Monday, February 27, 2012

Discipline

How do you discipline a kid who, up until this regression, has never done something she's not supposed to?  I honestly don't know if she knows there are rules in this world.  Up until the regression she smiled, flipped through her books, sat and played with toys, worked hard at therapy and achieved so many of our goals.  We encouraged her to get into stuff!  I remember one day before John left for work he opened one of our drawers in the kitchen and showed her how fun it would be to pull stuff out and make a mess.  A couple of times I put her in a time out for some small offense.  I came back to check on her and she had gotten out of the chair...all by herself.  Instead of telling her she needs to wait until I come and get her out of time out, I cheered for her.  Yea Emmy, you got out of that chair all by yourself...what a big girl!  The girl has never complained about not having a turn or been possesive over any toys.  She simply does not care about material things, other than her books.  As long as she's engaged with people, she's happy.  But this leads me to our current problem.  Since she's now unable to do things on her own, she wants somebody to engage her most of the time.  The only thing she can do independently is listen to music which she does A LOT when we're home and cooking, cleaning, living life.  So, I think she gets bored, restless, frustrated she can't just go over, sit down and look at her books.  It was not so long ago that she could.  Now, I need to help her get to the floor and hold the book.  I need to take both hands and help them flip.  Since I'm not available to assist her 24/7 AND she can't communicate with me she pretty much freaks out.  Since she's started regressing there has been a ton of head hitting, biting, flailing, screaming and otherwise uncontrollable fits.  Now, I'm used to a fit.  Ava was an expert fit thrower but Ava never hurt herself.  That's the part I have to watch carefully with Emmy.  And I'm in the dark about what the fit is about.  I would say maybe 10% of the time I know why she's upset.  The other 90 I'm guessing.  Does something hurt?  Is she feeling sick?  Did she bite her hand too hard or hit her head on something?  Or does she simply want me to change the song?  Maybe she's upset because she wants to sit on the potty...the list goes on.  I threw any and all discipline (like what I would have done with Ava) out the window.  I just wanted to make her happy.  And truthfully, when we found out she had Rett Syndrome and began to understand what she was going through my heart was breaking.  I started having a hard time just engaging her in simple floor play.  I was watching the skills disappear and it was just too hard to watch.  The situation just seemed (and still does) so cruel.  So I found myself, during these fits, crying right along with her.  I tried everything possible to sooth her.  I didn't tell her to stop biting or hitting.  If my body was failing me I'd probably bite and hit too.  But now we're all starting to get comfortable with her new limitations.  I'm so unbelievably thankful to have reached this point.  Losing the skills was the absolute worst for her and for us.  I am bracing myself for what may lie ahead but really the hard part (so far) was going from her having some independence to basically having none at all.  Even though she's more comfortable with what her body allows her to do she still has the uncontrollable fits.  I think improving communication is going to help A LOT and we're taking steps to help us be able to communicate with her better.  But that will take time.  We looked into helping with anxiety but the doctor didn't recommend medication.  He suggested behavioral therapy.  I know nothing about behavioral therapy and at the moment I'm too tired to start researching.  Any other Rett parents out there have suggestions?  Are there different types of behavioral therapy or is ABA the most commonly used with our girls?  And what the heck is ABA?  I've heard it described in broad terms but want to know what it would look like when you're trying to break self injuring behaviors.  I don't mind adding another therapy to the mix if it will calm my girly down.  So for now I just try and read her before the fit comes.  I try to communicate with her before she's too upset.  And if I'm not succesful and the fit is out of control I put the braces on her, surround her with pillows and let her flail.  I guess if she can't express herself with words then she needs to express herself through movement.  She needs to get out that frustration, anger and saddness.  We're just all thankful when it's over and we can move on with our day...until another one strikes!     

Friday, January 27, 2012

Dress Up Time

Around 4 pm or so these two start getting a little restless.  The hats, scarves, dish towels, safety pins, yarn, crayons, tape and other random household items come out and it's dress up time.  Emmy is such a trooper.  She pretty much goes along with whatever story line Ava has created...




Emmy mid-flick
 
For some reason dress up time with Ava always involves tape.








The flying fairy...


...and some kind of chinese princess


This is Rapunzel...with homemade hair.



And here's the prince...also with homemade hair!




Tuesday, January 24, 2012

My Therapists

There are so many therapists in my life...that work unpaid.  Mainly, my parents, sister and brother.  These four have listened patiently and loved unconditionally.  They've helped me wade through the deepest, scariest waters.  They've reassured me, telling me I can do this even when I think I can't.  And I am just beyond grateful.  I've realized that I'm not the, "pull up your big girl undies and move on" kind of person.  When the shock and saddness hit, I had to take the time to feel it.  I had to let myself get all the way to the bottom of it and rest there for a while.  And had I not taken that rest, I think I may have exploded.  I needed to call my family and repeat myself a million times and have them tell me it was going to be ok.   And now, after many months of digesting our new reality, the saddness has subsided a bit.  It still washes over me, knocks me down, but it takes less time for me to get back on my feet.

