Rachel also has a swing that she uses in physical therapy. It is used to help strengthen her core and her balance. I sat on it with her once and it is really relaxing. If only I had the type of house that we could install our own.
They alternate from swinging forward and backwards to side to side.
We took the girls on a fall hike recently. We all love this time of the year. (LOL as I think of the Facebook picture Steve posted about saying "pumpkin spice latte" three times into a mirror and a girl in yoga pants will jump out and tell you everything she likes about fall). The color of the leaves, the smell in the air, the crunch of leaves under your feet, pumpkins, apples and ect.
Meg, Rachel and Breanne
Love finding spina bifida daisies!
Alicia recatching her grasshopper.
The pint sized princess walked for part of the hike then rode on my back. I had added a yard of duck canvas to our baby carrier back in June to accomendate Rachel's size and at that time casts. I am glad I had altered the baby carrier and look forward to more family hikes this fall.
Yesterday Grandma and I spent a long morning with Rachel at Children's Hospital.This was the first time there in several months. The construction around Watertown Plank Rd is crazy. I never thought I would temporarily forget my way around Children's Hospital but I have to admit we road the elevator several times due to my forgetfulness. I will actually take that as a good thing meaning that Rachel has been healthy enough not to need to be there. Rachel had her annual urology testing. She started off with urodynamics testing. We had a great team helping with the test this time around. Rick and Molly explained everything they were doing.They also ran the test twice to ensure there were not any false positive results happening. And yes, Rick, I remember that you told Rachel she needed to buy Grandma and Mom a Starbucks once she is a working girl.( I am not sure when they started serving Starbucks at Children's but sure enough I saw the sign for at while walking on the 2nd floor). Rachel's fill rate for the urodynamics was at 15-which is based off of her weight. I apologize I forgot what the formula used was. To estimate pediatric bladder volume by age- take the age-add 2 and multiply by 30ml.
age 3 + 2 = 5 x 30ml = 150ml
Rachel then had a renal and bladder ultrasound. After her ultrasound, she had VCUG testing done.
Rachel was a great patient. She let out a few complaints but nothing earth shattering. Rachel the Brave was her name of the day.
Drumroll, please. Great news is that Rachel's bladder and kidneys look healthy. Her bladder is smooth, grew to the correct size for her age and her bladder volume is exactly where it should be also. Her kidneys also grew properly to the correct size for her age and look great! No hydronephrosis or kidney reflux!!!!!Hooray! She is still experiencing bladder spasms and sadly can not empty her bladder on her own. We will continue with catheterizing and will start using Vesicare to help with the spasms.
My nephew Max and brother Glenn dropped off a swingset that Max had outgrown. The story behind the swingset is that my grandparents in Green Bay found it. They picked up all of the pieces of this swingset that a family was throwing out. They delivered all the the pieces to my parents' house (which is about 2 hrs north of Green Bay). My dad sanded and repainted all of the pieces. After refurbishing the swingset, my dad brought it down and put it together for my nephew Max.My brother screened in the sand box and added a door to the sand box. Rachel is head over heels in love with this swingset.
No naughty kitties getting into this sandbox!
Look at this happy girl! She amazed me by showing me how she can get onto and off of the swing without any help. She still needs to work on moving her legs up and down- she pulls up her knees and then kicks her feet.
Look at Rachel's amazing arm strength! Yes!She lifted her entire body a good 4 inches above the seat of the swing to get into the swing. Embarrassing to say- I am no where near to being that strong in my arms. I tried to do a pull up on the monkey bars of the swing set and was an epic failure.
Rachel's hard work in therapy paid off. There is both a ladder and a rock climbing wall to climb up to go down the slide. She can climb up both without any assistance needed.
While these activities may seem like "no big deal" things to the average parent- to the parents of a special needs child, it is a like that happy moment when you are blowing out the candles on your birthday cake. It is that well needed reassurance that, yes, my child is more like his or her peers and getting further and further away from all of those horrible statistics you get bombarded with when your baby is diagnosed with having a disability. It is part of those "unseen" daily miracles that people often take for granted. I am blessed to watch my 3 yr old daughter show what a child with spina bifida at L4 can do and to see her inspire others.
I was unable to get a picture but the pint sized princess likes Pepper and me to ride on this seat with her. I am not sure how much Pepper enjoyed swinging but he will do anything for a Cheerio.
Rachel and Pepper are "monkey see monkey do" together. Somedays, I swear they conspire together to get me to clean up one mess while the other makes a different one. At least Pepper is consistent- he always takes his stolen items to chew to the shoe gathering in the sunroom.