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Hi, y'all

I'll be two years out January '01, with a total weight loss of 205,

(like to get another 10-15 off) ANYHOO...

I live in Iowa and last winter I really froze, it makes sense with

less insulation. I thought maybe my body would have adapted by this

winter....but it seems to be worse.

Of course with all the menopausal women in my office who are hot

flashing, my whining about being cold is not received well!! (I'm 47,

also)

So, my question is for some of you 4+ years out... does your body

ever adapt to the cold? Or do I make major investment in wool

sweaters and jackets, cuz this is a long term deal?

a

385/180/170

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<

>

a, I've been freezing in the Oklahoma winter cold ever since I had

surgery. I wear at least 2 pairs of socks (and sometimes layer them over a

couple of pairs of panty hose or tights) all winter long. Of course, I work

outside a lot, when I was a police officer, and still daily, with 20 horses

to care for. But I find that once I get cold, I STAY cold. The best socks

I've found for keeping feet warm are found at ski shops...up over the calf,

and insulated. I just buy bigger boots for winter, to get all those layers

inside. And the best way to stay warm is layering, but not tight. You need

the insulating effect of air trapped between the layers. If your shoes or

boots are too tight with a couple of pairs of socks inside, you're still

going to be cold.

Jac

mailto:jholdaway@...

http://www.pictureitdigitaldesigns.com/

http://members.cox.net/xxxfarmpaints

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a,

It hasn't gotten any better for me. I'm sitting my butt here freezing right

now with the heat on...Denmark today, high 2C. Even in Florida I was

telling myself...I've got to go further SOUTH. Dang, I musta taken a wrong

toin in Albuquerque...lol.

Dawn

Freezing my butt off

> Hi, y'all

> I'll be two years out January '01, with a total weight loss of 205,

> (like to get another 10-15 off) ANYHOO...

>

> I live in Iowa and last winter I really froze, it makes sense with

> less insulation. I thought maybe my body would have adapted by this

> winter....but it seems to be worse.

>

> Of course with all the menopausal women in my office who are hot

> flashing, my whining about being cold is not received well!! (I'm 47,

> also)

>

> So, my question is for some of you 4+ years out... does your body

> ever adapt to the cold? Or do I make major investment in wool

> sweaters and jackets, cuz this is a long term deal?

>

> a

> 385/180/170

>

>

> Homepage: http://groups.yahoo.com/group/Graduate-OSSG

>

> Unsubscribe: mailto:Graduate-OSSG-unsubscribe

>

>

>

>

>

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My WHOLE body is better than it was the first few years, but I have

Raynaud's, so nothing helps the fingers & toes.

I can get warm, with a few layers, but not those fingers & toes. Only warm

water or a heating pad can get blood back in once it's gone.

Thanks,

Vitalady T

www.vitalady.com

If you are interested in PayPal, please click here:

https://secure.paypal.com/affil/pal=vitalady%40bigfoot.com

Freezing my butt off

> Hi, y'all

> I'll be two years out January '01, with a total weight loss of 205,

> (like to get another 10-15 off) ANYHOO...

>

> I live in Iowa and last winter I really froze, it makes sense with

> less insulation. I thought maybe my body would have adapted by this

> winter....but it seems to be worse.

>

> Of course with all the menopausal women in my office who are hot

> flashing, my whining about being cold is not received well!! (I'm 47,

> also)

>

> So, my question is for some of you 4+ years out... does your body

> ever adapt to the cold? Or do I make major investment in wool

> sweaters and jackets, cuz this is a long term deal?

>

> a

> 385/180/170

>

>

> Homepage: http://groups.yahoo.com/group/Graduate-OSSG

>

> Unsubscribe: mailto:Graduate-OSSG-unsubscribe

>

>

>

>

>

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<

>

Guess what! Last year my PCP diagnosed me with Reynaud's. And it's a

syndrome, not a disease, and nobody knows any specific reason any specific

patient gets it or has it. You and I know it's probably because of WLS, and

my PCP does too. But in reality, Reynaud's means, " Your feet and hands are

cold all the time, and we don't know why, so we'll call it something. " He

even went so far as to send me to a cardiologist, and he did an ultrasound

on my legs and arms. My circulation and my heart are just fine. I'm just

cold.

