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Personal Pages

Categories:

See Also:
Sites:

» Alpha1 Antitrypsine Deficiency Open in a new browser window - One man's perspective and journey with A1AD and a list of links and other resources from the internet.
» Amelka's Page Open in a new browser window - Amelka was born in Warsaw, Poland with a complex of congenital anomalies. Photos, history and contact. [English/Polish]
» Ashly's Skeletal Dysplasia Open in a new browser window - A mom describes her daughters disorder which is thought to be a metabolic disease similar to mucopolysachharisdoses. Also links to other related sites.
» Caleb's Courage Open in a new browser window - A baby's fight with MPS I, Hurler Syndrome. Information on the disease and links to other children fighting disease.
» Joy's Page Open in a new browser window - Personal account about a daughter having Opitc Nerve Hypoplasia, Septo-Optic Dysplasia and had either a Congenital stroke or has schizencephaly.
» MCAD Angel Open in a new browser window - Dedicated to raising awareness of the genetic disorder known as MCAD deficiency and the importance of early detection.
» Maddy's Page Open in a new browser window - The story of Madison Wigglesworth who has hurler syndrome. Includes photo album and links to informative sites.
» Mowat-Wilson Open in a new browser window - Discussion site for mowat-wilson syndrome. Includes a links page, photos, a community page and a discussion area.
» Robert Kenneth Picklesimer Open in a new browser window - Born with Jeune Syndrome or Asphyxiating Thoracic Dystrophy in Louisville Kentucky. He underwent corrective surgery in San Antonio Texas, called the Titanium Rib Project.
» Story of Robert Purkis Open in a new browser window - A small boy's health problems, possibly Leigh's Syndrome, and how his parents have helped him improve his quality of life.
» Taryn's World: About Switches Open in a new browser window - Personal page for kids and parents about genetic disorders, especially mannosidosis.
» XXXXY Syndrome Open in a new browser window - Information on this rare chromosomal abnormality.


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Last Updated: 2007-02-09 04:25:45


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