feel the cold

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Re: feel the cold

Postby clairbear » Mon Nov 08, 2010 9:32 am

Hello!

I too am a chilly mortal - I am pleased to see that it is linked to EDS - everyone usually just thinks i am a wimp! I bought some really lovelt sheepskin slippers and some North Face thermal gloves over the weekend - as my usual gloves just aren't warm enough. The North Face gloves are being road tested this afternoon !

Clair
Confirmed EDS III Jan 2011 age 37
Not going to change my world but explains many of my peculiarities
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Re: feel the cold

Postby FIN1 » Thu Nov 11, 2010 4:32 pm

Hi

I'm constantly cold, my husbands thinks this is strange as I'm always wrapped up in my dressing gown or jumper. Then again he's the opposite and walks around in a t-shirt all year long without managing to get the cold! :)

The winter is a killer, I think it makes my joints feel worse and definitely stiffer.
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Re: feel the cold

Postby Stone » Tue Nov 23, 2010 2:40 pm

Agree with that, it's freezing already! Doesn't help I've got the patio doors open to try and dry some paint without stinking out the house...(don't ask)

I found my thick softshell gloves the other day which was a very happy moment! I normally wear fingerless ones if I'm getting a bit of a chill as they let you warm up a bit while still being able to write/type/do stuff :) My lower finger joints are worst in the cold so it works pretty well.

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Re: feel the cold

Postby everhopeful » Tue Nov 23, 2010 7:52 pm

As a Raynauds sufferer, I'm definately feeling the cold. I didn't break a sweat once, this summer, to my knowledge! I'm in the market for some new gloves cos my outer pair have sprung a hole and it's on one of my worst fingers regarding reactions. I wear the raynauds "silver" gloves under another pair and still my hands react (even on nifedipine). Not looking forward to the predicted chill down at the end of this week!!!

Liz
HMS and Raynauds (Diagnosed Sep 2009)
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Re: feel the cold

Postby sheppeyescapee » Tue Nov 23, 2010 10:26 pm

I have been freezing! Forgot to wear my gloves when I went out so I turned up to my slimming class with blue hands :duh: Feet have a habit of going blue too. When I was younger my nose used to go bright blue too :lol: I had a hot water bottle on my feet to warm them up and I couldn't even feel how hot it was, my feet were so numb and cold :wall: On my way back from slimming class it was so cold it felt like someone was stabbing me in the hip :roll:
J - 28,student,married to the lovely Em and live with 2 cats Bilbo and Pippin. Diagnosed with Aspergers, Dyspraxia, Dyslexia, EDS-HM, Mild Asthma, Chronic Pain, Chronic Fatigue, POTS, Syncope
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Re: feel the cold

Postby laracomps » Mon Jan 10, 2011 11:13 pm

Ah some fellow cold people...!

I've been utterly 'freezing' all day, I honestly feel like an ice block. I whacked the heating up, and have been sitting (well laying) on the sofa with the kids watching films today under my slanket, with my toddler laying on top of me with her thick fleecy blanket on, AND furry boot slippers and socks. I'm still freezing. :evil:

For me it seems to be connected to pain & tiredness. If I'm in a lot of pain it feels as though my body just shuts down, and I get this cold, nothing warms me up, and I get so tired that I can't keep my eyes open physically. It's horrible. Had it for such a long time now, when I was a teenager and pre-diagnosis, the Dr's thought I had ME.

Just another one of those 'things' you have to deal with with no magical cure or pill!

Off to warm/fry the wheat bag... :whistle:
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Re: feel the cold

Postby madmum » Mon Jan 10, 2011 11:38 pm

I find wearing mens thermal vest helps a lot. My right leg gets cold and goes purple so i wrap a blanket round it when sitting and keep my long boots on. Cannot wear a glove on my right hand due to the splint and the thumb pain.
Mum to son with hms,pain amplification,migraine,plantar fascitis,ibs.lactose intolerant,hayfever and numerous allergies. I have hms,arthritis,migraine,p.o.t.s,allergies,and others too numerous to mention. Acused of being mentally ill hence.....madmum.
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Re: feel the cold

Postby carolyn » Tue Apr 26, 2011 11:20 am

I wear thermals a lot, I'm always cold.
My friends thought I was nuts last year when we stayed in Vegas and in the night I had extra blankets on my bed and some days walked round in a hoodie. They were all sweating buckets.
Never thought before that it could be linked with EDS/HMS
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Re: feel the cold

Postby _Sara_ » Tue Aug 30, 2011 3:58 am

Reading this I am very very glad it isn't just me! What a relief :) Work are a pain at the moment as I am not allowed to wear my jacket and let me tell you it its freezing! :( My hands and feet are defiantly the worst effected also.
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Re: feel the cold

Postby Rosie » Tue Aug 30, 2011 1:52 pm

Hi Sara

If you have told your employee that you have a medical condition or are disabled then they have to make 'reasonable adjustment' for you, and this would include letting you wear your jacket or additional clothing as your condition causes you to feel cold.

