Home    Olivia's Story     About MPS Sanfilippo        Contact
 
 

Olivia's Wish - Back HomeAbout MPS Sanfilippo

For as complicated as it is to say, much less spell, Mucopolysaccharidoses Sanfilippo is fairly easy to understand.

When you think of your body as a whole, we take for granted how our body chemistry needs to work in concert with all it's essential parts. If one part is broken, the impact of the broken part is expidential in relationship to your total body chemistry.

Though Olivia is impacted by MPS Sanfilippo, Sanfilippo does not differ much from other MPS disorders. As cells in our body die they are processed and digested by enzymes. Olivia is missing an enzyme essential to processing and digesting these dead cells. Because the dead cells cannot be processed the body stores the cells it would otherwise digest in soft tissue organs and muscles throughout the body. As enough cells are stored the impacted organs begin to slow down, and eventually shut down.

The National MPS Society, Inc.

The Chidlren's Medical Research Foundation

The Sanfilippo Syndrome Medical Research Foundation

The Sanfilippo Children's Research Foundation

Canadian Society for MPS and related diseases

New Zealand Lysosomal Storage Support Group

United Kindom Society for MPS Diseases

Rare Diseases in Children

Family Village :Muchopolysaccharidosis

Duke Pediatric Medical Center (Olivia's home away from home)

 

 
       
© OliviasWish.com
BACK HOME
Site by Consistent Image Web Design