By Heather Morgan It is important to stop and process the news of Trisomy 18 before making any quick decisions. Maybe it was just this morning. You sat in the doctor’s office after your ultrasound. There had been too many long, awkward silences. You knew that something was wrong. Maybe it’s spina bifida. You’ve heard […]
“The Trisomy 18 Foundation was my life line. The staff there helped me through the darkest days of my life from the time our daughter was diagnosed with T18 until she died and even after. If anyone you know is pregnant with or has a T18 baby, tell them about the Foundation.”
— Wendy from Matlock, Derbyshire UK
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