In my experience parents are often handed their child’s diagnosis letter and then waved goodbye, without having the opportunity to learn what the diagnosis is, what it means for their family and how best they can support their child or young person.
Support doesn’t stop at the point of diagnosis either, parents know the type of help they give changes as their child grows; what is helpful at six, isn’t helpful at sixteen.
In fifteen years of clinical work and working with thousands of families, caregivers have always been consistent.
They want to know more, and they want to know how best they can help.
Parents tell me they want to know there are other people out there going through a similar journey as them and they aren’t alone as they look for answers.
The solution.
Parents and caregivers are the first part of the child’s village.
I am providing live and on-demand workshops, seminars, and education sessions for parents of neurodivergent children and young people.
Education topics include:
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Building awareness of pharmacological and non-pharmacological treatment options (co-presented with a Consultant Pharmacist).
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Understanding the senses, sensory profiles, and sensory accommodations available for your child and family.
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A guide to the hierarchy of regulation development.
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A guide to supporting parents to provide a safe space for their young person to explore gender and sexual identities.
Hit the button below to check out our upcoming sessions!