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  • 1 year later...
Guest guest

Dear Kathy in NC--

The Depo Provera shot which lasts 3 months does not take effect immediately.

The once a month shot Lunelle does. Atleast that is what my OB/GYN says.

And yes, I can understand the condom problem--I'm allergic to latex.

Caron

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Well i emailed the good Doc to help me out with this........i need sum help

SOOOOOOOOOOOOOOON..........i need another form of birth

control........condoms just not gonna cut it too much longer........sooo i

called my gyn and ask bout the shot and different things anyone here have

the shot? they said i would prolly gain weight i was likke

HUHHHHHHHHHHHH!!!!!!!! NO WAY!!!!!!! is true???!!! i need sum help

here.........and is the shot immediate??? or waitin period or what?

........i know i sound like im in desperate need here but everytime i stayed

off my bc pills for any period of time i got pregnants...(twice to be

exact).........dont want anymore rite nowwwwwwwwwwwww............

Kathy in NC

Danced with Dr R Val Day

397/370/307/??

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, I got an IUD. That is the nexy best method per my obgyn. It is 99

percent good. The pill will not work,it does not absorb correctly . any

more questions, let me know, believe me I have gone through this whole thing.

I have 1childand do not want another......

Janet mgb12/14/00

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Kathy,

I gained about 25 lbs on the shot in college right after I got

married. Also, you need to go read the manual about hormonal birth

control after the surgery. According to Dr R, after surgery with

sudden weight loss, only on hormonal birth control, you aren't

covered as well as you'd hope to be. IMHO it is too early only to

rely on hormonal birthcontrol. My husband has a low sperm count, and

we've had sex for years without anything without getting pregnant,

but now I've had surgery, we've started using condoms and spermicide.

> Well i emailed the good Doc to help me out with this........i need

sum help

> SOOOOOOOOOOOOOOON..........i need another form of birth

> control........condoms just not gonna cut it too much

longer........sooo i

> called my gyn and ask bout the shot and different things anyone

here have

> the shot? they said i would prolly gain weight i was likke

> HUHHHHHHHHHHHH!!!!!!!! NO WAY!!!!!!! is true???!!! i need sum help

> here.........and is the shot immediate??? or waitin period or what?

> .......i know i sound like im in desperate need here but everytime

i stayed

> off my bc pills for any period of time i got pregnants...(twice to

be

> exact).........dont want anymore rite nowwwwwwwwwwwww............

>

>

> Kathy in NC

>

> Danced with Dr R Val Day

> 397/370/307/??

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Guest guest

Kathy, I took the depo provera shot for many years and I studied, very

closely, to see if there was a correlation between the shots and my weight

and I found absolutely none, in fact, the week that I got the shot, I always

managed to loose a few lbs.

It is a WONDERFUL form of birth control as you only need a quick shot 4

times per year. The other side of it is that in the first year, you never

know when you will get a " breakthrough " bleeding issue; however, at the end

of the first you YOU STOP GETTING PERIODS!!! This part is wonderful.

It does work very quickly, but certainly consult your doctor on this. In

fact, if I remember correctly (I haven't had a shot for some time as I had a

hysterectomy) it is somewhat immediate, but they recommend that you use

protection as a backup for a little while. Good luck with this and I highly

recommend it.

Re: help needed

Well i emailed the good Doc to help me out with this........i need sum

help

SOOOOOOOOOOOOOOON..........i need another form of birth

control........condoms just not gonna cut it too much longer........sooo

i

called my gyn and ask bout the shot and different things anyone here

have

the shot? they said i would prolly gain weight i was likke

HUHHHHHHHHHHHH!!!!!!!! NO WAY!!!!!!! is true???!!! i need sum help

here.........and is the shot immediate??? or waitin period or what?

........i know i sound like im in desperate need here but everytime i

stayed

off my bc pills for any period of time i got pregnants...(twice to be

exact).........dont want anymore rite nowwwwwwwwwwwww............

Kathy in NC

Danced with Dr R Val Day

397/370/307/??

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Guest guest

Kathy, I'd like to suggest abstinence as a form of birth control. It's really a

very good way to prevent conception. And your husband will be so clean from all

the cold showers.

