About Leah
Our daughter Leah was born with a genetic condition called Achondroplasia (dwarfism). I decided to do this blog to share Leah’s incredible energy and zest for life. Ultimately our goal is to make people more aware of this condition and other physical and mental challenges that affect so many people in the world today, and to have people realize that we are all equal and special in different ways.
God Bless
The Kay Family……………
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Hi there, my name is Jaime and I am mom to 3 year old Caitlyn, who also has Achondroplasia. I can across your blog from another LP mom’s page. I would like to add a link to your blog from my page if that’s alright with you. Leah is absolutely adorable. I look forward to hearing from you and chatting some!
hi…my daughter was born also with achondroplasia. it’s been a hard road for the last 15 months (even though some may wonder why)and was only when a close beautiful friend of mine told me about your website and i read about your family, am I now able to find strength to face the world. i thank you for sharing your life, leah and your family. your insight into life with a child with achondroplasia has helped me immensely. leah is soooo beautiful and you truely are a wonderful family. i love her little moves video clip. thank you again for having the strength and courage, that has now passed on to me and no doubt, many other families. thank you and God Bless you all. x
I am new to the achondroplasia community. my daughter, Abby is 5 months old today and she is the only member of my family that has achondroplasia. I have 2 older sons. Your daughter is so beautiful and her looks are very similar to my Abby’s as I am sure they are to many other achondroplasia children. I would love to be in contact with other moms and to see what is in store for us. So far the doctors have said she will not need a shunt and we thank God for that. Thanks for having a site out here for all us newbies. God bless
You have a very beautiful daughter!
Hi Charmaine
It was great meeting you and your husband , we will certainly be there at the next meeting. We are together and a happy family , give Leah a big hug from Martinique, Enjoy your day Nicky and Mark
Hi, my story is quite similar to yours. I too have two older daughters and our third daughter(also hoping for a boy), Valentina was diagnosed with achondroplasia when I was 7 months pregnant. I also live in South Africa (Johannesburg) and would love to meet with you. I decided to join the UK support group and was told about your blog page. Your daughters are stunning! Your stories are really lovely, it is heart warming to know that someone else is experiencing the same as us. My baby is now 10 months old, and is really gorgeous. Her smile lights up the room, as you said, she really does melt hearts where ever we go. I would love to discuss a few things with you, and meet your lovely family.
What a cutie…you did a great job on this blog…I’m really trying to get ideas from blogs I see that are good…and this is! Come see mine and comment on how I can improve it.
http://theeverittjrfamily.blogspot.com/