Since I can't seem to gather my thoughts into one subject for a post, I thought I'd just do a bullet list of things that are going on with us. Here goes:
Ben had a great morning yesterday. He had PT and OT back-to-back which is very unusual since he only sees the OT every 2 to 3 months. We hadn't had a PT session in about a month due to various illnesses and scheduling conflicts so it had been awhile since we'd been to the hospital. He did really well at PT. He practiced going from sitting (on a bench) to standing and back to sitting for awhile. We then practiced STANDING ON HIS OWN! He was able to do it for 2 to 3 seconds. It was fantastic and he loved it. We left PT to head to OT. It's quite a walk through the hospital but Ben walked the whole way in his walker. OT went really well as well. He was able to do all the tasks presented to him and blew the OT away with his knowledge of numbers and letters. She didn't even bother to give us any homework. Ben then walked all the way from OT back to the car...another long walk. He did great. When I put him in his car seat, he looked at me and said "really fun Mommy". Too cute.
We've pretty much decided it's time for us to get a mini-van. I fought it for awhile but am now really ready for it. And excited about it. We've actually got one for the weekend to try out and I'm lovin' it! It's awesome. I can take both boys out to the van, open the sliding door, help Daniel in with one hand while holding onto Ben, put Ben in his carseat and then put Daniel in his carseat. With our CR-V, I would have to tell Daniel to hold onto my leg while I put Ben in and then put Daniel in...all the while worrying that Daniel will run off. No more worrying! Plus, there's tons of space for strollers, walkers, bikes, etc.
The end of tax season is only 2 weeks away! That means that the part-time job that I don't like will soon be over. As you may recall, I took on 2 part-time jobs back in February. Doing tax returns at my husband's office and being a Weight Watchers Leader. I really enjoy working for Weight Watchers and running meetings, but I'm not enjoying the return to the accounting world. Thankfully, that is almost over and I'll have more time for the boys. Yeah!
We're very strongly considering trying out Conductive Education for Ben this summer. The closest CE centre is 2 1/2 hours away but I think we're ready for it. We're going down in late May for an assessment. And then we'll make our decision. I'm pretty sure we'll try it out sometime this summer. I'm just not sure of the timing or how much we'll do yet, but I'll be sure to update you as we move along in this process. If you want to read more about Conductive Education, check out this post by Renee at Massagermommy.
Happy Saturday everyone!
Showing posts with label PT. Show all posts
Showing posts with label PT. Show all posts
Saturday, April 17, 2010
Monday, March 15, 2010
A typical PT session
(So I've been trying to do this post for a week now. I have a couple small videos of Ben's last PT session and I wanted to share them with you...but I cannot get the videos to load. So I will do this post with photos instead...it won't be as good but hopefully you'll get the main idea.)
Ben has PT twice a week - once at our local hospital and once by a private PT at home. I took some photos (and video) of his last PT session at the hospital for my own records, but also to share with all of you.
We are pretty consistent about making sure that Ben is stretched every morning so when we arrive for our PT session, we just jump right in. This week we started out "playing stickers". We've done this quite a few times, mainly because Ben loves it so much. And with a two-and-a-half-year-old, you just go with the flow!
This entails many, many plastic-sticker-like things that will stick on a mirror but will also peel right back off. He sits on a low bench so that his feet are firmly planted on the floor. The PT has his reach all over for the next sticker (over his head, on the floor, behind his back) and then he puts the sticker on the mirror...usually high up so he learns to stand and sit independently. He does awesome at it! And loves to tell us what each sticker is (there are dinosaurs, snowmen, butterflies, and lots of animals).

After this, he decided he wanted to walk. We used to practice using his walker, but we don't do that now since he's so good at it and gets to much practice at home. Instead, we decided that we would try "cruising along the wall"...which we've only ever tried once with no success. Well...this time...SUCCESS! Yes, he needed to be helped along and "spotted" but he did great. He walked all the way along the wall to the basketball net (which we moved to next).

Ben LOVES basketball...I don't think there is another kid out there that likes basketball as much as Ben does. Basketball almost always plays a part in his PT sessions at the hospital since they have a basketball hoop. In this part of the session, he's actually standing on his own in the corner (he's very good at this and we do it at home some). He then has to shoot the basketball. This takes a lot of balance and he does great. And he loves it as you can see.
