Emma is the kid of the month for August. We hope we can share her journey with others. We want to share her milestones and raise awareness for this RARE genetic disorder. We were excited to get her name and diagnosis out there. Please help us by sharing this blog on your Facebook pages, Instagram and Twitter. You can also share her Facebook page here is the link for that https://www.facebook.com/Embracelifeemma
Thanks again for all your love and support
*side note. Emma had her blood pressure check today and it went fantastic. They want to make sure the meds are being handled by her little body ok 😊
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