Well, it looks as though after much ado, Spring has finally arrived to North Dakota. Things have been going well and we continue to see positive changes and growth in Ethan. For the 1st time in his life, he's able to ride a bike. We were fortunate enough to have additional funds in Ethan's "Germany" account whereby we purchased a special bike that he was comfortable on and supported his needs. He picked out a lime green bike, with a little basket in the back that he can put things in. A video of his very 1st time can be seen below. That was on a Tuesday...by Sunday he rode 1.5 blocks while we took a walk along side him..He loves it! Now, all we need to get is some Toy Story decals to put on the bike and we'll be really set.
Outside of that, Ethan has decided to learn how to climb a ladder and proceeded to climb up the 5 rung ladder into our playhouse and then went down the slide (on his tummy) all by himself. Of course mom was having a heart-attack just waiting for a fall but as Ethan put it... "mom, I can do it--SEE???!!!" He's having a blast with his new found freedoms and the smile on his face really shows it.
In addition, he's growing like crazy as it seems I'm buying him new jeans all the time (my husband is convinced I'm just shrinking them). Its fun to see him stretching out and moving out of that "little boy" phase.
We see the orthopedic surgeon in mid-May regarding Ethan's progress and will be discussing Hamstring surgery as Ethan's hamstrings are still short from the past tone in his legs. Stretching helps some but will likely not be enough to get him stretched out to where he really needs to be in order to stand up straight and without support. For the time being however, he continues to get faster and faster with his crutches and his footing too has showing improvement over the last few months.
We're truly excited to see what the summer months bring...Stay Tuned! :-)
Well..that's its for now. Until later..
Lisa
My son Ethan has Cerebral Palsy-spastic diplegia.In July 2010 we had an adult stem cell treatment in hopes that our son would get his wish of having as he puts it "New Legs that Work". This blog is our story, adventure and progress.
A WORD TO READERS:
This Blog is intended to educate as many as possible. Our story is unique as is each story of a special needs child.
Thank you!
Lisa
Thank you!
Lisa
Wednesday, April 27, 2011
Tuesday, April 19, 2011
Friday, March 25, 2011
Snow, Spring and more Snow
Well, I can't believe the last "actual" update was February 6th! Wow--where does time go?
Ethan continues to do well! He has grown so much that its getting hard to carry him very far. He's getting extremely long and lanky. Its kind of fun to see his pants get shorter and shorter.
It seems that Spring will never arrive as we've had some nice weather with considerable melting and then mother nature decides that its not quite time for green grass and flowers and delivers another few inches of snow. Ethan is patiently waiting for the sidewalks to clear so that he can get out and play. He has informed us on a number of occassions that we can get rid of the wagon this year as he will be riding his bike and NOT in the wagon like other years. He makes me laugh and I can't help but admire his determined behavior. Needless to say we still have to get him a bike but have been waiting so not to torture the poor boy with having to simply "look" at his bike in the garage vs. riding it.
We also had another wonderful opportunity as a 3rd grade class from Henning MN interviewed me about Ethan. Based upon the Forum newspaper article they chose to write an essay on Ethan and what its like to have a disability. The essay is also part of a competition. The kids all wrote Ethan (and myself) "thank you" cards and included lots of words of encouragement... It was awesome and I can't wait to read the final story in April.
Other than that, its been life as we know it. Lots of therapy, lots of work and TONS of determination. Our goal is still on target for Disney World next year (feb/march) and we are sooo excited. Ethan has set yet another goal for himself and that is to take his first independent steps at Disney World... time will tell if he'll accomplish that goal but with lots of determination and work, I wouldn't disregard the thought that he'll be able to do it. He is a true trooper!
Thanks for everyone's continued prayers, emails and encouragement--Its truly appreciated.
Well..that's its for now. Until later..
Lisa
Ethan continues to do well! He has grown so much that its getting hard to carry him very far. He's getting extremely long and lanky. Its kind of fun to see his pants get shorter and shorter.
It seems that Spring will never arrive as we've had some nice weather with considerable melting and then mother nature decides that its not quite time for green grass and flowers and delivers another few inches of snow. Ethan is patiently waiting for the sidewalks to clear so that he can get out and play. He has informed us on a number of occassions that we can get rid of the wagon this year as he will be riding his bike and NOT in the wagon like other years. He makes me laugh and I can't help but admire his determined behavior. Needless to say we still have to get him a bike but have been waiting so not to torture the poor boy with having to simply "look" at his bike in the garage vs. riding it.
