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Concerns about your child's growth

This section of our website is dedicated to sharing information about childhood growth, support and information for those concerned their child is too small / is not growing, those who are concerned their child is too tall / is growing too quickly, and details of who to approach with your concerns and resources to help you.

Our Support Line

Need to speak to someone? Our nurse led Support Line is available to anyone concerned about their child’s growth or if they have a diagnosed growth condition. We are here to listen and support you. Call us on 020 8995 0257.

Our staff work on a part time basis and if we are not able to answer your call please leave a message and we will get back to you as soon as possible. Alternatively please email us at [email protected] to arrange a time to chat or complete our Support Line contact form.

By contacting the Child Growth Foundation Support Line you are providing consent for us to collect, process and store your data to provide you with the information or services you are contacting us about. Read our Support Line Privacy Statement for full details.

Visiting our site from outside the UK?

If you are living outside of the UK and have concerns about your child’s growth or a diagnosed growth condition, the information the CGF provides may help you in the conversations you have with your healthcare providers. However, healthcare systems across the world differ and it may be helpful to find local organisations and the appropriate medical teams who can support you to access the right care for your child.

The CGF are members of the International Coalition of Organisations Supporting Endocrine Patients (ICOSEP). ICOSEP are a group of patient support organisations and medical societies from across the globe, a list of these and their contact details can be found here.

We are also involved in the Overgrowth Syndromes Alliance, an international association of patient advocacy groups representing overgrowth-intellectual disability (OGID) disorders, which you can find out more about here.

If you are living in the USA, you can visit The MAGIC Foundation’s website or get in touch with their team.