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Stephanie Reece hasn't added a story.
Laynna is my daughter and has been diagnosed with Arthrogryposis. This genetic disorder along with her clubbed feet have enabled her the oppurtunity to walk. This disorder leads to weakness and giving a wasting appearance to the muscles. Due to the lack of fetal movement, the tendons that connect the muscles to the bone are not able to stretch to their normal length and this contributes to lack of joint mobility. It is a rare conginital disorder meaning no muscle development and/or absent muscle. This may also involve other internal abnormalties or central nurveous system conditions. This may lead to the need of multiple surgeries in the future along with more years of physical and occupational thearpy. Laynna has already been through one surgary and 17 months of thearpy. The time has come for our family to begin the process of getting Laynna a power operated wheel chair along with an accessable van. We are asking for the help of family and friends to spread the word so that anyone that has even a dollar or two, to donate that can help us reach our goal to get Laynna her chair and transportation.
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