Today, we had our specialist appointment at Children's Hospital with Dr. Peter Waters. He specializes in pediatric orthopedic surgery and handles many, many cases like ours. The visit was reassuring and we are very glad to have him on our team come October.Assuming things continue along as planned, we will not see him again until Ella is between 4-6 weeks old. At that point, he'll see what she is actually born with and will help make a plan going forward. Their focus will be on goals of either pinching or pushing with that hand. He agreed that it is huge that she has full wrist function.
Some interesting facts we learned today:
- Ella has what they call a trans-hand amputation, which is the 2nd most common kind of limb difference (second only to when the arm stop growing just past the elbow.)
- Limb differences occur in anywhere between 1 in 30,000 and 1 in 300,000, depending on the type of limb difference.
- Her arms will continue to grow proportionally, but they will both continue to grow. So, whatever the proportional difference is between her right and left arms at birth will likely continue into adulthood.
- Prosthetics are not where they need to be (cosmetically and functionally), especially for something like this, so most kids don't use them.
- The Department of Defense is the biggest leader in research for hand transplants and other missing hand solutions.
- Finding a good solution to missing a hand ranks in the top five for research goals.- There is absolutely nothing genetic about limb differences like these.
And finally...
- National studies have shown that kids with a limb difference actually grow up to be happier and more well-adjusted than so-called "normal kids"
That's it for now... we have a lull of a couple of weeks before our next doctor's appointment!

