Wednesday, February 1, 2012
A little video
FYI today is women in sports day that is why I posted the video stick around in march as I will be blogging a lot about CP that month because March is CP awareness month
Friday, January 27, 2012
rocky road
So the lack of blog post should single readers that I am back in school. but unlike last semester it has been really rocky thanks to OCD.
I behind on homework but if i get caught up I will cach up on here .
Anyway for the good news
basketball looks promising we have a tournament next weekend.
I love my biology class the teacher is super nice more on this soon.
I am also enjoying most of my other classes
I behind on homework but if i get caught up I will cach up on here .
If anyone has a facebook page click here for my blog page on facebook.
Tuesday, January 17, 2012
Guess who I met
So last Tuesday I went to San Francisco's pier at night. It was nice because it was not crowed or anything but I was not there to sight see. I was not there because I like the city but yet I was there to go the Aquarium by the bay but I was not there to see fish.
I was there to see a movie and not just a movie but a Q and A with the film maker do you know who yet?
I will give u a hint he is also a father,
He is a fabulous photo journalist his work has been in Time Magazine
got this from http://elmercqegs.files.wordpress.com/2011/03/time_magazine_logo.jpg |
It Was DAN HABIB OF INCLUDING SAM.
I was so excited to meet him and listen to him speak. He is soo good with presenting there were some kids there and it was really nice that he took the time to interact with him. He had recognized me and during the presentation asked me to stand up and I got a standing ovation. I really loved going it was soo cool because I finally got to 'meet' him . Of course we have been Facebook friends for a while now. I really love having IRLs. I was in my element going to stuff like this really solidifies that I want to be a disabled advocate on the rights of inclusion of students with disabilities. I am norm, something I am a part of is going to be having another youth summit and this time I will be attending. The best part was that the evening changed people's attitudes and got the conversation started. Thanks Dan for coming hope to see you again soon
Monday, January 16, 2012
MLK Poetry contest 2010
Happy MLK day
here is what I have to say to DR.King
Thank you Martin Luther King for paving the way for me. If it was not for you I would not have been born Thank you for laying the ground work for inclusion of those with disabilities wish you were alive to see how much closer we are to achieving your dream.
Ps when i do laundry I do the color load first then the whites
here is what I have to say to DR.King
Thank you Martin Luther King for paving the way for me. If it was not for you I would not have been born Thank you for laying the ground work for inclusion of those with disabilities wish you were alive to see how much closer we are to achieving your dream.
Ps when i do laundry I do the color load first then the whites
Friday, January 13, 2012
America 2012
I have never been to CHOP which stands for Children's Hospital of Philidelphia nor do i plan to donate a penny to them?
Why you ask
Meet Amelia she is a little girl whose needs a new kidney yet her parents were told by CHop that she can't because she has as the doctor's put it ever soo nicely. can you hear I am being sarcastic here Mental retardation and brain damage.
This is not fair as a advocate for those with disabilities It feels as if we are back to square one where kids with Intellectual disabilities yeah that is the right term are put into instutions. Socity has come to a census that this is wrong yet a DR can still say fthis in 2012 that is not fair.
As a person living with CP I feel deeply saden by the fact that this can still be said in 2012. I have been preaty lucky so far in that I have not needed and surgryies and would hate to think that someone would say no to me because I was not fit to live. Isn't that what Adolph Hitler did in Germany nearly 100 years ago. Isn't that what slave owners did to blacks when they treated them like horses during slavery. yeah that is exactly what they did but we now look back on that with same.
COME ON AMERICA WE CAN DO BETTER.
CLICK HERE TO HELP AMELIA BY SIGNING A PETION THEY NEED A LOT MORE VOTES
Why you ask
Meet Amelia she is a little girl whose needs a new kidney yet her parents were told by CHop that she can't because she has as the doctor's put it ever soo nicely. can you hear I am being sarcastic here Mental retardation and brain damage.
