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In reply to the discussion: Whoa! My Lynparza cost right at $15,000 a month. [View all]Meowmee
(9,212 posts)49. So sorry ๐ค๐ค๐ค ๐ข
It is insane and criminal that this can even happen. These people are crooks and criminals of the worst kind- who exploit sick people who have no choice. There should be controls on all hc costs etc.
I hope you find a way to get it paid for if you lose your insurance. Why are you losing your insurance? Definitely look into the whole medicaid route too.
I looked it up and something at the link talks about financial aid foundations, I don't know if this could help you. I am sure you probably read this already but I will link these just in case they can help you. I think the second or first link specifically has info on help for non insured patients from Astra Zeneca:
Who can apply?
People without health insurance
Medicare Part D and/or B recipients
Those who have recently experienced a financial crisis
Residents of the United States
Eligibility rules apply, please call an AZ&Me representative for more information at 1-800-AZandMe (1-800-292-6363).
https://www.everydayhealth.com/cancer/can-i-get-cancer-treatment-with-no-insurance/
https://www.myaccess360.com/patient/lynparza-olaparib/patient-affordability.html
https://www.lynparzahcp.com/patient-support/uninsured.html
In a much more minor story, I have been on Tymlos for the past 2 years or so after a spinal compression fracture. At first the copay was $25. I still got the company copay assistance and it was free. I knew that would not last because I have been through this before.
Then about 3 months later, the ins tells me the new copay is now $787! That is just the copay, for a one month pen. It is injected daily. I still have the copay assistance and it is free.
But I live in fear one day they are going to bill me that copay or thousands more etc. One month they messed up the billing and I was billed that copay- I had to call several times to get it straightened out. This is simply an injection pen for small dose abaloparatide- synthetic parathyroid hormone- which in small doses stimulates bone growth for those with osteoporosis. There is no reason for these prices except greed and criminality. It has to stop.
I have had severe hives to the point I had to get epi pens now and have stopped tymlos for now to see if it is involved plus I need a break as it was already causing a lot of other symptoms which were getting harder to tolerate.
I hope you find a way to get it paid for if you lose your insurance. Why are you losing your insurance? Definitely look into the whole medicaid route too.
I looked it up and something at the link talks about financial aid foundations, I don't know if this could help you. I am sure you probably read this already but I will link these just in case they can help you. I think the second or first link specifically has info on help for non insured patients from Astra Zeneca:
Who can apply?
People without health insurance
Medicare Part D and/or B recipients
Those who have recently experienced a financial crisis
Residents of the United States
Eligibility rules apply, please call an AZ&Me representative for more information at 1-800-AZandMe (1-800-292-6363).
https://www.everydayhealth.com/cancer/can-i-get-cancer-treatment-with-no-insurance/
https://www.myaccess360.com/patient/lynparza-olaparib/patient-affordability.html
https://www.lynparzahcp.com/patient-support/uninsured.html
In a much more minor story, I have been on Tymlos for the past 2 years or so after a spinal compression fracture. At first the copay was $25. I still got the company copay assistance and it was free. I knew that would not last because I have been through this before.
Then about 3 months later, the ins tells me the new copay is now $787! That is just the copay, for a one month pen. It is injected daily. I still have the copay assistance and it is free.
But I live in fear one day they are going to bill me that copay or thousands more etc. One month they messed up the billing and I was billed that copay- I had to call several times to get it straightened out. This is simply an injection pen for small dose abaloparatide- synthetic parathyroid hormone- which in small doses stimulates bone growth for those with osteoporosis. There is no reason for these prices except greed and criminality. It has to stop.
I have had severe hives to the point I had to get epi pens now and have stopped tymlos for now to see if it is involved plus I need a break as it was already causing a lot of other symptoms which were getting harder to tolerate.
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Can you get on disability and get Medicaid. I don't know if they would pay for expensive drugs.
kerry-is-my-prez
May 4
#65
That is obscene. I sure hope you don't lose your insurance. May The Universe protect you.
LoisB
May 3
#14
Maybe Jasmine Crockett could draw attention to your plight and shame your rep into helping
catrose
May 4
#56
I appreciate what he's doing, but I believe it's only for generic drugs that aren't "controlled" (needing a
LauraInLA
May 4
#52
Check if there are mfgr coupons, rebates, discounts, etc. Eliquis, Cequa and a bunch of others have them.
TheBlackAdder
May 3
#27
Agree mainly. But the prices charged are more based on profits/marketing/etc. than costs of research.
erronis
May 4
#55
To an organic chemist, it's pretty simple. No chiral centers. No fused rings. Two amide bonds. A hydrazone.
eppur_se_muova
May 4
#57
That's kind of weird, since it's a small molecule drug. However, I didn't know there was an effective treatment...
NNadir
May 4
#37
๐ It's terrifying, is what it is. Heartfelt hugs, hopes, wishes for your & our collective future โค๏ธ
Hekate
May 4
#42
I am so sorry you are going through this but I can certainly empathize. My husband has an incurable but
Nanjeanne
May 4
#51