Flo

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Guest guest

LMAO ty FLo i needed a good laff hehe.........

At 07:31 PM 5/26/2001 -0500, you wrote:

>Kathy, I'd like to suggest abstinence as a form of birth control. It's

>really a very good way to prevent conception. And your husband will be so

>clean from all the cold showers.

>

>Flo

>

>

>

>

>

>

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Guest guest

ty janet...the IUD and the shot are the two im lookin into rite now.

wonderin if anyone out there is using the shot rite now after the

MGB.........puhleeze respond if u are aned lemme know how things are

going.......if u recommend it or what.........

At 03:11 PM 5/26/2001 -0400, you wrote:

>, I got an IUD. That is the nexy best method per my obgyn. It is 99

>percent good. The pill will not work,it does not absorb correctly . any

>more questions, let me know, believe me I have gone through this whole thing.

>I have 1childand do not want another......

>Janet mgb12/14/00

>

>

>

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  • 3 weeks later...
Guest guest

Where is Trish's site? Must have missed it.

Bern

TX

> I would like to send Trish my before and after picture for her site

> but I am not sure how to do it with my scanner. If anyone could

help

> me it would be appreciated. Thanks, Liz

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  • 11 months later...
Guest guest

Hi Elaine,

> My entire digestive tract shut down for 3 days. My issue is my

> stomach is burning. I'm drinking aloe vera juice, colodial silver,

> acidophilis, glutamine. Anyone have suggestions as to what I can

do

> to help my poor stomach. I think that it is burned and possibly

> digested itself.

I HIGHLY recommend peppermint tea. It helps nausea, burning any

digestive symptoms I have. Also, mullein tea has helped my gut

alot. But peppermint with tea, you can't go wrong-it really is the

best.

By the way, it sounds like you may have gastritis. You may need to

let the md take a look (endoscopy). That is how I found I had

gastritis (burning, nausea, vomiting, gnawing feeling in my belly, I

couldn't take a vitamin C pill without throwing it up!!! ect.). The

proper diagnosis really helped me to heal my gut.

I hope this helps.

God bless,

KJ

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Guest guest

elaine. ive had the same thing happen to me. i found if i completely empty

my colon that the material in my stomache will move along. in other words it

happens when i get constipated. a couple enemas gives me relief very fast.

fred

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Guest guest

It's true peppermint is good for tummy terrors...but if you tend towards

reflux, know that peppermint relaxes the esophageal (SP?) sphincter....so

you might not want to drink it and then lie down. SaraLou

Re: help needed

> Hi Elaine,

>

>

>

> > My entire digestive tract shut down for 3 days. My issue is my

> > stomach is burning. I'm drinking aloe vera juice, colodial silver,

> > acidophilis, glutamine. Anyone have suggestions as to what I can

> do

> > to help my poor stomach. I think that it is burned and possibly

> > digested itself.

>

> I HIGHLY recommend peppermint tea. It helps nausea, burning any

> digestive symptoms I have. Also, mullein tea has helped my gut

> alot. But peppermint with tea, you can't go wrong-it really is the

> best.

>

> By the way, it sounds like you may have gastritis. You may need to

> let the md take a look (endoscopy). That is how I found I had

> gastritis (burning, nausea, vomiting, gnawing feeling in my belly, I

> couldn't take a vitamin C pill without throwing it up!!! ect.). The

> proper diagnosis really helped me to heal my gut.

>

> I hope this helps.

>

> God bless,

> KJ

>

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  • 2 months later...

Thanks Gordon what a nice lifting letter,My wife is

suffering so badly,She has HEP-C and a horriable case

of posorices all over her body and seratic artheritis

she is 46 and has been on S.S.disablaty for 2 years

now ,due to the Hep -c she can't take anything that

would help her becouse it would hurt her liver even

worse.Is there anything we can do ?She needs help!!

