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SERIESDONATE
Project ALS is the world’s first ALS organization to focus exclusively on research.We have raised over $100 million in 22 years to fund ALS research programs at leading academic institutions including Harvard University, Columbia University, UCSF, and the Salk Institute, and have made significant progress toward a cure for ALS. WHO WE ARE - PROJECT ALS They founded Project ALS as a non-profit 501 (c)3 in 1998, and set forth a new paradigm for ALS research. Project ALS-funded doctors and researchers were required to work together in small teams, toward a new standard of results-oriented accountability. Project ALS requires that its funded researchers communicate regularly, share data openlyOUR RESEARCH
Project ALS works collaboratively with its scientists to identify the most promising ALS research and, along with its Research Advisory Board (RAB), streamlines the research process with effective strategies. Project ALS assesses progress through regular meetings and reviews by the RAB. Project ALS engages in the ongoing recruitment of JOIN THE 2021 DON'T TALK-A-THON! How the Don’t Talk-a-Thon Started. Avery Niedrowski lost her Grandpa John to ALS when she was 6 years old. He was her rock. Two years later, Avery got busy. She chose to be silent for one whole day for the years her grandpa had been unable to speak due to ALS. In return, and in his honor, she asked people to donate money to Project ALSresearch.
PROJECT ALS INTRODUCES PROSETIN It took 6 years, and over 80 versions of the compound, to get to Prosetin: a drug that rescues motor neurons in cellular and animal models of ALS, crosses the blood-brain barrier with ease, and has been safe and well-tolerated in all of our tests to date. Notably, pathways that Prosetin targets have been identified by many other ALSresearchers
JENIFER’S LEGACY LIVES ON. Jenifer’s legacy lives on. May 6, 2021. Play Video. When Project ALS co-founder Jenifer Estess was diagnosed with ALS at the age of 35, her doctor told her to max out her credit cards, eat junk food, and just wait to die. Like most who find themselves in this situation, she wasappalled.
ONE FAMILY’S PASSIONATE FIGHT AGAINST NEURODEGENERATIVE One Family’s Passionate Fight Against Neurodegenerative Diseases. July 10, 2020. The Wasserman family has experienced first-hand the devastating effects of neurodegenerative diseases: Sandra Wasserman lost her beloved husband to Parkinson’s disease, and her son to glioblastoma. Now in her eighties, Sandra has friends experiencing the THE DON'T TALK-A-THON 2021 We really, really like you! And you really, really want to silence ALS. 100% of your $250 goes directly toward raising crucial funds for ALS research. Each person who registers for the #DontTalkAThon2021 and raises $250 or more will receive a Don't Talk-a-Thon hoodie for your generous donation and special shout outs! Fundraise. AT HOME WITH REBECCA LUKER Donate Now. Thank you for joining 3-time Tony nominee Rebecca Luker for an evening of song hosted by Santino Fontana and a conversation with Katie Couric. This event is sponsored by Playbill and the Actor's Fund. Rebecca is a highly-acclaimed, multi-Tony-nominated actress and singer. Her performances in Phantom of the Opera, The Secret Garden FUNDRAISING FOR PROJECT ALS Prosetin is a promising development that the ALS community is very excited about, and ProjectALS is working hard to develop and make this treatment accessible as fast as possible by working independently of the big Pharmaceutical industry. In order to do this they need ourhelp -
HOME - PROJECT ALSWHO WE AREABOUT ALSOUR RESEARCHGET INVOLVEDWEBINARSERIESDONATE
Project ALS is the world’s first ALS organization to focus exclusively on research.We have raised over $100 million in 22 years to fund ALS research programs at leading academic institutions including Harvard University, Columbia University, UCSF, and the Salk Institute, and have made significant progress toward a cure for ALS. WHO WE ARE - PROJECT ALS They founded Project ALS as a non-profit 501 (c)3 in 1998, and set forth a new paradigm for ALS research. Project ALS-funded doctors and researchers were required to work together in small teams, toward a new standard of results-oriented accountability. Project ALS requires that its funded researchers communicate regularly, share data openlyOUR RESEARCH
Project ALS works collaboratively with its scientists to identify the most promising ALS research and, along with its Research Advisory Board (RAB), streamlines the research process with effective strategies. Project ALS assesses progress through regular meetings and reviews by the RAB. Project ALS engages in the ongoing recruitment of JOIN THE 2021 DON'T TALK-A-THON! How the Don’t Talk-a-Thon Started. Avery Niedrowski lost her Grandpa John to ALS when she was 6 years old. He was her rock. Two years later, Avery got busy. She chose to be silent for one whole day for the years her grandpa had been unable to speak due to ALS. In return, and in his honor, she asked people to donate money to Project ALSresearch.
