Rezultati pretraživanja
  1. 16. pro 2019.
  2. : Learn what the accessibility lines are for. Hint: not carts, not motorcycles, not scooters, and not so you can park like an idiot.

  3. 12. kol 2019.

    Get popping with approval I received Nurown 7/2015 Still here! Want more! Co2,oxygen normal range, perhaps I could do more with more

  4. 1. lip 2019.

    Day 32 of ALS awareness month. Some believe it ended yesterday. I along with thousands of others still have it. Awareness doesn’t stop because we turned a page on a calendar. We stop when there’s a cure.

  5. 15. svi 2019.

    I feel so supported by my firm . They have developed a website and made a podcast with me to join us pALS in the battle.

  6. 10. lis 2019.

    "He's gonna find that cure." You've got that right . Thank you for spotlighting and our Kilt Walk for a Cure!

  7. 14. pro 2019.

    IAMALS is taking over Times Square on 12/17 to raise awareness for ALS and find a cure!

  8. 13. pro 2019.

    This guy has a heart of gold and so grateful for Khoi.

  9. 5. ruj 2019.

    We will fight with you to for your friend, my husband and so many others. Thank you!

  10. 27. stu 2019.

    Life is pretty great except for this one thing called ALS. Had a birthday yesterday and my only wish is that by next November we will be calling ALS a treatable chronic illness rather than a terminal illness.

  11. If you haven't heard of yet, you will. He's fighting to make his dream of finding a cure for ALS a reality. I'm proud to be part of that mission. I hope you'll join us.

  12. 4. velj

    30,000 ... # people in US w/ ALS 150 .... # of years w/ no effective treatment for ALS 10 ... # years NurOwn stem cell treatment pending FDA approval 2-5 ... # yrs survival for avg person w/ ALS 29 ... Eric Stevens' age at Dx

  13. 30. lis 2019.

    Absolutely - patients and caregivers drive change. We will be the reason that we look back at ALS protocol, trials and measurements and scratch our heads.

  14. 23. srp 2019.

    "Transparency"- a core ALSA mission statement item. Compensation was about $500k more than last year overall. The funny thing is, people would happily pay twice that amount (if we actually had RESULTS). Instead, groups like NME and have to go to DC to lobby the FDA. WHY?

  15. prije 17 sati

    Shri ji, I'm a patient suffering from I request you to go thru my appeal and help patients with such dreaded neuro degenerative diseases

    Prikaži ovu nit
  16. 14. pro 2019.

    "I AM ALS" "On the morning of December 17th our fight will be displayed on nearly a dozen screens in Times Square

  17. 17. pro 2019.

    We will change the world for ALS!

  18. Thank you Brian Wallach for your leadership and courage and calling on all of us to combat ALS. We are standing with you and Sandra

  19. I am an activist. I am a mom. I am ALS today and everyday until there is a cure. I stand with Brian and Sandra in this courageous battle. Join us!

  20. 19. pro 2019.

    FTP is proud to work with in honor of our Founding Partner Dan Tate, Jr. who is fighting ALS himself. Read more from Dan on the inspiring work the organization is doing and how we’re giving back: .

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