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it’s Rare for me
Stories
Guidelines
it’s Rare for me
Stories
Guidelines
Stories
Media Kit
To make the invisible
visible
, to
see
through another’s eyes, to
feel
through another’s heart.
All
ADA-SCID
Acromegaly
Alpha-Mannosidosis
Epidermolysis Bullosa
External
Fabry Disease
HoFH
Internal
LHON
Lipodystrophy
Nephropathic cystinosis
Sickle Cell Disease
Thalassaemia
Trailers
Ajda – Nephropathic Cystinosis
Alexandru – Fabry disease
Amber – Acromegaly
Ana – Epidermolysis Bullosa
Brian – Fabry disease
Chiara – Thalassaemia
Cindy – ADA-SCID
Elena – Lipodystrophy
Eliane – Leber hereditary optic neuropathy
Gianfranco – Leber hereditary optic neuropathy
Gina – Thalassaemia
Haiko – Alpha mannosidosis
Ismael – Sickle Cell Disease
Jakob – ADA-SCID
Jonathan – Acromegaly
Konstantinos – Nephropathic cystinosis
Lori – Fabry disease
Luis David – Epidermolysis Bullosa
Mandie – Fabry disease
Mary – Fabry disease
Matthew – Alpha mannosidosis
Maurice – Fabry disease
Moa – Cystinosis
Nadine – Leber hereditary optic neuropathy
Nicola – Thalassaemia
Paola – Leber hereditary optic neuropathy
Patricia – Lipodystrophy
Peter – Alpha mannosidosis
Phil – HoFH
Racquel – ADA-SCID
Ria – Fabry disease
Rosie- Lipodystrophy
Saffron – Alpha mannosidosis
Sandra – Fabry disease
Sarah – Alpha mannosidosis
Sebastian – Leber hereditary optic neuropathy
Storma – Sickle Cell Disease
Thomas – Alpha mannosidosis
Tyler – Sickle Cell Disease
Zina & Ray – ADA-SCID
zTrailers – It’s Rare For Me stories