PROJECT ALS INTRODUCES PROSETIN It took 6 years, and over 80 versions of the compound, to get to Prosetin: a drug that rescues motor neurons in cellular and animal models of ALS, crosses the blood-brain barrier with ease, and has been safe and well-tolerated in all of our tests to date. Notably, pathways that Prosetin targets have been identified by many other ALSresearchers
JENIFER’S LEGACY LIVES ON. Jenifer’s legacy lives on. May 6, 2021. Play Video. When Project ALS co-founder Jenifer Estess was diagnosed with ALS at the age of 35, her doctor told her to max out her credit cards, eat junk food, and just wait to die. Like most who find themselves in this situation, she wasappalled.
ONE FAMILY’S PASSIONATE FIGHT AGAINST NEURODEGENERATIVE One Family’s Passionate Fight Against Neurodegenerative Diseases. July 10, 2020. The Wasserman family has experienced first-hand the devastating effects of neurodegenerative diseases: Sandra Wasserman lost her beloved husband to Parkinson’s disease, and her son to glioblastoma. Now in her eighties, Sandra has friends experiencing the THE DON'T TALK-A-THON 2021 We really, really like you! And you really, really want to silence ALS. 100% of your $250 goes directly toward raising crucial funds for ALS research. Each person who registers for the #DontTalkAThon2021 and raises $250 or more will receive a Don't Talk-a-Thon hoodie for your generous donation and special shout outs! Fundraise. AT HOME WITH REBECCA LUKER Donate Now. Thank you for joining 3-time Tony nominee Rebecca Luker for an evening of song hosted by Santino Fontana and a conversation with Katie Couric. This event is sponsored by Playbill and the Actor's Fund. Rebecca is a highly-acclaimed, multi-Tony-nominated actress and singer. Her performances in Phantom of the Opera, The Secret Garden FUNDRAISING FOR PROJECT ALS Prosetin is a promising development that the ALS community is very excited about, and ProjectALS is working hard to develop and make this treatment accessible as fast as possible by working independently of the big Pharmaceutical industry. In order to do this they need ourhelp -
ABOUT ALS - PROJECT ALS ALS, also known as Lou Gehrig’s disease, is a brain disease that targets brain cells called motor neurons. Motor neurons send messages from the brain to muscles throughout the body. In ALS, as motor neurons die, a person progressively loses the ability to walk, speak, swallow, and breathe. ALS affects adults of all ages, from teens toseniors
PROJECT ALS
Throughout 2020, our top priority has been to minimize pandemic related delays on the pre-clinical development of prosetin. Led by a team of drug development experts, Project ALS continues to work each and every day toward an investigational new drug application—and a Phase I clinical trial—for prosetin. This opens in a new window. JENIFER’S LEGACY LIVES ON. Jenifer’s legacy lives on. May 6, 2021. Play Video. When Project ALS co-founder Jenifer Estess was diagnosed with ALS at the age of 35, her doctor told her to max out her credit cards, eat junk food, and just wait to die. Like most who find themselves in this situation, she wasappalled.
