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Hi MAzz,

will be thinking of you today at this sad time.

Hopefully it is nothing serious with Doug's ear but if it is a burst ear

drum which isn't uncommon (it has happened to me twice) it should be ok in

a couple of weeks time, I presume he is going to the Dr as soon as he can.

Take CAre,

Elaine

>-- Original Message --

>Central Coast Bandsters <centralcoastbandsters >,

>

>From: Mazz <starbug@...>

>Date: Fri, 27 Oct 2006 07:19:00 -0700

>Subject: hello

>Reply-

>

>

>To everyone who has been burning candles for my family I thank you very

>much. Today is going to be the tough day. Don's funeral is at 10.15

>this morning at Rookwood. So please think of Betty his wife, Narelle

>his daughter, Adam and his twin sons and also all his

>grandchildren and extended family at this time.

>

>Then would you believe of all days I have a team dinner with work that I

>

>have been planning for a couple of months now and I can not get out of

>it but I think it will be the medicine that I need after this week.

>

>I have Doug home from work today as he has a serious problem with his

>good ear. As most of you know Doug is deaf in one ear and blind in one

>eye because of his mum having had rubella when she was having him. Last

>

>night when having a shower dont ask me how or why he his ear got itchy

>and he put his finger in there to scratch it and he felt something crack

>

>and since then he has hardly been able to hear a thing. I am very

>worried about him and I home it is something structual done to the ear

>and not the eardrum or anything that will effect his hearing long term.

>

>Well talk to you all over the weekend. Have a great day.

>

>Cheers

>Mazz

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,

Good to see you : )

I also love to watch all of the children out and about. Several of them were incredibly polite without the prodding of their parents, which surprised me a bit. One family had their kids trick-or-treating, but the parents had sacks too...that was a bit odd.

Hugs,

-------------- Original message -------------- From: Potts <clonezfan100@...>

Hello everyone,Hope that you all are having a good week. Welcometo all of our new members. I hope that this growingfamily will provide whatever each of you may need.I'm & live in Cincinnati, OH. I deal withallergies/asthma/hypothyroidism on a daily basis. Myasthma is pretty well controlled. For fun I sing inmy church choir, read, and go to hockey games!It was fun tonight seeing the wide variety of agesof the kids out trick or treating, along with theircostumes. Unfortunately the weather (wet & cold)probably kept a lot of them home. If you all want to chat, I'm on-line most nightsfrom 9-10 PM, on Friday nights could be any time. MyAOL screen name is clonezfan. You all take care.Music is a gift from God__________________________________________________________Low, Low, Low Rates! Check out Messenger's cheap PC-to-Phone call rates BR>(http://voice.)

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one man had a bag for candy it was for his daughter she was afraid so he went around and got her candy mom said this was the last time we are doing this one kid really scared mom so she said thats the last time. heather how is your sore mine it itches but still red and the hole is still there josieheatherlkum@... wrote: , Good to see you : ) I also love to watch all of the children out and about. Several of them were incredibly polite without the prodding of their parents, which surprised me a bit. One family had their kids trick-or-treating, but the parents had sacks too...that was a bit odd. Hugs, -------------- Original message -------------- From: Potts <clonezfan100@...> Hello everyone,Hope that you all are having a good week. Welcometo all of our new members. I hope that this growingfamily will provide whatever each of you may need.I'm & live in Cincinnati, OH. I deal withallergies/asthma/hypothyroidism on a daily basis. Myasthma is pretty well controlled. For fun I sing inmy church choir, read, and go to hockey games!It was fun tonight seeing the wide variety of agesof the kids out trick or treating, along with theircostumes. Unfortunately the weather (wet & cold)probably kept a lot of them home. If you all want to chat, I'm on-line most nightsfrom 9-10 PM, on Friday nights could be any time. MyAOL screen name is clonezfan. You all take care.Music

is a gift from God__________________________________________________________Low, Low, Low Rates! Check out Messenger's cheap PC-to-Phone call rates < BR>(http://voice.)

