![]() |
| Here is some information on her condition Cockayne syndrome (also called Weber-Cockayne syndrome, or Neill-Dingwall Syndrome) is a rare autosomal recessive[1] congenital disorder characterized by growth failure, impaired development of the nervous system, abnormal sensitivity to sunlight (photosensitivity), and premature aging.[2]:575 Hearing loss and eye abnormalities (pigmentary retinopathy) are other common features, but problems with any or all of the internal organs are possible. It is associated with a group of disorders called leukodystrophies. The underlying disorder is a defect in a DNA repair mechanism.[3 One online support group for this condition can be found at http://www.amyandfriends.org/index.htmlhttp://www.amyandfriends.org/index.html Julia is a beautiful little girl, and if she has to pass early, it should not be in the dark confines of a crib, alone and with no one to care whether she lives or dies. Adopting Julia would be a true leap of faith, and a gift to her, just as it was for Chrissie Patterson. My prayers for this little girl!! |
![]() |
| Julia is another sweet little girl stuck in a "laying room". She has sandy brown hair and big brown eyes, and so longs to have a life outside the 4 walls of this crib. Her medical records indicate CP, strabismus, and something called Cockayne Syndrome. CS is a premature ageing disorder that leads to a shortened life expectancy. There are varying degrees of this syndrome and there are types I, II and III. |
Please pray!!!!


No comments:
Post a Comment