WEBINAR SERIES
Webinar with Richard Kind. Erin and Valerie chat with actor and long-time Project ALS supporter, Richard Kind. Richard is the host of this year’s Tomorrow is Tonight Virtual Gala, airing Thursday, October 22nd at 7:30 ET. Project ALS webinar with Senator Mike Braun and Corey Polen from Project ALS on Vimeo. THE HERMSTAD LEGACY: ADVANCES IN TREATMENTS FOR ALS The Hermstad Legacy: Advances in Treatments for ALS. January 25, 2021. On February 4th, we invite you to join special guest and ALS research advocate Ben Stiller, foremost ALS clinicians, leading researchers, and dedicated patient advocates to learn how Jaci and Alex Hermstad inspired the team effort that led to the development of jacifusen WE WILL W1N 4 ALS IN HONOR OF TOM KIRCHHOFF Tommy Kirchhoff, and best friend, Bobby Whalen, quarterbacks at Cedar Cliff and Trinity High schools in PA, raised nearly $250,000 for Project ALS this past football season through their campaign WE WILLW1N 4 ALS.
VALENTINE FOR A PIONEER Jaci and her horse Bud, March 2019 “Jaci is blazing a path that hopefully will not just cure her but set a course of treatment for countless others.” – Lori Hermstad, mother. February 14th is a significant day for the Hermstad family. On this day in 2011, Alex AT HOME WITH REBECCA LUKER Thank you for joining 3-time Tony nominee Rebecca Luker for an evening of song hosted by Santino Fontana and a conversation with Katie Couric. This event is sponsored by Playbill and the Actor's Fund. Rebecca is a highly-acclaimed, multi-Tony-nominated actress andsinger. Her
DONATE TO THE DON'T TALK-A-THON 2021 Thanks for helping us silence ALS. Thank you for your donation to Project ALS research. 100% of the money you donate will go straight toward cutting-edge, aggressive ALS research that aims to silence ALS once and for all. How often would you like to donate? One-timeMonthly. Choose a
WWW.PROJECTALS.ORG
www.projectals.org
HOME - PROJECT ALSWHO WE AREABOUT ALSOUR RESEARCHGET INVOLVEDWEBINARSERIESDONATE
Project ALS is the world’s first ALS organization to focus exclusively on research.We have raised over $100 million in 22 years to fund ALS research programs at leading academic institutions including Harvard University, Columbia University, UCSF, and the Salk Institute, and have made significant progress toward a cure for ALS. WHO WE ARE - PROJECT ALS They founded Project ALS as a non-profit 501 (c)3 in 1998, and set forth a new paradigm for ALS research. Project ALS-funded doctors and researchers were required to work together in small teams, toward a new standard of results-oriented accountability. Project ALS requires that its funded researchers communicate regularly, share data openlyOUR RESEARCH
Project ALS works collaboratively with its scientists to identify the most promising ALS research and, along with its Research Advisory Board (RAB), streamlines the research process with effective strategies. Project ALS assesses progress through regular meetings and reviews by the RAB. Project ALS engages in the ongoing recruitment of JOIN THE 2021 DON'T TALK-A-THON! How the Don’t Talk-a-Thon Started. Avery Niedrowski lost her Grandpa John to ALS when she was 6 years old. He was her rock. Two years later, Avery got busy. She chose to be silent for one whole day for the years her grandpa had been unable to speak due to ALS. In return, and in his honor, she asked people to donate money to Project ALSresearch.
PROJECT ALS INTRODUCES PROSETIN It took 6 years, and over 80 versions of the compound, to get to Prosetin: a drug that rescues motor neurons in cellular and animal models of ALS, crosses the blood-brain barrier with ease, and has been safe and well-tolerated in all of our tests to date. Notably, pathways that Prosetin targets have been identified by many other ALSresearchers
JENIFER’S LEGACY LIVES ON. Jenifer’s legacy lives on. May 6, 2021. Play Video. When Project ALS co-founder Jenifer Estess was diagnosed with ALS at the age of 35, her doctor told her to max out her credit cards, eat junk food, and just wait to die. Like most who find themselves in this situation, she wasappalled.
