Support for your patients

The patient leaflet, talking about testing, and where to signpost

Women told us that information up front made a real difference. Here you will find our patient leaflet, tips for talking about genetic testing, and trusted sources of support.

Being offered genetic testing after a third miscarriage can raise a lot of questions, often at a very difficult time. This page brings together what you need to support your patients: our patient leaflet to share, tips on talking about genetic testing based on what women told us, and trusted organisations to signpost to for information and emotional support.

You don’t need to be a genetics expert. Clear, kind information at the right time can make a real difference.

The patient leaflet

Our patient leaflet, ‘NHS Genetic testing after three miscarriages’ was co-written with women who have had recurrent miscarriages, and is co-branded with Miscarriage UK and the Association of Early Pregnancy Units. It explains who can have testing, how it works and what the results might mean. Please give it to anyone having their third miscarriage, or later.

Cover of the leaflet Genetic testing for Recurrent Miscarriage.

There are also patient webpages, which go into more detail: The biology, The genetic pathway, Support for you and FAQs. You can share the link with your patients.

Talking about genetic testing

Women told us that information up front made a real difference. These points come from what they told us.

Mention testing at the third loss, or later, before the tissue is sent away or disposed of. Many women only found out about testing by researching it themselves.

Testing can sometimes explain why a pregnancy ended and what it might mean for the future. Many women told us that just knowing was valuable.

A normal result doesn’t rule out other causes, and some samples can’t be tested.

The test can show the sex. Ask whether they want to know, but explain that a result involving the X or Y chromosome will need to be discussed.

The lab aims to report within 6 weeks. Tell them who will contact them with the result.

Point them to the leaflet, the patient webpages and the support organisations below.

Where to signpost

These are the most useful places to point patients to. The full list of patient links is on the patient pages.

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