Rosie
Diagnosed HEDS December 1st 2005. DD1 (20) HEDS and scoliosis (now corrected by surgery), diagnosed June 2006. DD2 (18) mild HMS. Son (11) some hypermobile joints, poor muscle strength and seems to be developing scoliosis as well, woopee!
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Re: feel the cold

Postby shirleytx7 » Tue Aug 30, 2011 2:43 pm

I too have always felt the cold. I live it Texas and it has been very hot here all summer from 90 to over 100 degrees. I hate the summer as the air conditioning is terrible and I have to wrap myself in a blanket at work to get through the day. Luckily no one seems to care.
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Re: feel the cold

Postby _Sara_ » Tue Aug 30, 2011 4:05 pm

Rosie wrote:Hi Sara

If you have told your employee that you have a medical condition or are disabled then they have to make 'reasonable adjustment' for you, and this would include letting you wear your jacket or additional clothing as your condition causes you to feel cold.

Rosie


Its gets nowhere to be honest with you, Iv been asking them for years to let me face in a certain direction with me being deaf but i never get anywhere :wall: Iv given up asking. Im sure they think I am making things up like when i say I have difficulty lifting heavy things they always try having me lift heavy things. I think its something I would have to get a form from the Dr's for? However my Dr knows very little also! Oh how nothing is ever easy for us :roll:
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Re: feel the cold

Postby Rosie » Tue Aug 30, 2011 7:16 pm

Hi again Sara

I think you may need to read up on your rights. It doesn't matter what your condition is, if you meet the definition of disabled within the law then your employer has obligations under law. Ignorance of the law does not mean they can pretend it doesn't exist, the onus is on your employer to know the law. There is a small amount about 'reasonable'adjustment here, or just google 'disabled employee rights', there are organisations that can help. One of these is Access to Work, who you can apply to as an individual, who wioll assess you in your workplace and make reccomendations, they will also partially fund some stuff. Another approach is to ask to be seen by your employer's Occupation Health (if they have one). Unfortunately it is often up to us as individuals to get things moving, but if your workplace is making you ill it is worth doing.
If all else fails, mentioning the Disability Discrimination Act may help.

Rosie

PS - anything you discuss with your employer or line manager, ask for it in writing.
Diagnosed HEDS December 1st 2005. DD1 (20) HEDS and scoliosis (now corrected by surgery), diagnosed June 2006. DD2 (18) mild HMS. Son (11) some hypermobile joints, poor muscle strength and seems to be developing scoliosis as well, woopee!
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Re: feel the cold

Postby louloutinks » Wed Aug 31, 2011 12:34 pm

I have an electric blanket on at night all year round but with the ANS stuff, I get hot, cold, hot cold, so it is on, off, on, off!!!
Me, 41...EDSIII, dysautonomia, POTS by Prof G but waiting tilt, fibromyalgia/CF

Son,8..autism, BJHMS, hypotonia, persistent anaemia

Mum...EDSIII
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Re: feel the cold

Postby Smol » Sun Sep 11, 2011 2:20 pm

Hi All
until I was put on tramadol I was constantly cold, even in summer, the only time I was ever comfortable was abroad. Then since the tramadol, my feet especially ,but hands too are still freezing while at the same time I'm alternately sweating cobs or shivering (feel a bit peri-menopausal) my hubby is always hot and is my own personal hot water bottle. The only time my feet are ever warm are while I'm in the bath or just when I wake up. Occasionally I have incredibly hot feet, which I just can't stand, they are so itchy and sore and red and make me realise how much I actually prefer for them to be cold

:bye:
Sarah

Finally diagnosed 6/12/11 with HMS, raynauds, Cervical Spondylosis (3 prolapsed discs and bone spurs) Bulging lumbar disc and SI dysfunction.
Blog here http://hypermobilitysyndrome.wordpress.com/
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