Lachlan was born in 2010. During our pregnancy we were given a 1:2 risk of trisomy 21 ( Down's Syndrome) or trisomy 18 ( Edward's Syndrome). We never confirmed this risk and it was only after birth we found out that Lachlan had trisomy 18. Lachlan continues to defy the odds. This is his journey
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Wednesday, 18 July 2012
Cardiology
Lachlan had a cardilogy check up today. His VSD is still there. It is pretty loud you can hear it easily. Thats a good thing because it means the hole is small. It hasn't changed in size over the last year approximately 2mm. The good news is that his heart is the right size and there is normal pressure in all chambers (no pulmonary hypertension) His cardiologist is happy to review in 2 years!! He was also very happy to see how happy Lachlan was.
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