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In a message dated 2/4/99 11:47:37 AM Eastern Standard Time,

springmountain@... writes:

<< I'm wondering if you have any

suggestions as to how to stop the condition to getting worse? What you

would do at my stage? >>

,

You are so lucky. And I'm happy for you cause there is stuff you can do to

help control rosacea. Just using a sun screen, even a hat, is a big help.

Being gentle with your skin - using products that make your skin say AAAHHH.

:) Keep tracking triggers and take them seriously. The more you can avoid

flushing, the milder your rosacea is. Find a derm who understands the

relationship between seb/derm and rosacea and will treat both. Aspirin helps

in a flare. Antihistamines are worth their weight in gold if you can take

them. I take Claritin daily and it's made a big difference to me. Zrytec

seems to be more effective, though.

Good luck.

Esther

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  • 1 year later...

First of all, welcome . I am sorry I am late welcoming you.

You have had such struggles. I hope that we can help you here. I send links and

information pages so that we can all read up on the illness. I will send some

tonight for you.

Glad to have you here.

List Moderator,

karen wrote:

>

>

> Hello everyoneI just joined your list tonight in hopes of finding some info

aboutthis disease that I was recently diagnosed with. I am 40 yrs. old andsince

Jan. 99 I was diagnosed with endometriosis after having apartial hyst in 1989.

In May of 99 I had additional surgery ofablation of endo and a presacral

neurectomy. at this point I had nouterus and no ovaries, but the gyn that

removed my ovaries in Jan. 99left ovarian remenants ehind and endo continued to

grow attaching mycolon and intestines to my pelvic floor. By may 99 I had stage

4 endodue to ignorance of the gyn who did my surgery in Jan. 99! Then inJuly 99

I had cystolcele and rectocele surgery because my bladderdropped and a herniated

rectum. Tried going back to work in Aug. 99and struggled till Dec.99 with muscle

and joint pain beyond beliefalong with sleeplessness, chronic fatigue! I was

diagnosed withfibromyalgia this month and I also believe that I am hypoglocemic

dueto hands trembling and shaking inside after eating

> sweets or evensausage gravy

>

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> Add or view links about fibro/CFS.

> http://www.onelist.com/links/

>

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> Go to: http://www.onelist.com/ Log in:

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> LIST OWNER:oa2@...

--

:0)

An argument with your spouse is a loving moment lost forever.

Mom to Bear, Wife to

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-

Welcome. You definitely have found a great place to get information on

fibro. My name is Tonya and I was diagnosed with possible fibro last month,

while my husband Marty was diagnosed a couple of years ago. There is a wide

variety of medications for pain. I take Darvocet and also Neurontin (for

Restless Leg Syndrome). Marty takes several things including Vicodin and

Celebrex. Unfortunately, there is no one thing that works for everyone. I

hope that you are able to find something that works for you.

Tonya

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  • 3 weeks later...
Guest guest

Dee

Thank you for that confirmation! I only use the darvocet when I

absolutely need it and I don't take it if I don't need it. I have only

been on darvocet for 3 months and out of a prescription of 90 I still

have more than half left. I am sure I would have taken more if I were

addicted to keep the pain down. The celebrex helps me for most of the

day till about 3:00 depending on how active I was that day. At this

point a little rest helps and when it doesn't and the calves of my leggs

spasm I have to take the darvocet or the spasms just get worse.

I then take two flexeril at bedtime and my morning stiffness is somewhat

better. Then I take my Celebrex every morning and the cycle begins

again. Sorry to be so long winded! I feel like you know where I'm coming

from! I hope you have had a good day!

The Mann's

and

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At 11:46 PM 3/10/00 -0500, you wrote:

>From: kgmann@...

>

>Dee

>

>Thank you for that confirmation! I only use the darvocet when I

>absolutely need it and I don't take it if I don't need it. I have only

>been on darvocet for 3 months and out of a prescription of 90 I still

>have more than half left. I am sure I would have taken more if I were

>addicted to keep the pain down. The celebrex helps me for most of the

>day till about 3:00 depending on how active I was that day. At this

>point a little rest helps and when it doesn't and the calves of my leggs

>spasm I have to take the darvocet or the spasms just get worse.

>I then take two flexeril at bedtime and my morning stiffness is somewhat

>better. Then I take my Celebrex every morning and the cycle begins

>again. Sorry to be so long winded! I feel like you know where I'm coming

>from! I hope you have had a good day!

>

>

>The Mann's

> and

>Sure do understand.....and glad it was reassuring. I have had a lot of

experience with " addictive " stuff....Valium is addictive they tell me but I

go days without it until I need it and never even think about it. I have

a friend on Demerol and it's the same for her....she has built up a bit of

tolerance for it but when she has minimal pain she skips it and doesn't

think about it....it just takes a bigger dose to cut the pain than it did

four years ago....so tell the Dr to get real!!!! Dee

>

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>

>

>VIP

>Add or view links about fibro/CFS.

>http://www.onelist.com/links/

>

>TO unsubscribe.

>Go to: http://www.onelist.com/ Log in:

>Go to this list: Click on your name: Select your choice.

>

>LIST OWNER:oa2@...

>

>

>

>

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  • 6 months later...
  • 1 year later...

Premindy:

Not everyone wears those socks ( Teds as we call them). I did not and

after one week I had no swelling nor need for them. My surgeon said that

they would not be necessary. No need for you to request the discomfort of

Teds if they are not necessary.

Vette

Oshkosh Wisconsin

USA

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  • 4 months later...
Guest guest

i wanted to introduce myself. i am foster mom to a 16yr old named

hassan. he has multiple medical problems and cerebral palsy. he has

been on a ketogenic diet for over 5 years. he has been fed the diet

via g-tube, which was placed in order to help him tolerate the diet.

hassan has had many major medical problems that started after he had

been on the diet for a few years, including nephratic syndrome,

aspirations, vomiting..had a fundo done a year ago, this spring he

was diagnosed with stomach dysmotility and now has j-tube. He spent

the last 21/2 months in the hospital on tpn feedings so was not on

ketogenic diet. went into status 4 times while in hospital and

multiple seizure each day. now that he is home he is having about 1

tc seizure a week mostly when in his sleep late at night. we have

never been able to wean him off the med, still on depakote, tegretol

and neurontin, in addition to diastat for prolonged seizures.

i am interested in talking to others who have experience with

children who have complex medical issues in addition to the seizure

disorder. i am also interested in chatting with folks who have had or

known someone on the diet for more then 3 years.

thanks for letting me be a part of your group

maggie

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