New Blog

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I will keep you up to date on all the newest deals and freebies I find.

NF Awareness Month

This is a letter that my cousin, Mia wrote to the local newspaper!
I am 11 years old, and I have a genetic disease. There is no cure or treatment for my disease. My genetic disease is called neurofibromatosis. I have many marks that look like birthmarks. This was the doctor's first clue that I have neurofibromatosis. I have to go to special doctors in St. Louis every year. What I get scared about is that it will hurt me some day. Sometimes I have bad dreams about what could happen to me. I don't know anyone else who has this. This is NF Awareness Month for all the people who might not know that. I am one of the kids who is part of this month, but I bet there are more people with what I have. I wanted to share this with you in case you did not know that May is NF Awareness Month.

MIA

So I know that I haven't blogged in like 4 months. I'd like to say that I've been to busy but I think I was too lazy. I think there's only like 2 people that ever read this so this is for you! Jase is getting so big and wild and funny! He is the cutesy little boy ever! He's started a new preschool and is learning so much! I've decided to go back to school and finish my degee. Ok, more later!

Happy Valentine's Day!

I love your fingers, I love your toes.

I love your mouth, I love your nose.

I love your eyes, I love your ears.

I love your laugh, I love your tears.

I love your touch, I love your smell.

I will protect you, I'll be your shell.

You give me love, You give me joy.

I love you, my baby boy!

HAPPY 2nd BIRTHDAY JASE!!!!!!!!!

It's hard to believe that my little baby boy is almost two! Wow, how the time has flown by. He is the most precious thing in the world and I thank God for him every day! I love you Jasey!!!