I have gelbert syndrome and i hope to find treatment
D
Dean
3 years ago
I suffer with Gilbert's and was diagnosed only a few months ago. Very late. But to have just one day to represent it is everything
Let's get people understanding
K
Kristi Orcutt
4 years ago
GS sucks and so many US doctors just shrug it off as nothing!
D
Deborah Yates
4 years ago
Hopefully a step towards international recognition of the impact Gilbert's Syndrome has on those who have it.
A
Andy Wiley
4 years ago
Gilberts Syndrome has changed my life, the things I loved to do now make the Gilberts unbearable at times, I am tired and foggy most of the time... sad times.
K
Karen
4 years ago
I was 63 when first diagnosed but I knew something was wrong since very young. Thought it was my thyroid and had a surprise you find it was GS.
E
Egidijus Gusčius
4 years ago
Help us feel better
A
Annika
4 years ago
Gilbert syndrome has been with me all my life, making me sad, anxious and tired. It would have been so important for me to know about it earlier. No child or teenager should have to experience the same. Education is everything.
K
Kanhai kumar
4 years ago
I am suffering from Gilbert syndrome
B
Birgitte M Carlsson
5 years ago
Jeg lider af Gilbert Meulengracht syndrom
S
Sara
5 years ago
I've been diagnosed with GS at 18 y/o (6 years now with GS). No one truly understands what is like to live with all the effects of this chronic (and invisible) illness (jaundice/fatigue/lack of concentration/bad digestion etc. etc.). We NEED more awareness and more medical research!
M
Morgan
5 years ago
Please help us!!
A
Angela MacRae
5 years ago
I was diagnosed with this yesterday and i totally believe we need to be heard
E
Ernesto Lopez
5 years ago
I have Gilbert's and it's hard to function some days.
D
David conway
5 years ago
GS Sufferer
L
Lee
5 years ago
I suffer fatigue, irritable bowel, abdominal pain and feeling weak in general frequently, I've got yellow in my eyes, and tinged yellow skin. Was only recently diagnosed with this syndrome and discovered that these symptoms are all common for Gilbert Syndrome suffers, but research is dismal. More research really needs to be done
J
Janis Gurutidis
5 years ago
WE NEED TO MAKE THIS HAPPEN!!
S
Sara Tucker
5 years ago
My son was diagnosed last year and so many things go on with him, and we are told well Gilbert's doesnt have symptoms, which we all know is a lie.
Me too.
I have gelbert syndrome and i hope to find treatment
I suffer with Gilbert's and was diagnosed only a few months ago. Very late. But to have just one day to represent it is everything Let's get people understanding
GS sucks and so many US doctors just shrug it off as nothing!
Hopefully a step towards international recognition of the impact Gilbert's Syndrome has on those who have it.
Gilberts Syndrome has changed my life, the things I loved to do now make the Gilberts unbearable at times, I am tired and foggy most of the time... sad times.
I was 63 when first diagnosed but I knew something was wrong since very young. Thought it was my thyroid and had a surprise you find it was GS.
Help us feel better
Gilbert syndrome has been with me all my life, making me sad, anxious and tired. It would have been so important for me to know about it earlier. No child or teenager should have to experience the same. Education is everything.
I am suffering from Gilbert syndrome
Jeg lider af Gilbert Meulengracht syndrom
I've been diagnosed with GS at 18 y/o (6 years now with GS). No one truly understands what is like to live with all the effects of this chronic (and invisible) illness (jaundice/fatigue/lack of concentration/bad digestion etc. etc.). We NEED more awareness and more medical research!
Please help us!!
I was diagnosed with this yesterday and i totally believe we need to be heard
I have Gilbert's and it's hard to function some days.
GS Sufferer
I suffer fatigue, irritable bowel, abdominal pain and feeling weak in general frequently, I've got yellow in my eyes, and tinged yellow skin. Was only recently diagnosed with this syndrome and discovered that these symptoms are all common for Gilbert Syndrome suffers, but research is dismal. More research really needs to be done
WE NEED TO MAKE THIS HAPPEN!!
My son was diagnosed last year and so many things go on with him, and we are told well Gilbert's doesnt have symptoms, which we all know is a lie.
Please help me. I need support.