Hi, my name is Kristen. My son Daniel is 11 months old and was born with unilateral PFFD in his right leg. I have never posted to this forum but I have found it to be so invaluable and look at it on a regular basis. This week I put together a blog for Daniel so that friends and family and other interested people can track Daniel's progress. I thought it would be worthwhile sharing it with the members of this blog as well so please feel free to take a look and forward it on to anyone else who may be interested.
Comments
What a great blog site!
Kristen,
My name is Shawna, I have a 2 month old son with PFFD of the right femur as well. I responded to your blog site, I would love to learn how your experience goes with the prosthesis fitting, Daniel learning to walk and the appointment with the Dr. in the USA (I am assuming from your blog site that you are talking about Dr. Paley out of Baltimore, MD).
Best of luck to you and your family with the upcoming prosthesis fittings, and with baby Daniel.
Shawna