Amanda, you said a mouthful!!!    I think many of us would think truer words 
were never spoken.   Thank you, janice
  ----- Original Message ----- 
  From: Amanda Diskey 
  To: [email protected] 
  Sent: Saturday, March 28, 2009 2:46 PM
  Subject: [TMIC] Thank you


  I just want to say that I am amazed at the amount of information I have 
gotten from you all about stem cell research and use! I never expected such a 
response, but I didn't know who else to ask. Of course my family and friends 
just want me to get better, and I want to be normal again so bad I would do 
anything to be that way. I miss playing with my kids, and cleaning my house, 
and driving, and going to work, using my hands, not wearing depends, and not 
being embarassed to go in public because of all of the above. I just want to be 
me again! I was looking for an easy fix, even if it cost 30,000, but thanks to 
this list I can make a more informed decision. This list is a wonderful place 
to go for information or support. I don't post a lot, but I always read the 
posts. Thank you all so much for understanding when no one else does!

  AMANDA




------------------------------------------------------------------------------
  From: "[email protected]" <[email protected]>
  To: [email protected]
  Sent: Thursday, March 26, 2009 10:03:50 PM
  Subject: tmic-digest Digest V2009 #200



  -----Inline Message Follows-----

  tmic-digest Digest                Volume 2009 : Issue 200

  Today's Topics:
    Re: [TMIC] going to DC                [ Lawrence King <[email protected] 
]
    Re: [TMIC] Embrionic Stem Cell Discu  [ Lawrence King <[email protected] 
]


  -----Inline Message Follows-----

  Try to find the Albert Einstein memorial near the Vietnam Vets Memorial & 
Constitution Ave.  we wanted to get there but the bone chilling cold 9F.  got 
the better of us and we gave up on both.  It's a site most tourists miss and 
don't know about.  and the museum of natural history is renovated and 
wonderful... you can see the hope diamond. 


  I want to hear about it when you get back!



  On Mar 26, 2009, at 9:09 PM, [email protected] wrote:


  Mindy the Artist



    Thanks Mindy
    I found the info on the tourmobile before we decided that I needed some 
sort of transport and I forgot about the wheelchair storage on the bus so that 
link was helpful. .  It will be perfect.  I found that it was the only bus 
through the cemetary - one of our desired stops.   I know we are going to use 
their two-day pass and see all of those sights.  Did you have a special spot 
that I might miis if I wasn't aware of it in advance?  I'm taking all the 
advice I can get.  
    Thanks
    Patti - Michigan  


    -----Original Message-----
    From: Lawrence King <[email protected]>
    To: [email protected]
    Cc: Lawrence King <[email protected]>
    Sent: Wed, 25 Mar 2009 2:38 pm
    Subject: Re: [TMIC] going to DC


    Hi Patti, 


    We went to DC in Jan for my father-in-laws funeral at Arlington Natnl.  
Cemetery and decided it was now or never to show the kids DC.  What ever your 
needs are I encourage you to take this tour bus:      
http://www.tourmobile.com/disability.php    and not the other ones.  I believe 
it cost us $32 per adult a day and we could get on and off at will.  I am 
walking wounded and would have been in agony if I had to walk from monument to 
monument.  I gave you the disability page so you can discuss your needs with 
them.  this is the only tour that has Natln. park service affiliation (and the 
monuments are a natnl. park)  and be happy there are accommodations at all the 
monuments to allow full access regardless of  your level of ability.  So enjoy 
yourself and wear an Obama button (the workers will be friendlier)






    Mindy the Artist


      Jeanne
      What a story!  You couldn't make that up if you tried and I think it's 
better (or worse) than anything I've seen on "House".  Your miracle is that you 
lived long enough to get to the right hospital and that they started you on 
steroids.  Thanks for sharing the details.

      You brought up the subject of maneuverability and I need help dealing 
with it. 