Get your email and see which of your friends are online - Right on the new .com

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My little girl (2) was in a wagon with Daddy pulling and she was a

pony, but she wouldn't get out. It was too cold. So I stood with my

son and got her a little candy. I don't think anyone minded.

Dawn

,

>

> Good to see you : )

>

> I also love to watch all of the children out and about. Several

of them were incredibly polite without the prodding of their parents,

which surprised me a bit. One family had their kids trick-or-

treating, but the parents had sacks too...that was a bit odd.

>

> Hugs,

>

>

>

> -------------- Original message --------------

> From: Potts <clonezfan100@...>

> Hello everyone,

> Hope that you all are having a good week. Welcome

> to all of our new members. I hope that this growing

> family will provide whatever each of you may need.

>

> I'm & live in Cincinnati, OH. I deal with

> allergies/asthma/hypothyroidism on a daily basis. My

> asthma is pretty well controlled. For fun I sing in

> my church choir, read, and go to hockey games!

>

> It was fun tonight seeing the wide variety of ages

> of the kids out trick or treating, along with their

> costumes. Unfortunately the weather (wet & cold)

> probably kept a lot of them home.

>

> If you all want to chat, I'm on-line most nights

> from 9-10 PM, on Friday nights could be any time. My

> AOL screen name is clonezfan.

>

> You all take care.

>

> Music is a gift from God

>

> __________________________________________________________

> Low, Low, Low Rates! Check out Messenger's cheap PC-to-Phone

call rates < BR>(http://voice.)

>

>

>

>

>

>

> ---------------------------------

> Get your email and see which of your friends are online - Right on

the new .com

>

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  • 4 weeks later...

Hi Lia,

Thank you for your introductory post. Welcome to battlefield

medicine. Grab a helmet and get political!

Lenny

List Co-host

>

> hi.. I subscribed a few weeks ago and have been lurking. I have a 15

, soon

> to be, son with pdd/nos who is hyperlexic. I am anti vaccine since

he was dx

> and I began to review his baby videos. My son seemed to be

afflicted in

> different ways... meaning the hyperlexia. He had exposure to a

round of chicken pox

> at 6 weeks of age... but then got a mystery rash at age 6 months..

a strange

> rash or blotches.. but they never crusted and scabbed.. no fever..

good

> appetite.. he would get these rashes out of the blue on and off for

the next 3.5

> years. He narrowed his appetite to anything white.. cheerios...

chicken

> breast... ff's.. BUT.. had normal play skills and loved thomas..

disney.. barney

> and imitated and created play. He did a lot of typical skill

development at

> typcial ages.. including self potty trained in both areas. BUT...

he was

> spelling, reading and not talking. limited eye contact... you all

know.. but no

> hand flapping , toe walking.. was a good sleeper.. and loved to be

around kids..

> but could not intereact. I could go on... with the good things..

BUT... his

> abstract language.. the W's questions.. he was in a foreign land in

the way

> of learning how to talk. HOW DOES THE MMR and he was vaccinated

with the HIB

> at age18 months and I see the slow downward progression as far as

eye contact

> and social skills one to one.. how does the VACCINES hit our kids?

too much?

> too little? no two kids are alike? I call it autism roulette.. I

tell every

> new mom... please read what is going on before vaccinating before

your child

> plays the AUTISM roulette ...why are some kids hit with more

symptoms than

> others? I want to scream... I have a son who is wonderful as all

others of

> yours. He is soo typical in so many ways.. but anyone can see the

horrible

> deficit of the language as I blame the vaccines!! peace , Lia

>

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thanks, lenny... I am not savvy in the political arena.. but I have a big voice and I know my way at an IEP table..I know one thing.. vaccines damaged my son... I want them to admit and become accountable for their damages and our hell... peace, Lia