Jac

mailto:jholdaway@...

http://www.pictureitdigitaldesigns.com/

http://members.cox.net/xxxfarmpaints

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I don't know the details of how you feel cold, but with me I feel

cold to the inside of my bones. The toes, nose, fingers all

extremities feel like they're going to freeze and break off. (thank

God I don't have a penis!) Even a ton of blankets doesn't help at

night. It's painful and horrible to be cold.

What DOES help is going to the gym in the morning and doing a good

workout. Now I know it sounds yucky, but it's the only thing that

gets me glowing. I've come to think of it as if my furnace is

shutting down because I'm losing weight. It wants to preserve

itself, so it goes on pilot light to conserve energy. I have to

forcibly stoke the fire and rev up the metabolism to get it burning

again. I feel normally warm for most of the rest of the day. Not

scientific by any means, but it works for me.

And just for the pure indulgence of it, I bought a stool to take and

leave in the gym shower. I turn the shower on as hot as I can stand

it and sit on the stool with the hot water gently pounding my

shoulders and back. I just sit there for about ten minutes and get

warm and relaxed. Huuh...heaven. And I earned it after that workout.

Vicki A.

> <

Raynaud's, so nothing helps the fingers & toes.>>

>

> Guess what! Last year my PCP diagnosed me with Reynaud's. And it's a

> syndrome, not a disease, and nobody knows any specific reason any

specific

> patient gets it or has it. You and I know it's probably because of

WLS, and

> my PCP does too. But in reality, Reynaud's means, " Your feet and

hands are

> cold all the time, and we don't know why, so we'll call it

something. " He

> even went so far as to send me to a cardiologist, and he did an

ultrasound

> on my legs and arms. My circulation and my heart are just fine. I'm

just

> cold.

>

> Jac

> mailto:jholdaway@c...

> http://www.pictureitdigitaldesigns.com/

> http://members.cox.net/xxxfarmpaints

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Well, Vickie, I have to say I'm too " lazy " to go to a gym. LOL. After I

spend the day taking care of 20 horses, lugging around 50 lb. Bags of feed

and 75 lb bales of hay (I go through 1/2 ton of feed and a ton of hay a

week), I'm too pooped to go workout, and I have a pretty healthy glow going

on when I get done. So really the only problem I ever REALLY notice is my

hands and feet, and after 20 years, I'm used to it. I think my doctor just

did the tests to ease his own mind. Incidentally, my mother, who had WLS in

May 1983 has the same problem too. Maybe this should be listed as a

side-effect of the surgery. I've never actually heard it mentioned or

associated before.

Jac

mailto:jholdaway@...

before and after pictures at:

http://hometown.aol.com/jrandjrholdaway

http://www.pictureitdigitaldesigns.com/

http://members.cox.net/xxxfarmpaints

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They refer to mine as syndrome also. When you start losing fingers & toes

(the circulation doesn't return), then they call it the disease. Kinda late

then.

BUT I had symptoms of this 10 yrs before surgery. It's just much worse now &

I didn't find out what was up with it til I had chill blains. I think only

the NE people will know what they are. NO ONE here knew what they were, inc

my docs, EXCEPT my podiatrist, who's a little on another station anyway, if

you catch my drift. But he knew what they were.

Anyway, same problem. The circulation shuts off, and that's it. My fingers

go absolutely waxy yellow/white. NO BLOOD AT ALL. It is the spookiest

thing. Right middle finger can go just by holding onto a glass of iced

protein too long. I usually use a mug with a handle for that reason. The

fastest way to get it back is to wash a few dishes, then it turns pink. In

public, I just go into the restroom and run warm water on it til the color

comes back.