      I decided it was time to go to Washington DC - a long-time desire of my 
hubby and myself.  I always use a cane and have a wheelchair that I loaned out 
a year ago, but could get back. I quit wearing my AFO after two years because 
my feet burn and I prefer to wear shoes that I can take off every time I sit 
down (even in public.)  I looked pitiful sitting with my brace beside me 
letting my feet breathe.  So, I will need to use a walker and/or be pushed in a 
wheelchair in Washington and am concerned about my hubby lifting the chair in 
and out of our car.  I have looked at 3 wheeled walkers that would be easier to 
maneuver in crowds, 4 wheeled walkers of all kinds, a 4 wheeled that turns into 
a transport chair ($400), and just a simple transport chair itself   A 
transport chair is a wheelchair for being pushed in, with (4) ten-inch wheels 
instead of the large wheels on the back for self-maneuvering.  The transport 
chair ! is about 12 lbs. lighter than my wheelchair and would be easier to get 
into my small car.  The 4 wheeled walker that turns into a wheelchair is $400 
on-line.  A transport wheelchair is $200 at Walmart.  I can buy a 3-wheeled or 
a 4-wheeled walker for $50 each on Craigslist.  What would YOU take to 
Washington DC?  What will I need?
      How will I feel using one for the first time? 

      I DON'T want to have to use any of them!  I'm ANGRY!

      Patti - Michigan

       



--------------------------------------------------------------------------
      Need a job? Find employment help in your area. 


    = 


----------------------------------------------------------------------------
    Need a job? Find employment help in your area. 




  -----Inline Message Follows-----

  Jim, 


  I have even more respect for your view now that you have explained it in such 
a personal way.   I haven't changed my own view but I love getting to wear the 
other persons moccasins (I'm Christian and my best friend is Buddhist).   I'm 
thrilled at how well this discussion has gone (can we talk about race next... 
just kidding)


  Mindy the Artist



  On Mar 26, 2009, at 8:02 PM, Jim Lubin wrote:


    They are just going to throw those unused blastocysts away only because 
someone is making the choice to do so. After they are created they remain 
frozen indefinitely until a decision is made by someone to remove them from 
their frozen state.

    I've seen the argument be made that they are going to die anyway so why not 
use them to help others, such as organ donation. I started thing about that 
reasoning a few years ago. As someone who is only being kept alive by a 
ventilator breathing for me I began thinking that "someone" could decide that 
if I was taken off the ventilator I would die anyway so why not use my organs 
to better someone else's life. Someone might decide that my heart, my liver, my 
lungs would be better used by someone else who might be more important or more 
productive, less of a burden cost wise, to society. I am not an organ donor.

    Remember the Terri Schiavo case in 2005? It was a big topic on the 
vent-users list. Her husband claimed she was in a Persistent vegetative state, 
her family said she was not. The media kept saying they want to remove her from 
"life support". She was not on life support, she had a feeding tube. Big 
difference. A ventilator is life support. Her feeding tube was removed and she 
was starved to death because nutrition was withheld. It was very scary to 
everyone who is on life support they way people were fighting to get her 
feeding tube removed. If people felt so strongly about her being removed what 
about us?

    I believe that human life begins at conception and that those blastocytes 
should be protected until natural death. Use them what they were created for or 
keep them frozen (i.e. on life support). I don't think these blastocytes should 
have been created in the first place, if a couple can't have a baby without 
intervention then it's not meant to be. That's just what I believe. Obviously 
it's legal so the world doesn't operate the way I believe. 

    Jim

    At 10:24 AM 3/26/2009, Westgold wrote:

      They just throw those unused blastocytes in the garbage, they end up in 
some medical waste dump somewhere.  Would you rather than that, than see those 
cells being used to help cure a lot of horrible diseases?  You say that you 
support organ donation -- isn't giving these blastocytes a chance to help save 
somoene's life similar to organ donation?  Don't you think they would rather do 
some good with whatever life they have, rather than just be thrown in a dump? 
    ----
    Jim Lubin               
    [email protected]
    http://makoa.org/jim 
    disAbility Resources: http://www.makoa.org








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