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Hi Mike,

I experienced frequent to constant nausea, started taking

promethazine, tried maranol (medical marijauna pill, tried some other

drugs and finally ended up on zofran twice a day, 8 mg which was the

most helpful so that I could keep up my nutrition. I also used the

promethazine for " breakthrough " nausea. I had huge battles with my

insurance and my doctor always groaned when she had to talk to

them.... she finally convince them that it was either the hospital for

IV zofran or the pills and they relented! I hope you don't have to go

to that extreme, but you should talk to your doctor. Its important to

keep up your nutrition.

Hope that helps,

Deb in Seattle

Tx 1/19/06 and walked 6 miles today in preparation for the Seattle

Half Marathon!!!!

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Hi Mike,

I experienced frequent to constant nausea, started taking

promethazine, tried maranol (medical marijauna pill, tried some other

drugs and finally ended up on zofran twice a day, 8 mg which was the

most helpful so that I could keep up my nutrition. I also used the

promethazine for " breakthrough " nausea. I had huge battles with my

insurance and my doctor always groaned when she had to talk to

them.... she finally convince them that it was either the hospital for

IV zofran or the pills and they relented! I hope you don't have to go

to that extreme, but you should talk to your doctor. Its important to

keep up your nutrition.

Hope that helps,

Deb in Seattle

Tx 1/19/06 and walked 6 miles today in preparation for the Seattle

Half Marathon!!!!

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Hi Mike,

I experienced frequent to constant nausea, started taking

promethazine, tried maranol (medical marijauna pill, tried some other

drugs and finally ended up on zofran twice a day, 8 mg which was the

most helpful so that I could keep up my nutrition. I also used the

promethazine for " breakthrough " nausea. I had huge battles with my

insurance and my doctor always groaned when she had to talk to

them.... she finally convince them that it was either the hospital for

IV zofran or the pills and they relented! I hope you don't have to go

to that extreme, but you should talk to your doctor. Its important to

keep up your nutrition.

Hope that helps,

Deb in Seattle

Tx 1/19/06 and walked 6 miles today in preparation for the Seattle

Half Marathon!!!!

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Zofran has worked for me when nothing else has, but it is very

expensive if you have no insurance coverage for Rxs. Last year I had

a major bout with labrythitis and its dizziness and found that

crystallized ginger slivers helped to quell the nausea. I've also

brewed " ginger tea " -- powdered ginger in hot water (to taste).

Phenergan works for some people, but it makes me so sleepy that I

swear I have no brain function -- and compazine doesn't work well for

me either. They may be options for you, however.

Penny

In , " kate ackerman " wrote:

> she finally convince them that it was either the hospital for

> IV zofran or the pills and they relented! I hope you don't have to go

> to that extreme, but you should talk to your doctor. Its important to

> keep up your nutrition.

>

> Hope that helps,

>

> Deb in Seattle

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Zofran has worked for me when nothing else has, but it is very

expensive if you have no insurance coverage for Rxs. Last year I had

a major bout with labrythitis and its dizziness and found that

crystallized ginger slivers helped to quell the nausea. I've also

brewed " ginger tea " -- powdered ginger in hot water (to taste).

Phenergan works for some people, but it makes me so sleepy that I

swear I have no brain function -- and compazine doesn't work well for

me either. They may be options for you, however.

Penny

In , " kate ackerman " wrote:

> she finally convince them that it was either the hospital for

> IV zofran or the pills and they relented! I hope you don't have to go

> to that extreme, but you should talk to your doctor. Its important to

> keep up your nutrition.

>

> Hope that helps,

>

> Deb in Seattle

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Zofran has worked for me when nothing else has, but it is very

expensive if you have no insurance coverage for Rxs. Last year I had

a major bout with labrythitis and its dizziness and found that

crystallized ginger slivers helped to quell the nausea. I've also

brewed " ginger tea " -- powdered ginger in hot water (to taste).

Phenergan works for some people, but it makes me so sleepy that I

swear I have no brain function -- and compazine doesn't work well for

me either. They may be options for you, however.

