Welcome to my blog about my journey through cranio with my youngest Denver. I write this blog to benefit myself by getting my feeling out and hope that someone may read this and get an understanding about what we go through as mums dealing with cranio. Some people thimk the journey of cranio ends after the 1st cranio surgery but that is far from the truth, this is a life changing journey that goes on for the life of the child and their family. I often write things I would never have the courage to say out loud to anyone, often the feelings are very raw and honest. So join me on my roller coaster ride through cranio and lets get through this together.

Friday, September 13, 2013

I have a son. He is 6 but turning 7 in 13 sleeps. He is cuddly. He is funny. He is clever, He is beautiful. He is energetnic. He is caring. He is testing. He is small. He is my baby. And he has craniosynostosis. And I am his mum. He is 2 years 5 months and 14 days since his CVR. and I feel like we are still at the beginning. He has been struggling for the past months with headaches, tiredness, concentration, hyperactivity, bodily functions and just being ok. And I have been struggling, to comfort him, hear him, encourage him to keep trying and learning even when his head hurts.  Next week we start the rounds of tests again to see if there is a reason an answer a way to fix it. Is there going to be an answer? Maybe Maybe not. I feel that cranio will never leave us. I long to think its all over he is fine we don't have to think about it anymore, go to more appointments, have meeting with his teachers. We can just be normal and not do all the cranio things. But it is not to be. I am not angry or bitter today I am just sad that he has to live with this. My sister had her first baby on Tuesday a Beautiful little boy. I took my kids to meet him and they all loved him. Towards the end of the visit Denver come over to me as I was holding the baby and asked 'is his head ok?' I said yes his heads ok, why do you ask? Denver answered because he has that bump across his head. I then explained how the bones in a babies head move so they can be born and then they slowly move and smooth out. He seemed reassured and like he had an understanding. The bump across the babies head is exactly where Denver's scar is. I felt sad that this would be a concern for him and on his mind, he just wants the baby to be ok and to have a 'normal' head.  I just wish he didn't have the knowledge within him of what cranio feels like. So I go into the eye test, brain pressure test, neuropsychological test, MRI scan with a heavy heart but a hope full one that we can fix what ever is going on. I pray for strength and calm as I hold him down for the needles, the drops the tests and pray that we will be smiling at the end of the day.

 

No comments:

Post a Comment