Ben has PT twice a week - once at our local hospital and once by a private PT at home. I took some photos (and video) of his last PT session at the hospital for my own records, but also to share with all of you.
We are pretty consistent about making sure that Ben is stretched every morning so when we arrive for our PT session, we just jump right in. This week we started out "playing stickers". We've done this quite a few times, mainly because Ben loves it so much. And with a two-and-a-half-year-old, you just go with the flow!
This entails many, many plastic-sticker-like things that will stick on a mirror but will also peel right back off. He sits on a low bench so that his feet are firmly planted on the floor. The PT has his reach all over for the next sticker (over his head, on the floor, behind his back) and then he puts the sticker on the mirror...usually high up so he learns to stand and sit independently. He does awesome at it! And loves to tell us what each sticker is (there are dinosaurs, snowmen, butterflies, and lots of animals).

After this, he decided he wanted to walk. We used to practice using his walker, but we don't do that now since he's so good at it and gets to much practice at home. Instead, we decided that we would try "cruising along the wall"...which we've only ever tried once with no success. Well...this time...SUCCESS! Yes, he needed to be helped along and "spotted" but he did great. He walked all the way along the wall to the basketball net (which we moved to next).

Ben LOVES basketball...I don't think there is another kid out there that likes basketball as much as Ben does. Basketball almost always plays a part in his PT sessions at the hospital since they have a basketball hoop. In this part of the session, he's actually standing on his own in the corner (he's very good at this and we do it at home some). He then has to shoot the basketball. This takes a lot of balance and he does great. And he loves it as you can see.
That was about it for that session. He's usually a little worn out, but he's still full of motivation and energy so he actually walks all the way back to the car in his walker when we're done now. (I don't let him walk TO the session since I don't want him too tired for the session.)
And just because I think my boys are so cute, here are a couple more recent photos.
Here are Daniel and Ben in Daniel's chair. Ben was sitting in it first, but Daniel always insists on climbing in behind him.
Here are Daniel and Ben in Daniel's chair. Ben was sitting in it first, but Daniel always insists on climbing in behind him.
Labels:
basketball,
Ben,
cruising,
Daniel,
PT,
sitting,
standing up
Thursday, April 23, 2009
All about Ben
I wasn't sure what I wanted to write about tonight. But I think it's time to tell you more about Ben's diagnosis. Ben has Spastic Diplegia Cerebral Palsy. He was diagnosed by a Pediatric Neurologist in September 2008...just a week after his first birthday. We really had no idea. We knew he had developmental delays but we really had no idea that it was any more than that. So, let me try to explain what this diagnosis means.
Ben's case is on the milder side of the spectrum. There is a classification system that classifies children affected by CP based on their gross motor skills (sitting, walking, and wheeled-mobility). You can see it here. Currently, both of Ben's PTs consider Ben to be a Level 2. This would indicate that Ben will someday be able to walk indoors unaided and walk outdoors with the use of a walker. This however is some time away but hopefully before he starts school.
Some more specifics about Ben:
1. We're not sure if the CP has affected his speech. He is somewhat delayed but not enough to cause any real concern at this point. He babbles constantly and can say some words (about 4) in the right context.
2. We don't think that the CP has affected his cognitive abilities. I am not sure but have heard that this will be assessed when he's around 3 years of age. Currently, his PT's think he's very bright.
3. His fine motor skills are really great at this stage. He saw an OT once a week for about 6 months. We only see her once a month now.
4. The spasticity in his legs seems to mostly affect his hamstrings and calves. His adductors are not as affected (the muscles on the inside of the thighs). Usually with Spastic Diplegia the adductors are affected which causes scissoring of the legs when walking or crawling. Ben had a bit of tightness in his adductors during a recent growth spurt but lately that tightness has lessened.