ONE FAMILY’S PASSIONATE FIGHT AGAINST NEURODEGENERATIVE One Family’s Passionate Fight Against Neurodegenerative Diseases. July 10, 2020. The Wasserman family has experienced first-hand the devastating effects of neurodegenerative diseases: Sandra Wasserman lost her beloved husband to Parkinson’s disease, and her son to glioblastoma. Now in her eighties, Sandra has friends experiencing the THE DON'T TALK-A-THON 2021 We really, really like you! And you really, really want to silence ALS. 100% of your $250 goes directly toward raising crucial funds for ALS research. Each person who registers for the #DontTalkAThon2021 and raises $250 or more will receive a Don't Talk-a-Thon hoodie for your generous donation and special shout outs! Fundraise. AT HOME WITH REBECCA LUKER Donate Now. Thank you for joining 3-time Tony nominee Rebecca Luker for an evening of song hosted by Santino Fontana and a conversation with Katie Couric. This event is sponsored by Playbill and the Actor's Fund. Rebecca is a highly-acclaimed, multi-Tony-nominated actress and singer. Her performances in Phantom of the Opera, The Secret Garden FUNDRAISING FOR PROJECT ALS Prosetin is a promising development that the ALS community is very excited about, and ProjectALS is working hard to develop and make this treatment accessible as fast as possible by working independently of the big Pharmaceutical industry. In order to do this they need ourhelp -
HOME - PROJECT ALSWHO WE AREABOUT ALSOUR RESEARCHGET INVOLVEDWEBINARSERIESDONATE
Project ALS is the world’s first ALS organization to focus exclusively on research.We have raised over $100 million in 22 years to fund ALS research programs at leading academic institutions including Harvard University, Columbia University, UCSF, and the Salk Institute, and have made significant progress toward a cure for ALS. WHO WE ARE - PROJECT ALS They founded Project ALS as a non-profit 501 (c)3 in 1998, and set forth a new paradigm for ALS research. Project ALS-funded doctors and researchers were required to work together in small teams, toward a new standard of results-oriented accountability. Project ALS requires that its funded researchers communicate regularly, share data openlyOUR RESEARCH
Project ALS works collaboratively with its scientists to identify the most promising ALS research and, along with its Research Advisory Board (RAB), streamlines the research process with effective strategies. Project ALS assesses progress through regular meetings and reviews by the RAB. Project ALS engages in the ongoing recruitment of JOIN THE 2021 DON'T TALK-A-THON! How the Don’t Talk-a-Thon Started. Avery Niedrowski lost her Grandpa John to ALS when she was 6 years old. He was her rock. Two years later, Avery got busy. She chose to be silent for one whole day for the years her grandpa had been unable to speak due to ALS. In return, and in his honor, she asked people to donate money to Project ALSresearch.
PROJECT ALS INTRODUCES PROSETIN It took 6 years, and over 80 versions of the compound, to get to Prosetin: a drug that rescues motor neurons in cellular and animal models of ALS, crosses the blood-brain barrier with ease, and has been safe and well-tolerated in all of our tests to date. Notably, pathways that Prosetin targets have been identified by many other ALSresearchers
JENIFER’S LEGACY LIVES ON. Jenifer’s legacy lives on. May 6, 2021. Play Video. When Project ALS co-founder Jenifer Estess was diagnosed with ALS at the age of 35, her doctor told her to max out her credit cards, eat junk food, and just wait to die. Like most who find themselves in this situation, she wasappalled.
