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Doc says I have a chance

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12 years 1 month ago #35562 by luca
Replied by luca on topic Doc says I have a chance
Sandi, thanks for the reply. What frustrates me the most is that the choice of the "next step" seems to be essentially trial and error! I do agree with many of the posts here that before I consider splenectomy, I really should get the indium screen, but that involves a trip to England and is definitely unsupported by my MD. Other than that step, it seems to be a toss up as to what med I try next, and no one seems to be able to make that call except me (since my MD is also VERY down on the immunosuppressants, although many on this site use them regularly).

A bit of positive news; my search of drug companies online reveals that at least one of the Canadian pharmacies can get Promacta at half of the US price ($2500 for 28 pills). It's still a lot to pay on the gamble that it may be "the drug" for me....
  • Sandi
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  • Sandi Forum Moderator Diagnosed in 1998, currently in remission. Diagnosed with Lupus in 2006. Last Count - 344k - 6-9-18
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12 years 1 month ago #35564 by Sandi
Replied by Sandi on topic Doc says I have a chance
I know, Luca. It's a roll of the dice. Most people try numerous things until they get to the point of the right treatment.

$2,500 for 28 pills? That's 30 grand a year!
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12 years 1 month ago #35568 by luca
Replied by luca on topic Doc says I have a chance
On another subject, I think it was Weird Jack who actually went to England recently and had the Indium scan. If you are still reading this forum, could you please send me some contact info and/or phone numbers of who you dealt with as I want to do the Indium before I make any further decisions on the splenectomy...
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12 years 1 month ago #35580 by Ann
Replied by Ann on topic Doc says I have a chance
12 years 1 month ago - 12 years 1 month ago #35583 by
Replied by on topic Doc says I have a chance

On another subject, I think it was Weird Jack who actually went to England recently and had the Indium scan


Not me. If I had the extra cash laying about to do that....well....I'd probably use it for more pressing issues.

Promacta is expensive because GSK can charge whatever they wish to charge. Same with Nplate.
Until the owners' lock on these two drugs expires and a generics surface, we're stuck with the cost. I don't expect a generic to happen anytime soon. There just aren't enough of us to warrant it. Had it not been for government research grants for 'orphan diseases' I doubt we'd even have Promacta and Nplate. Not that many people have ITP.
You must have looked at the 50mg dosage...I used to take 75mg and that was around $9,000 a month. My previous insurance covered Promacta nicely with a $40 co-pay. My current BCBS (mostly BS...as in Bu**Sh*t) insurance has a series of hoops to jump through...and if you succeed, they'll cover everything AFTER the the $4,000 annual max-out-of-pocket.
Or......I can take generic Cellcept at $10 a month co-pay and no hoops. Heck it's only around $40 without insurance.
Gee, guess which option I chose this year?

As Sandi inquired; What treatments have you tried so far?
ALL ITP treatment is trial and error.....ALL. Because all of us are different. Some folks get lucky and the first thing they 'try' works for them, some of us 'try' various things until we find one that works. And sometimes drugs just 'stop working'. I took Cyclosporine for a year or two, one day my counts dropped back to 4k and Cyclo would not do anything after that. I switched drugs. Hang in there....It's ALL trial and error.

16k can be perfectly livable if you are not bleeding, feel okay, and not bruising or covered in spots. A lot of us live just fine with what are considered low counts. The trick is finding a hematologist who will work with you....not just talk at you.
My most recent count was 19k. I stay in the 12k-20k range now with Cellcept. Had oral surgery a month ago and it was a non-event. We're all different....counts are just one indicator.

Keep your spleen as long as you can. It may not be much, but it's the only one you have.
100 years ago splenectomy for ITP was cutting edge....so was the Model T Ford, the Wright Flyer, Hollywood made its FIRST movie (Squaw Man), and Charlie Chaplin had just been signed with Mack Sennett. Penicillin hadn't even been discovered then and Prednisone was still 40 years in the future. Many things have changed over 100 years...including ITP treatments.

.
  • CindyAnn
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  • Diagnosed Jan 10, 2008. Rituxan treatment in May 2009. Treated with Prednisone off and on until 08/23/17 - 12.5mg Promacta as of 10/22/17
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12 years 1 month ago #35587 by CindyAnn
Replied by CindyAnn on topic Doc says I have a chance
www.pdsa.org/forum-sp-534/6-general-itp-discussion/10063-new-to-itp-my-story-attached-have-questions.html

this is the conversation that has information about the Indium scan very good read.

Cindy Ann
The following user(s) said Thank You: Sandi, luca