When Ben was diagnosed in September (7 months ago), he could roll from his tummy to back and back to tummy. He could roll both left and right. He was not comfortable hanging out on his tummy. He could not crawl in any form. He could not sit unassisted. He could not pull up. Just 7 months later, Ben can sit unassisted (although he still has some balance problems so we don't leave him unattended when sitting). He can army-crawl. He can get up on all fours. He can pull to a kneel. He can hang out on his knees. He loves to be on his tummy. He can use a walker with help. He can go up and down the 2 steps into our family room. HE IS AWESOME! What progress he has made! He is a very hard worker and gets such pleasure out of doing things himself! He amazes me every single day.
Cerebral Palsy ("CP") in the most basic terms means that there has been an injury to the brain (cerebral) that has caused the person to not be able to use their muscles in the normal way (palsy). CP is not progressive. It is not communicable. It is not curable. It is (somewhat) treatable.
There are 3 main types of CP:
1. Spastic
2. Athetoid
3. Ataxic
A person can also have a mix of these 3 types.
Spastic CP is the most common type (about 80% of CP cases are spastic). It basically means that the person has one or more tight muscles groups that limit their movements.
Diplegia is a type of CP that affects mostly the legs, but can affect the trunk and arms to a lesser extent.
Ben's case is on the milder side of the spectrum. There is a classification system that classifies children affected by CP based on their gross motor skills (sitting, walking, and wheeled-mobility). You can see it here. Currently, both of Ben's PTs consider Ben to be a Level 2. This would indicate that Ben will someday be able to walk indoors unaided and walk outdoors with the use of a walker. This however is some time away but hopefully before he starts school.
Some more specifics about Ben:
1. We're not sure if the CP has affected his speech. He is somewhat delayed but not enough to cause any real concern at this point. He babbles constantly and can say some words (about 4) in the right context.
2. We don't think that the CP has affected his cognitive abilities. I am not sure but have heard that this will be assessed when he's around 3 years of age. Currently, his PT's think he's very bright.
3. His fine motor skills are really great at this stage. He saw an OT once a week for about 6 months. We only see her once a month now.
4. The spasticity in his legs seems to mostly affect his hamstrings and calves. His adductors are not as affected (the muscles on the inside of the thighs). Usually with Spastic Diplegia the adductors are affected which causes scissoring of the legs when walking or crawling. Ben had a bit of tightness in his adductors during a recent growth spurt but lately that tightness has lessened.
When Ben was diagnosed in September (7 months ago), he could roll from his tummy to back and back to tummy. He could roll both left and right. He was not comfortable hanging out on his tummy. He could not crawl in any form. He could not sit unassisted. He could not pull up. Just 7 months later, Ben can sit unassisted (although he still has some balance problems so we don't leave him unattended when sitting). He can army-crawl. He can get up on all fours. He can pull to a kneel. He can hang out on his knees. He loves to be on his tummy. He can use a walker with help. He can go up and down the 2 steps into our family room. HE IS AWESOME! What progress he has made! He is a very hard worker and gets such pleasure out of doing things himself! He amazes me every single day.
Wednesday, April 15, 2009
Moving towards walking
At his last PT session, Ben got to try "walking" on his own for the first time. He absolutely loved it and did amazing. His PT thought he did fantastic and I just had to catch it on video. It won't be long before he's ready for his first walker. Check it out!
Sunday, April 12, 2009
The boys
Well. Now that you know lots about me, it's time to tell you about my boys.
My sweet, sweet boys are now almost 19 months old. Daniel and Benjamin were born on September 19th, 2007 at just 30 weeks and 2 days gestation. I had no complications with my pregnancy until 29 weeks when I started feeling some tightness and told my ob-gyn. Anyways, it turns out I was starting to dialate. A week later, I was dialated even more (even though I was not contracting). Both boys were breech and apparently they could feel Daniel's feet. They were very worried about cord compression and it was decided that an emergency c-section was in order.
So, within the hour, they had arrived. I was terrified. They were too young...just 30 weeks. They weighed 3 lbs 4 oz and 3 lbs 7 oz. They were of course taken right to the NICU after just a few pics with me.
They stayed in the NICU for 8 weeks and 1 day and came home together on November 15th, 2007. They both had rough hospital stays, but Ben definitely had the harder time. 24 hours after birth he was put on a ventilator. He was on it for 4 days. He spent the next 4 weeks going between CPAP and nasal canula. He got an infection. He required many blood transfusions. But finally, he got stronger and did better and got to come home.
