Tuesday, March 19, 2013

Lots of progress and lots of great news!!





   
 From Erik and Dawn:
We know, we know!!  It's been 3 months since this blog has been updated, and we thought about it often, but unfortunately, with a 17 year old, 14 year old, 12 year old, 19 month old and 3 month old, time is not exactly on our side. We do, however, take lots of pictures and videos, so our time is well documented.  (You can enjoy many of her short videos below.)
Analise has really been improving in all areas of her life.  She is really starting to use her voice now. Her vocabulary, although small, is expanding daily and her mimicking is really cute.  She actually understands almost everything we ask or tell her, but we are now working on the process of getting her to say those things on her own.  
Analise loves music and is even starting to sing some words and dance to the songs she loves.

Analise standing and dancing to Abuela singing:


   
Dawn and I noticed that her upper frenulum (skin between her upper lip and teeth) comes down very far and is attached between her two front teeth.  We found that several AMC kids had the same problem so it could be a part of the condition.  There are a few different options, but most revolve around waiting a couple of years to see what will happen.  The dentists actually say that the kids will eventually fall and the frenulum will tear with the fall. OUCH!!  Not exactly what we want to happen to Analise, especially since she won't be able to break the fall at all.  

Physically, Analise  is much more active.  She can scoot around the entire house in record time, and smiles the whole way.  She still has minimal active arm movement.  Her right index finger still has a strong twitch, but we are waiting for the others to follow suit.   


We are also trying electric stimulation on her forearms and biceps.  It's not easy (on her or us), but hopefully it will stimulate her muscles and help them to move.  We got some information from a fellow AMC father, Jason Coutee, about how the muscle stimulation has helped his son Jace.  Don't know if you remember Jason, but we posted some of the songs he has written about his son a while back.  I think you can also see them on his new blog:
http://amyoplasia.com/?page_id=93


Muscle stimulation time...hey this isn't that bad!! 

 

Analise finally got a "loaner" gait trainer from CCS until we work out the insurance for her own walker. This gait trainer is much better than the walker she was using because it supports all parts of her body, while promoting proper techniques for walking.  She loves roaming around the house and it's only been one day.  It was a great sight today, walking in the front door after a long day at work and seeing Analise walking around the house with a smile on her face.   We can't wait to see what she will do in the future.
Video of Analise on her new Gait Trainer:

 
Although her arms don't move "regularly", she finds a way to do everything!!  Some of the things she can do:  play the piano and xylophone, pick up small and large items, stack toys and blocks, put things away in containers, push buttons (especially on the remote control when I have sports on TV), tap rocks together to make music, and clap (in her own way).

Here are some short videos of Analise doing things her way:  
 
 Playing the Xylophone, as well as learning her colors!!

 
Putting her toys away, this way may take a little longer, but it gets done!!


Playing with blocks-She has learned how to say "help me".

Playing with puzzles-I can't believe she has figured out how to put the puzzle piece back in!!


Playing the keyboards 
(her cousin Bela is going to teach her how to play the piano)


Making "music" with Grandpa, she loves those rocks!!


Moving her arms with a little bit of help from Erik's invention


Turning the pages of her books, one at a time.



But I want to watch Laurie Berkner, not Football!!



 
  Analise is truly an amazing girl that doesn't give up.  Last week she also got her new AFO's (ankle foot orthotic)  and KAFO's (knee ankle foot orthoticts) that fit much better. The staff at Johnson's Orthopedic in Riverside are incredible and really do everything they can for Analise.  

THERE IS ALSO SOME MORE GREAT NEWS, WE'VE SAVED THE BEST FOR LAST!!:

Analise is getting fitted for a special Wilmington Robotic Exoskeleton (WREX), an arm orthosis that helps children with very little residual strength to move their arms in space.

We are very excited about this, especially since there are very few people in the world that have this orthosis!  In June, we are visiting Dr. vanBosse and Dr. Zlotolow in Philadelphia for her semi-annual checkups, and then we are headed to Delaware to get Analise fitted for the WREX.  WREX was even featured on a little girl with AMC named Emma during the New Year's Eve videos of 2012 on ABC. This is still very new for us, so as we find out more information, we will let everyone know.  

Check out a video with Emma and her Magic Arms:


What Erik rigged up in the meantime to help Analise move her arms...let's call it a very primitive WREX
 

We will also be attending the AMC convention in Las Vegas this July for the first time.  It will be exciting to finally meet all of the great people we hear and read about on Facebook and through Shriners in Philadelphia.  We can't wait!

Family update:  
Dawn has been back to work for a couple months now and feels very busy, as expected, but somehow keeps a smile on her face.  

Kaley is getting very close to turning 18 and graduating from high school.  She also bought a cute little car for herself, so she will be looking for work very soon.



--> Kyle has been playing high school lacrosse and is doing very well.  He has scored several goals and has had many assists in the programs' first year.  I am helping coach (even though I am still learning the sport) and having a blast.  I love high school sports and the excitement that comes with it.  I feel just as excited as Kyle during game days.  



 
--> Kassandra is doing extremely well in school (straight A's and A+'s for the second time in 7th grade) and is becoming a scoring machine in soccer.  Analise is even taking after her father and yelling "Kassandra" during the games.  



 
And the littlest one, Blake, he is as cute as can be.  Analise absolutely adores him and we are pretty sure he is going to think his name is "You're so cute!" because we say that about 100 times a day.  He is always happy and smiling and definitely brightens our family's day.  

Sorry if we have been a little out of the loop with everyone, but hopefully soon we will get back to "normal" hahahahaha.


Have a great Easter, and hope you had a wonderful Christmas!


5 comments:

  1. My little girl was born in Oct of 2012 and was diagnosed with AMC. Your blog was one of the first websites I found when looking up information. Seeing Analise's progress is wonderful! I don't know if you're interested but here is our blog to see pictures of our little girl Paige http://roleplayreallife.blogspot.com/

    It's truly amazing on how fast they grow and figure things out!

    ReplyDelete
    Replies
    1. We love sharing Analise's story in the hope that other AMC parents will be encouraged and inspired by her progress. It's also important for other parents to know that they are not out there by themselves. You are now part of the AMC family. Will you be going to the conference in Las Vegas in July? Analise's parents and siblings will be going as well as us, her grandparents. This will be the first conference have attended. Paige is BEAUTIFUL!! We read your blog and enjoyed getting better acquainted with you and Paige. Maybe we will see you at the AMC Conference. https://www.amcsupport.org/vegas_about.html
      Rich and Marti Russell

      Delete
    2. This comment has been removed by the author.

      Delete
    3. Checking out your blog again and just noticed your reply! Unfortunately we won't be making it this year to the conference (too much going on, wish we could have though we are only 4-5 hours away!). I'm hoping for next year when she's a little older too! Have fun and can't wait to hear all about it :)

      Delete
  2. Are you feeling like you do not have the car you deserve?
    This is because the salesman is trying to get a great commission out of you.
    Don't treat a salesperson like a friend. Continue reading for some valuable tips and information.

    my weblog :: cars

    ReplyDelete