We also had another wonderful opportunity as a 3rd grade class from Henning MN interviewed me about Ethan. Based upon the Forum newspaper article they chose to write an essay on Ethan and what its like to have a disability. The essay is also part of a competition. The kids all wrote Ethan (and myself) "thank you" cards and included lots of words of encouragement... It was awesome and I can't wait to read the final story in April.
Other than that, its been life as we know it. Lots of therapy, lots of work and TONS of determination. Our goal is still on target for Disney World next year (feb/march) and we are sooo excited. Ethan has set yet another goal for himself and that is to take his first independent steps at Disney World... time will tell if he'll accomplish that goal but with lots of determination and work, I wouldn't disregard the thought that he'll be able to do it. He is a true trooper!
Thanks for everyone's continued prayers, emails and encouragement--Its truly appreciated.
Well..that's its for now. Until later..
Lisa
Saturday, February 26, 2011
Sunday, February 6, 2011
Milestones, Interviews and more...
Hello everyone,
This past week was another busy week for us with a few unexpected opportunities and some 1st time events.
The week started out with Ethan staying home due to not feeling real well. It was nice to have him home with me for the day and in between working at home that day, we had some much missed snuggle time. Needless to say, after a few home-made chocolate chip cookies, he started to perk up and felt better by evening. As Ethan put it... "Mom...can I have 2 cookies? Cuz I'm really sick and they will make me feel better cuz you put love in them"... Who could resist that line so yes...he got the cookies.
The rest of the week went pretty smooth until Thrs when a friend of mine from MN called me (They too are schedule to go to the Xcell Center)and asked if I would share our story with a KSTP Channel 5 in Minneapolis. I was honored to share the spotlight with her and immediately agreed. So on Friday, I conducted a phone interview with KSTP...The story aired that night.
Also on Friday, Ethan was interviewed again by the Fargo Forum. We had to laugh as while it was after school and his sister was home; he quickly dismissed her to the basement and added "Just until after my interview, then we can play Wii"... We are anxiously awaiting the new story to come out and will post the link here.
Yesterday, Ethan decided to do a few 1sts... He went bowling for the 1st time ever (not counting Wii Bowling)and tied with his cousin Lauren...he was pretty excited about the 2 spares and 1 strike he got and he was just as excited when his sister, Ashlee got a strike as well. Then, he walked up stairs with his crutches...He also stood for 3 seconds last night and has been moving around furniture like crazy. At times however I have seen what appears to be the want to take independent steps--we just haven't seen him do it; but you can tell the thought is there.
Outside of that; Ethan continues to walk more and more with his crutches every day. He walks with them while shopping; in school; at church; and in the house...he loves the feel of independence and he's even getting really good at opening doors with them as well as turning the TV on/off. He can even go backwards!
We are anxiously awaiting for some of the snow to melt and for spring to arrive. The kids are getting antsy to ride bike and to be outside again. As spring nears, Ethan will get his own bike as well as a helmet/pads for the 1st time. He's desperately wanting a Toy Story 3 bike so I guess we'll see what we can find. :-)
As always...thank you to everyone, for the continued prayers and thoughts, they are being heard and felt--keep them coming. :-)
Well..that's its for now. Until later..
Lisa
This past week was another busy week for us with a few unexpected opportunities and some 1st time events.
The week started out with Ethan staying home due to not feeling real well. It was nice to have him home with me for the day and in between working at home that day, we had some much missed snuggle time. Needless to say, after a few home-made chocolate chip cookies, he started to perk up and felt better by evening. As Ethan put it... "Mom...can I have 2 cookies? Cuz I'm really sick and they will make me feel better cuz you put love in them"... Who could resist that line so yes...he got the cookies.
The rest of the week went pretty smooth until Thrs when a friend of mine from MN called me (They too are schedule to go to the Xcell Center)and asked if I would share our story with a KSTP Channel 5 in Minneapolis. I was honored to share the spotlight with her and immediately agreed. So on Friday, I conducted a phone interview with KSTP...The story aired that night.
Also on Friday, Ethan was interviewed again by the Fargo Forum. We had to laugh as while it was after school and his sister was home; he quickly dismissed her to the basement and added "Just until after my interview, then we can play Wii"... We are anxiously awaiting the new story to come out and will post the link here.
Yesterday, Ethan decided to do a few 1sts... He went bowling for the 1st time ever (not counting Wii Bowling)and tied with his cousin Lauren...he was pretty excited about the 2 spares and 1 strike he got and he was just as excited when his sister, Ashlee got a strike as well. Then, he walked up stairs with his crutches...He also stood for 3 seconds last night and has been moving around furniture like crazy. At times however I have seen what appears to be the want to take independent steps--we just haven't seen him do it; but you can tell the thought is there.