Daniel fared better but still had a long haul. Although he never had anything really serious happen, he just took a long time to get over his A's & B's and take all his feeds on his own. Maybe he was just waiting for his brother to be ready to go home too.
When they came home healthy, I really thought we were in the clear. The only worry I had related to their "preemieness" was RSV. They only left the house to go to the pediatrician. We were living in NY then and didn't have any family or friends nearby. This turned out to be a blessing since no one came to visit and therefore didn't bring their germs with them. The boys didn't get sick the whole winter.
By March, I knew that Ben was developmentally delayed. But there was nothing I could do about it yet. We were moving home in May and I already knew that it took upwards of 6 weeks to get a PT to start seeing him.
Ben finally saw a PT in July. She came to the house and agreed that he was very delayed. At that point he was 9 months old (7 months corrected). Her assessment put him at about a 3 month level developmentally. Unfortunately she was going on holiday for 6 weeks and was only able to give us some tips on what to do. In August, Ben finally got in to see the PT at our local hospital on a weekly basis.
At this point, I still didn't have any idea that Ben had CP. Well, I should say my head had no idea. My gut knew something was up. All last summer, I was a wreck. I would say that I was depressed. I was overwhelmed. All I wanted to do was sleep.
The week after their 1st birthday, we went to a children's hospital a few hours away for the boys to have EEG's. Daniel had had a "shaky episode" and their pediatrician wanted both boys to have EEG's to rule out epilepsy. After their EEG's, we met with the neurologist. He told us that Daniel was fine and was likely having "shudder attacks". These are common in young children and usually go away within the first 2 years. Then he talked to us about Ben. He told us that Ben has spastic diplegia cerebral palsy. He told us that he didn't know if Ben would walk, run or play sports. He told us that Ben was obviously very intelligent and that the CP didn't affect his cognitive abilities. He told us that Ben was lucky to have a twin brother and that Daniel was lucky to have Ben. We just sat there. I don't think we asked even one question.
Then we drove home. We hardly talked on the way home. I'm pretty sure I cried. The whole drive home I was just itching to get on my laptop and start googling.
It's now 6 months since "diagnosis day". Ben is making great progress. He can sit up quite well, army-crawls everywhere, and can pull up to kneel (he's close to pulling up to stand). His fine motor skills are great and his OT now sees him just once a month. Just last week, he started training for his first walker. He did absolutely amazing and walked everywhere he could. His PT was thrilled with how well he did.
I am doing OK. Most days are good. Some days are hard. Some moments are really hard. Luckily, I have Daniel too so I have to face Ben's delays everyday and I can't be naive about how delayed he is. This makes it much easier to go to playdates and see other kids doing "normal" things. But sometimes, no matter how prepared I think I am, it catches me. I see Ben laying on the floor playing (because he can't get into sitting on his own) and all the other kids walking and running around him and it just gets to me.
But Ben is so much more than his diagnosis. He loves to be chased and tickled. He's a picky eater (he likes red pepper but not apples?). He has the most gorgeous eyes and the most wonderful smile in the whole world. He loves his daddy more than anything (even more than mommy). He loves Tupperware. He doesn't really like it when Daniel kisses him. But he loves to kiss Elmo. He is so determined and so hard working that it amazes me everyday.
And Daniel. He's small but a bully. He loves to take Ben's toys. But loves to kiss him too. He prefers mommy to daddy but would probably rather just have his blankie. His favourite word is "cracker". He loves to look out the window at the cars. He'll eat just about anything as long as you're eating it too. He has the bluest eyes.
So that's it. Those are my kids. I hope you enjoyed getting to know them.
My sweet, sweet boys are now almost 19 months old. Daniel and Benjamin were born on September 19th, 2007 at just 30 weeks and 2 days gestation. I had no complications with my pregnancy until 29 weeks when I started feeling some tightness and told my ob-gyn. Anyways, it turns out I was starting to dialate. A week later, I was dialated even more (even though I was not contracting). Both boys were breech and apparently they could feel Daniel's feet. They were very worried about cord compression and it was decided that an emergency c-section was in order.