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My step-daughter has had Crohn's since she was a small

child. It took a long time to get it diagnoses and she

had to go through a lot to get it under control. I

know how she hates prednisone. I've been on it at

doses much smaller than what she had. Hope you can be

off steroids soon. Speak up more often ; )

Willow

--- solwitchstanny <solwitchstanny@...> wrote:

> just wanted to say hi to all.Had Crohn`s for the

> past 19 years.Had a

> right hemicolectomy in 1986.currently on steroids

> AGAIN

>

>

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My step-daughter has had Crohn's since she was a small

child. It took a long time to get it diagnoses and she

had to go through a lot to get it under control. I

know how she hates prednisone. I've been on it at

doses much smaller than what she had. Hope you can be

off steroids soon. Speak up more often ; )

Willow

--- solwitchstanny <solwitchstanny@...> wrote:

> just wanted to say hi to all.Had Crohn`s for the

> past 19 years.Had a

> right hemicolectomy in 1986.currently on steroids

> AGAIN

>

>

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Hi and welcome! I'm and see my sig for my main health problems. FYI I was readmitted to the behavioral health unit the day before Thanksgiving and released this past Tues. I have been trying to catch up on email since. and get my meds straightened out. I am now on Geodome, seroquel and trilithium or something like that for the new dx of bipolar. Right now I have to let my husband take charge of my meds as I didn't od but took few pills when I wasn't supposed to, not enough to hurt myself but you know how they are, they think everyone is suicidal.

I hope you write more soon about your Chron's and the surgery and if you have difficulty with prednisone--I certainly do....btw if anyone objects to my sig I can change it.

all ways love, all ways Jesus! your sis, age 46 w/fibro asthma allergies etc,bipolar depression anxiety etc.mom of Nick age 24 wonderful adorable young man & pharm techAng age 22 college student doing great but happens to be blessed with this crazy thing called cfwife of , 48, trying to help fix us.(we aren't broken)and Lucy age 4 the dog

hello

just wanted to say hi to all.Had Crohn`s for the past 19 years.Had a right hemicolectomy in 1986.

..

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Dear ,

Sorry you hit a bump in the road. Glad you're back.

Seroquel worked magic on my bipolar. I was rapid

cycling and that stopped quickly. I can sleep which I

never could before. I don't see anything wrong with

your sig.

Welcome back,

Willow

My Challenges:

Scoliosis, Radiation Injury to my Brain, Ministrokes, Memory Problems, Cluster

Migraine Headaches, Osteoporosis with Multiple Broken Bones, Fibromyalgia,

Chronic Pain and Fatigue, Depression, PTSD, Bipolar Type II Rapid Cycling,

Anxiety, Chronic Insomnia, Sleep Apnea, Spinal Stenosis, TMJ injury, Thyroid

Cancer X3, Skin Cancer, Loss of Salivary Glands due to Thyroid Radiation Tx,

Teeth Destruction with Loss of Salivary Glands, Obesity, Restless Leg Syndrome,

Alpha Wave Intrusion on Delta Sleep plus many other Sleep Anomalies,

vonWillebrand's disease (genetic bleeding disorder), Hypertension, High

Cholesterol and Triglycerides, Chronic Allergies, Asthma, Peripheral Neuropathy,

Chronic Gastritis, GERD, Adult ADD, Overactive Bladder,

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>

> Hi and welcome! I'm and see my sig for my main health

problems. FYI I was readmitted to the behavioral health unit the day

before Thanksgiving and released this past Tues. I have been trying

to catch up on email since. and get my meds straightened out. I am

now on Geodome, seroquel and trilithium or something like that for

the new dx of bipolar. Right now I have to let my husband take

charge of my meds as I didn't od but took few pills when I wasn't

supposed to, not enough to hurt myself but you know how they are,

they think everyone is suicidal.

>

> I hope you write more soon about your Chron's and the surgery and

if you have difficulty with prednisone--I certainly do....btw if

anyone objects to my sig I can change it.