ONE FAMILY’S PASSIONATE FIGHT AGAINST NEURODEGENERATIVE One Family’s Passionate Fight Against Neurodegenerative Diseases. July 10, 2020. The Wasserman family has experienced first-hand the devastating effects of neurodegenerative diseases: Sandra Wasserman lost her beloved husband to Parkinson’s disease, and her son to glioblastoma. Now in her eighties, Sandra has friends experiencing the THE DON'T TALK-A-THON 2021 We really, really like you! And you really, really want to silence ALS. 100% of your $250 goes directly toward raising crucial funds for ALS research. Each person who registers for the #DontTalkAThon2021 and raises $250 or more will receive a Don't Talk-a-Thon hoodie for your generous donation and special shout outs! Fundraise. AT HOME WITH REBECCA LUKER Donate Now. Thank you for joining 3-time Tony nominee Rebecca Luker for an evening of song hosted by Santino Fontana and a conversation with Katie Couric. This event is sponsored by Playbill and the Actor's Fund. Rebecca is a highly-acclaimed, multi-Tony-nominated actress and singer. Her performances in Phantom of the Opera, The Secret Garden FUNDRAISING FOR PROJECT ALS Prosetin is a promising development that the ALS community is very excited about, and ProjectALS is working hard to develop and make this treatment accessible as fast as possible by working independently of the big Pharmaceutical industry. In order to do this they need ourhelp -
ABOUT ALS - PROJECT ALS ALS, also known as Lou Gehrig’s disease, is a brain disease that targets brain cells called motor neurons. Motor neurons send messages from the brain to muscles throughout the body. In ALS, as motor neurons die, a person progressively loses the ability to walk, speak, swallow, and breathe. ALS affects adults of all ages, from teens toseniors
PROJECT ALS
Throughout 2020, our top priority has been to minimize pandemic related delays on the pre-clinical development of prosetin. Led by a team of drug development experts, Project ALS continues to work each and every day toward an investigational new drug application—and a Phase I clinical trial—for prosetin. This opens in a new window. JENIFER’S LEGACY LIVES ON. Jenifer’s legacy lives on. May 6, 2021. Play Video. When Project ALS co-founder Jenifer Estess was diagnosed with ALS at the age of 35, her doctor told her to max out her credit cards, eat junk food, and just wait to die. Like most who find themselves in this situation, she wasappalled.
WEBINAR SERIES
Webinar with Richard Kind. Erin and Valerie chat with actor and long-time Project ALS supporter, Richard Kind. Richard is the host of this year’s Tomorrow is Tonight Virtual Gala, airing Thursday, October 22nd at 7:30 ET. Project ALS webinar with Senator Mike Braun and Corey Polen from Project ALS on Vimeo. THE HERMSTAD LEGACY: ADVANCES IN TREATMENTS FOR ALS The Hermstad Legacy: Advances in Treatments for ALS. January 25, 2021. On February 4th, we invite you to join special guest and ALS research advocate Ben Stiller, foremost ALS clinicians, leading researchers, and dedicated patient advocates to learn how Jaci and Alex Hermstad inspired the team effort that led to the development of jacifusen WE WILL W1N 4 ALS IN HONOR OF TOM KIRCHHOFF Tommy Kirchhoff, and best friend, Bobby Whalen, quarterbacks at Cedar Cliff and Trinity High schools in PA, raised nearly $250,000 for Project ALS this past football season through their campaign WE WILLW1N 4 ALS.
VALENTINE FOR A PIONEER Jaci and her horse Bud, March 2019 “Jaci is blazing a path that hopefully will not just cure her but set a course of treatment for countless others.” – Lori Hermstad, mother. February 14th is a significant day for the Hermstad family. On this day in 2011, Alex AT HOME WITH REBECCA LUKER Thank you for joining 3-time Tony nominee Rebecca Luker for an evening of song hosted by Santino Fontana and a conversation with Katie Couric. This event is sponsored by Playbill and the Actor's Fund. Rebecca is a highly-acclaimed, multi-Tony-nominated actress andsinger. Her
DONATE TO THE DON'T TALK-A-THON 2021 Thanks for helping us silence ALS. Thank you for your donation to Project ALS research. 100% of the money you donate will go straight toward cutting-edge, aggressive ALS research that aims to silence ALS once and for all. How often would you like to donate? One-timeMonthly. Choose a
WWW.PROJECTALS.ORG
www.projectals.org
HOME - PROJECT ALSWHO WE AREABOUT ALSOUR RESEARCHGET INVOLVEDWEBINARSERIESDONATE
Project ALS is the world’s first ALS organization to focus exclusively on research.We have raised over $100 million in 22 years to fund ALS research programs at leading academic institutions including Harvard University, Columbia University, UCSF, and the Salk Institute, and have made significant progress toward a cure for ALS. WHO WE ARE - PROJECT ALS They founded Project ALS as a non-profit 501 (c)3 in 1998, and set forth a new paradigm for ALS research. Project ALS-funded doctors and researchers were required to work together in small teams, toward a new standard of results-oriented accountability. Project ALS requires that its funded researchers communicate regularly, share data openly ABOUT ALS - PROJECT ALS ALS, also known as Lou Gehrig’s disease, is a brain disease that targets brain cells called motor neurons. Motor neurons send messages from the brain to muscles throughout the body. In ALS, as motor neurons die, a person progressively loses the ability to walk, speak, swallow, and breathe. ALS affects adults of all ages, from teens toseniors
