Siennas Development

Hi, my name is Janey Bain. Norman Bain and my daughter Sienna Bain is extremely developmentally delayed. She is almost 2 and not crawling, walking, talking, standing by herself, eating solid foods, feeding herself, and many more.

We currently have her in physical therapy, occupational therapy, developmental therapy, and are soon to start speech therapy. We also have appointments with her pediatrician and a developmental pediatrician at Riley’s children’s hospital on November 16th.

We haven’t gotten many answers yet, we’ve been told that it is possibly a genetic issue that causes muscle weakness like turners syndrome, muscular dystrophy, or cerebral palsy and we also suspect autism. Im hoping we will get some real answers soon and a medical diagnosis. We believe that she will be able to walk and get caught up but we are just not sure.

We haven’t asked for help in the past but since my husband has been out of work since December of 2020 due to a lung infection that almost killed him we’ve been solely relying on my income and have fallen behind.

We would be so grateful if you could donate to help cover the costs of her medical care, travel costs, sensory toys costs, and just the overall living costs for our family because we are really struggling to keep a roof over our heads. Having a child with special needs gets expensive. 

Thank you so much for the love and continued support, even if you can’t donate we are still so grateful for having all of you in our lives.