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I just joined this group and thought I'd add my story. I've had asthma

all my life - 47 years. Been in and out of the hospital, tried

everything from allergy shots to yoga. The leukotriene inhibitors and

atrovent were the only thing besides prednisone that helped at all,

and they didn't do much for me. I had gotten to the point where I was

on the evil candy all the time and it was unlikely I would get off.

They were considering supplemental oxygen at night because my 02 sats

were going way down even with a CPAP. The constant prednisone had

given me diabetes and arthritis. I have become hypersensitive to

albuterol; it gives me heart palpitations and headaches.

I found Xolair on the web and asked about it three years ago. My

doctor went to bat for it even though he isn't a respiratory

specialist (I live in a small town). He managed to get it through my

insurance. I am one of the truly lucky ones. I was weaned from the

prednisone, plus all my other asthma meds over time. I now use my

Xopenex inhaler once in perhaps two weeks, and then for

exercise-induced symptoms. A week ago, there was an advisory in the

valley where I live saying that we had the highest pollen count in the

world! I didn't even have a stuffy nose!

I have a higher quality of life now than 20 years ago. I am still

diabetic, but as I lose the steroid weight, I gain greater control of

that.

But now I have a dilemma. I lost my job in April. I have been able to

keep up payments on my COBRA benefits so far and should be fine

through the end of the year, but I really fear losing my health

insurance. There is no way I could pay for this drug without

insurance. I have applied at a number of places, and I hope to get a

job soon. But losing this drug would be like losing my life.

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Genentech has a program for folks who can't afford Xolair and don't

have insurance. I think Pat (screen name momma something) posted

information how to get an application or whatever in the last 6

months or so. Go back through the message logs if someone doesn't

post that again.

-Addy

--- In , " lurkitty117 " <scruffy@...>

wrote:

>

> I just joined this group and thought I'd add my story. I've had

asthma

> all my life - 47 years. Been in and out of the hospital, tried

> everything from allergy shots to yoga. The leukotriene inhibitors

and

> atrovent were the only thing besides prednisone that helped at all,

> and they didn't do much for me. I had gotten to the point where I

was

> on the evil candy all the time and it was unlikely I would get off.

> They were considering supplemental oxygen at night because my 02

sats

> were going way down even with a CPAP. The constant prednisone had

> given me diabetes and arthritis. I have become hypersensitive to

> albuterol; it gives me heart palpitations and headaches.

>

> I found Xolair on the web and asked about it three years ago. My

> doctor went to bat for it even though he isn't a respiratory

> specialist (I live in a small town). He managed to get it through

my

> insurance. I am one of the truly lucky ones. I was weaned from the

> prednisone, plus all my other asthma meds over time. I now use my

> Xopenex inhaler once in perhaps two weeks, and then for

> exercise-induced symptoms. A week ago, there was an advisory in the

> valley where I live saying that we had the highest pollen count in

the

> world! I didn't even have a stuffy nose!

>

> I have a higher quality of life now than 20 years ago. I am still

> diabetic, but as I lose the steroid weight, I gain greater control

of

> that.

>

> But now I have a dilemma. I lost my job in April. I have been able

to

> keep up payments on my COBRA benefits so far and should be fine

> through the end of the year, but I really fear losing my health

> insurance. There is no way I could pay for this drug without

> insurance. I have applied at a number of places, and I hope to get

a

> job soon. But losing this drug would be like losing my life.

>

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Guest guest

Quite a dilemma you have. I am glad to hear you are much better after 20

years. This gives a lot of us hope there is a light at the end of the

tunnel.

I have not done any research into this idea but I wonder of those of us

on Xolair could join together as a group and present this to BCBS or

some other insurance provider or even purchase insurance on our own.

More and more persons seem to be using Xolair every day. Would this make

it less expensive for all of us. I am not an expert in insurance by any

means but I though I would present this idea and see what others had to

say about it.