I feel like I've found a way to grieve but still live life.  Be sad about Emmy's struggles but still find joy. There was a time when I wondered if I would ever feel joy again.  It felt like no matter what I was doing a piece of my heart was dark.  Nothing felt complete.  But over time I am getting better at pushing the Rett monster aside and trying to focus on whatever small joy may be presenting itself at the moment.  Rett Syndrome will be there, it doesn't need my immediate attention all the time.

Never have I had to deal with a difficult situation that I wasn't able to push out of my mind, if even for a brief couple of minutes.  There has always been some distance.  But Rett Syndrome is an every day, in your face, kind of struggle.  And to top it off the person who is struggling is someone who owns a piece of your soul.  It has just taken me a while to figure out how to live with this battle and still find joy.  During one of the MANY converstations I've had with my dad throughout this time he told me that living with joy is a choice you make.  Ok, easy to say, harder to do when you're watching your daughter regress.  Then he shared a story with me...a piece of his childhood that I never fully understood.  Throughout his childhood his father had heart attacks year after year after year.  He had a host of medical problems that left him unable to work and in pain.  My grandma worked long, hard hours and my dad went off to school each day.  He said when they returned home they were never quite sure what they'd find.  This went on for years.  As a young boy he had to figure out a way to live life, enjoy life and focus on all the goodness that surrounded him.  This story not only gave me a little insight into what has made my dad, my dad...it gave me strength.

My therapists, whether it's my family, other rett moms, neighbors or friends have sat with me and listened.  It's really remarkable.  They haven't tried to 'fix' things... they haven't offered up one liners like "It's God's plan" and walked away.  They've sat by my side and let me grieve, letting me know it's ok to feel.  Really, what would I do without these people?  I just hope I can be that person for somebody else.  That I can be a good enough friend to just sit by their side and listen.   




  

Thursday, January 12, 2012

Winter Walk

Ava has been asking if it's really winter.  There has been pretty much NO SNOW in Chicago until today.








They all came in with smiley, red faces.  John said at one point the sled flipped over and they both went face first into the snow.  He thought Emmy would start screaming.  Nope.  She was just happy to eat snow without having to make her hands cooperate!

Friday, January 6, 2012

Holidays

Christmas, New Years and all the days in between had a different feel this year.  There were some emotional ups and downs but overall not as hard as I thought it would be.  Surprising, I know!  When we celebrated Emmy's 3rd birthday in August I had talked myself into being excited about her little family party and I thought it would be great.  Well, when the day came it was HARD.  Much harder than I thought it would be.  I've come to understand that the saddness hits at very unexpected times.  I never know what will trigger it (might have something to do with pregnancy hormones too).  But thankfully we were surrounded by our families throughout the holidays and just being with people who love and care about our little foursome seemed to make everything better.

We spent Christmas at John's parent's house...wish I had a bunch of pictures to share but just didn't get around to finding the camera.  Pure laziness!  I spent my time there sleeping in, enjoying A LOT of wonderful food and just hanging out with his family.  We went to Christmas Eve mass with the kids and both girls did amazing.  Emmy usually has a hard time at church but she just snuggled with John and was all smiles!  The message given at the service was one of hope...it was just what I needed to hear.  

 
Ava and Emmy love their Mimi and Grandpa's cat, Jack.  This cat is the most even tempered animal I've met.  He sits on his little perch while Emmy attempts to pet him.  Her attempts usually resemble hitting or flicking and he just stays put and takes it!  The look on his face says it all.

The following Friday John got home from work and we made a last minute decision to drive down to my parent's house (near St. Louis) for New Years.  It's about five hours in the car so I brought along my huge body pillow and tried to stretch out the best I could.  I'm so tired by Friday that I passed out with the girls early in the trip and John chugged his coffee to stay awake. 

Again, I took no pictures...boo.  But we did have a wonderful time!  New Year's Eve night my mom made a huge Mexican feast, we played dominos (although my dad secretly wanted to be playing bridge : ) and I actually made it until midnight.  My brother, his wife and three boys came over and the cousins ran wild together.  Uncle Kyle is always the entertainment...playing all sorts of chasing games the kids love.  One day I'll get a video of the action, it's pretty hysterical!

I did manage to get my act together and get out a Christmas card AND it's a picture of our whole family.  Getting a picture of the four of us is a daunting task so I usually just send out a picture of the girls.  So I'll leave you with the Foster Four, soon to be FIVE...I'm starting to get a little nervous about that!




 



Wednesday, November 30, 2011

Going on 24 Weeks!

Finally a belly bump picture!  I've been feeling great other than the usual stuff, occasional heartburn, backaches, whatnot.  I'm feeling lots of little (and not so little) kicks which I think is the best part of pregnancy.  John felt his first kick the other day too : )  I know we've got about half way to go but I'm getting pretty excited to meet this little girl!  

Wednesday, November 9, 2011

Also in October...


messy hair emmy in her tinker bell jammies

Master Tigeress (many thanks to Grandma E. for making her costume!)

and the Dragon Warrior!


Wearing her Cardinals shirt, enjoying some World Series action!  This is about the fourth inning ;)
Sorry dad


After trick or treating bonfire at the Rossi's

the girls discovered pixie sticks...yikes!
apple picking


Emmy at school!