Michael Joseph Moscatello
Michael was born at 29 weeks with a PVL. When he was 12 months old he was diagnosed with Cerebral Palsy. This is our life and how we get by day to day!
Friday, April 6, 2018
Tuesday, August 19, 2014
Saturday, May 24, 2014
Tuesday, April 29, 2014
Tuesday, April 8, 2014
Mikey did it :)
Mikey has been working so hard and he finally can get himself sitting up. It takes him time and hard work but if you tell him to sit up he can :) I'm so proud.
Friday, March 21, 2014
A grandmas love is the most precious thing.
Grandma Rose loved Mikey so much. You can see it in her face. Such a proud great grandma. She will be missed. We love you grandma.
Monday, October 22, 2012
Saturday, October 20, 2012
Mikey's first pumpkin he helped paint
We had fun doing this project. Mikey wanted to rub the paint on the pumpkin so next time I think I will get finger paints :) happy Halloween
Life is so hectic
I want to post here all the time and I seem to always forget. I read a blog from a mom who has I believe 9 children most with special needs she writes daily. This should be cake for me lol
Mikey's doing well since his Botox. He has a better range of motion which is helping him try to do more things. Like getting in his knees :)
He's loving school and we just got his wonderful new bed. Everything is going well on our end. Now for some pictures.
Mikey's doing well since his Botox. He has a better range of motion which is helping him try to do more things. Like getting in his knees :)
He's loving school and we just got his wonderful new bed. Everything is going well on our end. Now for some pictures.
Wednesday, August 1, 2012
Summer begins for Mikey
Mikey is done with school till September 5th. He will be spending lots of time with grandma and grandpa and then 2 weeks with mommy and 1 with daddy :)
Friday, June 8, 2012
Hawthorne lions club ramp project
Amazing men are building a ramp for Mikey. We can't even begin to say thank you.



Tuesday, June 5, 2012
Apparently 2012 Im not doing any better with blogging!! Maybe by 2013 lol. Mikey is doing very well. His progress is slow but hes making progress. We are set to have botox done on September 21, 2012. Hoping this helps him to sit better and start to stand.
Hes holding his cup much better then ever. He loves school. I promise to upload pictures soon.
Trying to cope one day at a time is challenging sometimes. Some days are easy some days are so hard. This is our life whether we like it or not. Anything I have to face is nothing compared to what Michael has to face every day. He has a life journey ahead of him and hes has to always push. Life isnt going to be easy for him but with his great personality Im sure he will be just fine.
Friday, December 23, 2011
So far behind...
I wanted to keep this blog up to date but its been hard to do. I will try harder in 2012. This was a rough year for me emotionally. I was finally able to face reality that my son is handicap. I went threw the denial phase the anger phase and I finally think Im at acceptance. I keep saying one day at a time. I feel so much love for this little boy and will do whatever I have to make his life the best it can be.
Merry Christmas to everyone and I promise more pictures soon. I have them all on facebook :-) Its much easier for me to keep up there for some reason.
Merry Christmas to everyone and I promise more pictures soon. I have them all on facebook :-) Its much easier for me to keep up there for some reason.
Tuesday, November 8, 2011
Monday, July 25, 2011
Bath seat has arrived / Eye Check up

I am so glad we finally got Mikeys bath seat. Tonights bath was no picnic for me. Since Mike wasnt home it was just me trying to figure this thing out. The poor baby wasnt to comfortable but I think he liked having more room. I promised him tomorrow we would have more fun. Ive been dying to have fun bath time but it never happened because he didnt have the room to move and he wasnt sitting. Now we have much more room!! Hope tomorrow is better :-)
Today was also Mikeys 6 month check up with Dr. Mickey. He said everything was great! Good news is the best news!! Hes impressed at how well the surgery corrected his turn. He said to come back in 6 months just for a follow up.
It was hard waiting for the Dr because there were kids in the waiting room looking at Mikey like he was different. I guess because hes our child he doesnt seem any different to us but to a stranger they are wondering why is that kid not walking or talking or sitting up? It was hard and its just the begining ... but we will face these things and get threw them one day at a time.
Signing off... time for some mommy and daddy time which we rarely get :-)
Monday, July 4, 2011
Happy 4th of July
Sunday, June 26, 2011
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