Hope to hear from you Thanks tommy Wilkens

__________________________________________________

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Tommy I cleared Hep C a few years ago but still have Cirrhosis. My Primary

Dr. has been giving me Darvocet for my aching for a few years now saying I

couldn't take anything else. Now my lower back hurts so bad I told her

Darvocet not working so she finally referred me to Rhuemy Dr. I ran out of

the Darvocet this month in only 2 weeks so I finally started taking my

hubby's 800 mg Ibuphron. I've taken a bunch of tests but don't go back to

Rhuemy till a week from tomorrow. The Ibuphron actually worked so I e-mailed

my Heptolgist and asked him about it. He said if I'm taking it as prescribed

my liver should be fine. I did write back to tell him the amount I'm taking

though but haven't heard back yet. I've told my Primary and Heptologist

there is a questions of quality of life, and I refuse to hurt. If I can't

take anti inlammatorys than give me pain pills. Make sure you also talk to

her liver Dr. about how much pain she is in they WILL give her something for

pain. I have alot of friends with Hep C and Arthritis and they are being

treated with at least pain meds.

Peace/Love

Randi

> Thanks Gordon what a nice lifting letter,My wife is

> suffering so badly,She has HEP-C and a horriable case

> of posorices all over her body and seratic artheritis

> she is 46 and has been on S.S.disablaty for 2 years

> now ,due to the Hep -c she can't take anything that

> would help her becouse it would hurt her liver even

> worse.Is there anything we can do ?She needs help!!

> Hope to hear from you Thanks tommy Wilkens

>

>

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Tommy,

Thanks for your reply (and others as well), I know a number of us have been

feeling pretty miserable of late and I thought a message of lighter note and

peace would help. I am sure the group will respond better than I can to

your wife's need for help. This group is such a forum of hope and support.

Regards, Gordon

Re: [ ] Help needed

> Thanks Gordon what a nice lifting letter,My wife is

> suffering so badly,She has HEP-C and a horriable case

> of posorices all over her body and seratic artheritis

> she is 46 and has been on S.S.disablaty for 2 years

> now ,due to the Hep -c she can't take anything that

> would help her becouse it would hurt her liver even

> worse.Is there anything we can do ?She needs help!!

> Hope to hear from you Thanks tommy Wilkens

>

>

> __________________________________________________

>

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Randi,

I am not an MD (far from it) but I am not sure I agree with your heptologist

about the ibuprofen being OK as long as you take it as directed. I took

naproxyn exactly as directed and, thankfully my rhuemy does routine liver

profiles, and discovered that I had impaired function. It wouldn't hurt to ask

your rhuemy at your next appointment. Do you have blood work regularly?

Eva in AR

Faithfulhope7@... wrote:Tommy I cleared Hep C a few years ago but still

have Cirrhosis. My Primary

Dr. has been giving me Darvocet for my aching for a few years now saying I

couldn't take anything else. Now my lower back hurts so bad I told her

Darvocet not working so she finally referred me to Rhuemy Dr. I ran out of

the Darvocet this month in only 2 weeks so I finally started taking my

hubby's 800 mg Ibuphron. I've taken a bunch of tests but don't go back to

Rhuemy till a week from tomorrow. The Ibuphron actually worked so I e-mailed

my Heptolgist and asked him about it. He said if I'm taking it as prescribed

my liver should be fine. I did write back to tell him the amount I'm taking

though but haven't heard back yet. I've told my Primary and Heptologist

there is a questions of quality of life, and I refuse to hurt. If I can't

take anti inlammatorys than give me pain pills. Make sure you also talk to

her liver Dr. about how much pain she is in they WILL give her something for

pain. I have alot of friends with Hep C and Arthritis and they are being

treated with at least pain meds.

Peace/Love

Randi

> Thanks Gordon what a nice lifting letter,My wife is

> suffering so badly,She has HEP-C and a horriable case

> of posorices all over her body and seratic artheritis

> she is 46 and has been on S.S.disablaty for 2 years

> now ,due to the Hep -c she can't take anything that

> would help her becouse it would hurt her liver even

> worse.Is there anything we can do ?She needs help!!

