Why we started this blog

Our daughter (we will call her Sydney) was born with Fibular Hemimelia, a club foot, and 4 toes in July, 2011. We've been staying on top of posting about her journey and wanted to create a new blog specifically for this to help anyone who might be on a similar journey.

We hope this is helpful and informative. We are happy to answer any questions you may have so please reach out if we can be of any help. Good luck on your journey!!

Our next post will be a summary of the journey up to this point which has led us to the decision to have a Syme's amputaiton performed on our daughter in June of 2015. Then all of our following posts will be the chronological history of her journey up until now.