>

> all ways love, all ways Jesus! your sis,

> age 46 w/fibro asthma allergies etc,bipolar depression

anxiety etc.

> mom of Nick age 24 wonderful adorable young man & pharm tech

> Ang age 22 college student doing great but happens to be blessed

with this crazy thing called cf

> wife of , 48, trying to help fix us.

> (we aren't broken)

> and Lucy age 4 the dog

> hello

>

>

> just wanted to say hi to all.Had Crohn`s for the past 19

years.Had a

> right hemicolectomy in 1986.

>

> Recent Activity

> a.. 9New Members

> Visit Your Group

> New Message Search

> Find the message you want faster. Visit your group to try out

the improved message search.

>

>

>

> Share feedback on the new changes to Groups

> .

>hi brenda this is Terri b i have lived with khron's for many years

and in 2002 i finally had to have a iliostomy done i waqs salways so

sick and i just could not bear it any more my dr really worked with

me to try to prevent the surgery since this was my 3rd

colosotomy/iliostomy since i was born i'm 45 now and i'm in my 19th

years total and my krhon's was so out off control i weight like

95pound then i went up to 212 pounds because i became so toxic and

not having contol of my bowels was horrible i was wearing diapers my

husband left me and i was not looking foward to living the rest of

my life with a bag but almost 5 years later i'm glad i had the

surgery at least now i have some control with the bag and i still

have to take meds to keep it under control kindof what i'm saying is

make sure you get at least 3 dr opion and that you trust the doctor

who is treating you do your reshearch i went to the book store and

bought the paper back (they are cheaper) and make the most informed

choise for you i choose the wrong dr to do the surgery and i have a

lot of problems because of that and i would hate to see anyone go

through what i'm going through .some dr are to quick to just cut you

and go and you are left to pick up the pieses .living with krhon's

is hard you will be in my prayes .also even with the sugery i still

have khron's i gpo into remission and then bingo it's back this year

alone i have lost 94pounds i'm at 118 because of it but aleast i had

the wieght to lose so please please do your research o.k that care

Terri B

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Hi Jerri. I know the alone thing...it kinda' sucks in the sense that you get tired of tellin' yerself how bad you feel.. haha Seriously, you do want another opinion cause your not feelin' safe about what if you fall asleep and not realize that you need to breath and etc...... The TX did that to me. I'm stage 1 2b with ESLD and on the LIST... I tried tx twice only got to 5 weeks before an infection set's in I'm sorry your hurting...Keep an eye on the temp. and the more water you drink will only go towards promoting a nice, shiny coat and killing fleas....OH! wrong group!! OK.. that was weak... I've given my staff the day off, along with the driver, so I will be here all day, If you wanna' talk mail me....what sre your stats??? Deliman Jerri Neely

<all4jerri@...> wrote: Hi,My name is Jerri and I am new to this group. I began my Interferon treatment on November 24th and it is already hard. I have been really sick for the past 4 days and was wondering if anyone can tell me if it is going to get better or if this is as good as it gets.I live alone and at this point am unsure if I will be able to do this. I guess I am just scared. Any advise would be helpful.thanks,Jerri

Check out the all-new beta - Fire up a more powerful email and get things done faster.

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Hi

Jerri. Welcome to our family. I’m De. I did treatment (tx) thru 2004. It was harder

for me in the beginning and the end and easier in the middle, although I did

have some problems throughout. Attitude is everything. There was a

point when we talked about stopping because my blood count was going too low

and the insurance wouldn’t approve Epogen, but I told the doc I’d

come to far to quit, so I had my count checked every week to be sure I was

still safe to keep going. I was bound and determined to finish & I

did and it has paid off for me so far. I’m almost 2 years clear.

What

kind of sides are you having and we’ll see what helpful hints we can give

you to deal with them.