OUR RESEARCH
Project ALS works collaboratively with its scientists to identify the most promising ALS research and, along with its Research Advisory Board (RAB), streamlines the research process with effective strategies. Project ALS assesses progress through regular meetings and reviews by the RAB. Project ALS engages in the ongoing recruitment of JOIN THE 2021 DON'T TALK-A-THON! How the Don’t Talk-a-Thon Started. Avery Niedrowski lost her Grandpa John to ALS when she was 6 years old. He was her rock. Two years later, Avery got busy. She chose to be silent for one whole day for the years her grandpa had been unable to speak due to ALS. In return, and in his honor, she asked people to donate money to Project ALSresearch.
PROJECT ALS INTRODUCES PROSETIN It took 6 years, and over 80 versions of the compound, to get to Prosetin: a drug that rescues motor neurons in cellular and animal models of ALS, crosses the blood-brain barrier with ease, and has been safe and well-tolerated in all of our tests to date. Notably, pathways that Prosetin targets have been identified by many other ALSresearchers
ONE FAMILY’S PASSIONATE FIGHT AGAINST NEURODEGENERATIVE One Family’s Passionate Fight Against Neurodegenerative Diseases. July 10, 2020. The Wasserman family has experienced first-hand the devastating effects of neurodegenerative diseases: Sandra Wasserman lost her beloved husband to Parkinson’s disease, and her son to glioblastoma. Now in her eighties, Sandra has friends experiencing the THE HERMSTAD LEGACY: ADVANCES IN TREATMENTS FOR ALS The Hermstad Legacy: Advances in Treatments for ALS. January 25, 2021. On February 4th, we invite you to join special guest and ALS research advocate Ben Stiller, foremost ALS clinicians, leading researchers, and dedicated patient advocates to learn how Jaci and Alex Hermstad inspired the team effort that led to the development of jacifusen THE DON'T TALK-A-THON 2021 We really, really like you! And you really, really want to silence ALS. 100% of your $250 goes directly toward raising crucial funds for ALS research. Each person who registers for the #DontTalkAThon2021 and raises $250 or more will receive a Don't Talk-a-Thon hoodie for your generous donation and special shout outs! Fundraise. AT HOME WITH REBECCA LUKER Donate Now. Thank you for joining 3-time Tony nominee Rebecca Luker for an evening of song hosted by Santino Fontana and a conversation with Katie Couric. This event is sponsored by Playbill and the Actor's Fund. Rebecca is a highly-acclaimed, multi-Tony-nominated actress and singer. Her performances in Phantom of the Opera, The Secret Garden HOME - PROJECT ALSWHO WE AREABOUT ALSOUR RESEARCHGET INVOLVEDWEBINARSERIESDONATE
Project ALS is the world’s first ALS organization to focus exclusively on research.We have raised over $100 million in 22 years to fund ALS research programs at leading academic institutions including Harvard University, Columbia University, UCSF, and the Salk Institute, and have made significant progress toward a cure for ALS. WHO WE ARE - PROJECT ALS They founded Project ALS as a non-profit 501 (c)3 in 1998, and set forth a new paradigm for ALS research. Project ALS-funded doctors and researchers were required to work together in small teams, toward a new standard of results-oriented accountability. Project ALS requires that its funded researchers communicate regularly, share data openly ABOUT ALS - PROJECT ALS ALS, also known as Lou Gehrig’s disease, is a brain disease that targets brain cells called motor neurons. Motor neurons send messages from the brain to muscles throughout the body. In ALS, as motor neurons die, a person progressively loses the ability to walk, speak, swallow, and breathe. ALS affects adults of all ages, from teens toseniors
OUR RESEARCH
Project ALS works collaboratively with its scientists to identify the most promising ALS research and, along with its Research Advisory Board (RAB), streamlines the research process with effective strategies. Project ALS assesses progress through regular meetings and reviews by the RAB. Project ALS engages in the ongoing recruitment of JOIN THE 2021 DON'T TALK-A-THON! How the Don’t Talk-a-Thon Started. Avery Niedrowski lost her Grandpa John to ALS when she was 6 years old. He was her rock. Two years later, Avery got busy. She chose to be silent for one whole day for the years her grandpa had been unable to speak due to ALS. In return, and in his honor, she asked people to donate money to Project ALSresearch.