~STEVE ZIMMERMAN, CPM, CVOM~

________________________________

From: [mailto: ]

On Behalf Of lurkitty117

Sent: Tuesday, July 11, 2006 1:22 AM

Subject: [ ] My story

I just joined this group and thought I'd add my story. I've had asthma

all my life - 47 years. Been in and out of the hospital, tried

everything from allergy shots to yoga. The leukotriene inhibitors and

atrovent were the only thing besides prednisone that helped at all,

and they didn't do much for me. I had gotten to the point where I was

on the evil candy all the time and it was unlikely I would get off.

They were considering supplemental oxygen at night because my 02 sats

were going way down even with a CPAP. The constant prednisone had

given me diabetes and arthritis. I have become hypersensitive to

albuterol; it gives me heart palpitations and headaches.

I found Xolair on the web and asked about it three years ago. My

doctor went to bat for it even though he isn't a respiratory

specialist (I live in a small town). He managed to get it through my

insurance. I am one of the truly lucky ones. I was weaned from the

prednisone, plus all my other asthma meds over time. I now use my

Xopenex inhaler once in perhaps two weeks, and then for

exercise-induced symptoms. A week ago, there was an advisory in the

valley where I live saying that we had the highest pollen count in the

world! I didn't even have a stuffy nose!

I have a higher quality of life now than 20 years ago. I am still

diabetic, but as I lose the steroid weight, I gain greater control of

that.

But now I have a dilemma. I lost my job in April. I have been able to

keep up payments on my COBRA benefits so far and should be fine

through the end of the year, but I really fear losing my health

insurance. There is no way I could pay for this drug without

insurance. I have applied at a number of places, and I hope to get a

job soon. But losing this drug would be like losing my life.

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  • 6 months later...

well one of the side effects of AMN107 is

constipation. I never had that in my life and did not

know how serious it could be. I went to the emergency

after about 5 days and they did nothing in fact I

think they were afraid to do anything as my counts

were low. My doctor was away so I went to another

doctor and he again did nothing. after 9 days I had

to go in for a transfusion to Medical Day Unit and the

nurse took one look at me and called a doctor. I then

started to throw up blood etc I ended up in the

hospital for 6 days. And now the people that make

AMN107 know just how serious it can be.

But it was a warning on the write up that they give

all who go on an experimental drug. which by the way

I send Zavie a copy of all the side effects ..just in

case someone wanted to know..Thanks for your kind

words I had a lot of requests for that story but due

to my unique circumstances of 29 years I was not

willing to worry people with all my low counts but I

dropped to zero pleatelets and Zav asked his doc about

it and She said that yes it is serious but people can

functions on low counts... so I though I would write

that little history and keep track of my counts to

encourage anyone interested..

Skip

--- doveh12 <deh12@...> wrote:

> Congratulations, Skip. You're now a " blogger. " I

> enjoyed your

> first entry. May I ask you what was the bad

> reaction you had in the

> beginning of AMN-107 treatment?

>

> I like what you said about just being " along for the

> ride. " We

> never know what plans God has for us, do we?

>

> Warm regards.

>

>

>

>

> >

> > Hello Group,

> > after careful consideration I have put my history

> on a

> > web page.. I have asked Zaviem to check it out to

> see

> > if it is suitable. I must remind anyone that

> reads it

> > that my case is a bit different than most.

> > So just keep in mind that low counts are ok.. In

> fact

> > when I zero platelets Zaviem asked his new doc

> about

> > that and she confirmed that low counts do not mean

> as

> > much as we all think.

> >

> > My web page is at

> > http://easyskip.tripod.com

> > if you wish just leave a message in the guest book

> and

> > I will try to answer all question although I am

> not

> > the brightest leaf on the tree.

> > SkipD

> > DX'ed when the dead sea was just ill.

> >

> >

> >

> >

> >

>

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> >

>

>

>

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