De

Hello

Hi,

My name is Jerri and I am new to this group. I began my Interferon

treatment on November 24th and it is already hard. I have been really

sick for the past 4 days and was wondering if anyone can tell me if it

is going to get better or if this is as good as it gets.

I live alone and at this point am unsure if I will be able to do

this. I guess I am just scared. Any advise would be helpful.

thanks,

Jerri

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Hi De,

Thanks for the email. I am taking Pegasus (weekly)

and Ribaviron (400 mg in am and 600 mg in pm). As far

as symptoms go I feel like I have the flu, stuffy

head, muscle aches and stomach issues (I can't eat

anything except crackers).

I also have developed a rash on my elbows. I know

that they said that you might get a rash I just didn't

think that it would be this soon.

Had some anxiety last week and haven't been sleeping.

Other than that it is all great:)

Worried about being able to work tomorrow. Were you

able to continue working?

Jerri

--- Motley <dmotley@...> wrote:

> Hi Jerri. Welcome to our family. I'm De. I did

> treatment (tx) thru 2004.

> It was harder for me in the beginning and the end

> and easier in the middle,

> although I did have some problems throughout.

> Attitude is everything.

> There was a point when we talked about stopping

> because my blood count was

> going too low and the insurance wouldn't approve

> Epogen, but I told the doc

> I'd come to far to quit, so I had my count checked

> every week to be sure I

> was still safe to keep going. I was bound and

> determined to finish & I did

> and it has paid off for me so far. I'm almost 2

> years clear.

>

>

>

> What kind of sides are you having and we'll see what

> helpful hints we can

> give you to deal with them.

>

>

>

> De

>

> Hello

>

>

>

> Hi,

>

> My name is Jerri and I am new to this group. I began

> my Interferon

> treatment on November 24th and it is already hard. I

> have been really

> sick for the past 4 days and was wondering if anyone

> can tell me if it

> is going to get better or if this is as good as it

> gets.

>

> I live alone and at this point am unsure if I will

> be able to do

> this. I guess I am just scared. Any advise would be

> helpful.

>

> thanks,

> Jerri

>

>

>

>

________________________________________________________________________________\

____

Have a burning question?

Go to www.Answers. and get answers from real people who know.

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Hi Jerri,

I was on tx twice & worked through both times. That was the old tx, I hear the new one isn't as bad but I haven't tried it so I can't say from personal experience. I had a lot of side effects. Spent four months feeling like I had the flu, lost some weight & my sense of smell went weird - perfume that I'd liked before made me gag. My doctor dx'd (diagnosed) me with COPD while I was on tx but it went away when tx stopped. When I checked the list of side effects there was one - lung infiltrates - I guess that's what that was. There were more but I can't remember, it's 10 years ago & my memory doesn't go that far back (if it works at all)

Hugs,

SuZie

Next time I'm coming back as a cat

----- Forwarded Message ----From: jerri neely <all4jerri@...>Hepatitis CSupportGroupForDummies Sent: Sunday, December 3, 2006 8:14:25 PMSubject: RE: Hello

Hi De,Thanks for the email. I am taking Pegasus (weekly)and Ribaviron (400 mg in am and 600 mg in pm). As faras symptoms go I feel like I have the flu, stuffyhead, muscle aches and stomach issues (I can't eatanything except crackers).I also have developed a rash on my elbows. I knowthat they said that you might get a rash I just didn'tthink that it would be this soon.Had some anxiety last week and haven't been sleeping.Other than that it is all great:)Worried about being able to work tomorrow. Were youable to continue working?Jerri--- Motley <dmotleybellsouth (DOT) net> wrote:> Hi Jerri. Welcome to our family. I'm De. I did> treatment (tx) thru 2004.> It was harder for me in the beginning and the end> and easier in the middle,> although I did have some problems throughout.

