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Emmerdale’s Down’s abortion plot shows disability education is severely lacking in Britain Edel Harris © Provided by The Independent Thirty-three years ago, I gave birth to a baby boy with what was described then as a “development delay”.  For the first five years of his life as new parents, we muddled through.   We had no diagnosis until my son was five years old and that came in the form of a letter that arrived on a Saturday morning in the post from the local hospital genetics clinic.   We were in shock. We lacked any information and desperately needed somebody to talk to. Thank goodness for the Fragile X Society where another parent took my call that Saturday morning. For many years we accidently stumbled across information, usually from another parent of a child with a learning disability who in passing mentioned “benefits” or “respite”. We began to appreciate that there was support for families like ours.

Chris bissonCharlotte bellamyChildren campaignFragilex societyMencap early yearsMencap early years surveyTreat me wellகிறிஸ் பிசன்சார்லோட் பெல்லாமிகுழந்தைகள் பிரச்சாரம்உபசரிப்பு என்னை நன்றாக