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Hello. I might've missed something, but what side effects does Medrol have?

Are they like Prednisone? Did you find that it works just as good as the

Prednisone?? I'm looking for ANYTHING but Prednisone!! Please let me

know!! Thanks!!

Philadelphia, PA

>From: " Bozena Patin " <bpatin@...>

>Reply-

>< >

>Subject: [ ] To Patty

>Date: Fri, 31 Aug 2001 14:40:48 -0000

>

>Hi Patty,

>

>Thanks for the input. I will certainly ask my doctor about the Medrol -

>anything has to be better than the Prednisone. He just loooovees it when I

>ask about stuff I've learnt from this group! BTW I would join you in that

>bonfire anytime ......even from down under!

>

>Sounds like you're doing really well!

>

>Regards, Bozena

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  • 2 months later...

Patty:

I'm sorry to hear that you are not feeling well. You definitely need to go on

with your life. I was recently diagnosed in June of this year and was 100% on

the pity pot, could not stop thinking about the illness, was crying all the time

etc. and was on prednisone for two weeks, when my GI called and said " you're

levels are normal and by the way, you are pregnant, so stop taking the meds " .

(My husband and I had tried for years to have a baby with no luck). I thought

why now? I could only conclude that God was giving me a sign to get on and over

it and off the pity pot! Now, at 5 months pregnant, I feel wonderful! and my

levels have been normal! Who knows how I will feel later, but I'm going to

remain upbeat and beat it! The point, if you can, try to think and focus on the

positive..your mental definitely effects your physical...at least in my case.

Good Luck and Congratulations on your future with .

Toni P (AIH 6-01 and pregnant:) )

>>> pattyeady@... 11/01/01 03:40AM >>>

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Toni

I am so happy for you on your wonderful news. Keep the faith.

Gloria AIH 9/01

>From: " Antonia Ponder " <amp@...>

>Reply-

>< >

>Subject: [ ] Re: To Patty

>Date: Thu, 01 Nov 2001 11:01:34 -0600

>

>Patty:

>

>I'm sorry to hear that you are not feeling well. You definitely need to go

>on with your life. I was recently diagnosed in June of this year and was

>100% on the pity pot, could not stop thinking about the illness, was crying

>all the time etc. and was on prednisone for two weeks, when my GI called

>and said " you're levels are normal and by the way, you are pregnant, so

>stop taking the meds " . (My husband and I had tried for years to have a

>baby with no luck). I thought why now? I could only conclude that God

>was giving me a sign to get on and over it and off the pity pot! Now, at 5

>months pregnant, I feel wonderful! and my levels have been normal! Who

>knows how I will feel later, but I'm going to remain upbeat and beat it!

>The point, if you can, try to think and focus on the positive..your mental

>definitely effects your physical...at least in my case.

>

>Good Luck and Congratulations on your future with .

>

>

>Toni P (AIH 6-01 and pregnant:) )

>

> >>> pattyeady@... 11/01/01 03:40AM >>>

>

>

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  • 3 months later...

Patty,

Yes BC is great for people who love nature !!!!

" J. " <scott_p@...> wrote:

, I live as far away fromCanada as is possible in the States I am in Miami. I did live in Port Huron Michigan back in 1977-1979 and worked in Sarnia Ontario, I also vacationed in toronto & montreal last year. Beautiful country if you skip no--april or don't mind freezing your shnuggilies off. I want to go hiking in Banft and skiing in BC!

Patty

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" J. " <scott_p@...> wrote:

from Canada,

I will respond even though you asked Gayle not me. I was on & off prednisone for almost 20 yrs when I had my transplant. Also I had chirrosis on my first biopsy in 1982.

At the same time I think everyone is different. I have friends who were never dx prior to complete liver failure [the ICU type] and needed immediate tx. You have to accept the differences. They are prominent among us. To a our new member FATIGUE IS THE WORST heng in there this group is the place to be.

Patty Miami

Patty,

Thank you for sharing this with me. Just the fact that you are telling me that you lived with cirrhoses for so long without a transplant is encouraging to me. For some reason it is less scarry to me, if it comes later... That means to me that I can go on with my life without being scared that it will happen tomorrow. What i'm saying might not make sense to you but to me it's like confirming what my doctor said; If the med goes well you could go on living with the cirrhoses...

Thanks again and take care of yourself

from Canada

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  • 1 year later...
Guest guest

Bozena,

At least your Dr has a sense of humor, replace your liver and everything

will be OK. The transplant surgeons talk in a way that makes you feel like

it's an oil change in a car. His explanation of the prednisone withdrawal

makes sense to me. Hopefully they will lessen. So many things result in

night sweats, they may go away and you'll never know. (Sounds good to me!)

