Help Levi Through the next few months of Severe Hemophilia A
The Coulsons have just found out their little boy Levi has Severe Hemophilia A. Lets help them through this tough few weeks.
Otago
Levi Was Diagnosed with Hemophilia A on thursday 12th November.This is a lifelong disorder and will need continual treatment.
Hemophilia A. <1% of FVIII in the blood. People with severe hemophilia A experience bleeding following an injury and may have frequent spontaneous bleeding episodes, often into their joints and muscles.
Sam and Dave are off to Christchurch with Levi this week to have a port, typically a Port-A-Cath, a small device that is surgically implanted under the skin, usually in the upper chest above the heart. This is to receive the FVIII without trying to find a vein in a baby (no easy task)
We would just love to help them out anyway we can over the coming few months while they learn all they can to help Levi.
Meron Blakey's involvement (page creator)
They are Great friends of ours and we just want to make the next few months easier for them while they learn how to look after Levi without worrying about how to pay the rent, bills and childcare.
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We Thank You all 20 November 2015
If I could express just how blown away by the support and friendship that has been shown over the last few days i can not express the Gratitude that Sam and Dave are feeling right now! They are just beyond thankful.
I know in time they will thank every single one of you personally but for now….." thank you all so so much, with all our love Sam and Dave "
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