Friday, June 18, 2010

Medical Update

I guess its time for a medical update. Conditions/Problems/Resolutions/blah blah

Hydrocephalus: Carter's pressure is under control and shunt is working nicely for now. His shunt anniversary is January 4, 2008. Its pretty rare for a long shunt life, especially a shunt thats been recalled. But his is doing well. Many shunts fail due to blockage and infection. Bodies are designed to fight off foreign items especially long plastic tubes in the brain. We feel blessed to have such a long shunt life so far. Many of our Hydro buddies have had hundreds of shunt revisions.

Macrocephaly: Well the definition of this is just simply a large head and a few other traits, so needless to say Carter still suffers from this. The only way to fix this is a Neuro Cranial Reconstruction Surgery. At this point, it would be mearly cosmetic with huge risk, so we are passing on this for now.

Cortical Vision Impairment: We just went to our Ophthalmologist who we see every few months. He just declared Carter's CVI totally resolved! Carter's had eye muscle surgery in January 2009 for ocular misalignment which worked beautifully and he now has super straight eyes. They usually veer back but Carter's hasn't so far. He's been patched for about a year. He's also had vision therapy once a week since he was 3 months old. Something must have worked because CVI is now resolved!

Hearing: I just posted this but here goes again. Carter just got tubes placed April 2010 then a few weeks ago he passed a very extensive group of hearing tests with flying colors! NO hearing loss, wheew. Crossed this off the worry list.

Physical Therapy: We are still going to Shriners, but we took a few months off to let development kick in. I am a big fan of letting Carter do most of his learning and exploring in a natural environment instead of a therapy room. We mostly get direction from our therapists and then we practice in a natural environment just like all other children learn these valuable things. Here's our milestones
~1st Smile: 5 weeks
~Rolling over: 6 months
~1st Word: 11 months
~Holding Up Head: 15 months
~Sitting Independently: 16 months
~Pull to Stand: 18 months
~Cruising: 19 months
~Crawling: 20 months
~Walking: 2 yrs 4 months
~Running: 2 yrs 4.5 months :)

Feeding Therapy: Feeding is always our battle, he's eating a bit more then before. All food must be of slight texture and must be dry. He's still staying alive on Ensure bottles. Lots of Cheetos, dry cereal, crackers and on a lucky day he'll try my cooking. Sometimes Eric and Jordan are brave enough to try my cooking as well.

Speech Therapy: Carter is very behind on speech, he said a bunch of words at about 12 months old and one day he quit saying all words. He's back to saying about 4 words now, just since the tubes. We are seeing speech therapy twice a month.

Occupational Therapy: This is still an important part of our week, we try to put Carter in a group setting with other children or in a chaotic setting (such as the Luau) and he has a total meltdown. The sensory part of his brain doesn't know how to filter so chaos over loads his system. We work with our wonderful OT to teach him how to handle this kind of stress. This is a big task for Carter. Needless to say he has a hard time really going anywhere. He's also very schedule oriented. If we throw off his normal schedule he has a hard time recovering.

Beans: He had double Hydrocele Inguinal Hernia surgery in January 2009. All is well in that department, he gets embarrassed if we talk about this too much.

Developmental Delay: He tests on about an 18 month old level in most areas. There are a few areas that he is on target with a two year old but there are a few areas of development that he tests much lower. But for the overall test scores he's real close to 18 months old.

3 comments:

Jenny Lawless said...

You guys are amazing and so is Carter! Every time I check out your blog I get teary eyed just thinking of how special he is!

Anonymous said...

Looks like Carter is doing great! I am so glad he is hitting so many milestones. I just went to the hydro conference. It was great! If I can pass on any information let me know. Chantel K

KimN said...

Just stumbled across your blog. I have an almost 15 mth old that was born with hydrocephalus as well. His milestones look amazing! What a cute little guy too!