Tuesday, May 31, 2011

Memorial Weekend in Pictures (with a Few Updates)

Playtime with Daddy on a lovely warm and sunny Memorial day. William is using his special Childrite chair to practice sitting!!
My big boy sitting tall in his chair.
Our newly planted Garden with a pathway for the dogs (currently training them to use it ;-) because they like to run right through the flowers to our side door. The white fence is a work in progress but coming along nicely. Before our new neighbors arrival; their Realtor informed us of their "deathly fear" of dogs. We had been planning a privacy fence for some time but this was the true motivator to begin building. As it turns out the new neighbor and her four year old daughter are wonderful and actually tolerating the dogs. Over the weekend Ella played at their house for the first time; I was thrilled ;-) The woman was born in India, she moved to the United States 10 years ago, she cooks delicious smelling traditional Indian food, and has traveled extensively... which I find fascinating. For as long as I can remember I have owned a wall size world map and have always dreamed of visiting exotic lands and cultures. India is one of those places, among many, that I have yet to see.


Ella giving William a little push in his Pony gait trainer... "Go William GO"...
Modeling mommy's glasses in her new summer pajamas.
There was a frosted cupcake on the plate in front of William!; he's very happy to be eating a variety of foods again since stopping the Ketogenic diet. Unfortunately, he is once again having multiple seizures every day. Last week he had an EEG (two dozen wires glued to his head for over an hour) which was very stressful for us both and the technician. He cried and fought nearly the entire time; very difficult to watch. ( I think that will be the last one for a long while). Today we had a follow up appointment at Strong hospital with the Neurologist. Our Neurologist is a kind man and extremely intelligent but not very aggressive with treating William's seizures. He maintains an outlook that because of the severity of Will's brain malformation seizures will be a constant during his life and that it won't harm him to let the seizures happen (to some degree). I of course keep asking if the seizures can elicit more "seizure pathways" and interfere with potential development; and if so shouldn't we be proactive to gain control. He insists that the seizures will not do further damage to the brain and should not hinder development. I fear that he does not have great expectations for William's potential development based on his MRI. I do not want to limit my son's capabilities and am also very aware that seizures are uncomfortable and upsetting for my son. I can imagine they are not a pleasant experience to be having daily. Yet at the same time anti-epileptic medications can be highly sedative and have side effects; so it is a balancing act from hell. In conclusion and ending the appointment the Neurologist tells me that, " watching William have seizures daily must be very difficult so I will be as aggressive in treatment as you would like." Which means that he is willing to work with us but throwing the ball back into my court so to speak. So here we go changing medications and increasing doses again at my request... wish us luck....

Tuesday, May 24, 2011

Bits and Pieces from May

The twins and I love visiting Grandma and Grandpa's house; especially during hot Spring and Summer days. Grandma's gardens are looking lovely and sumptuous already in May.......
One of my favorites plants; my mothers bleeding hearts are looking much better than my own. My flower gardens are finally planted... pictures to come soon. I don't especially relish digging in the dirt but love splashes of color throughout my yard and watching the beautiful plants bloom. I planted some red tubular plants in hope that hummingbirds will visit this year.

A few months ago I pulled a muscle in my back lifting William; nothing serious but enough to make further lifting difficult for many days. At that point I decided I was a little too plumpy and out of shape. So my personal vision is to be strong and toned to feel great but also because it is simply what my lifestyle demands. William depends on me for all movements; everyday, and he is not a small kid anymore. Yet, not only are the workouts great for strength but I find them incredibly stress relieving. My parents well equipped home gym allows me the chance to workout while still watching the kids. They allow a few bins of toys to be stashed under the stairs and have a t.v equipped with netflix via the Wii near the workout area; great distractions for the twins so I can focus on running or lifting weights.
The picture above is one of the most challenging exercises (for my busted abs anyway). The goal is to hang from the ceiling with the black arm straps/slings and do crunches without swinging. Your body naturally wants to swing so it is a workout in and of itself just to keep still before drawing the legs up. Core strength is key though for lifting.

Last week Ella ended her first year of preschool with a class trip to the Seneca Park Zoo. Her favorite part of the trip was a giant log carved into a bench. In the picture above she is in a contemplative mood; watching the crowds of people trying to entice the tiger out of his cool hiding spot. I can't blame the tiger; personally I would hide too with all those people waving cameras and shouting at me......



William styling the 3 E love wear..... 3E Love is a disability awareness clothing line and marketing company founded in 2007 by siblings Annie and Stevie Hopkins and their family & friends. The mission of the company is simple; to create and market products and services that embrace living life no matter the obstacles, and by doing so, educate society and empower those with disabilities to love life (taken from their website). The wheelchair heart is their fabulous symbol shown along with the 3 E's; Embrace. Educate. Empower. Embrace diversity, Educate your community, and Empower each other. Learn more or purchase products to spread the cause at this website 3E Love Store — ABOUT 3E LOVE and like on facebook!!!

My kids and I often get quick glances or even stares while out in the community. Before my pregnancy and the twins I was just an average person in a crowd; obscure and not used to attention. Which suited me fine since I was the timid wall flower type. So it was a shock during my late 2nd and 3rd trimester of pregnancy to receive attention and even comments practically everywhere I went. When grocery shopping during my 3rd trimester strangers would let me go ahead of them in line... people would nervously ask how far I was past my due date; as if they feared I would go into labour in the middle of the store. When the kids were babies people used to stop us and exclaim, "twins, oh how cute... " and so forth. Now we mostly get stares or comments because my handsome boy is so big (he and Ella are still the same size; weight and height) and not walking or talking. More often than you would think; strangers will stop us and ask questions. Just last week at the zoo a woman asked how old William was and if he was in a special stroller. SO..... since we seem to get this attention; I love the idea of expressive tees, bags, and yes even a bumper sticker to spread the message of love and acceptance for all people regardless of varying abilities. Spread the 3 E love!!!!





Some Random pictures from the month of May and Memorial Day weekend.....

Oh how we love delicious Avocados....
Ella during her dance recital this past week!! She is the blond in pink smack in the middle of the princesses.
A modest selection of flowers Ella and I planted this weekend.
Love birds.... and finally the men in the "family".....