> Hope to hear from you Thanks tommy Wilkens

>

>

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Eva, I have an appt. with Rheummy next tues. and yes I will ask for something

else. In fact I may see if I can refill the darvocet. My primary gave me 3

refills of 50 and wrote take l every 6 hours and I've needed them every 6

hours. Anotherwards, following drs. scrip I took them as prescribed so its

ok to refill now? I'll call my pharmacist tomorrow and check, not sure if

its an insurance thing or what. I never did hear back from my Heptologist

I'll try him again tomorrow. It just seems that for years now everyone has

been so concerned about my liver that they hadn't listened to how much I

ached. I finally got through to Primary 6 weeks ago.

I see the Rhuemmy on Tues. and the Dermatologist on Wed. They better figure out

something I can take. I saw a neurololgist today and had a EMG test done for

Neuropathy, I also have numb and tingly toes. They said I had to get results

from Rhuemmy hmmm. That test was really different I had never felt anything

like it before. Definitely shocking... they like send elec. from your muscle to

foot and see how long it takes lol. I'm also waiting to get results of xrays

to knees, hips and lower back. I have one fingernail that has a pit,

and pssorias on elbows, 2 fingers and I think a little on scalp. I feel like

a scab or something but I can't see it. I'm still waiting for official PA

diagnoisis or whatever else is causing me so much discomfort.

Thanks for letting me ramble

Peace/Love

Randi

>

> Randi,

> I am not an MD (far from it) but I am not sure I agree with your

> heptologist about the ibuprofen being OK as long as you take it as

> directed. I took naproxyn exactly as directed and, thankfully my rhuemy

> does routine liver profiles, and discovered that I had impaired function.

> It wouldn't hurt to ask your rhuemy at your next appointment. Do you have

> blood work regularly?

> Eva in AR

> Faithfulhope7@... wrote:Tommy I cleared Hep C a few years ago but still

> have Cirrhosis. My Primary

> Dr. has been giving me Darvocet for my aching for a few years now saying I

> couldn't take anything else. Now my lower back hurts so bad I told her

> Darvocet not working so she finally referred me to Rhuemy Dr. I ran out of

>

> the Darvocet this month in only 2 weeks so I finally started taking my

> hubby's 800 mg Ibuphron. I've taken a bunch of tests but don't go back to

> Rhuemy till a week from tomorrow. The Ibuphron actually worked so I

> e-mailed

> my Heptolgist and asked him about it. He said if I'm taking it as

> prescribed

> my liver should be fine. I did write back to tell him the amount I'm

> taking

> though but haven't heard back yet. I've told my Primary and Heptologist

> there is a questions of quality of life, and I refuse to hurt. If I can't

> take anti inlammatorys than give me pain pills. Make sure you also talk to

>

> her liver Dr. about how much pain she is in they WILL give her something

> for

> pain. I have alot of friends with Hep C and Arthritis and they are being

> treated with at least pain meds.

>

> Peace/Love

> Randi

>

> > Thanks Gordon what a nice lifting letter,My wife is

> > suffering so badly,She has HEP-C and a horriable case

> > of posorices all over her body and seratic artheritis

> > she is 46 and has been on S.S.disablaty for 2 years

> > now ,due to the Hep -c she can't take anything that

> > would help her becouse it would hurt her liver even

> > worse.Is there anything we can do ?She needs help!!

> > Hope to hear from you Thanks tommy Wilkens

> >

> >

>

>

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Hi Eva,

I'm new to this site as well, I've posted one message but I've been reading all

of this stuff and I have a question. I was diagnosed with PA about four years

ago and apparantly went into remission, or whatever it's called, during my last

pregnancy. It came back with a vengeance after I had my baby last year. My Dad

was diagnosed with pancreatic cancer the month after the baby was born. I've

spent this last year trying to save his life and he died last month. I think my

flare had something to do with stress.

But I've been controlling the pain with 600 mgs of Ibuprofen three times a day

for this whole year, except for the two months I was on Celebrex and the one

month I was on Vioxx (and neither helped). The rheumy prescribed methotrexate

after doing blood work, but before he got the results. I then had an

appointment with my endocrinologist who gave me the results of my blood work.

