Messages of Support

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Welcome to the "Walking with Giants Foundation" messages of support page. Here you can leave message(s) of support or feedback about our site. Please note we reserve the right to delete/amend any entries that may be deemed offensive or unsuitable, as we would like this area of the " Walking With Giants Foundation" site to represent a "Family Friendly" environment.


Justine Tuesday, 12 July 2011 16:02 | Melbourne, australia
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Just been introduced to Charlotte in the tiniest girl in the world special. Overcome by how beautiful she and her family is. They posses the kind of strength and love most people only pray for. I hope she, and you all, continue to grow both physically and emotionally.
Would love if you could update the website to tell us how she's doing now.
Charlotte you have fans all over the world.
Love and thanks

Toni Saturday, 18 June 2011 16:06 | Tamworth, England
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After watching the 'Tiniest Girl in the world' one night, I decided to do my charity English assessment presentation on the WWGF - and out of the 25(ish) different charity presentations that our class did, when we voted on the best, the WWGF tied first with Water Aid! Hope Charlotte et al. are getting on o.k - Toni

Lacy Monday, 23 May 2011 17:10
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Hello Charlotte. You are so beautiful!! You are an inspiration to me. You are kept in my prayers daily, and I hope your life is full of joy.
Love, lacy

Joanna Fuller Wednesday, 18 May 2011 19:05 | Massachusetts, USA
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Stumbled upon "The Tiniest Girl in the World" on the TLC channel. Am so glad I did. Between the "Tiniest Girl" and your website, I am no longer ignorant about the experiences of these sweet children, their loving families, and the inspiration they provide to all of us. Thank you.

Meghan Monday, 21 March 2011 02:56
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Thank you for allowing me access to information about Kenadie and Charlotte. After seeing their television specials, I have often wondered how they are getting on. They are amazing little girls. I wish them the best.


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Entries in guestbook

Our Aims

Hold a yearly international event to bring families together to celebrate life and allow them to meet experts from around the world.

Provide trips out and events during the annual convention and also breaks for families needing respite.

Source out and financially assist with specialist equipment, toys, custom made clothes, costumes and furniture.

Create opportunities to allow individuals affected by Primordial Dwarfism to reach their full potential in life.

Facilitate research into the causes of Primordial Dwarfism and the complex life threatening medical issues faced by individuals affected by Primordial Dwarfism.

Raise awareness amongst the general public, medical professions, support services and other interested parties.

Facilitate family support meetings and connections to highlight life issues, concerns and remove the isolation families feels.

Identify those with Primordial Dwarfism and bring them into contact with other individuals, families and specialists.