As time goes on, it gets worse. I have 5 fingers (and they go in a certain

order) AND 5 toes (also a certain order) that will lose the blood & not come

back without my taking steps. They don't just " warm up " . The chill blains

represent 3 months of pain & peeling skin. SO, I am now a lot quicker to

get my feet out of the cold than I usta be.

Thanks,

Vitalady T

www.vitalady.com

If you are interested in PayPal, please click here:

https://secure.paypal.com/affil/pal=vitalady%40bigfoot.com

RE: Freezing my butt off

> <

Raynaud's, so nothing helps the fingers & toes.>>

>

> Guess what! Last year my PCP diagnosed me with Reynaud's. And it's a

> syndrome, not a disease, and nobody knows any specific reason any specific

> patient gets it or has it. You and I know it's probably because of WLS,

and

> my PCP does too. But in reality, Reynaud's means, " Your feet and hands are

> cold all the time, and we don't know why, so we'll call it something. " He

> even went so far as to send me to a cardiologist, and he did an ultrasound

> on my legs and arms. My circulation and my heart are just fine. I'm just

> cold.

>

> Jac

> mailto:jholdaway@...

> http://www.pictureitdigitaldesigns.com/

> http://members.cox.net/xxxfarmpaints

>

>

>

>

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Good Lord Jac!

The gym seems like a country club compared to your workout! I had to

carry 50 lb. bags of sugar for my kid's food drive yesterday and my

shoulder still hurts!

Smiles,

Vicki A.

> Well, Vickie, I have to say I'm too " lazy " to go to a gym. LOL.

After I

> spend the day taking care of 20 horses, lugging around 50 lb. Bags

of feed

> and 75 lb bales of hay (I go through 1/2 ton of feed and a ton of

hay a

> week), I'm too pooped to go workout, and I have a pretty healthy

glow going

> on when I get done. So really the only problem I ever REALLY notice

is my

> hands and feet, and after 20 years, I'm used to it. I think my

doctor just

> did the tests to ease his own mind. Incidentally, my mother, who

had WLS in

> May 1983 has the same problem too. Maybe this should be listed as a

> side-effect of the surgery. I've never actually heard it mentioned

or

> associated before.

>

> Jac

> mailto:jholdaway@c...

> before and after pictures at:

> http://hometown.aol.com/jrandjrholdaway

> http://www.pictureitdigitaldesigns.com/

> http://members.cox.net/xxxfarmpaints

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Share on other sites

And you still detest the heat? Strange little thing, ain'tcha?

Alice

The Loon

RNY 12/28/00

> They refer to mine as syndrome also. When you start losing fingers

& toes

> (the circulation doesn't return), then they call it the disease.

Kinda late

> then.

>

> BUT I had symptoms of this 10 yrs before surgery. It's just much

worse now &

> I didn't find out what was up with it til I had chill blains. I

think only

> the NE people will know what they are. NO ONE here knew what they

were, inc

> my docs, EXCEPT my podiatrist, who's a little on another station

anyway, if

> you catch my drift. But he knew what they were.

>

> Anyway, same problem. The circulation shuts off, and that's it. My

fingers

> go absolutely waxy yellow/white. NO BLOOD AT ALL. It is the

spookiest

> thing. Right middle finger can go just by holding onto a glass of

iced

> protein too long. I usually use a mug with a handle for that

reason. The

> fastest way to get it back is to wash a few dishes, then it turns

pink. In

> public, I just go into the restroom and run warm water on it til

the color

> comes back.

>

> As time goes on, it gets worse. I have 5 fingers (and they go in a

certain

> order) AND 5 toes (also a certain order) that will lose the blood &

not come

> back without my taking steps. They don't just " warm up " . The chill

blains

> represent 3 months of pain & peeling skin. SO, I am now a lot

quicker to

> get my feet out of the cold than I usta be.

>

>

> Thanks,

>

>

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I know. Believe me, I drive myself crazy, too. LOL!