He said that the liver enzymes were elevated a little, and that back in 1996

they were also elevated (which no one ever told me), but that they were even

higher now. I wonder why my rheumy didn't reconsider the methotrexate. Also,

my real question is, could the elevation be caused by the Ibuprofen? If not,

what could it be caused by? I'm waiting to get in to see another rheumy so that

I can get a second opinion. I have a tremendous family history of cancer and

I'm afraid to use methotrexate because I've read that it can actually cause

cancer. The rheumy I just saw is at the University of Kentucky and he's all by

himself, he doesn't even have a nurse I can call and talk to. I don't know what

I should do. My choices of rheumatologists are pretty slim in Lexington,

Kentucky so I am trying to find one in a surrounding state. Also, my children

are all due for their chicken pox vaccine in September. I'm thinking I can't be

on the methotrexate at that time either. So, I don't know what to do about

controlling my pain in the meantime if the Ibuprofen is elevating my liver

enzymes. Does anyone have any suggestings for any of these complications?!

Thanks,

Cheryl

Re: [ ] Help needed

Randi,

I am not an MD (far from it) but I am not sure I agree with your heptologist

about the ibuprofen being OK as long as you take it as directed. I took

naproxyn exactly as directed and, thankfully my rhuemy does routine liver

profiles, and discovered that I had impaired function. It wouldn't hurt to ask

your rhuemy at your next appointment. Do you have blood work regularly?

Eva in AR

Faithfulhope7@... wrote:Tommy I cleared Hep C a few years ago but still

have Cirrhosis. My Primary

Dr. has been giving me Darvocet for my aching for a few years now saying I

couldn't take anything else. Now my lower back hurts so bad I told her

Darvocet not working so she finally referred me to Rhuemy Dr. I ran out of

the Darvocet this month in only 2 weeks so I finally started taking my

hubby's 800 mg Ibuphron. I've taken a bunch of tests but don't go back to

Rhuemy till a week from tomorrow. The Ibuphron actually worked so I e-mailed

my Heptolgist and asked him about it. He said if I'm taking it as prescribed

my liver should be fine. I did write back to tell him the amount I'm taking

though but haven't heard back yet. I've told my Primary and Heptologist

there is a questions of quality of life, and I refuse to hurt. If I can't

take anti inlammatorys than give me pain pills. Make sure you also talk to

her liver Dr. about how much pain she is in they WILL give her something for

pain. I have alot of friends with Hep C and Arthritis and they are being

treated with at least pain meds.

Peace/Love

Randi

> Thanks Gordon what a nice lifting letter,My wife is

> suffering so badly,She has HEP-C and a horriable case

> of posorices all over her body and seratic artheritis

> she is 46 and has been on S.S.disablaty for 2 years

> now ,due to the Hep -c she can't take anything that

> would help her becouse it would hurt her liver even

> worse.Is there anything we can do ?She needs help!!

> Hope to hear from you Thanks tommy Wilkens

>

>

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In a message dated 08/15/2002 11:57:01 AM Eastern Daylight Time,

troycheryl@... writes:

> Also, my real question is, could the elevation be caused by the Ibuprofen?

Hi Cheryl - my rheumy checks my enzymes every 3 months even after being off

the MTX because I'm on anti-inflammatories (vioxx), which of course ibuprofen

is as well. So I guess it's possible you could have elevated enzymes from

that. In my opinion, you do need a DMARD though to protect your joints from

further deteriation. Have you asked your rheumy about Remicade? The enbrel

still seems to be a problem to get, but maybe he/she could get you on

remicade or arava if you are afraid of the MTX. I also have a family history

of cancer (I don't think I can name one person on my dad's side who hasn't

had it in some form) but I did use MTX for 2 yrs. - Had to go off for my

liver elevations.

As far as the chicken pox vaccine goes, I believe that if the vaccine is a

" dead " vaccine, it can't hurt you if you have lowered immunity - but check

with your doctor.

Take care,

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My sympathy to you. My PA started three months after my father was

diagnosed with pancreatic cancer. Once diagnosed, I know I had symptoms

before then, but never severe. I thought my PA would go into remission once

my father's suffering was over--but a few months after his death, my mom was

diagnosed with breast cancer. She is now in remission after surgery and

treatment. I am working part-time starting this week. I hope the reduction

in work load and a healthy family will get me back on track with PA.

