Welcome to the website of the Child Growth Foundation (CGF), the UK’s leading charity focusing on children’s growth and endocrine issues
2014 CGF Christmas Cards available via www.justgiving.com/cgfchristmascards
On this site, you can find helpful information whether you are a parent whose child has a suspected or diagnosed growth problem, an adult or family member of someone with a growth or endocrine disorder, or a medical professional.
We aim to:
- Support and encourage all children or adults with growth disorders, and their families, in every way we can
- Promote and fund research into the causes and cure of growth and endocrine disorders, and publish the results
- Educate the public, especially medical professionals, in the challenges those with growth and endocrine disorders are likely to face
- Encourage medical professionals at all levels to monitor growth and development. We provide training and equipment to ensure that all growth measuring is undertaken accurately and appropriately
If you would like more information on the activities of the Foundation, or have any concerns and would like some advice please contact us.
1st Achondroplasia Symposium
As Chair of the Child Growth Foundation, I would like to join with the Chairs of The Dwarf Sports Association, The Little People of Ireland, Little People UK, The Restricted Growth Association and Short Stature Scotland in announcing an important agreement that our organisations reached unanimously at the 1st Achondroplasia Symposium held in Newcastle on the 20th and 21st of September.
We have agreed to work with Dr. Michael Wright of Newcastle Hospitals and Dr. Melita Irving of the Evelina London Children’s Hospital to support a group of clinicians who wish to improve the quality of healthcare services available to all people of restricted growth in the UK and Ireland. We will work collectively with this group of clinicians and each of our organisations will have a representative on the group. The first piece of work will focus on the needs of adults with achondroplasia but the information and services developed will be of relevance to all of our members.
We will work together to produce information endorsed by all of our organisations which will be made available on a single website.This will provide a single point of access to our organisations and will ensure that there is clarity about what each of our organisations has to offer.
We will work together to the benefit of those to whom we provide services and those who need our support but have not yet found us. We will be supportive of each organisation and will seek to collaborate wherever possible. We will refrain from inappropriate criticism of individuals and of other organisations.
We will meet on a regular basis to discuss areas for future collaboration.
We encourage all of our members to recognise the importance of this initiative and to work with us to ensure its success.
The Child Growth Foundation is pleased to announce that it will now be offering advice and support for families and individuals with Weaver Syndrome.
'New triggers discovered in formation of pituitary tumours in children'
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Looking for Growth Equipment and Charts?
Visit our shop for all of your growth monitoring equipment requirements.
If you are looking for a good summer read, combined with helping a good cause, take a look at 'My Bermuda Namesakes'
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