> Attitude is everything.> There was a point when we talked about stopping> because my blood count was> going too low and the insurance wouldn't approve> Epogen, but I told the doc> I'd come to far to quit, so I had my count checked> every week to be sure I> was still safe to keep going. I was bound and> determined to finish & I did> and it has paid off for me so far. I'm almost 2> years clear.> > > > What kind of sides are you having and we'll see what> helpful hints we can> give you to deal with them.> > > > De> > [Hepatitis CSupportG roupForDummies] Hello> > > > Hi,> > My name is Jerri and I am new to this group. I began> my Interferon > treatment on November 24th and it is already hard. I> have been really > sick for the past 4 days and was wondering if anyone> can tell me if it > is going to get better or if this is as good as it> gets.> > I live alone and at this point am unsure if I will> be able to do > this. I guess I am just scared. Any advise would be> helpful.> > thanks,> Jerri> >

> > ____________ _________ _________ _________ _________ _________ _Have a burning question? Go to www.Answers. and get answers from real people who know.

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Hi Jerri I'm d aka dannegrl I'm 33 and in texas. I an type 1a. I am a 2 time non-responder to treatment. I had alot of side effects from tx but the dr I had didn't know a thing about hep c at all. I would take 2 tylenol before my shot. then my hubby did the shot for me and I would go to bed. I was only able to eat yougart for the first few months of tx. Then my dr said try other cold and creamy foods since they seemed to work good for me. If you are not a big water drinker lots of us here drink CRYSTAL LITE the store brand is great too. oh Jello was another thing I could eat. lol go figure. And still now 2yrs later i love cold creamy foods. While I was a non responder, my husband Mitch was on tx for 52 weeks. He has been undetectable since he was at his 6 month labs on tx. He is coming up on his 3rd year since finishing his pegintron/rebatol.. Honey don't give up. we are all here and It helps to know the things you are going through , we

understand. love and welcome djerri neely <all4jerri@...> wrote: Hi Gail,Thanks for the information. I found that I wasfeeling better by this afternoon. I took my shotFriday night so I am hoping that I can still get towork.I will have to pick up some Ensure as crackers aren'tcutting it anymore. Thanks again for the advise,Jerri . The art of living lies not in eliminating but in growing with troubles. -Bernard M. Baruch

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Jerri MAKE SURE YOU SHOW YOU DR THE RASH. we was told to show them rashes, because it could be an allergic reaction. Better to be safe. djerri neely <all4jerri@...> wrote: Hi Suzie,I'm glad to hear that your treatment worked. I knowwhat you mean about the sense of smell. I will walkinto someones house and it is horrible although I knowthat there isn't anything there. I smell smoke all ofthe time and no one smokes. Weird.Got a crazy rash on my elbows yesterday. It

seemslike every day something new comes up.Day 11 is over 336 more to go :)Thanks againJerri . The art of living lies not in eliminating but in growing with troubles. -Bernard M. Baruch

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>

> Hi Jerri I'm d aka dannegrl I'm 33 and in texas.

Jerri, did you tell me you knew of some good doctor's in Tyler? My

daughter really needs to find a new one and I'm not sure where to send

her. On my way there today, she's having an exploratory surgery..

Thanks!

Debi in Austin

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Debi I Have Had The Best Luck With A Group Of Doctors Thru Physicians First Its

A Group Of Doctors Located Across The Street From East Texas Medical Center. The

Center Is On Olympic Plaza. I Will See About Getting You Names And Numbers. Love

D

[debi_inaustin@...] wrote:

>

> Hi Jerri I'm d aka dannegrl I'm 33 and in texas.

Jerri, did you tell me you knew of some good doctor's in Tyler? My

daughter really needs to find a new one and I'm not sure where to send

her. On my way there today, she's having an exploratory surgery..

Thanks!

