Hello! My name is Natalie. I’m 20 years old and my daughter, Alitzel, will be 3yrs old in a couple of days. My husband, Alitzel’s father, is 20, and is in the Marine Corps. We had Alitzel when I was 16 years old. She was born with Arthrogryposis in both her upper and lower extremities. Alitzel has limited mobility as this condition affects her shoulders, elbows, wrist, fingers, knees and she also has Bilateral Clubfoot in both of her feet. She has already had surgery, castings, and goes through extensive therapies. We would so appreciate donations so we can go back out to the Paley Institute in Florida to get Alitzel seen by the AMC specialist, Dr. Feldman. With his treatment, our hope is to get her walking and make improvements on her ability to use her upper extremities. These Arthrogryposis specialists treat kids like Alitzel everyday and their specialized understanding makes a huge difference. We want her in the best care so that she has the best chance to become . Not many medical professionals are familiar with Arthrogryposis. She hasn’t been back to Paley since she was a baby. They recommend we come back when she turns 3. We could use all the help we can get for her medical bills, daily uber/lyft, food expenses, etc. while we are in Florida. Thank you in advance for your support. Anything over the asked amount will allow me, her mother take time off work for a longer stay, intense therapy, more medical treatments. We will keep sharing her journey in Florida too! Here is Alitzel’s facebook page so you can follow her journey: Alitzel’s AMC Journey
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