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.



  IF  I  WERE  A CARTOON  I  WOULD LOOK LIKE THIS  
   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 

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.

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.

Friday, January 6, 2012

My MIddle School Memories Introduction

  Hi guys      I  just want to let you know that    I  will be training to  blog about  my mid school     years from the best of  my  memory.  There are a few  reasons  for doing this.

   1  The  people  I started  blogging with   now  have kids that are  almost middle school  age

2  It was a  rough  years  for   me

3 I hope  my story can  improve   other   middle school, or  future  middle school  students.

  So   have a  great  weekend    and  be sure to  tuin in  Monday  to read  about  orientation to   sixth    grade.

Monday, January 2, 2012

Something that has been on my mind since the new year o

      So    we had a  New  Years  day party at my house   yesterday.  I had a great time  ; however    some  one said  something about Dick  Clark


  Dick Clark   and  new years  eve  have been    a  package deal   most of the time since  i  was born.      , It is  only  recently that  I  became aware  of the  person who  has  hosted for a long time   apparently  to  long   for some  people.

 here is  what I heard  by two  people  say about  Dick Clark.

  Dick Clark  should not be  on  tv anymore.  I could not  understand  him.


   First off  Dick  Clark  had a stroke   that caused  his speech to be slurred  but  HE  IS  THE ONE  WHO CAME UP  WITH THE  NEWS  YEAR  EVE.  When  he started  if  ,40 years ago  he  was  abled  body the only thing  that happend  is  he  had  a  stoke.  What would have happend   if  Dick Clark had   the stork  around the time he was born ie  Cp,  Well  back then   his  parents would have been advised to  put him  in a institution  and    the   New  York  new years   thing would have not existed.

 So  here is  my option  on the matter.   Mr.Clark should get to contiue   bringing in the new years as  long as  he wants to. It is  a good   awareness    for people with  strokes.    Having a stroke  should not hinder  anyone  from   having   a  fun   New  Year.  Happy  New  Year  Everyone

Saturday, December 31, 2011

2011 Year in Review



 
   It seems  like  yesterday I  did a  2010  year   in  review  now it is  time to  do  it for  2011  and  before you  know it  will  be time  for a 2012  year in  review.  I  honestly love  doing these it is  a chance to  reflect on all the  great  things  that  happend    during the  year  so  without  further  delay  here  it is.


 January 2011:   I  had a   my  first  long  winter break  and  started taking college level  classes   at  my local  community college .  Book gal   started  her last semester  of high school.
 C, me and R  2/2011
February 2011 :    I  made  a  buzzer  short  my  cousin  came to vist
 March  2011:    The  college  thing  just  clicked  for me.   It  took long enough


 April 2011:       I   actually  aced  a  college   essay.   I     competed  in the Menlo  Games .Book Gal gets  accepted  to UMass Boston.


May  2011:  Book Gal  turns   18. I  go to a job   intake  but  it did not work  out  yet I  had  fun  in the process. .






My  Dad and I  fourth of  July 2011
June 2011:  Book Gal  graduates  high school  we  celebrate with  friends and  family,.  My grandma comes   up and  My  parents  grandma and  me    take a  day  trip to   Monterey.  I    became a  Hope Solo  fan   watching the Women's world Cup.


July 2011; Celebrated    our country  independence   day  in  sacramento  with my   mom's   family Book  gal  leaves  for  college .  My  big  brother turned  27  and my  dad  had  his  b day as well
   "Sexy" minni mouse Halloween  2011  
 August 2011:   I  saw  my  old aid in the park,  Princess turns   17 and starts her senior year .   I    begin my  second year  of  college.
  September 2011:  I turn   two  decades   old   how   did that  happend


 October 2011 :   I  met  Steve  Wampler and   rocked out at  the 25 annual  bridge school   concert.     I also attended  my  first buddy walk


  November2011:      I  got  to be a goalie in  the  special olympics  tournament   and watch   power soccer at the Ability  expo  in  san  jose .  Princess   became  the  first     African  american   to win  homecoming    at  her high school


December   2011 :  My parents  celebrate 21 years  of  marriage . My  dog has been  in our family for seven  years  Christmass  eve   I enjoy  Mario  games on my  three Ds.  My mom and I had   a Comical  Costco  trip.


 
  Me and  Santa  at the Christmass  tree farm   December 2011 






Disability Awareness  post  that  you  do not want to miss




Stumbo Family Story




















   Having  CP  is not the end  of the world
    Value of  my  Life 
    My  name is  AZ not  az








 Happy New Year  Everyone
   



 Got  image  from :
ehttp://www.2dolphins.com/images/blogpix/snoopy_happy_new_year.png

Friday, December 30, 2011

A Comical Casco trip

   It all started   earlier today  my mom and I  were   in  Costco  we are having a New Years Day party at our house sunday   so   we need  some  Sparkling apple cider.    My  mom    needed  this  drink and  had been  looking all  over  for  it   no   luck.  i ask someone  he  tells me it is  in the  asile  we come to this  






 it is  up  high   we    get  it  down  After  we  got  it done someone  told us it was   here


  behind    us  on the  table


      Other things that made me laugh   on the Cosco  trip
 The jacket   we  wanted to buy  did not have a tag in it

and   my mom left  her  card    at the cash regster
Costco
  will never be the  same

  Any  Funny things happend to you  guys  today


   Stick  around   for   year in  review  coming  soon