Patrick & Henry...
Sydney really wanted to feed Sullivan...patrick . amy . sullivan . henry & murphy
Patrick & Henry...
Sydney really wanted to feed Sullivan...Posted by patrick & amy at 7:05 AM 0 comments
Labels: Lunch with the Danz family
Yesterday late afternoon we went to physical therapy for Sullivan...it turns out all of our hard work is paying off FAST! His therapist was amazed at his flexibility..range of motion, neck position etc. I guess when you do a stretching routine 8 + times a day... change happens! Pretty cool. Sullivan also wanted to show off a bit and he rolled over unassisted for the first time during his session...that was fun to see!
Friday we get fitted for his DOC band.... hopefully he will make fast progress there too.
Today Patrick's mom will be visiting after she gets off from work... that will be fun... the boys are excited! We like visitors!
Posted by patrick & amy at 7:33 AM 0 comments
Labels: a good report
Oops... its been a week since my last post...that's a first for me...I am usually pretty good. Things have been ultra busy and I have lots to post! I just wanted to drop a quick note in case you check in and wonder if what we're up to!
Right now I am enjoying watching Henry & Sullivan jump and play in their new jumping toys.
Oh, by the way Henry rolled over yesterday unassisted.. very impressive!
Posted by patrick & amy at 5:37 AM 0 comments
Labels: its been a week
Posted by patrick & amy at 7:21 PM 1 comments
Labels: sunday in georgetown
We almost forgot to take a picture! That explains why this is taken in a parking garage... Henry was sleeping so we snuck a picture with Sullivan who decided to stay awake! We met up at Tysons II for a few hours... this girl and I could have talked for three weeks to catch up! It had been way too long!
Posted by patrick & amy at 8:49 AM 0 comments
Labels: karen jones
Posted by patrick & amy at 8:38 AM 0 comments
Labels: erin, pat and dianes bday
Today we went to our first session of physical therapy for Sullivan's neck.... it went really well. We learned several stretches that will help his torticollis...we will need to do the series of stretches at least 8 times a day in addition to weekly therapy sessions at the hospital. Our therapist's name is Jeannie...she was really good with Sullivan and let Henry join in too... we didn't want him to feel left out. Basically, I learned by watching her stretch Sullivan and practicing on Henry... lucky him! I guess it will get easier as I learn the stretches and he gets used to stretching. We had some tears today but not as many as when I stretch him at home...we learned how to stretch him so that he has some fun in the process. They predict he will need to be in therapy for 4-6 months to treat the tight muscles. If it goes untreated it can lead to some significant motor delays. We don't want that. Our neurologist appointment got moved until Friday of this week it was supposed to be Wednesday... Tomorrow we go to Cranial Technologies for our 3-D images of Sullivan's head.... these will be needed in order for them to make his DOC band. Any who... that is the update from here...
oh, if you are reading this now and wonder what all of this means you can go back and read a past post titled "perks of being baby a"... enjoy!
Posted by patrick & amy at 6:05 PM 0 comments
Labels: physical therapy
Posted by patrick & amy at 9:28 AM 0 comments
Labels: my mom's visit
Posted by patrick & amy at 9:14 AM 0 comments
Labels: sweet potatoes
Posted by patrick & amy at 6:33 PM 0 comments
Labels: tysons with the girls
We've learned a lot in the last week about issues that can arise when you're lucky enough to be baby A! :) We found out Sullivan has Torticollis and Plagiocephaly. Basically, Sullivan has occipital and frontal flattening, a slight ear shift and bi-temporal flattening as a result of being baby A. Baby A (Sullivan) was head down and in my pelvis for months without the ability to move freely as Baby B (Henry) was able to do throughout their residency in utero! This position resulted in torticollis, tightening of the neck muscles so he slightly tilts his head to the left. So, based on that we will treat the muscular issues with physical therapy and to correct the "structural issues" we will purchase a DOC Band. Basically it looks like a white plastic helmet...but it isn't really a helmet of the sorts that I'm sure you are thinking. It is to help his head correct itself by encouraging growth in some areas while slowing growth in others... We want Sullivan to be as happy and healthy as possible so we have decided to go forward with this. He will wear the DOC Band 23 hours each day for approximately three months...might be shorter or longer but that is the average. In case you want to read about treatments or other cases you can visit http://www.cranialtechnologies.com/. We will keep you updated with the progress and of course more pictures of our little man as he sports his new "hat"!
Posted by patrick & amy at 12:52 PM 2 comments
Labels: Sullivan update
Posted by patrick & amy at 12:24 PM 0 comments
Labels: Meet Dr. Nies
henry is wearing ann's sunglasses....i think we need a pair!
Posted by patrick & amy at 6:40 PM 0 comments
Labels: play date
Posted by patrick & amy at 7:04 PM 0 comments
Labels: jumpin around