Childhood Stroke, Hemiplegia, Constraint Therapy, Selective Dorsal Rhizotomy, ESES, Epilepsy, Hemispherectomy and more!
Wednesday, September 3, 2014
Sunday, August 17, 2014
Harbor Lights Cruise
Byron loves New York City, and so do we! Tonight we took the Harbor Lights cruise on the circle line with Bob's Sister and Brother-in-law Karen and Chris. The weather was beautiful and the visuals were stunning!
Sunday, June 22, 2014
Sunday, June 8, 2014
Swimming!
For two years now I have wondered if Byron would ever gain the confidence to swim unaided in a pool. This year, on a trip to Captiva Island, he met a 9 year old boy named Matthew who was an excellent swimmer. Matthew was very patient with Byron's inability to swim and played with him in the shallow waters happily. One day Matthew was unavailable to play and Byron surprised us all by not only jumping into the shallow end unaided, but the deep end as well. He even swam across the pool! Byron was so proud to show Matthew what he had learned later that day. I am certain that the SDR surgery also made it possible for Byron to more freely move his leg. In the video you can see some nice movement there. Go Byron! (and thank you Matthew!!)
Thursday, June 5, 2014
Wednesday, June 4, 2014
Thursday, May 22, 2014
Before and After - Stairs
I have very few before and after videos. Here is a new video of Byron walking down stairs - no braces. Now look at the video below. That was with full bracing shortly after the surgery - his toe was pointed WAYYYY in. Great to see good progress!
Byron First Dorsal Rhizotomy Follow Up - Columbia
Today Byron had his 6 months follow up to the SDR surgery. It was the first time we have seen his surgery and recovery team since November 2013. The appointment was at Columbia Presbyterian at the Spasticity Clinic.
The comparison of the before with the after testing was very promising. His spasticity numbers had decreased which was very good. What was most surprising was their reaction to Byron himself. One therapist said "He seems like a totally different kid!"
Byron was cooperative, friendly and relaxed. This was in stark contrast to several of his earlier visits with this team. Each time he visits there he is asked to walk, run, jump and they play a lot with his legs and arms. This time he really seemed to enjoy it.
The BEST news is that he no longer has to wear a leg brace. They could see no difference between the SMOs, the AFO and nothing at all. Needless to say this is awesome!
Byron is walking better but he still has a long way to go. His ankle is still really tight so they showed me two excellent stretches I can do before he goes to bed. Byron seemed to tolerate the stretch so I look forward to trying it.
Another piece of good news is no PERC surgery, which is the heal cord lengthening, is needed. Phew!
Everyone, including me, is now focusing on his arm. It seems his arm has little to no spasticity, no change since the surgery. And no more Botox needed which is great. We stayed for a while today to have a custom hand splint made. It should arrive in about three weeks.
It is always so wonderful to work with experts in the field. I hope we can work with this team more often. There is a fairly good constraint therapy camp in New Jersey, so who knows, maybe this blog will go back to it original title - A Constraint Therapy Journal!
The comparison of the before with the after testing was very promising. His spasticity numbers had decreased which was very good. What was most surprising was their reaction to Byron himself. One therapist said "He seems like a totally different kid!"
Byron was cooperative, friendly and relaxed. This was in stark contrast to several of his earlier visits with this team. Each time he visits there he is asked to walk, run, jump and they play a lot with his legs and arms. This time he really seemed to enjoy it.
The BEST news is that he no longer has to wear a leg brace. They could see no difference between the SMOs, the AFO and nothing at all. Needless to say this is awesome!
Byron is walking better but he still has a long way to go. His ankle is still really tight so they showed me two excellent stretches I can do before he goes to bed. Byron seemed to tolerate the stretch so I look forward to trying it.
Another piece of good news is no PERC surgery, which is the heal cord lengthening, is needed. Phew!
Everyone, including me, is now focusing on his arm. It seems his arm has little to no spasticity, no change since the surgery. And no more Botox needed which is great. We stayed for a while today to have a custom hand splint made. It should arrive in about three weeks.
