New doctor at surgery just told me Gilberts doesn't cause many problems?
C
Caroline lanigan
10 years ago
Needs to be addressed for better understanding for my child.
P
Patrik Hermansson
10 years ago
Gilberts syndrome needs to be taken seriously. It's is not an illness without symptoms and can be debilitating for the suffers. My wife suffers from Gilberts and every week I see her suffer!
A
Anonymous
10 years ago
Yes GS and people who have it need more surport.
C
Catherine hatton
10 years ago
I've been living with the fatigue and brain fog for years now and only recently been diagnosed. I want it to be recognised rather than pushed under that carpet that gs had no symptoms
M
Mary Long
10 years ago
U.S.
M
Menaa Mohamed El Achraf
10 years ago
I have this G'S
and am tired of being tired
Thanks for all what you are doing
Peace
D
Debs Swan
10 years ago
Feeling less tired, or at least knowing for sure what to do to help eliviate the symptoms would be amazing!
S
Sarah Hopkins
10 years ago
It's most definitely time for GS to be recognised as a debilitating disorder.
B
Bernadette Mclean
10 years ago
I work with children with SEN and feel that this a good cause to offer my support
A
Amber
10 years ago
My life! Ho hum!
S
Susan Hull
10 years ago
Research is needed urgently.
Y
Yuri suazo
10 years ago
We need help
K
Kelly
10 years ago
For Elli
C
Cari
10 years ago
Signed
J
Julie O'Maley
10 years ago
My daughters young life is blighted with this disease. It's limiting the person she can be . She deserves help as she battled through every day .
T
Tilde Okeke
10 years ago
Please recognise the symptoms of GS as real and present!!
Signed j.lee
God provides
New doctor at surgery just told me Gilberts doesn't cause many problems?
Needs to be addressed for better understanding for my child.
Gilberts syndrome needs to be taken seriously. It's is not an illness without symptoms and can be debilitating for the suffers. My wife suffers from Gilberts and every week I see her suffer!
Yes GS and people who have it need more surport.
I've been living with the fatigue and brain fog for years now and only recently been diagnosed. I want it to be recognised rather than pushed under that carpet that gs had no symptoms
U.S.
I have this G'S and am tired of being tired Thanks for all what you are doing Peace
Feeling less tired, or at least knowing for sure what to do to help eliviate the symptoms would be amazing!
It's most definitely time for GS to be recognised as a debilitating disorder.
I work with children with SEN and feel that this a good cause to offer my support
My life! Ho hum!
Research is needed urgently.
We need help
For Elli
Signed
My daughters young life is blighted with this disease. It's limiting the person she can be . She deserves help as she battled through every day .
Please recognise the symptoms of GS as real and present!!
I was diagnosed at age 17.