Frequently Asked Questions

Application update in progress and will resume applications as soon as complete!

A: Due to high volume of applications that we receive with each cycle, we prefer that you wait until you receive your confirmation e-mail from us. If you don’t receive a confirmation email within 4-6 weeks of submitting your application please send a follow up to ask.helpcurehd@gmail.com.

A: There are no fees to apply for our application, however we do require a background check that incurs an $18.00 charge per individual applicant.

A: These tests are different from each other. PGT-A is to identify embryos affected by chromosomal abnormalities. PGT-M is to identify gene specific disorders.

A: Each application is reviewed on a case by case scenario and many variables are taken into consideration.

A: Test results from the affected person, or their mom or dad. 

Death certificate from the mom or dad showing HD as the cause of death.

Or medical records from the doctor showing a HD diagnosis.

A: HelpCureHD is partnered with various clinics across the US and those clinics will be our first choice (exceptions can be considered.)

A: Applicants will be responsible for consultation and diagnostic tests prior to the start of the IVF cycle.

A: The IVF needs to be started within 6 months of being awarded.

A: No, services will only be paid from the date the grant was awarded.

A: RGI, Cooper Genomics, iGenomix, Prediction genomics.

A: No, we do not share your HD status with employers, insurance, or references.

A: US & Canada .

A: We cover embryo storage during the cycle, once transferred it is the applicant’s responsibility.

A: For liability purposes we do not.

A: HelpCureHD’s mission and goal is to help eradicate HD from family genealogy, any infertility related procedures will be at the cost of applicant. Infertility will not disqualify you, but any related procedures are the applicant's responsibility.