What a fab day it has been today! Shay is 3 years old now and he has enjoyed a full weekend with a birthday party on Saturday. This year Shay knew it was his birthday. He was getting very excited knowing it was very near and kept saying 'Me birthday'. Even though it was his birthday today, Shay still had to have his blood taken. It's a shame this fell on such a special day for him. Saying this when he saw not one but three nurses turn up at the door with helium happy birthday balloons for him, his face said it all. They especially went out of their way for Shay and it really made his day.
Normally Shay has a transfusion every 6 weeks. This time he is a week under and will be having a transfusion this week. It is very disappointing as we thought maybe his blood lines were improving but we will just have to wait and see.
Results:
Hb - 8.3
Platelets - 97
Wbc - 3.21
Neutrophills - 0.47
About Me
- Shay
- London, United Kingdom
- Welcome to Shay's story and thank you for taking the time to find out how Shay is doing. It is a place to share our hopes, sadness and the happy times that our little man has. Shay in April 2008 was diagnosed with Pearson's Syndrome a Mitochondrial disease with no cure. Pearson syndrome is very rare, less than a hundred cases have been reported worldwide. It characteristically present in early infancy with pallor, failure to thrive, pancytopenia and diarrhoea. Additional manifestations often include progressive external ophthalmoplegia, proximal myopathy with weakness, and neurologic disturbances. Multiple organ involvement is quite variable. Most infants die before age 3, often due to unremitting metabolic acidosis, infection, or liver failure. Those few individuals who can be medically supported through infancy may experience a full recovery of marrow and pancreatic function. These children eventually undergo a transformation from Pearson's syndrome to Kearns-Sayre syndrome with the development of ptosis, incoordination, mental retardation and episodic coma. Life as we use to know it I cannot remember. We have to live in hope that a miracle will happen for our son.
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