Penny

In , " kate ackerman " wrote:

> she finally convince them that it was either the hospital for

> IV zofran or the pills and they relented! I hope you don't have to go

> to that extreme, but you should talk to your doctor. Its important to

> keep up your nutrition.

>

> Hope that helps,

>

> Deb in Seattle

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Mike,

I took ginger root capsules for years, followed by a HUGE glass of water (to avoid heartburn like symptoms), and when that stopped working I was given a Rx for compazine and for Tigan suppositories when the compazine failed me. Earlier this year the compazine stopped doing the job, and due to a UC flare the Tigan was of no use, so I am now taking Zofran. I would ask your doctor about Phenergren, Compazine, Tigan or Zofran. Suffering with nausea is not necessary, when there are so many things they can prescribe for relief.

Good luck in finding what works for you!

(MO)PSC & UC '84, chronic pancreatitis '97, listed for tx 06/05for details see www.caringbridge.org/visit/melaniejs

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Mike,

I took ginger root capsules for years, followed by a HUGE glass of water (to avoid heartburn like symptoms), and when that stopped working I was given a Rx for compazine and for Tigan suppositories when the compazine failed me. Earlier this year the compazine stopped doing the job, and due to a UC flare the Tigan was of no use, so I am now taking Zofran. I would ask your doctor about Phenergren, Compazine, Tigan or Zofran. Suffering with nausea is not necessary, when there are so many things they can prescribe for relief.

Good luck in finding what works for you!

(MO)PSC & UC '84, chronic pancreatitis '97, listed for tx 06/05for details see www.caringbridge.org/visit/melaniejs

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Mike,

I took ginger root capsules for years, followed by a HUGE glass of water (to avoid heartburn like symptoms), and when that stopped working I was given a Rx for compazine and for Tigan suppositories when the compazine failed me. Earlier this year the compazine stopped doing the job, and due to a UC flare the Tigan was of no use, so I am now taking Zofran. I would ask your doctor about Phenergren, Compazine, Tigan or Zofran. Suffering with nausea is not necessary, when there are so many things they can prescribe for relief.

Good luck in finding what works for you!

(MO)PSC & UC '84, chronic pancreatitis '97, listed for tx 06/05for details see www.caringbridge.org/visit/melaniejs

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Penny and Deb,

Many thanks for your prompt responses regarding the treatment of

nausea, I'll give your suggestions a try.

Mike

> > she finally convince them that it was either the hospital for

> > IV zofran or the pills and they relented! I hope you don't have to go

> > to that extreme, but you should talk to your doctor. Its important to

> > keep up your nutrition.

> >

> > Hope that helps,

> >

> > Deb in Seattle

>

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Penny and Deb,

Many thanks for your prompt responses regarding the treatment of

nausea, I'll give your suggestions a try.

Mike

> > she finally convince them that it was either the hospital for

> > IV zofran or the pills and they relented! I hope you don't have to go

> > to that extreme, but you should talk to your doctor. Its important to

> > keep up your nutrition.

> >

> > Hope that helps,

> >

> > Deb in Seattle

>

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Penny and Deb,

Many thanks for your prompt responses regarding the treatment of

nausea, I'll give your suggestions a try.

Mike

> > she finally convince them that it was either the hospital for

> > IV zofran or the pills and they relented! I hope you don't have to go

> > to that extreme, but you should talk to your doctor. Its important to

> > keep up your nutrition.

> >

> > Hope that helps,

> >

> > Deb in Seattle

>

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Although I don't have constant nausea, when it hits

it's bad. I also have itching...and I was prescribed

Zofran. It is a very very expensive anti-nausea med

used primarily for chemo/radiation patients.

Baudoux-Northrup

__________________________________________________

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Although I don't have constant nausea, when it hits

it's bad. I also have itching...and I was prescribed

Zofran. It is a very very expensive anti-nausea med

used primarily for chemo/radiation patients.

Baudoux-Northrup

__________________________________________________

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Although I don't have constant nausea, when it hits

it's bad. I also have itching...and I was prescribed

Zofran. It is a very very expensive anti-nausea med

used primarily for chemo/radiation patients.

