For the people asking me what our situation is..here it is. Skylar hasn’t been able to fully walk on her bare feet. We have been battling this issue for 2 years now maybe even longer. We have been through 3 doctors and finally saw one at OU Children’s who we are with now. This doctor happens to be a surgeon and told us this. Skylar’s muscles and tendons are cable tight and is causing her an immense amount of pain each day. I believe it cause I stay up all day and night rubbing her legs or icing them. She has been through braces, special shoes and a little bit of PT. Nothing has helped. So here we are today and she is wearing two casts to basically hold her feet in a flat position. Her pain levels are constant and it is a true struggle everyday. Her muscles/tendons have now affected her bowels to where I HAVE to give her a suppository every now and then to help her bowels move. -Update 11/19/2024: Skylar’s brain scan didn’t go as expected and her left side of her brain is damaged. We are still moving forward and praying each day. She will be doing long term PT, OT, speech and whatever program she needs to help her along the way🤍 We truly appreciate all the calls, texts, messages and gifts from everyone💕 For the people that have asked about what they could get for her..I really don’t like asking for handouts and I know I am being stubborn. We really appreciate everyone so much. We will think about what she needs though…mostly prayers 🤍🙏🏻🧎🏻‍♀️‍➡️