For our last Probably Nothing episode of the series we are joined by Helen White, who years after her diagnosis of womb cancer found out she has Lynch Syndrome. Helen asked for genetic testing after seeing our #LetsTalkLynch campaign and after speaking to Dr Neil Ryan (who works on Lynch Syndrome) at our Trek to Remember a few years ago.
Since then Helen has been a big advocate for Lynch Syndrome and genetic testing, and works on patient involvement groups.
We will be chatting to Helen about her womb cancer diagnosis and treatment, why she went for genetic testing, and what it was like finding out she had Lynch Syndrome.
To see more about Probably Nothing, and catch up with all old episodes, visit our website, eveappeal.org.uk/probablynothing.
If you have any questions or concerns about Lynch Syndrome and cancer risk, you can also get free and confidential advice from Ask Eve, our nurse-led information service, on nurse@eveappeal.org.uk or 0808 802 0019.
#ProbablyNothing #LynchSyndrome #Lynch #WombCancer #BowelCancer #OvarianCancer #AskEve #EveAppeal #TheEveAppeal
Негізгі бет Probably Nothing- Living with Lynch Syndrome
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