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RE: Cellcept

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I'm not sure anyone in this group has taken Cellcept. If anybody has, let us

know if you can. As far as I can tell, most members in this group tend not

to have the rapidly progressive type of gn where drugs like Cellcept might

be called for.

Pierre

Cellcept

> Has anyone else tried a cycle of Cellcept yet? Did you have any side

> effects?

>

>

>

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I did take it. I did a two months cycle to see how it would affect my test

results. On April 11 I will see my Neph and post what difference it made.

> Re: Cellcept

>

>

> I'm not sure anyone in this group has taken Cellcept. If anybody

> has, let us

> know if you can. As far as I can tell, most members in this group tend not

> to have the rapidly progressive type of gn where drugs like Cellcept might

> be called for.

> Pierre

>

> Cellcept

>

>

> > Has anyone else tried a cycle of Cellcept yet? Did you have any side

> > effects?

> >

> >

> >

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Will, Byron

We are using Cellcept for one month, 1g twice a day, without noticeable side

effect. This is short term experience. Cellcept is part of a complete

treatment with corticoid and ACE. Will, are you getting what you expected

from Cellcept?

Is it used used as IGAN treatment or post renal transplant?

Thanks

jean Claude

Will Cayo28/03/01 21:05wcayo@...

> Byron,

>

> I am on 1g of Cellcept twice daily. I have been on Cellcept for about six

> months and have noticed no side effects.

>

> Will

>

> Cellcept

>

>

> Has anyone else tried a cycle of Cellcept yet? Did you have any side

> effects?

>

>

>

>

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They put me on it to treat IGAN. It is to early to tell if it is doing the

job

or not.

Will

Cellcept

>

>

> Has anyone else tried a cycle of Cellcept yet? Did you have any side

> effects?

>

>

>

>

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I had done a two month cycle, and I the only side effect was that I became

very sensative to the sun. I burned easily and my eyes were very sensative.

My neph told me it was all in my head but I checked with a pharmacist and

that is a possible side effect.

On a side note, do people with IGAN get a lot of sore throats? I always do.

I get a sore throat with flu like symtoms about three times a year.

-Byron

> Cellcept

> >

> >

> > Has anyone else tried a cycle of Cellcept yet? Did you have any side

> > effects?

> >

> >

> >

> >

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Lucky you! I get flu like symptoms from day to day. Today however is my

day off, I have a blood nose instead!

Reply-To: iga-nephropathy

To: <iga-nephropathy >

Subject: RE: Cellcept

Date: Tue, 3 Apr 2001 14:29:41 -0400

I had done a two month cycle, and I the only side effect was that I became

very sensative to the sun. I burned easily and my eyes were very sensative.

My neph told me it was all in my head but I checked with a pharmacist and

that is a possible side effect.

On a side note, do people with IGAN get a lot of sore throats? I always do.

I get a sore throat with flu like symtoms about three times a year.

-Byron

> Cellcept

> >

> >

> > Has anyone else tried a cycle of Cellcept yet? Did you have any side

> > effects?

> >

> >

> >

> >

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Hi

I too suffer from flu like symptoms a fair bit, not daily like yourself, but

every 3-4 weeks or so. I saw an ENT consultant last year, who gave me a

full work-up including CT scan of the head. His conclusions were, that the

virus I had (which has been bandied about was the cause of my IGAN!), which

hospitalised me for 10 days, had damaged my sinus canals, it had also

damaged my right inner ear, and I have lost 30% hearing in that ear.

Surgery was an option, but came with so many risks, that I chose to pass on

it, It also came with no guarantee that it would last.

Nowadays I suffer from irritatingly regular nose-bleeds, and sneezing fits.

Prior to this I never had any problems in this area. Puzzling isn't it?

Regards

Cellcept

> >

> >

> > Has anyone else tried a cycle of Cellcept yet? Did you have any side

> > effects?

> >

> >

> >

> >

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Indeed , indeed! My current symptoms are ususally mild which I think

is probably better than being really sick once a month like I was. Even so,

on some days I think that if I was in the farming area I'd be standing

amoungst the cows and sheep saying " pick me, pick me. " (Has it really only

been 6 weeks since the first outbreak?) You probably remember that I don't

want to do the steroid thing until I've been 2 months with out any

symptoms... And you probably remember my opinion of London... I have

thought about seeing an ENT when I get back to Australia (have to be

proactive now that I know my new kidney is going to be be a pizza topping).

I still think that it's just one big flu that is not going away. Your

experiences reinforce just how delicate our bodies really are. It will be

interesting to find out more if anyone ever does any serious research.

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LOL , now come on surely a mouth full of ulcers, pus filled nostrils,

cant be more favourable than flu!!!! Seriously yes only six weeks, and no

sign of abating, horrid stuff.

Yes I recall your opinion of London, and cant really blame you for that. As

to serious research, if you recall my Neph is doing a study into the fatigue

aspect, and to which I volunteered. Shock horror, I was not accepted why?

Because my condition is not advanced enough!!!! They obviously want someone

so sick, they are bound to be fatigued aren't they. Pretty poor excuse if

you ask me, the real reason being my ability to question them, they want

someone who will be totally submissive and unquestioning. That rules me out

then LOL!!!!

Keep well, and promise keep in touch when back in Oz ok.

Best wishes

RE: Cellcept

Indeed , indeed! My current symptoms are ususally mild which I think

is probably better than being really sick once a month like I was. Even so,

on some days I think that if I was in the farming area I'd be standing

amoungst the cows and sheep saying " pick me, pick me. " (Has it really only

been 6 weeks since the first outbreak?) You probably remember that I don't

want to do the steroid thing until I've been 2 months with out any

symptoms... And you probably remember my opinion of London... I have

thought about seeing an ENT when I get back to Australia (have to be

proactive now that I know my new kidney is going to be be a pizza topping).

I still think that it's just one big flu that is not going away. Your

experiences reinforce just how delicate our bodies really are. It will be

interesting to find out more if anyone ever does any serious research.

_________________________________________________________________________

Get Your Private, Free E-mail from MSN Hotmail at http://www.hotmail.com.

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, I can't believe they rejected you for the research! What is it they

actually want to know? We are all tired surely that deserves investigation

no matter how advanced the situation. Makes me so mad!

I had a video conference interview for a job in my company in Oz yesterday

(it was awful - I had to be in the office at 0700). Seemed to go well so I

have my fingers crossed, but if it doesn't happen I will just quit when the

time comes!

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, has your neph ever admitted that this is connected to IGAN?

> Cellcept

> > >

> > >

> > > Has anyone else tried a cycle of Cellcept yet? Did you have any side

> > > effects?

> > >

> > >

> > >

> > >

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No he hasn't Byron. At first I thought it was something to do with giving

up smoking, but neph treats it as co-incidence. I don't think he likes me

because I said I wouldn't take the steroids until I could go a couple of

months without a cold - he gave me the kind of look that indicated he

thought I was mentally incompetant. In his letter to the GP he said that I

was resistant to the idea of steroids so he obviously doesn't feel that it

is significant. GP understands (I will be sad to leave him behind).

Reply-To: iga-nephropathy

To: <iga-nephropathy >

Subject: RE: Cellcept

Date: Wed, 4 Apr 2001 08:49:57 -0400

, has your neph ever admitted that this is connected to IGAN?

> Cellcept

> > >

> > >

> > > Has anyone else tried a cycle of Cellcept yet? Did you have any

side

> > > effects?

> > >

> > >

> > >

> > >

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