There is a desperate need for palliative care for children
C
Chantelle Macalagh
3 years ago
Children in South Africa has the same rights as an Adult to Palliative Care.
T
TIVA YVONNE JAMELA
3 years ago
Children's Palliative care to be roll out in all Hospitals.
T
Thandeka Gwala
3 years ago
Free services for all
A
Albert Smit
3 years ago
If we don't love and care for our children, who will ??
This is basic human rights.
J
Jessica
4 years ago
Children's Palliative care is needed now.
G
Garth Leech
6 years ago
Urgent need of full implementation.
M
Migena
6 years ago
God is always with people in need.
A
Anxhela Qirinxhi
6 years ago
Wishing we will reach the million signs as soon as possible
I
Irena
6 years ago
help the children, they need to live till the end without suffering!
L
Liz Tanner
6 years ago
Every human being should be entitled to recieve the care they need when they need it.
M
Maryann
6 years ago
Support.
L
Lee Last
6 years ago
It's an absolute disgrace that so many children do not have access to palliative care. The Government is failing dismally in its duty to provide health care for our children and should be deeply ashamed.
M
Mark Heywood
7 years ago
Mark
M
Myrtle Williams
7 years ago
Children have the right to palliative care.
G
Gavin Bruce Ferrier
7 years ago
I believe every child must be given the care they need.
P
Phindi
7 years ago
Every child deserves quality care for a lifetime....
N
Nicky GunnClark
· petition starter
7 years ago
Natasjha - its not clear what assistance you need. Please send an email to the PatchSA website with specifics, and I will try to help further http://patchsa.org/#contact-us.
It may interest you to know that our PatchSA newsletter of Nov 2016 shared news that at a Rare Diseases Conference (RareX) held at Spier, Stellenbosch, Lara Bloom, co-executive director of the Ehlers-Danlos society, attended, and was keen for an Ehlers-Danlos support group to be started in South Africa. She writes:
The Ehlers-Danlos Society is keen to help the setup of an EDS support group in South Africa. As the international umbrella organisation we are committed to making sure geography doesn’t determine your quality of life. Utilising our experience and networks we can help willing and able advocates to set up a registered charity so that patients in South Africa have somewhere to turn for advice and support. Please contact Lara Bloom directly if you are interested at [email protected]
You can also contact Rare Diseases South Africa, led by Kelly du Plessis and ask if an EDS support group was ever set up. https://www.rarediseases.co.za/about Hope that is helpful Natasjha - but please send an email to PatchSA if you need further assistance, and we can try to help
M
Mriga Moodliar-Pillay
7 years ago
Children's palliative care welcomed with open arms
There is a desperate need for palliative care for children
Children in South Africa has the same rights as an Adult to Palliative Care.
Children's Palliative care to be roll out in all Hospitals.
Free services for all
If we don't love and care for our children, who will ?? This is basic human rights.
Children's Palliative care is needed now.
Urgent need of full implementation.
God is always with people in need.
Wishing we will reach the million signs as soon as possible
help the children, they need to live till the end without suffering!
Every human being should be entitled to recieve the care they need when they need it.
Support.
It's an absolute disgrace that so many children do not have access to palliative care. The Government is failing dismally in its duty to provide health care for our children and should be deeply ashamed.
Mark
Children have the right to palliative care.
I believe every child must be given the care they need.
Every child deserves quality care for a lifetime....
Natasjha - its not clear what assistance you need. Please send an email to the PatchSA website with specifics, and I will try to help further http://patchsa.org/#contact-us. It may interest you to know that our PatchSA newsletter of Nov 2016 shared news that at a Rare Diseases Conference (RareX) held at Spier, Stellenbosch, Lara Bloom, co-executive director of the Ehlers-Danlos society, attended, and was keen for an Ehlers-Danlos support group to be started in South Africa. She writes: The Ehlers-Danlos Society is keen to help the setup of an EDS support group in South Africa. As the international umbrella organisation we are committed to making sure geography doesn’t determine your quality of life. Utilising our experience and networks we can help willing and able advocates to set up a registered charity so that patients in South Africa have somewhere to turn for advice and support. Please contact Lara Bloom directly if you are interested at [email protected] You can also contact Rare Diseases South Africa, led by Kelly du Plessis and ask if an EDS support group was ever set up. https://www.rarediseases.co.za/about Hope that is helpful Natasjha - but please send an email to PatchSA if you need further assistance, and we can try to help
Children's palliative care welcomed with open arms
It’s a no brainer