It is always so wonderful to work with experts in the field. I hope we can work with this team more often. There is a fairly good constraint therapy camp in New Jersey, so who knows, maybe this blog will go back to it original title - A Constraint Therapy Journal!
Friday, May 16, 2014
Saturday, December 14, 2013
Happy Holidays!!!
The best Christmas present ever - Byron is home !! We are so happy to have our family reunited and everyone happy, healthy and strong. Thank you to all who have sent your blessings to Byron and our family and read this blog. We LOVE you!!!!!
Friday, December 13, 2013
Last therapy sessions
Therapy has been so amazingly helpful here. Their therapy village is really high tech. Here is a short video of byron on a machine that helps him shift his weight correctly. Mom & Dad will miss these daily therapies. Byron has progressed so far.
Thursday, December 12, 2013
Teachers Pet
This is Byron's teacher. Her name is Jen. She is always so happy to see Byron each day. Wednesday was her birthday and Byron gave her stickers. She was overjoyed! Then we sang happy birthday. Byron really likes school here. He is doing so well.
New Dressing Speed Record
This morning Bryon was challenged by his OT (Sheri) to dress is less than 10 minutes! Could it be possible? - YES !!!
He dressed himself in 5 minutes with only a tiny bit of help starting his sox.
He dressed himself in 5 minutes with only a tiny bit of help starting his sox.
Bye Maureen
Byron had his last PT session with Maureen. She is taking off today and Friday to use up her vacation for the year. She was so sweet in her goodbye. She will coordinate with his therapists at school and at the center for discovery. Byron really liked her as was doing everything she asked during therapy. Thank you Maureen!
Wednesday, December 11, 2013
Byron will be a little sad to leave
Today at lunch Bryon said that he likes school here a little bit. (great praise!). He also likes having recreation with all the other kids. He has become friends with most of the kids on the floor. They circle like sharks while waiting for req. It is great fun every day.
Tuesday, December 10, 2013
Here is therapy
Byron is doing great at therapy. Today was an obstacle course. And stairs. He is doing very well.
Monday, December 9, 2013
So Happy He's Coming Home!
Just finished my "shift" at Blythedale. I can't wait until the family is all together again!
Byron had therapy in a very complicated computer device today. He said he didn't like it but secretly I know he did. You shift your weight to get a little cake to stay in a box on a computer screen. Then the computer tells the therapist what Byron needs to work on to improve his balance and weight distribution. Very cool!
Byron had therapy in a very complicated computer device today. He said he didn't like it but secretly I know he did. You shift your weight to get a little cake to stay in a box on a computer screen. Then the computer tells the therapist what Byron needs to work on to improve his balance and weight distribution. Very cool!
Saturday, December 7, 2013
The wheelchair is "normal"
Tonight I was speaking with some parents about their son Moshe, who had the same surgery Byron had but is still not allowed by the hospital to use anything but a wheel chair.
I saw him walk the other day and he walks quite well, but he still has far to go. Moshe's mom told me that he walked and ran before the surgery, but just on his toes. I said to her that it must be so hard for Moshe to be confined to a wheel chair here, but that I had noticed that he seems perfectly ok with it. Then she said something interesting. She said that here in Blythedale, everyone is in a wheelchair, so it's the normal way to be.
When Byron goes to recreation, he stays in his wheelchair the entire time, even though he's perfectly free to walk. At Blythedale you stay in a wheelchair if you wan to fit in, to be "normal".
What a strange and wonderful thing that is.
I saw him walk the other day and he walks quite well, but he still has far to go. Moshe's mom told me that he walked and ran before the surgery, but just on his toes. I said to her that it must be so hard for Moshe to be confined to a wheel chair here, but that I had noticed that he seems perfectly ok with it. Then she said something interesting. She said that here in Blythedale, everyone is in a wheelchair, so it's the normal way to be.
When Byron goes to recreation, he stays in his wheelchair the entire time, even though he's perfectly free to walk. At Blythedale you stay in a wheelchair if you wan to fit in, to be "normal".
What a strange and wonderful thing that is.
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