Baudoux-Northrup

__________________________________________________

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Something that alleviated most of my

nausea symptoms was changing the way I drink my medication around.

I take Rifampicine(locally sold as,

amongst others: Rimactaine) and Utro. (Locally sold as Ursotan).

Originally my Px indicated that I have to

drink the Rifampicine in the mornings, 300mg.

Eventually, after experimenting I found

that by taking it in the evenings before bed-time, the nausea also didn’t

recur in daytime hours – and because I am asleep after taking it –

I am not aware of it at nights.

Regards,

-SJ

South Africa

Dx PSC UC April 2005

From: [mailto: ] On Behalf Of hist.prof

Sent: 16 September 2006 19:01 PM

To:

Subject: nausea

& PSC

I'm new to the group - just joined a couple weeks ago.

I (male, 57)was

diagnosed with PSC about a month ago after an emergency ERCP. My

biggest complaint so far is almost constant nausea and a mild stomach

ache which has led to weight loss (30 lbs. over th lst 6 months). Has

anyone else had this symptom and any suggestions on how to deal with it?

Thanks in advance.

Mike

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Something that alleviated most of my

nausea symptoms was changing the way I drink my medication around.

I take Rifampicine(locally sold as,

amongst others: Rimactaine) and Utro. (Locally sold as Ursotan).

Originally my Px indicated that I have to

drink the Rifampicine in the mornings, 300mg.

Eventually, after experimenting I found

that by taking it in the evenings before bed-time, the nausea also didn’t

recur in daytime hours – and because I am asleep after taking it –

I am not aware of it at nights.

Regards,

-SJ

South Africa

Dx PSC UC April 2005

From: [mailto: ] On Behalf Of hist.prof

Sent: 16 September 2006 19:01 PM

To:

Subject: nausea

& PSC

I'm new to the group - just joined a couple weeks ago.

I (male, 57)was

diagnosed with PSC about a month ago after an emergency ERCP. My

biggest complaint so far is almost constant nausea and a mild stomach

ache which has led to weight loss (30 lbs. over th lst 6 months). Has

anyone else had this symptom and any suggestions on how to deal with it?

Thanks in advance.

Mike

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Share on other sites

Something that alleviated most of my

nausea symptoms was changing the way I drink my medication around.

I take Rifampicine(locally sold as,

amongst others: Rimactaine) and Utro. (Locally sold as Ursotan).

Originally my Px indicated that I have to

drink the Rifampicine in the mornings, 300mg.

Eventually, after experimenting I found

that by taking it in the evenings before bed-time, the nausea also didn’t

recur in daytime hours – and because I am asleep after taking it –

I am not aware of it at nights.

Regards,

-SJ

South Africa

Dx PSC UC April 2005

From: [mailto: ] On Behalf Of hist.prof

Sent: 16 September 2006 19:01 PM

To:

Subject: nausea

& PSC

I'm new to the group - just joined a couple weeks ago.

I (male, 57)was

diagnosed with PSC about a month ago after an emergency ERCP. My

biggest complaint so far is almost constant nausea and a mild stomach

ache which has led to weight loss (30 lbs. over th lst 6 months). Has

anyone else had this symptom and any suggestions on how to deal with it?

Thanks in advance.

Mike

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Yes, I was having the same symptoms around the time they listed me

for my transplant. I went to see an acupuncturist. I explained to her

that I had liver problems and that I was constantly nauseous and that

I had no appetite. I would go twice a week to see her. It was a bit

expensive (most insurance companies only cover a small portion if

anything) but I feel that it is what keep me strong until I got my

transplant.

Pat

>

> I'm new to the group - just joined a couple weeks ago. I (male, 57)

was

> diagnosed with PSC about a month ago after an emergency ERCP. My

> biggest complaint so far is almost constant nausea and a mild

stomach

> ache which has led to weight loss (30 lbs. over th lst 6 months).

Has

> anyone else had this symptom and any suggestions on how to deal

with it?

