When your child develops ME/CFS (Myalgic Encephalomyelitis/Chronic Fatigue Syndrome) everything feels uncertain, but you don’t have to face it alone.
If your child is exhausted, struggling to attend school, and you’re searching for answers, guidance, and someone who truly understands - you’re in the right place.
I support parents of children with the condition to understand, navigate the challenges, and feel more confident about the path ahead.
You're not alone in this
When a child develops ME/CFS, it can feel overwhelming for the whole family.
Many parents find themselves asking:
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Why did this happen to my child?
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Will they recover?
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Should they rest or try to stay active?
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How do we manage school, friendships, and daily life?
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Why does no one seem to understand what they’re going through?
The uncertainty, worry, and constant searching for answers can be exhausting.
I work with parents facing these challenges, helping them understand the condition and navigate this journey with more clarity, confidence, and reassurance.
Because when a child is living with this parents need support too.
How I help families
Parents are often left trying to navigate a complex and poorly understood illness without the support they need.
I help them:
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Understand it and what their child is experiencing
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Make sense of symptoms, energy limits, and setbacks
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Learn practical ways to support their child’s wellbeing
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Navigate challenges with school, daily life, and family impact
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Feel more confident in the decisions they are making
Most importantly, I provide a space where parents feel heard, understood, and supported.
With the right understanding and guidance, the journey can feel far less overwhelming.
Is this right for you?
You may be here because your child has developed this condition and everything suddenly feels uncertain.
Perhaps your child is struggling with overwhelming exhaustion, missing school, or no longer able to do the things they once loved.
You may be searching for answers, trying to understand what is happening, and wondering how best to support them.
Many parents I speak to feel:
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Confused about what IT really is
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Unsure how much their child should rest or how to balance activity
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Worried about school and their child’s future
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Frustrated by conflicting advice or lack of understanding
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Emotionally exhausted from trying to hold everything together
Does this sound familiar?
With the right support and guidance, families can begin to feel more confident and supported in the journey ahead.
You don't have to figure this out on your own
If your child has developed ME/CFS and everything feels uncertain, having someone who understands can make all the difference.
I’m here to listen, support you, and help you feel more confident in the steps ahead.