Second Annual All4Adam Fundraiser Coming Soon

On May 18, the Anderson family will hold a fundraiser, the Second Annual All4Adam, at the VFW to raise awarenes of, and raise money for research of, MECP2 Duplication Syndrome.

MECP2 Duplication Syndrome is a rare genetic condition first discovered in 2005. Peter and Elin Anderson of North Andover learned their son Adam had this condition when he was 3.

With MECP2 Duplication Syndrome, the patient -- mostly found in boys -- has an area of the X chromosome, including the MECP2 gene, erroneously duplicated.

Symptoms of MECP2 Duplication Syndrome include "infantile hypotonia, mild dysmorphic features, developmental delay, absent to minimal speech, recurrent infections, progressive spasticity especially of the lower limbs, ataxia, autistic features and seizures," according to the Rhett Syndrome Research Trust.

MECP2 Duplication Syndrome is not to be confused with Rhett Syndrome itself, however, in which the MECP2 gene is mutated or deleted.

In February 2012, the 401Project (www.401project.com) was launched by more than 200 families from across the globe united by MECP2 Duplication.

And on Saturday, May 18, from 7 p.m. to 12 a.m., the Andersons will host the "All4Adam" fundraiser at the VFW Post 2104, 32 Park St.

All 4 Adam will feature live entertainment, raffles, auctions, refreshments and more. Tickets are $25 and can be purchased by emailing all4adam2012@gmail.com. Tickets will also be available at the door.

Money will go to the 401Project.