Outside of that; Ethan continues to walk more and more with his crutches every day. He walks with them while shopping; in school; at church; and in the house...he loves the feel of independence and he's even getting really good at opening doors with them as well as turning the TV on/off. He can even go backwards!
We are anxiously awaiting for some of the snow to melt and for spring to arrive. The kids are getting antsy to ride bike and to be outside again. As spring nears, Ethan will get his own bike as well as a helmet/pads for the 1st time. He's desperately wanting a Toy Story 3 bike so I guess we'll see what we can find. :-)
As always...thank you to everyone, for the continued prayers and thoughts, they are being heard and felt--keep them coming. :-)
Well..that's its for now. Until later..
Lisa
Saturday, January 29, 2011
Thursday, January 13, 2011
Ethan's new legs...that work
Hello everyone,
Sorry I haven't updated our blog for a while but its been a little bit of a whirlwind lately with all of Christmas activities.
Well I'm not one for suspense...and from the title of my entry...I'm sure your wondering what news I'll be passing along to you so i'll pass along the news.
Ethan decided that he's had enough of his walker and started using his crutches this past week. He was scared to death the 1st time but a few days later decided to walk across the room a few times with them and all with complete ease. Yesterday in school, he continued to practice too in the hallways. The excitement that he shows...is unmeasurable. He still uses his walker and chair to get around longer distances but his walking is sooo much nicer with his crutches as he has to go slower than he does with his walker.
Needless to say, I've been in touch with our travel agent about starting to plan for the much promised trip to Disney World next year (2012). The kids are sooo excited.
Who would have thought that just a few short months ago Ethan was in a wheelchair and today...using crutches. Miraculous...
We also joined up with a local group called HOPE INC (watch the January 2nd episode of Extreme Home Makeover to get to know the family who heads the group and what HOPE Inc is.)...
Last Saturday we played Sled Hockey for the 1st time...Connor and Ashlee too got to participate. Mom pushed the sled for an hour and thought I was going to bed ridden the next day due to sore legs but...overall it was a blast and weather permitting we'll be back this Saturday. Ethan and Connor had a great time-Ethan scored 3x and Connor 1x...Ashlee wasn't too sure about it.
Our journey truly continues... Ethan continues to make definite progress. His tone reduction has been compared to that of what one might see with after having a rhizotomy surgery... He still likes to pull up on his toes a bit but we are confident that with stretching and strength building some of that should be resolved however due to short hamstrings, we may have to have a hamstring lengthening surgery in the future but we'll cross that bridge when we get there...For now, we are thrilled with the progress Ethan has made and continue to see daily miracles.
That's all for now...stay tuned!
Lisa
Sorry I haven't updated our blog for a while but its been a little bit of a whirlwind lately with all of Christmas activities.
Well I'm not one for suspense...and from the title of my entry...I'm sure your wondering what news I'll be passing along to you so i'll pass along the news.
Ethan decided that he's had enough of his walker and started using his crutches this past week. He was scared to death the 1st time but a few days later decided to walk across the room a few times with them and all with complete ease. Yesterday in school, he continued to practice too in the hallways. The excitement that he shows...is unmeasurable. He still uses his walker and chair to get around longer distances but his walking is sooo much nicer with his crutches as he has to go slower than he does with his walker.
Needless to say, I've been in touch with our travel agent about starting to plan for the much promised trip to Disney World next year (2012). The kids are sooo excited.
Who would have thought that just a few short months ago Ethan was in a wheelchair and today...using crutches. Miraculous...
We also joined up with a local group called HOPE INC (watch the January 2nd episode of Extreme Home Makeover to get to know the family who heads the group and what HOPE Inc is.)...
Last Saturday we played Sled Hockey for the 1st time...Connor and Ashlee too got to participate. Mom pushed the sled for an hour and thought I was going to bed ridden the next day due to sore legs but...overall it was a blast and weather permitting we'll be back this Saturday. Ethan and Connor had a great time-Ethan scored 3x and Connor 1x...Ashlee wasn't too sure about it.
Our journey truly continues... Ethan continues to make definite progress. His tone reduction has been compared to that of what one might see with after having a rhizotomy surgery... He still likes to pull up on his toes a bit but we are confident that with stretching and strength building some of that should be resolved however due to short hamstrings, we may have to have a hamstring lengthening surgery in the future but we'll cross that bridge when we get there...For now, we are thrilled with the progress Ethan has made and continue to see daily miracles.
That's all for now...stay tuned!
Lisa
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