IF I WERE A CARTOON I WOULD LOOK LIKE THIS |
As a person living with CP I feel deeply saden by the fact that this can still be said in 2012. I have been preaty lucky so far in that I have not needed and surgryies and would hate to think that someone would say no to me because I was not fit to live. Isn't that what Adolph Hitler did in Germany nearly 100 years ago. Isn't that what slave owners did to blacks when they treated them like horses during slavery. yeah that is exactly what they did but we now look back on that with same.
COME ON AMERICA WE CAN DO BETTER.
CLICK HERE TO HELP AMELIA BY SIGNING A PETION THEY NEED A LOT MORE VOTES
Tuesday, January 10, 2012
Cerebral Palsy is not hopeless
I have many memories of watching 60 minutes . It has been a tradition that has been happening for a long time in my household . I loved seeing Andy Rooney at the end and I am sad that he died. He passed away the day of my softball torment last year.
So On sunday when I was on face book and someone posted that 60 minutes would speak about CP I do what I normally do. I sneak into my parent's room and watch TV as was the case Sunday night. I really like how 60 minutes so far has portrayed people with disabilities up until this point but the piece was a exception.
The way the reporter talked about CP painted a very sad picture of my disability. The story starts out with phrases such as "hopeless disease." Sorry but I have CP and no it is not hopeless nor a disease, its a disability.I invite anyone who thinks that Cp is hopeless to come spend some time at my place. Laughter is a common thing in my house and I have played sports gone to school attend college. I am really funny . yes I have a disability but it is not the end the world.
This brings up the whole point of the article. The article talks about wanting to "cure" CP and other disabilities using illegal stem sells. I find it wrong because I have CP and I do not want to be cure of CP. It is apart of who I am . It is not hopeless nor is it the end of the world. My advice to parents of kids with CP is step back take a deep breath and do not go to other countries to get stem cells because having CP is not that bad. As of January 2012 stem cells can not help Cp yet CP is not hopeless. I am living proof that therapy and lots of love will do wonders. For whatever reason I have disabilities and you know what I am normal. This is my normal.
So On sunday when I was on face book and someone posted that 60 minutes would speak about CP I do what I normally do. I sneak into my parent's room and watch TV as was the case Sunday night. I really like how 60 minutes so far has portrayed people with disabilities up until this point but the piece was a exception.
The way the reporter talked about CP painted a very sad picture of my disability. The story starts out with phrases such as "hopeless disease." Sorry but I have CP and no it is not hopeless nor a disease, its a disability.I invite anyone who thinks that Cp is hopeless to come spend some time at my place. Laughter is a common thing in my house and I have played sports gone to school attend college. I am really funny . yes I have a disability but it is not the end the world.
This brings up the whole point of the article. The article talks about wanting to "cure" CP and other disabilities using illegal stem sells. I find it wrong because I have CP and I do not want to be cure of CP. It is apart of who I am . It is not hopeless nor is it the end of the world. My advice to parents of kids with CP is step back take a deep breath and do not go to other countries to get stem cells because having CP is not that bad. As of January 2012 stem cells can not help Cp yet CP is not hopeless. I am living proof that therapy and lots of love will do wonders. For whatever reason I have disabilities and you know what I am normal. This is my normal.
Monday, January 9, 2012
Sixth grade part one : orientation
I remember going to school for orientation. I would be in Pod 2. My sixth grade class was split up into Pods. This meant that a group of kids would have the same English Math and Science class. This would be my first time rotating classes as well. This system seemed to be a good idea because all the teachers were next door to each other. This was also a good idea because the kids in each class had the potential to become great friends. I stay potential because it never really worked out. Due to social skills problems I never really had friends without disabilities from middle school on up. Let me say that at least I knew everyone name by the end of the year.
During ordination I would come to find that my pod was the cool advanced pod. Our pod had a mascot the sea horse which none of the other pods had as well as fun math. I did not do very much math that year instead we did art projects it was cool. My teacher was very old in fact back in 2003 he had some former students children. He is now retiring at the end of this school year 2011. I was the only one from my family to have him. Book gal went to a private school and Princess was in a different pod. He had some disabilities but that did not prevent him from teaching math science and PE as well as coach sports.
Anyway after orientation I went out breakfast with DD, we were friends all throughout middle school, I had no idea what w to as to come that year.
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