the fatigue where even breathing wears you out!! I've been doing the anti-inflammatory Paleo diet, so I've been doing my bit and looking after myself. My Dr (not rheumy) has decided to reduce my steroids. I have come down from 15mg to 10 but struggling on 10mg. My next rheumy appt not till November and summer months are the only time I'm semi-able. So I've decided today to book privately to see my rheumatologist that helped me initially before linking me back into the NHS here, 7 months is too long to wait for an appointment, especially when they are weaning you off the only med that has been any help!! Dr wants me down to 7.5mg. What a difference being well makes all round hey? The ability to do things without pain and fatigue is a mood lifter in itself!! I'm not prepared to give up my summer which is my only reprieve, the last 2 years have been extremely hard, there have been no birthday parties for my children as I have been too ill - this year I have been making it happen come hell or high water. It took a year of being totally incapacitated before being prescribed meds and a further year to get the meds right before seeing improvement, not to mention a spell in hospital that left me unable to care for my self or my family!! My general Dr has changed 2 or 3 times recently and this one and I will end up locking horns. Mainly because this is my life and I'm fighting hard for it - they have no idea what we go through - with there good health whilst shuffling you out the door because they have other patients to see!!! Sorry - for the outpour - I'm struggling, but also know I have GP battle commencing, next week and need to keep my wits about me and be assertive. Whilst finding myself some proper help!! I understand how you feel about the family not always understanding - I generally feel that only other sufferers understand the full extent of our tiredness, pain and inability to plan things. At the moment I am psyching myself up to cook dinner for the family - my whole body is screaming 'Nooooo' but I will still make myself do it!! Sending love and light xx

Natura profile image
Natura

Jo...feel like that every night. Dinner is a real effort sometimes. Right now my eyes are burning and I did three big things already today (bike ride, mowed lawn, picked up my sister from a dr appt), and the day is only half over. I have an art class at the library, dinner to make and then a concert tonight. I don't mean to complain, these are all good things. Just too much crammed into one day. I am tired just thinking about the rest of my day. Feel better...good luck with party. I totally understand. Why I don't have parties anymore. Too much work, and I collapse at the end. Not fun for me. Only more work.

GEISHAGAL profile image
GEISHAGAL

Where's my post at? Was workin on it, then nada

Not what you're looking for?

You may also like...

Does lupus affect tendons

The. Last few days I have been having pain in my Achilles. Today while taking my dogs for a walk, I...

Cold Weather and pain

I don't know about anyone else but I am in excruciating pain. In bed and when I get off I can't...
Rosebud13 profile image

Does Plaquenil affect your temperament?

Hi, guys. Am looking hopefully to get an answer or at least maybe some guidance. After 10 of...
MandieR profile image

How does lupus affect the nervous system?

I'm flaring at the moment. I'm trying to get my head around how lupus affects the nervous system...
Maya23 profile image

Does SLE affect your general immune system?

I was diagnosed with SLE 15 years ago and have managed my symptoms successfully since then. I'm...
jennylee profile image

Moderation team

See all
Debbie_kinsey profile image
Debbie_kinseyAdministrator
chelseawong profile image
chelseawongAdministrator
michaellasmith profile image
michaellasmithAdministrator

Top community tags

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.