The MAGIC Foundation
Rating: 4.98 stars 50 50 reviews
6645 W. North Avenue Oak Park IL 60302 USA
The MAGIC Foundation Mission: The MAGIC Foundation is a national non-profit organization created to provide support services for the families of children afflicted with a wide variety of chronic and/or critical disorders, syndromes and diseases that affect a child's growth. Since its inception the Foundation has grown to include support services for adults who were also impacted by these disorders. The MAGIC Foundation Vision: Our commitment and vision is, to reduce the emotional and physical trauma caused by growth disorders, resulting in healthier, happier children and consequently, adults. Our Motto: Children have a short time to grow and a lifetime to live with the results!
Children affected with Endocrine Disorder that affect physical growth, and adults with Endocrine Disorders.
Geographic areas served:
Support of parents & affected adults
An Annual Educational Convention, On-line social media via Facebook, Twitter & Instagram, Physician Referrals, Insurance Appeals Assistance, Medical Brochures for Affected Disorders.
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Reviews for The MAGIC Foundation
I remember when I found MAGIC: it was November 2002 in the middle of the night-the only opportunity I had time to research online. Back then, Internet resources weren't what they are today. The middle of the night was my only opportunity to research because during the day I was constantly feeding my daughter or taking her to numerous doctor appointments.
The night I found the MAGIC website and read about a child with RSS changed our lives.
Since then, MAGIC is our #1 priority for charitable donations. I hope every parent who is struggling with a child who has a rare growth disorder finds this organization.
We tell people "that is when the clouds parted and the sun came out" for our family. The resources MAGIC has provided us are amazing: medical, emotional, and financial (help with insurance issues) not to mention the life-long relationships!
Thank you MAGIC!
I found the Magic Foundation after it was found that my daughter had a rare form of dwarfism called Meier-Gorlin Syndrome. We attended the annual convention that Magic holds in Lombard, IL the year of our diagnosis. The group welcomed us with open arms. My daughter was 9 years old at the time and was getting to the age where other kids started noticing the difference in her size. Spending the weekend with other kids that had Primordial Dwarfism was great for her. It was a place she felt safe and unjudged. Magic has also been an outstanding resource for me as well. I have received helpful information on insurance matters, education on Growth Hormone use, and many other useful tips and tricks. It is amazing to have a place to turn that truly understands our families struggles. We LOVE the Magic foundation and all it has done for our family.