PROJECT ALS INTRODUCES PROSETIN It took 6 years, and over 80 versions of the compound, to get to Prosetin: a drug that rescues motor neurons in cellular and animal models of ALS, crosses the blood-brain barrier with ease, and has been safe and well-tolerated in all of our tests to date. Notably, pathways that Prosetin targets have been identified by many other ALSresearchers
ONE FAMILY’S PASSIONATE FIGHT AGAINST NEURODEGENERATIVE One Family’s Passionate Fight Against Neurodegenerative Diseases. July 10, 2020. The Wasserman family has experienced first-hand the devastating effects of neurodegenerative diseases: Sandra Wasserman lost her beloved husband to Parkinson’s disease, and her son to glioblastoma. Now in her eighties, Sandra has friends experiencing the THE HERMSTAD LEGACY: ADVANCES IN TREATMENTS FOR ALS The Hermstad Legacy: Advances in Treatments for ALS. January 25, 2021. On February 4th, we invite you to join special guest and ALS research advocate Ben Stiller, foremost ALS clinicians, leading researchers, and dedicated patient advocates to learn how Jaci and Alex Hermstad inspired the team effort that led to the development of jacifusen THE DON'T TALK-A-THON 2021 We really, really like you! And you really, really want to silence ALS. 100% of your $250 goes directly toward raising crucial funds for ALS research. Each person who registers for the #DontTalkAThon2021 and raises $250 or more will receive a Don't Talk-a-Thon hoodie for your generous donation and special shout outs! Fundraise. AT HOME WITH REBECCA LUKER Donate Now. Thank you for joining 3-time Tony nominee Rebecca Luker for an evening of song hosted by Santino Fontana and a conversation with Katie Couric. This event is sponsored by Playbill and the Actor's Fund. Rebecca is a highly-acclaimed, multi-Tony-nominated actress and singer. Her performances in Phantom of the Opera, The Secret Garden ABOUT ALS - PROJECT ALS ALS, also known as Lou Gehrig’s disease, is a brain disease that targets brain cells called motor neurons. Motor neurons send messages from the brain to muscles throughout the body. In ALS, as motor neurons die, a person progressively loses the ability to walk, speak, swallow, and breathe. ALS affects adults of all ages, from teens toseniors
GET INVOLVED
Temporary Mailing Address: 4330 Camp Kaufmann Road Huntingtown, MD 20639. 801 Riverside Drive, Suite 6G New York, NY 10032. Phone: (212) 420-7382. Fax: (646) 559-9290WEBINAR SERIES
Webinar with Richard Kind. Erin and Valerie chat with actor and long-time Project ALS supporter, Richard Kind. Richard is the host of this year’s Tomorrow is Tonight Virtual Gala, airing Thursday, October 22nd at 7:30 ET. Project ALS webinar with Senator Mike Braun and Corey Polen from Project ALS on Vimeo. JENIFER’S LEGACY LIVES ON. Jenifer’s legacy lives on. May 6, 2021. Play Video. When Project ALS co-founder Jenifer Estess was diagnosed with ALS at the age of 35, her doctor told her to max out her credit cards, eat junk food, and just wait to die. Like most who find themselves in this situation, she wasappalled.
