Child Growth Foundation

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Child Growth Foundation Making a difference wherever growth is a concern.

πŸƒβ€β™€οΈπŸƒβ€β™‚οΈ Good luck to our fantastic Royal Parks Half Marathon runners taking on the challenge tomorrow! πŸ’™πŸ’›We are so grat...
10/10/2026

πŸƒβ€β™€οΈπŸƒβ€β™‚οΈ Good luck to our fantastic Royal Parks Half Marathon runners taking on the challenge tomorrow! πŸ’™πŸ’›

We are so grateful to Iona, Kristen, Alex, Peter and Joshua for running in support of the Child Growth Foundation. Your dedication, training and fundraising efforts mean so much to our community.

If you'd like to support our amazing runners, there's still time to donate:

πŸ’™ Iona: https://www.justgiving.com/page/iona-stretton-3
πŸ’™ Kristen: https://www.justgiving.com/page/krissy-yusuf-3
πŸ’™ Alex: https://www.justgiving.com/page/alexander-wright-2
πŸ’™ Peter: https://www.justgiving.com/page/peter-morris-25519
πŸ’™ Joshua: https://www.justgiving.com/page/matilda-flain-1

Thank you to each and every one of you for helping us raise awareness and vital funds for the Child Growth Foundation. We'll be cheering you on every step of the way! πŸŽ‰πŸ‘

πŸ’™πŸ’›πŸ…

Spaces still available to join the CGF community of parents affected by undergrowth conditions such as Silver Russell sy...
06/10/2026

Spaces still available to join the CGF community of parents affected by undergrowth conditions such as Silver Russell syndrome , SHOX, GHD, IUGR/SGA, Precocious Puberty, PIGF1 deficiency, Hypopituitarism for an information based webinar with Behaviour Consultant, Helen Crosby.

Helen will deliver a presentation on the subject 'supporting your child's emotional well-being' with an opportunity to ask questions and connect with other families.

This event is open to CGF members who have full paying membership.

Register now by completing this form-

https://forms.cloud.microsoft/e/Gw1tc6fYeT

Please note spaces are limited to a maximum of 12 attendees.

If you have any questions about this event, please email us- [email protected]

04/10/2026

πŸ’™πŸ… A huge thank you to Sophie for taking on the AJ Bell Great Scottish Run Half Marathon today in support of the Child Growth Foundation!

We are so incredibly grateful for your dedication, commitment, and fundraising efforts. Every mile you've run and every pound you've raised will help us continue supporting children, young people, and families affected by growth conditions.

Sophie, thank you for being part of and for helping to make a difference. We hope you're feeling proud of your amazing achievement today! πŸŽ‰πŸ‘

If you'd like to support Sophie and help her reach her fundraising goal, please visit her fundraising page here: https://www.justgiving.com/page/sophie-parry-17

πŸ’™πŸ’›

October is Pituitary Awareness month so we’re shining a light on the tiny gland that has a huge role to play in our heal...
01/10/2026

October is Pituitary Awareness month so we’re shining a light on the tiny gland that has a huge role to play in our health.

The pituitary gland is a small gland at the base of the brain that helps control important functions including growth, metabolism, stress responses and water balance.

Our website contains lots of information www.childgrowthfoundation.org and for those with multiple pituitary hormone deficiency, our dedicated webpage can signpost you to further peer support and the opportunity to read personal stories from other families https://childgrowthfoundation.org/conditions/hypopituitarism/

πŸ“ž Need Support? We're Here for You.The Child Growth Foundation offers a free nurse-led support line for families affecte...
29/09/2026

πŸ“ž Need Support? We're Here for You.

The Child Growth Foundation offers a free nurse-led support line for families affected by growth conditions. Whether you have questions, concerns about your child's growth, or simply need someone to talk to, our team is here to help.

We also have bookable support call slots available, allowing you to arrange a convenient time to speak with a member of our support team.

πŸ‘‰ Book a support call here:
[email protected]/?ismsaljsauthenabled" rel="ugc" target="_blank">https://bookings.cloud.microsoft/book/[email protected]/?ismsaljsauthenabled

πŸ’™ If you're worried about your child's growth, trust your instincts and reach out for support.

Spaces still available to join the CGF community of parents affected by an overgrowth condition such as Sotos syndrome, ...
28/09/2026

Spaces still available to join the CGF community of parents affected by an overgrowth condition such as Sotos syndrome, SKS, TBRS or Weavers syndrome, for an information based webinar with Behaviour Consultant, Helen Crosby.

Helen will deliver a presentation on the subject 'Behaviours that Challenge' with an opportunity to ask questions and connect with other families.

This event is open to CGF members who have full paying membership.

Register now by completing this form-

https://forms.cloud.microsoft/e/CX2Qa2Qm1m

If you have any questions about this event, please contact [email protected]

πŸ’œ I'm proud to be running in support of the Child Growth Foundation (CGF)! πŸƒβ€β™€οΈThe Child Growth Foundation has been an i...
25/09/2026

πŸ’œ I'm proud to be running in support of the Child Growth Foundation (CGF)! πŸƒβ€β™€οΈ

The Child Growth Foundation has been an incredible source of support for our family as we've navigated our son's journey with Growth Hormone Deficiency.

Since starting treatment, he has done amazingly well. His growth, health and confidence have improved so much, and we're incredibly proud of the bravery, resilience and positivity he has shown every step of the way.

