The Story of My April Butterfly: A Blessing

Saturday, November 15, 2008

A Blessing

Maggie has had the blessing of a very special substitute for a few weeks now.
This is a very good friend of ours, and her smile and loving ways have been a huge blessing in Maggie's life. Every day that I see this beautiful face there to welcome Maggie, allows me to leave that day feeling at peace. I know that Maggie is being loved and cared for... What an awesome blessing God has given us in our good friend above!

Thank you, Lord.

2 comments:

Anonymous said...: Yes, Heidi, it is a ture blessing.
Love you all,Mom; November 15, 2008 at 2:39 PM
Jen said...: Heidi

Maggie looks so great and so happy! I am glad things are working out so well!; November 17, 2008 at 3:13 AM

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Maggie spent the first three weeks of her life in the NICU... first to investigate an irregular heartbeat- cleared with a diagnosis of a wandering pace-maker and sent home at 5 days old. She stopped breathing 2 hours after we had been home... we gave her rescue breaths, called 9-1-1 and Maggie was transfered by ambulance to the NICU, again. At 20 days old Maggie was sent home with a diagnosis of mild Laryngomalasia (floppy windpipe) and an apnea monitor to wear for 6 months. At one year of age Maggie was diagnosed as Hypotonic and spent the next 6 months of her life being seen by a Neurologist, a Genetic Counselor and Occupational Therapists. She began early intervention for her developmental delays. At age 3 she began attending a Special Education Preschool. She attended a typical Kindergarten class with RSP help for fine motor delays. Beginning in 1st grade she began her journey through Special Education for intensive help with many developmental and cognitive delays. Beginning in 3rd Grade I decided to Homeschool Maggie through a local charter school. She still received Special Ed. services, but I was in charge of her daily curriculum. We began her 5th grade year by enrolling her back in public school. This year will either prove to be a great stepping stone to the rest of her education, or it will be a year to revisit other options. This is our journey living with a child who is Hypotonic.