Thanks,

Vitalady T

www.vitalady.com

If you are interested in PayPal, please click here:

https://secure.paypal.com/affil/pal=vitalady%40bigfoot.com

Re: Freezing my butt off

> And you still detest the heat? Strange little thing, ain'tcha?

> Alice

> The Loon

> RNY 12/28/00

>

>

> > They refer to mine as syndrome also. When you start losing fingers

> & toes

> > (the circulation doesn't return), then they call it the disease.

> Kinda late

> > then.

> >

> > BUT I had symptoms of this 10 yrs before surgery. It's just much

> worse now &

> > I didn't find out what was up with it til I had chill blains. I

> think only

> > the NE people will know what they are. NO ONE here knew what they

> were, inc

> > my docs, EXCEPT my podiatrist, who's a little on another station

> anyway, if

> > you catch my drift. But he knew what they were.

> >

> > Anyway, same problem. The circulation shuts off, and that's it. My

> fingers

> > go absolutely waxy yellow/white. NO BLOOD AT ALL. It is the

> spookiest

> > thing. Right middle finger can go just by holding onto a glass of

> iced

> > protein too long. I usually use a mug with a handle for that

> reason. The

> > fastest way to get it back is to wash a few dishes, then it turns

> pink. In

> > public, I just go into the restroom and run warm water on it til

> the color

> > comes back.

> >

> > As time goes on, it gets worse. I have 5 fingers (and they go in a

> certain

> > order) AND 5 toes (also a certain order) that will lose the blood &

> not come

> > back without my taking steps. They don't just " warm up " . The chill

> blains

> > represent 3 months of pain & peeling skin. SO, I am now a lot

> quicker to

> > get my feet out of the cold than I usta be.

> >

> >

> > Thanks,

> >

> >

>

>

>

> Homepage: http://groups.yahoo.com/group/Graduate-OSSG

>

> Unsubscribe: mailto:Graduate-OSSG-unsubscribe

>

>

>

>

>

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Yeah, I am freezing my BUTT off too. So, we bought a hot tub. LOL Now we

have serious discusions about how HOT to keep the hot tub. I want it all

the way up to the max which is 102. wants it around 99 which is

way too cold for me. Naturally we actually bought the hot tub so I could

do hydro-therapy for my knees. I even have a prescription for it!!

Debbie in Gig Harbor

ladybostons@...

www.paws2print.com

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MMMMMmmmmmm, hot tub! I am with you, though, hotter is better, although I can't

stay in it as long. I think the whirlpool at the gym is set to 106, so 102 does

not seem outrageous to me.

Reminds me of Joanne's home waterbirth though... they filled the rented birth

tub with water from the washing machine connection until they ran the hot water

heater out, and then they started heating water on the stove. My sister and the

doula worked like galley slaves to get it full enough for me to get into it.

Being 289 pounds and hot-natured at the time, the first thing I said when I got

in was " TOO HOT! " LOL I could have gotten in it 10 or more minutes sooner if

we'd agreed on a cooler temperature beforehand. My skinny and much

colder-natured husband had to get out of it, he was too cold. But I guess I was

working harder than he was, too. ;-)

Z

Open RNY 09/17/01

310/128/125

________________________________

From: Debbie McNeice-Schuyler

Sent: Sat 12/14/2002 7:22 PM

To: Graduate-OSSG

Subject: RE: Re: Freezing my butt off

Yeah, I am freezing my BUTT off too. So, we bought a hot tub. LOL Now we

have serious discusions about how HOT to keep the hot tub. I want it all

the way up to the max which is 102. wants it around 99 which is

way too cold for me. Naturally we actually bought the hot tub so I could

do hydro-therapy for my knees. I even have a prescription for it!!

Debbie in Gig Harbor

ladybostons@...

www.paws2print.com

Homepage: http://groups.yahoo.com/group/Graduate-OSSG

Unsubscribe: mailto:Graduate-OSSG-unsubscribe

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