My Nonprofit Reviews

My son was diagnosed with unilateral ONH when he was 3 months old. I was so confused about this diagnosis and what we would have in store for him in the future. I felt so alone learning how rare this condition is and I broke down in tears often thinking this was all my fault somehow. Becoming a member of the MAGIC Foundation FB group page has been life changing! I not only have received proper information to make sure my son gets all the attention and appointments that he needs, but I no longer feel alone. I know I stand tall and strong with a big group of other brave warriors who also struggle with this condition or raise a kiddo with it. My experience with my first born has been so much easier knowing I have support and a group that I can always reach out to for advice and information. This group is HEAVEN SENT! Thank you from the bottom of my heart! 💜