Are there any foundations that can help with out of pocket expenses? I have insurance but copays for specialists and meds are expensive

[weezy81]

[Mazcd Partner MPNVoice]

Hi Weezy81, can you tell me what MPD you have and where you live? You say you have insurance, what exactly does this pay for? I will try and find out what I can for you.

Kind regards, Maz.

[weezy81 in reply to Mazcd]

I have polycythemia vera, thrombocyotosis, Myeloproliferative neoplasm, & lymphadenopathy. I live in Champaign, Illinois. My copay is for dr.is $35 and my meds are on a tier system. Anywhere from $3 -$69, until I reach my donut hole. I am on SSD and have a very limited income.

[Mazcd Partner MPNVoice in reply to weezy81]

Hi Weezy81, I am not sure if this will help, but you could get in touch with the MPN Research Foundation in the US, this is the link to their site, mpnresearchfoundation.org/ they have a support group in Illinois with a contact number and email address, they may be able to help you. Maz