Please do more research I am in South Africa would be appreciated here as well thanks
M
Marisol C
7 years ago
My 10 year son were diagnosed for 4 weeks ago. I feel so lonely as a parent here in Sweden... lots of ppl don’t know about this
diseases and health care are themselves uncertain about any diet. Together we must increase our knowledge and understanding and avoid the ignorance that exists!
H
Hannah Roy
7 years ago
Sufferer of GS, diagonosed 5 years ago and drs still have no idea how to help
N
Nathalie Nilsson
7 years ago
Time to do a proper research about this condition, as it has so many side effects that has a major impact on daily life for GS sufferers
J
Jodie
7 years ago
So many side effects from this. Which can make leading a normal life hard.
P
Pallavi
7 years ago
More research needed on Gilbert syndrome
C
Charlie
7 years ago
Suffered from chronic fatigue for a very long time, took me a year and a half to get diagnosed for this syndrome and another liver disease. We need research !
R
Richard
7 years ago
Signed
J
Julian
7 years ago
#dream
L
Lorna Harrison
8 years ago
We need to raise awareness of GS and it recognised as being symptomatic. It can be treated by following a good diet & looking after yourself
E
ewa aymer
8 years ago
gilbert syndome has ruined my life tok away all joy ad happiness
M
Marina
8 years ago
Gilbert’s syndrome sufferer
M
Marion Marshall
8 years ago
Grandson has it
N
Natasha marshall
8 years ago
Thank god someone is fighting for this. So sick of doctors telling me GS isn’t affecting my child who has all of the above symptoms and worse!
B
Bas van der Meijden
8 years ago
I see it affect my friend every day
D
Dorian Good
8 years ago
i just want to support people with this condition . especially my friend Melissa
K
Kathleen
8 years ago
Living with Gilberts Syndrome I always feel sick, fatigued and have a number of bouts of raised Belirubin, jaundice skin and eyes, and abdominal pain. More study is needed to assist those living with the condition.
N
Nina Ayres
8 years ago
GPs in UK do not recognise the symptoms of Gilbert's syndrome, but so many of us seem to share them!
Please do more research I am in South Africa would be appreciated here as well thanks
My 10 year son were diagnosed for 4 weeks ago. I feel so lonely as a parent here in Sweden... lots of ppl don’t know about this diseases and health care are themselves uncertain about any diet. Together we must increase our knowledge and understanding and avoid the ignorance that exists!
Sufferer of GS, diagonosed 5 years ago and drs still have no idea how to help
Time to do a proper research about this condition, as it has so many side effects that has a major impact on daily life for GS sufferers
So many side effects from this. Which can make leading a normal life hard.
More research needed on Gilbert syndrome
Suffered from chronic fatigue for a very long time, took me a year and a half to get diagnosed for this syndrome and another liver disease. We need research !
Signed
#dream
We need to raise awareness of GS and it recognised as being symptomatic. It can be treated by following a good diet & looking after yourself
gilbert syndome has ruined my life tok away all joy ad happiness
Gilbert’s syndrome sufferer
Grandson has it
Thank god someone is fighting for this. So sick of doctors telling me GS isn’t affecting my child who has all of the above symptoms and worse!
I see it affect my friend every day
i just want to support people with this condition . especially my friend Melissa
Living with Gilberts Syndrome I always feel sick, fatigued and have a number of bouts of raised Belirubin, jaundice skin and eyes, and abdominal pain. More study is needed to assist those living with the condition.
GPs in UK do not recognise the symptoms of Gilbert's syndrome, but so many of us seem to share them!
tired of being tired
Tired of being tired...