Hypochondroplasia kid: The Little Couple

What is hypochondroplasia?

Hypochondroplasia is a form of short-limbed dwarfism. This condition affects the conversion of cartilage into bone (a process called ossification), particularly in the long bones of the arms and legs. Hypochondroplasia is similar to another skeletal disorder called achondroplasia, but the features tend to be milder.

All people with hypochondroplasia have short stature. The adult height for men with this condition ranges from 138 centimeters to 165 centimeters (4 feet, 6 inches to 5 feet, 5 inches). The height range for adult women is 128 centimeters to 151 centimeters (4 feet, 2 inches to 4 feet, 11 inches).

People with hypochondroplasia have short arms and legs and broad, short hands and feet. Other characteristic features include a large head, limited range of motion at the elbows, a sway of the lower back (lordosis), and bowed legs. These signs are generally less pronounced than those seen with achondroplasia and may not be noticeable until early or middle childhood. Some studies have reported that a small percentage of people with hypochondroplasia have mild to moderate intellectual disability or learning problems, but other studies have produced conflicting results.

Wednesday, June 15, 2011

The Little Couple

I have come to love the show Little Couple. I am so proud that they are a married, successful, happy, adjusted couple. So me and Coleman watched it together for the first time last night and I tried to see if he understood that they were little people. I said to him "Some people are littler than others...do you have any questions about this show?" He said "well, I'm big like Carter, I'm not little." Well maybe I'll bring this subject up next year but I am glad though that he didn't notice they were different. I'm so proud of my kids. They have confidence and pride in themselves and yet compassion and equality for others I wish for everyone.
So this conversation will happen but he is not ready yet.

2 comments:

Smilen ChampJuly 4, 2011 at 10:19 PM
Hi
My name is Jenna and I came across your site. I have a rare bone disease called Chondroplasia Punctata, and I am a Little person. I love it when people sign my guestbook. Coleman is an inspirational hero. www.miraclechamp.webs.com
ReplyDelete
Replies
A pathologically information hungry motherJuly 10, 2011 at 11:44 AM
Hi Kirsten,
I have been to your blog a few times. My new baby is 6 weeks old and she has been diagnosed with hypo. I am going to start a blog with information and about our family. Pls let me know if it OK to list your page as a blog I read?
ReplyDelete
Replies