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 Hi, I am Danni-Lea Sandland, mom of Clay Bishop.
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 Clay has a condition called Stat-1 Gain of Function Mutation, only 660 people in the world diagnosed.
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 He has to go through so much medical treatments, tests, and appointment which for an 8 year old is an awful thing to have to go through all the time.
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 We recently found out he needs a surgical line fitted for a treatment lasting 4-8 weeks. He has an extreme phobia of needles and every appointment is traumatic for him.
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 <br>
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 Im setting this up, suggested by someone, to get him some treats and presents for being such a brave strong boy. I don’t know how to write these and I hate asking for anything but I’m just trying for my little boy.
</div><img alt="" src="https://d2g8igdw686xgo.cloudfront.net/108838839_1791540642869980_r.jpg" width="100%">
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Anonymous

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Support Clay for being so brave

Just £66£ to go! Make an impact.

Support Clay for being so brave

Just £66 to go!
Make an impact.