Good luck.

Ks Di

Re: [ ] Help needed

Hi Eva,

I'm new to this site as well, I've posted one message but I've been reading

all of this stuff and I have a question. I was diagnosed with PA about four

years ago and apparantly went into remission, or whatever it's called,

during my last pregnancy. It came back with a vengeance after I had my baby

last year. My Dad was diagnosed with pancreatic cancer the month after the

baby was born. I've spent this last year trying to save his life and he

died last month. I think my flare had something to do with stress.

But I've been controlling the pain with 600 mgs of Ibuprofen three times a

day for this whole year, except for the two months I was on Celebrex and the

one month I was on Vioxx (and neither helped). The rheumy prescribed

methotrexate after doing blood work, but before he got the results. I then

had an appointment with my endocrinologist who gave me the results of my

blood work. He said that the liver enzymes were elevated a little, and that

back in 1996 they were also elevated (which no one ever told me), but that

they were even higher now. I wonder why my rheumy didn't reconsider the

methotrexate. Also, my real question is, could the elevation be caused by

the Ibuprofen? If not, what could it be caused by? I'm waiting to get in

to see another rheumy so that I can get a second opinion. I have a

tremendous family history of cancer and I'm afraid to use methotrexate

because I've read that it can actually cause cancer. The rheumy I just saw

is at the University of Kentucky and he's all by himself, he doesn't even

have a nurse I can call and talk to. I don't know what I should do. My

choices of rheumatologists are pretty slim in Lexington, Kentucky so I am

trying to find one in a surrounding state. Also, my children are all due

for their chicken pox vaccine in September. I'm thinking I can't be on the

methotrexate at that time either. So, I don't know what to do about

controlling my pain in the meantime if the Ibuprofen is elevating my liver

enzymes. Does anyone have any suggestings for any of these complications?!

Thanks,

Cheryl

Re: [ ] Help needed

Randi,

I am not an MD (far from it) but I am not sure I agree with your

heptologist about the ibuprofen being OK as long as you take it as directed.

I took naproxyn exactly as directed and, thankfully my rhuemy does routine

liver profiles, and discovered that I had impaired function. It wouldn't

hurt to ask your rhuemy at your next appointment. Do you have blood work

regularly?

Eva in AR

Faithfulhope7@... wrote:Tommy I cleared Hep C a few years ago but

still have Cirrhosis. My Primary

Dr. has been giving me Darvocet for my aching for a few years now saying I

couldn't take anything else. Now my lower back hurts so bad I told her

Darvocet not working so she finally referred me to Rhuemy Dr. I ran out

of

the Darvocet this month in only 2 weeks so I finally started taking my

hubby's 800 mg Ibuphron. I've taken a bunch of tests but don't go back to

Rhuemy till a week from tomorrow. The Ibuphron actually worked so I

e-mailed

my Heptolgist and asked him about it. He said if I'm taking it as

prescribed

my liver should be fine. I did write back to tell him the amount I'm

taking

though but haven't heard back yet. I've told my Primary and Heptologist

there is a questions of quality of life, and I refuse to hurt. If I can't

take anti inlammatorys than give me pain pills. Make sure you also talk

to

her liver Dr. about how much pain she is in they WILL give her something

for

pain. I have alot of friends with Hep C and Arthritis and they are being

treated with at least pain meds.

Peace/Love

Randi

> Thanks Gordon what a nice lifting letter,My wife is

> suffering so badly,She has HEP-C and a horriable case

> of posorices all over her body and seratic artheritis

> she is 46 and has been on S.S.disablaty for 2 years

> now ,due to the Hep -c she can't take anything that

> would help her becouse it would hurt her liver even

> worse.Is there anything we can do ?She needs help!!

> Hope to hear from you Thanks tommy Wilkens

>

>

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Thanks so much for the replys. I'll see what I can do.

