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Little Miss Hannah Foundation

Support for Families of Children Diagnosed with Rare, Life-Limiting, or Complex Medically Conditions. Childhood Rare Disease Advocacy.

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Personal Story

May 9, 2012 by Carrie Ostrea

Food Allergies: A Common Problem with an Uncommon Level of Severity

Severe Food Allergies

With the prevalence of food allergies today, you would probably not consider a child with food allergies to have a rare disease.   With the diagnosis of food allergies, as long as the child does not ingest the food that they are allergic too, they will be fine.  This doesn’t seem like anything to worry about…

Filed Under: Blog Tagged With: Personal Story

April 16, 2012 by Carrie Ostrea

Shades of Grey

By the time Texas residents Nicole and Bill Morris celebrated the birth of their fourth son, they were no strangers to childhood illnesses. Their careers – Bill as a pediatric nurse and Nicole as a special education teacher – taught them about health issues that affect kids. Things hit home, however, when at 11 days…

Filed Under: Blog Tagged With: Personal Story

April 6, 2012 by Carrie Ostrea

Aqua Therapy

My son, Bertrand‘s first aqua therapy session was a success! Not only did he have fun and do well in the water, the results were carried forward on land the rest of the day. Aqua therapy will definitely become a part of his therapy regimen. Aqua therapy is also known as Aquatic Therapy, Pool Therapy,…

Filed Under: Blog Tagged With: Personal Story

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10624 S. Eastern Avenue, Suite A-847
Henderson, NV 89052
Phone: (702) 608-2488
Fax: (702) 541-9957

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Little Miss Hannah Foundation is a 501(c)(3) tax-exempt nonprofit corporation, EIN# 45-3993921