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Raynaulds

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I came very close (with my feet), but have learned to NEVER let them

get cold, and if they do, get em warm asap. I know it hurts, but

every minute counts. And keep em moving, just bend them every time

you think about it, under warm water helps too, it dilates the

vessels. I got some Nitro ointment(Rx), that will open those vessels

right up, but will also give you an instant headache unless you're

very stingy with it. I take a lot of hot baths instead. One dr put me

on blood pressure med, that makes the vessels relax, but I had low

blood pressure to begin with, and it knocked me for a loop every time

I changed position. I hope you are getting some help with it- dr????

Unfortunately, a necessary evil sometimes. lol

> anyone suffering with finger ulcers that wo'nt heal?

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  • 5 years later...
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Deb,

I was first diagnosed with Raynaulds about six years ago... I was

first told that it was primary, but we've now discovered that it is

actually secondary... Yuck!

Raynaulds can be controled through channel blockers and taking asprin

as a daily regiment... Beyond that, its best to just keep all of your

extremities as warm as possible. I have learned to wear gloves in the

freezer section in the grocery store. I also frequently wear gloves

with the finger tips cut out so that I can type, and I almost always

have a space heater near by. Since all my other issues have come to

the surface, I've actually noticed the raynaulds taking a back seat as

I have less raynaulds attacks then what I was use to...

Best advise I can give is to check out the Raynaulds Association at

http://www.raynauds.org/index.cfm They are a great group of people

and can advise you as to some really great products as well.

Surprisingly, many on this site have other conditions as well. If

nothing else, you can read the latest articles and studies that get

posted there in the news section...

Stay warm

Bonnie R.

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Thanks. I feel like I went from this pretty healthy work horse of a person

to a chronically ill person I don't recognize. I know the prednisone is

making me more emotional than usual but this is so distressing to me.

especially at work. I am a good nurse but it is becoming so hard to do my

job properly. Thanks for the info and just for listening. My hubby thinks I

am getting too much info but I need it. I want to know as much as I can

before facing that rheumy for the first time!

On Thu, May 29, 2008 at 7:36 AM, Bonnie <tiredtaz@...> wrote:

> Deb,

> I was first diagnosed with Raynaulds about six years ago... I was

> first told that it was primary, but we've now discovered that it is

> actually secondary... Yuck!

> Raynaulds can be controled through channel blockers and taking asprin

> as a daily regiment... Beyond that, its best to just keep all of your

> extremities as warm as possible. I have learned to wear gloves in the

> freezer section in the grocery store. I also frequently wear gloves

> with the finger tips cut out so that I can type, and I almost always

> have a space heater near by. Since all my other issues have come to

> the surface, I've actually noticed the raynaulds taking a back seat as

> I have less raynaulds attacks then what I was use to...

> Best advise I can give is to check out the Raynaulds Association at

> http://www.raynauds.org/index.cfm They are a great group of people

> and can advise you as to some really great products as well.

> Surprisingly, many on this site have other conditions as well. If

> nothing else, you can read the latest articles and studies that get

> posted there in the news section...

> Stay warm

> Bonnie R.

>

>

>

--

Deb N

" If you can dream it, you can do it. Always remember that this whole thing

was started with a dream and a mouse "

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I've had Reynauds for a few years. Its very painful whenever my hand touches

something cold. I get this burning aching pain that makes tears run down my

cheeks. I've since learned not to go shopping or in frozen foods without

gloves. Otherwise I pay the price for a big attack. I can even get it just

sitting in a room with a fan going and especially the AC in the warmer months.

Bonnie <tiredtaz@...> wrote: Deb,

I was first diagnosed with Raynaulds about six years ago... I was

first told that it was primary, but we've now discovered that it is

actually secondary... Yuck!

Raynaulds can be controled through channel blockers and taking asprin

as a daily regiment... Beyond that, its best to just keep all of your

extremities as warm as possible. I have learned to wear gloves in the

freezer section in the grocery store. I also frequently wear gloves

with the finger tips cut out so that I can type, and I almost always

have a space heater near by. Since all my other issues have come to

the surface, I've actually noticed the raynaulds taking a back seat as

I have less raynaulds attacks then what I was use to...

Best advise I can give is to check out the Raynaulds Association at

http://www.raynauds.org/index.cfm They are a great group of people

and can advise you as to some really great products as well.

Surprisingly, many on this site have other conditions as well. If

nothing else, you can read the latest articles and studies that get

posted there in the news section...

Stay warm

Bonnie R.

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