My daughter is 19 and was born with fibular hemimelia resulting in amputation of her left foot at 11 months and subsequent 7 other surgerys to the most resent this year to shorten her residual limb for better fitting prosthesis. I didn't know what to do or where to go 19 years ago, but throughout this journey, I've learned a few things. You, too, may have some lessons to share that will help me and others who have watched their children adapt to this diffence. I hope to hear from you.
Started by Yaritza on 02/02/2009 in Mom's Of Children With Limb Differences.
Last update on 02/02/2009 by Yaritza