So, within the hour, they had arrived. I was terrified. They were too young...just 30 weeks. They weighed 3 lbs 4 oz and 3 lbs 7 oz. They were of course taken right to the NICU after just a few pics with me.
They stayed in the NICU for 8 weeks and 1 day and came home together on November 15th, 2007. They both had rough hospital stays, but Ben definitely had the harder time. 24 hours after birth he was put on a ventilator. He was on it for 4 days. He spent the next 4 weeks going between CPAP and nasal canula. He got an infection. He required many blood transfusions. But finally, he got stronger and did better and got to come home.
Daniel fared better but still had a long haul. Although he never had anything really serious happen, he just took a long time to get over his A's & B's and take all his feeds on his own. Maybe he was just waiting for his brother to be ready to go home too.
When they came home healthy, I really thought we were in the clear. The only worry I had related to their "preemieness" was RSV. They only left the house to go to the pediatrician. We were living in NY then and didn't have any family or friends nearby. This turned out to be a blessing since no one came to visit and therefore didn't bring their germs with them. The boys didn't get sick the whole winter.
By March, I knew that Ben was developmentally delayed. But there was nothing I could do about it yet. We were moving home in May and I already knew that it took upwards of 6 weeks to get a PT to start seeing him.
Ben finally saw a PT in July. She came to the house and agreed that he was very delayed. At that point he was 9 months old (7 months corrected). Her assessment put him at about a 3 month level developmentally. Unfortunately she was going on holiday for 6 weeks and was only able to give us some tips on what to do. In August, Ben finally got in to see the PT at our local hospital on a weekly basis.
At this point, I still didn't have any idea that Ben had CP. Well, I should say my head had no idea. My gut knew something was up. All last summer, I was a wreck. I would say that I was depressed. I was overwhelmed. All I wanted to do was sleep.
The week after their 1st birthday, we went to a children's hospital a few hours away for the boys to have EEG's. Daniel had had a "shaky episode" and their pediatrician wanted both boys to have EEG's to rule out epilepsy. After their EEG's, we met with the neurologist. He told us that Daniel was fine and was likely having "shudder attacks". These are common in young children and usually go away within the first 2 years. Then he talked to us about Ben. He told us that Ben has spastic diplegia cerebral palsy. He told us that he didn't know if Ben would walk, run or play sports. He told us that Ben was obviously very intelligent and that the CP didn't affect his cognitive abilities. He told us that Ben was lucky to have a twin brother and that Daniel was lucky to have Ben. We just sat there. I don't think we asked even one question.
Then we drove home. We hardly talked on the way home. I'm pretty sure I cried. The whole drive home I was just itching to get on my laptop and start googling.
It's now 6 months since "diagnosis day". Ben is making great progress. He can sit up quite well, army-crawls everywhere, and can pull up to kneel (he's close to pulling up to stand). His fine motor skills are great and his OT now sees him just once a month. Just last week, he started training for his first walker. He did absolutely amazing and walked everywhere he could. His PT was thrilled with how well he did.
I am doing OK. Most days are good. Some days are hard. Some moments are really hard. Luckily, I have Daniel too so I have to face Ben's delays everyday and I can't be naive about how delayed he is. This makes it much easier to go to playdates and see other kids doing "normal" things. But sometimes, no matter how prepared I think I am, it catches me. I see Ben laying on the floor playing (because he can't get into sitting on his own) and all the other kids walking and running around him and it just gets to me.
But Ben is so much more than his diagnosis. He loves to be chased and tickled. He's a picky eater (he likes red pepper but not apples?). He has the most gorgeous eyes and the most wonderful smile in the whole world. He loves his daddy more than anything (even more than mommy). He loves Tupperware. He doesn't really like it when Daniel kisses him. But he loves to kiss Elmo. He is so determined and so hard working that it amazes me everyday.
And Daniel. He's small but a bully. He loves to take Ben's toys. But loves to kiss him too. He prefers mommy to daddy but would probably rather just have his blankie. His favourite word is "cracker". He loves to look out the window at the cars. He'll eat just about anything as long as you're eating it too. He has the bluest eyes.
So that's it. Those are my kids. I hope you enjoyed getting to know them.
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