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Uploaded by on Oct 15, 2007

A startling fact about ALS is that well over 90% of the people afflicted with this disease opt to die rather than use a ventilator to breathe for them when the diaphragm becomes too weak to pump the lungs. A significant reason for this is that the perception of life on a vent is pretty dismal. Across the country, the only places to provide care to a vented person are hospitals (or worse) - not an inviting living environment. The Steve Saling ALS Residence was the result of the planning described here. Opened in March 2010, the ALS Residence will prove that ALS does not have to be fatal anymore.

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Uploader Comments (smoothsaling)

  • What a outrage asking for money to build a nursing home, then they will have the gall to charge the patients $400. a day to be in the nursing home till the patients savings is taken. Then the nursing home will rip off the tax payers Medicaid for the patients. Do Not Donate Any Money Let It Fail Vote For Community Care Act. Care In Peoples On Homes Not Nursing Homes. Even Spouces are paid. ADAPT will help to get community choice act passed
  • @The391956 I applaud your effort to advocate for community care legislation. It is critically important that we deinstitutionalize long term care of our elders and disabled population. Home Care can be provided more economically in the home and most people would prefer to stay in their homes.

  • @The391956 In many situations, home care is not viable or appropriate. The Leonard Florence Center for Living is a nursing home our society can be proud of and should be the model for how to provide long term care when community care is not an option.

  • @The391956 LFCL is the first urban GreenHouse model of nursing home in the country. I live in a private residence of 10 people, with a private bedroom and bath. I have a normal residential kitchen and a spacious living room. My home is as nice as most 5-star hotels and, because of the built-in automation, I have total control over my environment despite being paralyzed and speechless from ALS.

  • @The391956 If you want to see how to live residentially in a skilled service residence, check out LeonardFlorenceCenter dot organization

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All Comments (37)

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  • Me too.Saw it with my mother.

  • @canada930 There are a lot of people who agree with you and they tend to do so within 5 years. But since ALS does not affect the mind, it is possible to utilize technology to restore the functions that ALS steals away. That is really good news for those of us determined to live. Until medicine proves otherwise, technology IS the cure. The ALS Residence proves it.

  • 나는 여기써있는 글들은 다이해할수가 없다. 그러나 이들이 말하는것이 무엇이며 무슨말을 하는지는 어렴풋이 알수가있다. 그어느누구보다도 잘알수가 있다. 왜냐면 현재 나도 2006 년 시작돼 지금은 상태가 많이 안조은 시기까지 왔기때문이다. 그러나 이제는 눈물도 감정도 많이 닳아없어졌다. 그래서 이들의 고통과 슬픔을 누구보다도 잘알수가있다. 목소리도 잘나오지않고 몸도가누기 힘들어졌지만 그래도 아직 키보드 를 두두릴수 있음을 하나님께 감사드림니다. 그리고 지금 루게릭을 같이 앓고있는 환우들 우리모두 이글이라도 쓰고 읽을수 있음을 감사하기로합시다.. 우리마지막은 생각하지말고 오늘은 또오늘은 그리고 또오늘은 하면서 살기로 합시다.

    모든분들께 하나님 은혜가 있으시기를 기도합니다.

    여기까지 적는데 너무시간이 오래걸렸습니다.영어로 쓰지못해 죄송합니다.

    new york 에서.....

  • My Father my Superman got ALS

    Thank God we live in Sweden and Finland with public healthcare and LOT of handicap rights ..I have the luxury to move back home to my mom and dad parttime

    cuz my dad will be at he´s own home as long as we can <3

  • For those of the people that have ALS, is it basically the destruction of nerve fibers which, even though the brain works perfectly fine, is unable to receive messages fully? Or are there other components. It's so sad knowing that these illnesses exist and we haven't found a cure for them or anything to slow down the progression. Bless all the people that were present in this video.

  • @smoothsaling

    I am so sorry that you are paralyzed and speechless from ALS

    ALS is a awful illness., I lost my Grandmother from ALS.

    I am sorry I cursed your nursing home,

    My grandmother was in a very bad one.

  • I see you wrote to me

    Why do 90% not want to be on ventilators?

    Are Hospitals Any Worse Then A Nursing

    Home, That is strange

    Do Most ALS patients want home care

    instead of Hospital

    I do not understand

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