I would love to start my own website and call it "THE DIFFERENT FACES OF HETEROTAXY". A place where moms and dads can come and share pictures and stories of their little ones with Heterotaxy with polysplenia or asplenia. I want to raise awareness of this rare (confusing) syndrome. Hopefully, in the next few months, I will be able to start working on my website. If anyone has any ideas for my website please leave your comment. Any input is welcomed.
Update on Chloe: Chloe has been doing well. She is getting over her sinus infection. She was put on Zithromax for five days then for 3 weeks she'll be on IC Cefdinir. I am in a hurry for summer. Chloe seems to do better in the summer months.
2 comments:
I think that sounds like a great idea.
GREAT IDEA!!!!
_JTinMD
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