Debi in Austin

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HEY JERRI, WELCOME TO GROUP LIKE OTHERS HAVE SAID THIS IS A NICE GROUP YOU CAN GET ALL THE ANSWERS TO YOUR QUESTIONS LOTS OF SUPPORT AND HAVE A GOOD TIME IM KATHY (KAT) I DONT HAVE HEP C ITS MY HUBBY THAT HAS IT HIS GENOTYPE IS 4 WITH CIRRHOSIS HE DID TX BACK IN 2003 FOR A YEAR HE WAS ON NIGHTLY SHOTS HE IS AN NONRESPONDER IT DID CUT VL IN HALF AT THE PRESENT HE IS TO SICK TO REDO TX BUT TO WELL FOR TRANSPLANT SO WE GET TO PLAY THE WAITING GAME. WE HOPE THAT YOU DO WELL WITH TX AND HAVE GOOD RESULTS BUT YOU HAVE TO EAT RIGHT AND DRINK YOUR WATER KATJerri Neely <all4jerri@...> wrote: Hi,My name is Jerri and I am new to this group. I began my Interferon treatment on November 24th and it is already hard. I have been really sick for the past 4 days and was wondering if anyone can tell me if it is going to get better or if this is as good as it gets.I live alone and at this point am unsure if I will be able to do this. I guess I am just scared. Any advise would be helpful.thanks,Jerri

Access over 1 million songs - Music Unlimited.

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Hi Suzie,

Sorry for the misunderstanding. Also sorry to hear

that your tx didn't work. May I ask how long they

kept you on the treatment?

Thanks for giving me a smile today with your cat

story. Where do you live. I haven't been around snow

in years. So Cal for me.

:)

Jerri

--- suzie <suzieandsandy@...> wrote:

> Hi Jerri,

> Sorry , you misunderstood me. I worked through

> both attempts at tx but it didn't work for me. I'm

> what they call a non-responder, nothing happened. I

> got side effects but no effects. They say my liver

> got a break while I was on tx but I don't know.

> Anyways, I'm still here & so's the HCV darn it. I'm

> on disability now.

> I'm thinking of sending SpYke out to find a job -

> anyone need a crackerjack mouse catcher? He's

> pissed at me right now. Won't look at me but

> expresses his disgust with just the back of his

> furry little head. He wanted to go out so I took

> him out while I was shoveling the front walk & no

> Pattycakes, I didn't dump snow on him, he supervised

> from the stairs. When I finished he wanted to go

> for a walk so off we went. Well guess what - he got

> his feet wet! And it's all my fault. Amazing how

> short your memory is when you're a cat.

> SuZie & Sir SpYke the wet footed

>

>

>

>

>

>

>

>

>

>

>

> Next time I'm coming back as a cat

>

>

>

>

>

>

>

>

>

>

>

>

> [Hepatitis CSupportG roupForDummies]

> Hello

> > >

> > >

> > >

> > > Hi,

> > >

> > > My name is Jerri and I am new to this group. I

> > began

> > > my Interferon

> > > treatment on November 24th and it is already

> hard.

>

=== message truncated ===

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Hi d,

Thanks so much for your email. I am sorry that the

treatment didn't work for you but happy for your

husband.

I am also type 1A. My liver is between stage 2 and 3

right now. I live in San Pedro, CA and am 50 years

old (sounds old for some reason today). Guess I

should be greatful to have reached this age.

Thanks for the tips on what to eat. I will have to

stock up before my shot on Friday. I am able to eat a

little now. Actually had a sandwich yesterday.

Thanks for the support.

Hugs,

Jerri

--- dannegrl <dannegrl2003@...> wrote:

> Hi Jerri I'm d aka dannegrl I'm 33 and in texas. I

> an type 1a. I am a 2 time non-responder to

> treatment. I had alot of side effects from tx but

> the dr I had didn't know a thing about hep c at all.

> I would take 2 tylenol before my shot. then my hubby

> did the shot for me and I would go to bed. I was

> only able to eat yougart for the first few months of

> tx. Then my dr said try other cold and creamy foods

> since they seemed to work good for me. If you are

> not a big water drinker lots of us here drink

> CRYSTAL LITE the store brand is great too. oh Jello

> was another thing I could eat. lol go figure. And

> still now 2yrs later i love cold creamy foods.

