Archive for the 'ALS' Category

They Stare at My Mouth

Friday, August 27th, 2010

They stand in front
They, up above
Looking down
At only my mouth
I am pinned
Wings long withered
Flattened under gravity’s glass
Head jerking toward what I need
Foot in the air
Stretched and pointing with toes
Follow my eyes!
Please!
Head jerking!
Toes pointing!
Eyes screaming!
And they only stare at my mouth

I don’t know what you want
They say
Calm down
They say
Just tell me what you want
They say
I can’t help you
They say
Until you tell me
What you want
And they stare at my mouth
See nothing else
Head jerking!
Toes pointing!
Eyes screaming!
Gestures
My language
Hear with your eyes and your mind!
Language is so much more
Than words!

Still they stare at my mouth
Waiting

-kara 8/27/10

What Kind of Life is This Anyway?

Saturday, May 15th, 2010

I am imprisoned in the downstairs of my house. The downstairs consists of a living room and kitchen. No bathroom. The living room is cut in half by a long child gate. My 5-year-old son gets the half with the TV, sofa, and big windows. I remember snuggling on that sofa with him, watching movies together, looking at books, playing iPod games, making phonecalls, or just giggling and being silly. Now that I cannot walk, I have no access to my son’s side. The little office chair I scoot around in cannot get thru the opening in the gate. My side of the room is cluttered with my electric bed, computer, humidifiers, fax machine, suction, cough assist, nebulizer… the ugly equipment of this heavy existence… none of it child-proof.

I scoot my chair up to the gate, hang my head over the bars, and hope he will come over and hug me. He rarely does. I try to schedule time for the aide to bring him to me and sit him on my lap. But there is little time. Why does it take all damn day for the aide to take care of me? Sponge baths in the kitchen are laborious, but 2+ hours is ridiculous. It seems my days are merely a job and I am just the subject of that job. I’m a limp product, being lifted, positioned, dressed, pottied, wiped, fed, undressed, washed, dressed, fed, pottied, wiped, fed, pottied, wiped, fed, lubed, oiled, maintained, but never driven. I start up every day, but go nowhere. I see the sunshine only thru windows. I am never taken outside. It’s too much work.

I am 90% maintenance, 10% human, and find myself asking, “What kind of life is this?”

-kara

Cold hard rules from ALSA Greater New York

Wednesday, March 31st, 2010

Here is what they told me:

We do require that patients who receive wheelchairs from our loan closet be in the process of getting a custom chair funded by their insurance.  Our loaner chair is meant to be something that is used while you are waiting for your chair that is on order.

Funny… my $$ donations didn’t have rules and requirements attached. I thought my donations would be used on ANY pALS in need. So, people who have to wait for their chair to be ordered, or those without insurance, or who cannot afford the co-pay, cannot borrow a wheelchair from ALSA Greater New York. How exclusive, and just wrong! I will not be donating my equipment to ALSA. There are other organizations without such rules.

Quality of Life

Wednesday, March 31st, 2010

Quality of life
I think it’s in the toilet
The one I can’t access anymore.

Paralyzed Housewives: Happiness

Saturday, March 13th, 2010

Happiness…

Protected: die

Saturday, January 9th, 2010

This post is password protected. To view it please enter your password below:

Reactions to the NY Times Article

Tuesday, September 15th, 2009

“Medicare Would Rather Buy $8000 Computer than $150 iPhone App”
Read post on GIZMODO The Gadget Blog.

“This is a very powerful article. As the cost of helpful technology drops, companies are finding it hard to compete and keep up.”
Read post on A Jew in Reindeer’s Clothing.

Chris Parandian says:
“insurance companies would rather spend $8000 on a bulky PC device that requires disabling most of the functionality of the PC instead of $300 on an iPhone that can change someone’s life.”
“we’ve lost two family friends to A.L.S., this is an outrage…”

ALS Is Front-And-Center In The New York Times Again!
“This time there is an excellent article on covered technology, ALS, and common sense (and how they don’t converge). People with ALS have much to contribute to the discussion of healthcare reform and healthcare delivery.”
-ALS Advocacy

“Need another reason to hate insurance companies? Even their computers suck.”
-LiVEJOURNAL

This one is my favorite:
“The NY Times listens to those who struggle to use their voice…”
-All Together We Can

“Medicare/Medicaid won’t pay for the iPhone or the app because the iPhone has more than one function. It can be used for purposes other than treating a disability, so they won’t cover it. This is absolute insanity.”
-I4U NEWS

“Insurers Fail To Keep Up With Speech Technology, Deny Funding For Devices That Multi-Task.”
-Medical News TODAY

“Woman replaces $8,000 medical gear with iPhone”
-Telecom Asia
my note: I actually did unlock my $8,000 speech generating device for $45. I still found it useless. My home computer is an ordinary Mac Powerbook. After my disappointment with the dinosaur-like device that Medicare and my secondary insurance provider approved and paid for, I footed the bill myself to turn my own computer into a fully functioning AAC device complete with dual switch access; a superior layout program for customizing or designing my own on-screen keyboards, functions, mouse behaviors, etc., all accessible by any input device or by various scanning methods; a switch program to run all the scannable keyboards/panels; an excellent communication program for speech; some of the highest quality voices to use as my voice; an on-screen keyboard program with the most amazing and intelligent word/phrase prediction and completion I have ever experienced. The result was a great computer that is also a highly sophisticated AAC device. I spent less than $900 to turn an ordinary computer into an alternative access speech generating device. That was two years ago. Since then, I purchased an iPhone and an app called Proloquo2Go. This is what portability is all about!

“Text-to-Speech Technology Reaches an Inflection Point”
-Bits Blog, New York Times

-kara

The NY Times on AAC, New Technology, & Medicare Coverage

Tuesday, September 15th, 2009

Aiden and I appear on the front page of the NY Times today. I’m using my iPhone to speak while snuggling with my beautiful boy who uses his iPod Touch to play music, videos, educational games, and slowly, but surely, to communicate with Proloquo2Go!

This is an important article that addresses Medicare’s reluctance to recognize new technology (and great cost saving) for people with speech impairments,.

Full article is here:
http://www.nytimes.com/2009/09/15/technology/15speech.html

-kara

iPhone App Gives Voice to Those Without

Thursday, July 16th, 2009

Proloquo2Go in the news:

Story and video here.

My Nephew to Walk for pALS

Friday, July 3rd, 2009

My nephew Josh will walk to raise money for his local ALS Association chapter in Atlanta on November 14, 2009. I have friends with ALS all over the world. I am so touched that Josh will walk in my honor. The ALS Association provides much needed services and equipment to patients and their families. My sister Kelly raised over a thousand dollars for our local New York chapter in just a few days! Way to go Kelly! Rock on Josh!

Sponsor Josh at his Personal Fundraising Page