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Here is his contact info:

Dr. Pierre Blais

Innoval

496 Westminster Ave.

Ottawa, Ontario

Canada K2A 2V1

613-728-8688

Good luck, they are nice people when I talked to them on the phone I

was impressed!

In @y..., " Beverley Smalley " <kokomo@b...> wrote:

> How can I get ahold of him?

> Beverley Smalley

> ----- Original Message -----

> From: <cjheer@i...>

> < @y...>

> Sent: Friday, November 09, 2001 6:01 PM

> Subject: Re: confused!!!

>

>

> > he can analyze them but I am not sure if they would show anything

if

> > they have been in the fridge or handled, unfortunatly they are not

> > supposed to be kept cold, it kills things I think.

> >

> > Check out some of the posts further back I think his info is

there I

> > think it is around 200 or 300 bucks and it depends on how much you

> > want done.

> >

> >

> >

> >

> >

> >

> > In @y..., " Beverley Smalley " <kokomo@b...> wrote:

> > > Can Dr. Blais analyze my implant that I have had for over 3

years

> > and kept

> > > in the refrigerator? (nice when you have company) What is the

> > procedure and

> > > the cost?

> > > Beverley Smalley

> > > ----- Original Message -----

> > > From: <cjheer@i...>

> > > < @y...>

> > > Sent: Friday, November 09, 2001 2:32 PM

> > > Subject: Re: confused!!!

> > >

> > >

> > > > First of all I would contact Dr blais and find out how he

wants

> > them

> > > > sent to him, second I would talk to your explanting surgeon

> > > > beforehand to make sure he knows that you want your implants

to be

> > > > packaged properly after explant so that they can be sent to Dr

> > Blais

> > > > for ananlysis, I would be sure that he understands you want

> > pictures

> > > > of the implants with the capsules on them before they are sent

> > > > anywhere, if he is offended by this I wouldn't trust him to

do the

> > > > job right. I would explain to him that you have heard of

women not

> > > > having capsules taken out and getting sicker and that you just

> > want

> > > > to be extremely careful, also get it in writting.

> > > >

> > > > I wouldn't worry so much about the time scheduled as I would

about

> > > > all this other stuff, because if the surgery runs over

schedule

> > they

> > > > are usually prepared for that, however if you are having any

> > second

> > > > thoughts about this PS I would be careful, you do not want to

> > have to

> > > > have more surgeries down the road.

> > > >

> > > > Call him and discuss these issues asap, to put your mind at

ease,

> > and

> > > > yes usually an explant and capsulectomy would take longer

than an

> > > > hour and a half, but who knows, most of us had lifts too.

> > > >

> > > > What incision is he using?

> > > >

> > > > Good luck and keep us posted!

> > > >

> > > >

> > > >

> > > >

> > > >

> > > >

> > > >

> > > >

> > > >

> > > >

> > > > In @y..., cpannarale@y... wrote:

> > > > > Hello!

> > > > >

> > > > > I am slightly confused at what I should do for my

explantation.

> > > > >

> > > > > First, are my implants and capsules sent to a pathologist

> > > > > automatically or do I do this?

> > > > >

> > > > > Next, does dr. blais do this or does he just examine the

> > implants

> > > > > after pathology or before?

> > > > >

> > > > > Finally, I don't know if I missed the post but did Dr. Kolb

post

> > > > how

> > > > > long an explantation usually takes? Because I'm suppose to

be

> > > > having

> > > > > a complete capsulectomy no mastopexy and it's only scheduled

> > for 1

> > > > > 1/2 hours while most of you seem to have had 3 hour

> > surgeries!!!!

> > > > >

> > > > > Can I expect my surgeon to be offended by asking him to take

> > > > pictures

> > > > > or videotaping the procedure? Whats the best way of trying

to

> > > > > guarantee that the capsules be taken out?

> > > > >

> > > > > Thanks,

> > > > > Charlene

> > > >

> > > >

> > > >

> > > >

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  • 1 year later...

The pain in your right side is REAL and is called Upper Right

Quadrant Pain. The liver is encased in a membrane..which has nerve

endings. When the liver is inflammed, it pushes against that membrane

and causes the pain. It is widely accepted that this is not an

imaginary pain.

As for your White blood cells, the Ribavirin WILL cause them to drop.

Are you not getting copies of your labs? If not, tell your Doctor you

want copies from now on, and get the past copies. This way you can

keep tabs on what is going on.

If your white blood cells drop below 5.0, they should either stop the

Ribavirin completely, or lower the dosage. The white blood cells WILL

come back up once the Ribavirin is stopped, or lowered. Many people

have to take a lower dosage of the pills because of this.

As for your attorney, call him twice a day until you speak to him.

Better yet, go to his office and sit in the waiting room until he

sees you. Check in your city for any kind of assistance programs you

may qualify for. There must be something or someway that can help

you.

Have you flied for Social Security yet? If you have at least Stage 3

fibrosis, you may qualify.

Hope this helps,

LeighAnn

http://www.geocities.com/1Leighann

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As I said before, responding to treatment really depends on your

Genotype. If your doctor hasn't done this test, tell him you want

one. Even if you only have a 50% chance of responding, while you are

on treatment it will stop the liver from being damaged more.

When I first started treatment in 1998, there was a 14% chance of

responding. I didn't. I've done every treatment out there, and have

not responded to any of them.

BUT...I can tell you that in the last 2 years, since I did the

Pegasys and Ribavirin, my liver did not become more damaged. I know

the treatment will help your liver, and whether or not we have the

virus should be second to stopping liver damage that could wind up

causing us to have a transplant.

So hang in there with the treatment. Let the dr lower the Ribavirin

and watch the labs closely. Better to take a smaller dosage than none

at all.

LeighAnn

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As I said before, responding to treatment really depends on your

Genotype. If your doctor hasn't done this test, tell him you want

one. Even if you only have a 50% chance of responding, while you are

on treatment it will stop the liver from being damaged more.

When I first started treatment in 1998, there was a 14% chance of

responding. I didn't. I've done every treatment out there, and have

not responded to any of them.

BUT...I can tell you that in the last 2 years, since I did the

Pegasys and Ribavirin, my liver did not become more damaged. I know

the treatment will help your liver, and whether or not we have the

virus should be second to stopping liver damage that could wind up

causing us to have a transplant.

So hang in there with the treatment. Let the dr lower the Ribavirin

and watch the labs closely. Better to take a smaller dosage than none

at all.

LeighAnn

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