very cute!Good luck tomorrow! Sending lots of prayers!
We are all thinking and praying for Megan and for your family. You will all make it through this and be stronger for it.
Hi. A mutual friend sent me a link to your blog so I thought I would take a peek. My daughter is a couple of months younger than Megan and has a severe form of epilepsy and global delays. She's in several genetic studies across the country. We've tried HBOT. We've been through ACTH. I can relate to a lot of what you have gone through, as you explain it on your blog. I'm SO saddened to hear what you and your family are experiencing now. I'm very interested in your project, the special needs park. I live in the Northdale area of Tampa and would like the chance to chat with you once your family's lives settle down a bit and when Megan is doing better. Feel free to email me at firstname.lastname@example.org. My prayers are with you.
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