>

> Thanks in advance.

>

> Mike

>

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Yes, I was having the same symptoms around the time they listed me

for my transplant. I went to see an acupuncturist. I explained to her

that I had liver problems and that I was constantly nauseous and that

I had no appetite. I would go twice a week to see her. It was a bit

expensive (most insurance companies only cover a small portion if

anything) but I feel that it is what keep me strong until I got my

transplant.

Pat

>

> I'm new to the group - just joined a couple weeks ago. I (male, 57)

was

> diagnosed with PSC about a month ago after an emergency ERCP. My

> biggest complaint so far is almost constant nausea and a mild

stomach

> ache which has led to weight loss (30 lbs. over th lst 6 months).

Has

> anyone else had this symptom and any suggestions on how to deal

with it?

>

> Thanks in advance.

>

> Mike

>

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Yes, I was having the same symptoms around the time they listed me

for my transplant. I went to see an acupuncturist. I explained to her

that I had liver problems and that I was constantly nauseous and that

I had no appetite. I would go twice a week to see her. It was a bit

expensive (most insurance companies only cover a small portion if

anything) but I feel that it is what keep me strong until I got my

transplant.

Pat

>

> I'm new to the group - just joined a couple weeks ago. I (male, 57)

was

> diagnosed with PSC about a month ago after an emergency ERCP. My

> biggest complaint so far is almost constant nausea and a mild

stomach

> ache which has led to weight loss (30 lbs. over th lst 6 months).

Has

> anyone else had this symptom and any suggestions on how to deal

with it?

>

> Thanks in advance.

>

> Mike

>

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Thanks Pat, sounds like a good idea.

Mike

> >

> > I'm new to the group - just joined a couple weeks ago. I (male, 57)

> was

> > diagnosed with PSC about a month ago after an emergency ERCP. My

> > biggest complaint so far is almost constant nausea and a mild

> stomach

> > ache which has led to weight loss (30 lbs. over th lst 6 months).

> Has

> > anyone else had this symptom and any suggestions on how to deal

> with it?

> >

> > Thanks in advance.

> >

> > Mike

> >

>

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Thanks Pat, sounds like a good idea.

Mike

> >

> > I'm new to the group - just joined a couple weeks ago. I (male, 57)

> was

> > diagnosed with PSC about a month ago after an emergency ERCP. My

> > biggest complaint so far is almost constant nausea and a mild

> stomach

> > ache which has led to weight loss (30 lbs. over th lst 6 months).

> Has

> > anyone else had this symptom and any suggestions on how to deal

> with it?

> >

> > Thanks in advance.

> >

> > Mike

> >

>

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Thanks Pat, sounds like a good idea.

Mike

> >

> > I'm new to the group - just joined a couple weeks ago. I (male, 57)

> was

> > diagnosed with PSC about a month ago after an emergency ERCP. My

> > biggest complaint so far is almost constant nausea and a mild

> stomach

> > ache which has led to weight loss (30 lbs. over th lst 6 months).

> Has

> > anyone else had this symptom and any suggestions on how to deal

> with it?

> >

> > Thanks in advance.

> >

> > Mike

> >

>

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,

Thanks for the suggestions - this is all so new to me but it sure

helps knowing others are going throught the same things. Looks like

it's going to be a long haul which is a lot better than a short haul!

Best,

Mike

>

> Mike,

> I took ginger root capsules for years, followed by a HUGE glass of

water (to

> avoid heartburn like symptoms), and when that stopped working I

was given a Rx

> for compazine and for Tigan suppositories when the compazine

failed me.

> Earlier this year the compazine stopped doing the job, and due to

a UC flare the

> Tigan was of no use, so I am now taking Zofran. I would ask your

doctor about

> Phenergren, Compazine, Tigan or Zofran. Suffering with nausea is

not

> necessary, when there are so many things they can prescribe for

relief.

>

> Good luck in finding what works for you!

> (MO)

> PSC & UC '84, chronic pancreatitis '97, listed for tx 06/05

> for details see www.caringbridge.org/visit/melaniejs

>

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