As members of CGF, we've benefited from their specialist nurse-led support service, peer support groups and trusted information resources. Having somewhere to turn for advice and understanding, while connecting with other families facing similar challenges, has made a real difference to us.

That's why I'm delighted to be raising funds and awareness for this fantastic charity. Their work helps ensure that families affected by growth conditions never have to face their journey alone.

πŸ’œ If you'd like to support me and help CGF continue its vital work, please consider donating via my JustGiving page:

πŸ‘‰ https://www.justgiving.com/page/krissy-yusuf-3

Every donation, no matter the size, will help the Child Growth Foundation support more children and families affected by growth conditions.

Thank you for your support, and please share this post to help raise awareness of growth conditions and the support available to families. πŸ’œ

In few weeks' time, I'll be running the Royal Parks Half Marathon for the Child Growth Foundation... and I'm slightly te...
23/09/2026

In few weeks' time, I'll be running the Royal Parks Half Marathon for the Child Growth Foundation... and I'm slightly terrified! πŸƒβ€β™€οΈπŸ’œ

My husband, James, has always said that the motto of our family is "Ambition outstrips ability." I've always disagreed, but in this case, he might actually be right.

When the Child Growth Foundation asked if I'd run the Royal Parks Half Marathon, my thought process was simple:

βœ… I can run.
βœ… The charity is amazing.
βœ… What could possibly go wrong?

Since saying yes, I've remembered a few important details:

β€’ I haven't run properly in over seven years.
β€’ I've had two children since then.
β€’ A half marathon is 21km, not 10km. πŸ€¦β€β™€οΈ

So here I am, training, questioning my life choices, and counting down the days!

But there is a much bigger reason why I'm doing this.

When our daughter Eva was two years old, after numerous tests, hospital appointments and even an overnight stay at GOSH, she was diagnosed with growth hormone deficiency. At the time, James and I decided not to share her diagnosis widely. We never wanted people to see limitations before they saw her.

We wanted people to see what we see every day: a confident, happy, determined little girl.

Nearly four years later, Eva continues to thrive with daily growth hormone treatment, and we've realised that her diagnosis does not define her. More importantly, we never want her to feel that it is something that needs to be hidden.

That's why I'm sharing our story today.

The Child Growth Foundation provides vital support, information and advocacy for children and families affected by growth conditions. Until Eva's diagnosis, we had never heard of the charity. Now we know just how important their work is.

So, in four weeks' time, I'll be taking on 21km to help raise awareness and support their incredible work.

πŸ’œ If you'd like to support me and help the Child Growth Foundation continue its vital work, please consider making a donation via my JustGiving page:

πŸ‘‰ https://www.justgiving.com/page/iona-stretton-3

Every donation, no matter the size, will help the Child Growth Foundation support more children and families affected by growth conditions.

Please also help by liking, sharing and commenting on this post to spread awareness.

Thank you for your support. πŸ’œ

Have you been inspired by Child Growth Awareness Day and would like to share your journey to help others?Your story coul...
22/09/2026

Have you been inspired by Child Growth Awareness Day and would like to share your journey to help others?

Your story could make a real difference to families who are facing similar challenges. Whether it's your child's growth journey, diagnosis, treatment, or the support you've received along the way, we'd love to hear from you.

We are looking for personal stories to feature in our newsletter and on our website to help raise awareness and support others in our community.

πŸ“§ Please get in touch at [email protected]

Together, we can help more families feel informed, supported, and less alone.

The CGF website has a huge variety of information and support resources on growth including our 𝘊𝘩π˜ͺ𝘭π˜₯𝘩𝘰𝘰π˜₯ 𝘎𝘳𝘰𝘸𝘡𝘩: 𝘈 π˜—π˜’π˜³π˜¦...
20/09/2026

The CGF website has a huge variety of information and support resources on growth including our 𝘊𝘩π˜ͺ𝘭π˜₯𝘩𝘰𝘰π˜₯ 𝘎𝘳𝘰𝘸𝘡𝘩: 𝘈 π˜—π˜’π˜³π˜¦π˜―π˜΅ 𝘊𝘒𝘳𝘦𝘳 𝘎𝘢π˜ͺπ˜₯𝘦 available at: https://childgrowthfoundation.org/wp-content/uploads/2025/10/Childhood-growth-A-parent-carer-guide-DIGITAL.pdfand and our π˜—π˜’π˜³π˜¦π˜―π˜΅ 𝘊𝘒𝘳𝘦𝘳 𝘎𝘢π˜ͺπ˜₯𝘦 𝘡𝘰 𝘎𝘳𝘰𝘸𝘡𝘩 𝘊𝘰𝘯𝘀𝘦𝘳𝘯𝘴 available at:https://childgrowthfoundation.org/wp-content/uploads/2024/07/A-parent-carer-guide-to-concerns-about-a-childs-growth-July-2024.pdf

Please see the website for all our resources including for those already diagnosed with a growth condition www.childgrowthfoundation.org

Address

C/o Kinnair Associates Limited, Aston House Redburn Road
Newcastle Upon Tyne
NE51NB

Opening Hours

Monday 9:30am - 4pm
Tuesday 9:30am - 4pm
Wednesday 9:30am - 4pm
Thursday 9:30am - 4pm
Friday 9:30am - 4pm

Telephone

+442087982139

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