Story
My 16 year old son developed chronic migraines aged 11 which was finally diagnosed as PoTS (Postural Tachycardia Syndrome). Family life changed and our role as parents changed.
For the first 3 years no health professional told us we were carers and no one pointed us in the direction of Carers in Beds.
Over the last 2 years we have been supported by their cafes, monthly meetings, treatments, training such as managing stress, Emotional 1st Aid.
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