Here I am the morning before surgery finding it hard to sleep I decided to blog... I still have a few more hours until I have to wake Scott and the boys up but I'm getting my pre-surgery jitters out. I have been through a ton of testing and imaging with Landen all needing various sedation or anesthesia so I know he does well. But you can't help as a mother to still get a little nervous every time they take your little one back into the OR without you. I'm really excited for this I have worked endlessly for Landen to receive his cochlear implant and its finally time!
We have been so busy lately between CI stuff and getting him re-established with many of the doctors down here. Last week we meet with a new geneticist at Primary Children's who was so nice and seemed to know everyone. Including our geneticist in Arizona, Dr Zellweger whom the PBD spectrum is named after, and Dr Braverman who we see with the GFPD he knew when she was just training in genetics. We really enjoyed meeting him and he has already gone above and beyond in helping find resources answers to some of our questions.
Yesterday Landen got a new set of braces his old AFOs still fit but we were not getting the results we wanted with them. I had previously discussed with the OT in Flagstaff that there might be a need to put him in a taller brace since he was hyper extending his knees, walking on his toes and leaning back too far when he tried to walk. The OT we see now in Logan suggested the same thing. He is really good at explaining why Landen's needs things and exactly how it will help him. We agreed and fitted him for a new braces and we picked them up yesterday. The manufacture didn't quite fit them right and they are too tight and already are causing some red spots and irritation on his feet. So we are actually getting new ones made and only using these ones to get him use to the idea of the taller brace. I love how as soon as we put them on we could tell a difference. He stands straighter and the few timid steps he took were heal to toe instead of toe to hill which is what we were going for. They are also at a different angle because he spends so much time with his toes pointed he was loosing some of the range of motion in his ankles and this will force his feet into a position that will stretch the muscles and prevent the tightening we already see a little of.
Also yesterday he was fitted for his first adaptive stroller. This is a stroller we are getting through our insurance company that will be able to fit him and his needs for many years to come. We no longer need the double stroller and his poor little feet practically drag on the ground in the single stroller we have. Plus his school has requested it since they have to carry him from place to place if he refuses to use his walker. Its tiring I know cuz I do it! He is so small yet he isn't small anymore... if that makes sense.
I look at Landen two different ways sometimes I guess depending on my mood. Sometimes I look at him and see how big he is and how much he has grown. Looking back at pictures a year or more ago and compare him to himself. This is when my heart swells and I'm so proud of him! What accomplishments he has made and how wonderful it is to see him grow! Then there are the times I can't help but compare him to others. Mostly Brayden who has now slightly outgrown him and other four year olds. The he is so small... I really try to avoid this but sometimes its hard. Especially being around friends who have four year olds. People I was pregnant with and I was so excited to see our kids grow up together. I see them running and dancing and playing and going off to school. I see them interacting with their family and making friends knowing I will never have that kind of interaction with Landen. Usually it doesn't really bother me Landen is Landen and I love him. But every once and a while I can't help but feel a little jealous or heartbroken over missing out. Today is not a sad day though today is a happy day. Today is a day where I'm so proud of my little Landen! I'm proud of my family and my husband. It has been so much work getting here. I have worked through frustration and stupidity and my own tears to get to this point. My little Landen is getting his cochlear implant and in a few weeks (the 27th and 28th) they will be activated and he will be able to hear! Can you believe it! What a miracle this is for our Landen. I know it sounds dramatic but this will change everything! It gives him one more way to experience his world and he has so few ways now. I love my Landen! I will post as soon as I can about the surgery but now I think I will try and grab one more hour of sleep or maybe a relaxing bath.
Shortly after his second birthday our Little Landen was diagnosed with a Proxisomal Biogenesis Disorder (or PBD) a rare yet fatal genetic disorder. It hasn't been easy for us to share and this site has been created to help us keep everyone updated with doctors news, information and what is going on in our journey. We know we have tons of family and friends support and love. We hope and pray that we are blessed with many more years to watch our sweet baby grow!
My Little Landen
This blog has been created to help others keep up to date and follow our journey. I will post as often as I feel there is new news in his condition or our family be it good or bad.
Wednesday, March 13, 2013
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