PGD patient pathway

Double helix

Stage 1

Medical referral and registration as a CARE patient.

Stage 2

Obtain mutation analysis, if possible.

Stage 3

Attend consultation and counselling at CARE.

Stage 4

Design and optimisation of PGD test using blood samples or cheek swabs.

This can take up to 12 weeks depending on the disease and the mutation.

Stage 5

If the disease is one for which CARE are already licensed to test for, we would arrange a PGD Review Consultation to proceed with treatment.

If the disease is one for which we do not already hold a license then an HFEA application would be required. Approval can take up to 3 months following submission. When received, we would then book a PGD Review Consultation to proceed with treatment.

Stage 6

This is the first stage of the IVF cycle up to the second day after egg recovery (Day 2).

Stage 7

Embryo Biopsy (Day 3)

Stage 8

Genetic Analysis

Stage 9

Transfer of embryos identified as being free of the inherited genetic disease (usually Day 5).

Stage 10

Pregnancy testing at 14-16 days after embryo transfer.

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Support Organisations

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Support Organisations

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Genetics Story