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Idiopathic Thrombocytopenic Purpura

Status
Identified

Approved and Donation Ready

This fund has been developed in response to patients who have contacted PAF for help with their medication expenses and could not find help. While this fund has been fully designed and we are ready to provide needed support to these patient communities, this fund is not yet able to accept applications for assistance as we are still working to secure charitable donations that will allow us to open it.

If you, or someone you know, would like to contribute to this fund, please visit our Donors page for more information on how to provide critical support for patients in need.

Fund Type

Co-pay, Co-Insurance & Deductible

Maximum Award Level

$3,500 Per Year

Eligibility Requirements
  • Household Income Requirements 400% or less of Federal Poverty Guideline (FPG) (adjusted for Cost of Living Index (COLI) and number in household)
  • Insurance Requirements Patient must be insured and insurance must cover the medication for which patient seeks assistance.
  • Must reside and receive treatment in the United States.

About Idiopathic Thrombocytopenic Purpura

“Idiopathic thrombocytopenic purpura (ITP) also called immune thrombocytopenia, is a rare bleeding disorder characterized by the immune system mistakenly attacking and destroying blood platelets, which can lead to excessive bruising and bleeding. The cause of the immune reaction is unknown in almost half of the cases, so these cases are classified as “idiopathic”. Thrombocytopenia refers to a decrease in platelets (thrombocytes). Purpura pertains to purplish areas in the skin and mucous membranes and outer lining of organs where bleeding has occurred as a result of decreased platelets.
ITP can occur in anyone at almost any age, but women younger than 40 have a two to three times higher chance of developing ITP than men. There are two types of ITP, acute and chronic. Acute ITP is most commonly seen in young children, with boys and girls being equally affected. This is the most common form of ITP. Symptoms often, but do not necessarily, follow a viral infection. About 85 percent of children recover within 1 year and the problem doesn’t return. Chronic ITP can occur at any age, the symptoms last a minimum of six months to several years. This form usually occurs in adults, but can also occur in adolescents. Chronic ITP can recur and requires continual follow-up care.

Idiopathic Thrombocytopenic Purpura Resources
Medication & Financial Assistance Resources
The Patient Advocate Foundation's (PAF) Co-Pay Relief (CPR) Program does not review the information contained on the website links provided for content, accuracy or completeness. Use of and access to this information is subject to the terms, limitations and conditions as outlined on the accessed websites. PAF Co-Pay Relief Program makes no representation as to the accuracy or any other aspect of the information contained on any website accessed from the CPR website, nor does PAF Co-Pay Relief Program necessarily endorse the website information provided. The information presented on the PAF Co-Pay Relief website is provided for general information only and is not intended as a substitute for medical care. Please talk with your healthcare provider about any information you acquire from this or any other website accessed through the PAF Co-Pay Relief program website.
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