The long road to diagnosis: Pitt-Hopkins Syndrome

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Congenica announced as a finalist for MIT Solve’s Horizon Prize

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Living with a rare disease in perspective: Lynsey’s Rare Journey

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How we learnt about Menkes Syndrome

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Discovering Glut1 Deficiency Syndrome

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Diagnosing CALFAN syndrome after years of uncertainty

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Raising awareness of Dravet Syndrome

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Our story of Norrie Disease

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How Schinzel-Giedion Syndrome (SGS) has changed our lives

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Dr Charles Steward joins as “friend” of the UK Infantile Spasms Trust

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Our CHAMP1 journey

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1

The long road to diagnosis: Pitt-Hopkins Syndrome

Read More

Congenica announced as a finalist for MIT Solve’s Horizon Prize

Read More

Living with a rare disease in perspective: Lynsey’s Rare Journey

Read More

How we learnt about Menkes Syndrome

Read More

Discovering Glut1 Deficiency Syndrome

Read More

Diagnosing CALFAN syndrome after years of uncertainty

Read More

Raising awareness of Dravet Syndrome

Read More

Our story of Norrie Disease

Read More

How Schinzel-Giedion Syndrome (SGS) has changed our lives

Read More

Dr Charles Steward joins as “friend” of the UK Infantile Spasms Trust

Read More

Our CHAMP1 journey

Read More
1