Save the date From the 23rd February until the 1st March we are asking all members to help us raise awareness of Oesophageal Atresia and
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 Are you the father of a child born with OA/TOF? Are you looking to support a male caregiver? Do you wish to talk more about |
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2 events, 28 February is Rare Disease DayRaising awareness and generating change for the 300 million people worldwide living with a rare disease, their families and carers. |
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 Calling all adults born with OA/TOF. You’re invited for a virtual cuppa and chat with other adults born with OA/TOF. This informal meet-up is led |
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 Calling all adults born with OA/TOF. You’re invited for a virtual cuppa and chat with other adults born with OA/TOF. This informal meet-up is led |
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TOFS 2026 Seminar Important Update:We’ve been made aware that there is a part closure on the Piccadilly Line on Saturday. Depending on which direction you’re |
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 Are you the parent or carer of a child born with OA/TOF? Do you wish to meet others in a similar situation? Join us for |
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 Don’t miss your chance to meet up with other OA/TOF parents and families in the West Midlands, for a cuppa, chat and some Easter crafts! |
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