Hang in there!

Patty

RE: J, Jeanette, Anita, Patty and Celuch

>

> Bozena,

> The hot flashes became night sweats as I got closer to transplant. In

> the few weeks before I slammed into the ground with total liver

> failure I was actually changing the sheets several times during the

> night. It was bad. After the transplant nothing. Patty

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  • 7 months later...

Patty,

Where in northern V irginia are you? We're in Fairfax County.Who do you see for rheumatology?

Liz

Re: First Posting/OT?/G.

In a message dated 12/10/03 9:30:44 PM Eastern Standard Time, cpgarafalo@... writes:<< Hi, Patty - which part of the country are you in?I hope not Nebraska! >>Hi Chris:Nope, not Nebraska. We are in Northern VA. We were fortunate to find one so soon (after repeatedly calling them) and one so close.Take care.PattyTo leave this mailing list, send request to: -unsubscribe

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  • 4 weeks later...

In a message dated 1/6/04 8:33:00 AM Eastern Standard Time,

nikki228@... writes:

<< Patty

Just to throw my 2 cents in here Patty. I understand

completely how you feel; but, remember as these kids are

having flare ups the arthritis is attacking their bodies

too - obviously their joints. This can cause different

damage to them down the line. So you want to remember that

you need to stop the deterioration and progression of the

disease as well.

Tammy

>>

Exactly. I even mentioned the DMARDs today to her rheumy. He will use them

if he thinks, but right now he doesn't want to start with them. We go again

in 3 weeks and he will address it again.

Thanks Tammy.

Patty

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  • 2 years later...

Hi Patty,

Sorry I took so long to answer your question about event monitors.

" EventMonitors:

Event monitors are small devices that are used by patients over a

longer period (weeks to months, typically one month). Two stickky

patches (electrodes) on the chest connect two wires to the event

recorder. The monitor is always on but will only store the patient's

rhythm when the patient or caregiver pushes the button. Most

monitors will save the rhythm for several seconds of rhythm before

the button is even pushed. The rhythm is also saved for a period

after the button is pushed. A few specialized monitors are used

only after the patient has symptoms. The intent is for most monitors

to be worn as much as possible every day to increase the chances of

recording the patient's rhythm when he/she has symptoms. "

They " help to identify irregular beats, called arrhythmias

to further evaluate arrhythmias noted on a resting EKG

to evaluate other signs and symptoms which may be heart-

related, such as fatigue, shortness of breath, dizziness, or

fainting. "

Mine was sent to my house, but I haven't started the proceedure yet.

Patty, good luck on your fast...if you go from water to juice let me

know and I will join you with a lemon juice fast.

Love, Shirley

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Hi Shirley,

Thanks for the ansswer on event monitors. Let us know how you do

with it.

I have started the juices. Yesterday afternoon I had some fresh

juiced pineapple juice. YUM! I also had 2 kiwi's and some broth,

so I had a little more than I had planned, but I am determined to

stay on an all plant diet.

I'll be doing juices today and for as long as I can. That fresh

pineapple juice is the best! I decided on that because of the anti-

inflammatory enzymes it provides.

I am glad you want to join me!

Patty

>

> Hi Patty,

>

> Sorry I took so long to answer your question about event monitors.

>

> " EventMonitors:

>

> Event monitors are small devices that are used by patients over a

> longer period (weeks to months, typically one month). Two stickky

> patches (electrodes) on the chest connect two wires to the event

> recorder. The monitor is always on but will only store the

patient's

> rhythm when the patient or caregiver pushes the button. Most

> monitors will save the rhythm for several seconds of rhythm before

> the button is even pushed. The rhythm is also saved for a period

> after the button is pushed. A few specialized monitors are used

> only after the patient has symptoms. The intent is for most

monitors

> to be worn as much as possible every day to increase the chances

of

> recording the patient's rhythm when he/she has symptoms. "

>

> They " help to identify irregular beats, called arrhythmias

> to further evaluate arrhythmias noted on a resting EKG

> to evaluate other signs and symptoms which may be heart-

> related, such as fatigue, shortness of breath, dizziness, or

> fainting. "

>

> Mine was sent to my house, but I haven't started the proceedure

yet.

>

> Patty, good luck on your fast...if you go from water to juice let

me

> know and I will join you with a lemon juice fast.

>

> Love, Shirley

>

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