> While I was a non responder, my husband Mitch was

> on tx for 52 weeks. He has been undetectable since

> he was at his 6 month labs on tx. He is coming up on

> his 3rd year since finishing his pegintron/rebatol..

>

> Honey don't give up. we are all here and It helps

> to know the things you are going through , we

> understand.

> love and welcome

> d

>

> jerri neely <all4jerri@...> wrote:

> Hi Gail,

>

> Thanks for the information. I found that I was

> feeling better by this afternoon. I took my shot

> Friday night so I am hoping that I can still get to

> work.

>

> I will have to pick up some Ensure as crackers

> aren't

> cutting it anymore.

>

> Thanks again for the advise,

> Jerri

>

>

>

> .

>

>

>

>

>

> The art of living lies not in eliminating but in

> growing with troubles.

> -Bernard M. Baruch

>

>

>

> ---------------------------------

> Cheap Talk? Check out Messenger's low

> PC-to-Phone call rates.

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Hi Debi,

I don't know anyone in Texas. I live in Southern

California. Hope all is well. Safe traveling

Jerri

--- debi_inaustin <debi_inaustin@...> wrote:

>

> >

> > Hi Jerri I'm d aka dannegrl I'm 33 and in texas.

>

> Jerri, did you tell me you knew of some good

> doctor's in Tyler? My

> daughter really needs to find a new one and I'm not

> sure where to send

> her. On my way there today, she's having an

> exploratory surgery..

> Thanks!

> Debi in Austin

>

>

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Hi Kat,

Thanks for the support. Sorry to hear about your

husband. I am genotype 1. Off to the doctors today

for labs and to see about my rash.

Talk soon,

Jerri

--- KATHY SHELNUTT <kathyshel2000@...> wrote:

> HEY JERRI,

> WELCOME TO GROUP LIKE OTHERS HAVE SAID THIS IS A

> NICE GROUP YOU CAN GET ALL THE ANSWERS TO YOUR

> QUESTIONS LOTS OF SUPPORT AND HAVE A GOOD TIME

> IM KATHY (KAT) I DONT HAVE HEP C ITS MY HUBBY THAT

> HAS IT HIS GENOTYPE IS 4 WITH CIRRHOSIS HE DID TX

> BACK IN 2003 FOR A YEAR HE WAS ON NIGHTLY SHOTS HE

> IS AN NONRESPONDER IT DID CUT VL IN HALF AT THE

> PRESENT HE IS TO SICK TO REDO TX BUT TO WELL FOR

> TRANSPLANT SO WE GET TO PLAY THE WAITING GAME.

> WE HOPE THAT YOU DO WELL WITH TX AND HAVE GOOD

> RESULTS BUT YOU HAVE TO EAT RIGHT AND DRINK YOUR

> WATER

>

> KAT

>

> Jerri Neely <all4jerri@...> wrote:

> Hi,

>

> My name is Jerri and I am new to this group. I began

> my Interferon

> treatment on November 24th and it is already hard. I

> have been really

> sick for the past 4 days and was wondering if anyone

> can tell me if it

> is going to get better or if this is as good as it

> gets.

>

> I live alone and at this point am unsure if I will

> be able to do

> this. I guess I am just scared. Any advise would be

> helpful.

>

> thanks,

> Jerri

>

>

>

>

>

>

> ---------------------------------

> Access over 1 million songs - Music

Unlimited.

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>

> Debi I Have Had The Best Luck With A Group Of Doctors Thru

Physicians First Its A Group Of Doctors Located Across The Street From

East Texas Medical Center. The Center Is On Olympic Plaza. I Will See

About Getting You Names And Numbers. Love D

that would be super! She's working with Trinity now and not very

happy.

> Thanks!

> Debi in Austin

>

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