Cheryl

Re: [ ] Help needed

In a message dated 08/15/2002 11:57:01 AM Eastern Daylight Time,

troycheryl@... writes:

> Also, my real question is, could the elevation be caused by the Ibuprofen?

Hi Cheryl - my rheumy checks my enzymes every 3 months even after being off

the MTX because I'm on anti-inflammatories (vioxx), which of course ibuprofen

is as well. So I guess it's possible you could have elevated enzymes from

that. In my opinion, you do need a DMARD though to protect your joints from

further deteriation. Have you asked your rheumy about Remicade? The enbrel

still seems to be a problem to get, but maybe he/she could get you on

remicade or arava if you are afraid of the MTX. I also have a family history

of cancer (I don't think I can name one person on my dad's side who hasn't

had it in some form) but I did use MTX for 2 yrs. - Had to go off for my

liver elevations.

As far as the chicken pox vaccine goes, I believe that if the vaccine is a

" dead " vaccine, it can't hurt you if you have lowered immunity - but check

with your doctor.

Take care,

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  • 10 months later...
Guest guest

Hi I am Ray Kennedy in the UK. Send and E Mail to Bob at

acts@... and he will talk to you about alternative treatments, they are

not expensive.

Ray Kennedy

[ ] HELP NEEDED

THANK YOU FOR AN EXCELLENT FORUM. I HOPE SOMEONE OUT THERE CAN BE OF

ASSISTANCE. I HAVE READ OF A THERAPY THAT COULD BE OF GREAT USE, NOT

AS A TREATMENT, PER SE, BUT TO HELP STIMULATE THE IMMUNE SYSTEM AFTER

RADIATION OR CHEMO. THE THERAPY IS RELATIVELY CHEAP, BUT THE PROBLEM

IS THAT A PRESCRIPTION IS NECESSARY FOR IT. UNFORTUNATELY, I AM

DISABLED AND CAN'T AFFORD TO SEE AN ALTERNATIVELY MINDED DOCTOR, WHO

WOULD BE OPEN TO PRESCRIBING THIS. I LIVE ON LONG ISLAND, IN NEW

YORK AND WOULD BE VERY APPRECIATIVE TO ANYONE WHO COULD HELP.

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Guest guest

I heard of a so called recent breakthrough devised here in Australia

where they block the production of sex hormones in the body, and this

is said to lead to stimulation of the immune system. You and I can

probably forget it though for two reasons:

1. A course of treatment is reported to cost $2000AUD,

2. Given the cost of treatment, it must involve the use of

drugs, and thus would have unacceptable side effects.

If your MD is not " open " , wouldn't it be nice if we were able to

pries them open. Good luck in finding someone to write that script.

Les Catterall

--

mal19782002 wrote:

>

> THANK YOU FOR AN EXCELLENT FORUM. I HOPE SOMEONE OUT THERE CAN BE OF

> ASSISTANCE. I HAVE READ OF A THERAPY THAT COULD BE OF GREAT USE, NOT

> AS A TREATMENT, PER SE, BUT TO HELP STIMULATE THE IMMUNE SYSTEM AFTER

> RADIATION OR CHEMO. THE THERAPY IS RELATIVELY CHEAP, BUT THE PROBLEM

> IS THAT A PRESCRIPTION IS NECESSARY FOR IT. UNFORTUNATELY, I AM

> DISABLED AND CAN'T AFFORD TO SEE AN ALTERNATIVELY MINDED DOCTOR, WHO

> WOULD BE OPEN TO PRESCRIBING THIS. I LIVE ON LONG ISLAND, IN NEW

> YORK AND WOULD BE VERY APPRECIATIVE TO ANYONE WHO COULD HELP.

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  • 1 year later...

I just completed six applications of Rituxan and had no side effects whatsoever.

I am 66 and had six rounds of chemo before the Rituxan. I even had a low WBC

(2,300) when getting my last application. Hope your husband comes through as

easily as I did.

Dave

----- Original Message -----

From: jackie liddell Nov 13

My husband was diagnosed with non curable non Hodgkin's lymphoma in September.

....Next Tuesday he starts on a course of rituxin...Can anyone suggest anything

I can use or do to minimize the toxic effect of the rituxin.

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