Graeme's LPA Membership & Expenses

Graeme Theodore was born on January 8, 2015.   We were super excited to meet our baby boy.  When he was born, the doctors noticed that his limbs seemed short and his head was large.  They performed an ultrasound for his head and did x-rays of his limbs.  We were referred to a geneticist, who did more x-rays and diagnosed Graeme with achondroplasia, the most common form of dwarfism, when he was 7 weeks old.  This means a few more doctor visits and health concerns, but overall Graeme will be completely normal, just small.  We're trying to raise some money to pay for his lifetime membership to LPA (Little People of America) and for some unexpected medical bills for his x-rays and CT scan that weren't covered by our insurance.  Any help (including prayers) is greatly appreciated!

To read more about Graeme, visit our blog:
The Little Things in Life

To learn more about dwarfism, LPA, and the benefits of membership (such as access to the medical advisory board), visit Little People of America