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INTERNATIONAL DAY OF GILBERT'S SYNDROME

473 Comments

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Nicola
9 years ago

For my son xx who knows all these symptoms we understand and support him- need GS to be a recognised medical condition that DOES causes symptoms

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Debbie
9 years ago

This touches my heart for everyone who has this disease. My son was finally diagnosed about a year ago after suffering for many years. I so agree that there needs to be alot of research done so that there will be help and relief for those who suffer with this. We need a cure!

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Dawn
9 years ago Featured

My 14 year old son has missed the last 6 months of school. The only diagnosis is Gilbert's Syndrome and even our paediatrician admits she's never seen someone so debilitated by GS. Originally she said it is symptomless (despite all his symptoms).

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Kevin Dunlap
9 years ago

My son has GS

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Breanne Renaud
9 years ago

Struggling With symptoms of Gilbert daily.

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Elaine Venter
9 years ago

Please do as much research as possible to find treatment and a cure for this health issue. Thank You

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Rebecca McKenzie
9 years ago

My daughter has this and doctors can't give much info, at least we have a diagnosis

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Anonymous
9 years ago

Please do as much research as possible to find treatment and a cure for this health issue. Thank You

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Durga sapkota
9 years ago

I am suffering from Gilbert syndrome and every time I visit doctor with some problem like tiredness, hunger craving, tinnitus but they tell me Gilbert syndrome does not create problem ! I wish more research should be done in this !

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Leah Moss
9 years ago

I was diagnosed about a year ago.

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Bernadette McInerney
9 years ago

Adding my support for an international day for Gilbert's Syndrome.

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Samantha barrett
9 years ago

I know two kids with this.

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Lauren-Joy Rosenbach
9 years ago

Think sideways and find a cure.

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wendy kruger
9 years ago

Tired of drs telling me my kids have a benign condition... We need more research done to find out why they have these awful symptoms.

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Lanie Stoneman
9 years ago

Just been told diagnosis but apparently dr's knew I've had it for over 3 years from previous blood test but never told me until now.

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Dale Kerans
9 years ago

Needs to be more research into this to help those who have it have a better quality of life.

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Philippa Abbiss
9 years ago

I am fed up of being told this condition is symptomless and to get on with my life. I'm tired of being tired!!

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Lyn Radley
9 years ago

This disease is not known about by most people unless it effects yourself or a family member and it can be very life changing

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J Hill
9 years ago

It's a hidden illness that few recognise with debilitating fatigue, abdominal pain and severe itchy skin.

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Zoe armstrong
9 years ago

Please let the medical profession understand how we feel. It's not all in our heads!!