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When my son was diagnosed with Dypraxia I had to carry out loads of research and find out more about the condition. Jake struggles with his speech, remembering simple instructions, and coordination . He cannot ride a bike, kick a football, and lags severely behind his peers at school.
Without the Dypraxia Foundation I would not have had the essential knowledge and support from therapists, consultants, and other sufferers to help my son Jake through the difficulties he has faced since he was 2 yrs old. Dyspraxia is not rare, there are thousands of undiagnosed sufferers, children and adults without the necessary support to help them carry out everyday tasks and learn simple things that the rest of take for granted..
The Dyspraxia foundation can only continue to help those sufferers in need through people donating time and money. It is essential that this support network is allowed to flourish and continue help the those individuals that need much needed support to adapt to their condition and lead as normal lives as possible.