THE HUNT FOR ALS BIOMARKERS: FAT? 2. Disease stratification biomarkers: ALS is a complicated brain disease, made more challenging to treat because of its heterogeneity. Research has identified more than 50 genes that can cause ALS, and multiple biological processes are involved. Even with research advances, it largely remains a mystery that some ALS starts in thethroat, and
VALENTINE FOR A PIONEER Jaci and her horse Bud, March 2019 “Jaci is blazing a path that hopefully will not just cure her but set a course of treatment for countless others.” – Lori Hermstad, mother. February 14th is a significant day for the Hermstad family. On this day in 2011, Alex AT HOME WITH REBECCA LUKER Thank you for joining 3-time Tony nominee Rebecca Luker for an evening of song hosted by Santino Fontana and a conversation with Katie Couric. This event is sponsored by Playbill and the Actor's Fund. Rebecca is a highly-acclaimed, multi-Tony-nominated actress andsinger. Her
FUNDRAISING FOR PROJECT ALS We are taking a vow of silence for ALS Awareness month starting on May 22nd in honor of all individuals diagnosed with ALS. DONATE TO THE DON'T TALK-A-THON 2021 Thanks for helping us silence ALS. Thank you for your donation to Project ALS research. 100% of the money you donate will go straight toward cutting-edge, aggressive ALS research that aims to silence ALS once and for all. How often would you like to donate? One-timeMonthly. Choose a
DONATE TO TEAM CHRIS COMBS Team Chris Combs. Thank you for supporting Project ALS. 100% of your donation will go to aggressive, groundbreaking Project ALS research that's working to identify the first effective treatments—and ultimately a cure—for ALS. How often would you like to donate? HOME - PROJECT ALSWHO WE AREABOUT ALSOUR RESEARCHGET INVOLVEDWEBINARSERIESDONATE
Project ALS is the world’s first ALS organization to focus exclusively on research.We have raised over $100 million in 22 years to fund ALS research programs at leading academic institutions including Harvard University, Columbia University, UCSF, and the Salk Institute, and have made significant progress toward a cure for ALS. WHO WE ARE - PROJECT ALS They founded Project ALS as a non-profit 501 (c)3 in 1998, and set forth a new paradigm for ALS research. Project ALS-funded doctors and researchers were required to work together in small teams, toward a new standard of results-oriented accountability. Project ALS requires that its funded researchers communicate regularly, share data openly ABOUT ALS - PROJECT ALS ALS, also known as Lou Gehrig’s disease, is a brain disease that targets brain cells called motor neurons. Motor neurons send messages from the brain to muscles throughout the body. In ALS, as motor neurons die, a person progressively loses the ability to walk, speak, swallow, and breathe. ALS affects adults of all ages, from teens toseniors
OUR RESEARCH
Project ALS works collaboratively with its scientists to identify the most promising ALS research and, along with its Research Advisory Board (RAB), streamlines the research process with effective strategies. Project ALS assesses progress through regular meetings and reviews by the RAB. Project ALS engages in the ongoing recruitment of JOIN THE 2021 DON'T TALK-A-THON! How the Don’t Talk-a-Thon Started. Avery Niedrowski lost her Grandpa John to ALS when she was 6 years old. He was her rock. Two years later, Avery got busy. She chose to be silent for one whole day for the years her grandpa had been unable to speak due to ALS. In return, and in his honor, she asked people to donate money to Project ALSresearch.
PROJECT ALS INTRODUCES PROSETIN It took 6 years, and over 80 versions of the compound, to get to Prosetin: a drug that rescues motor neurons in cellular and animal models of ALS, crosses the blood-brain barrier with ease, and has been safe and well-tolerated in all of our tests to date. Notably, pathways that Prosetin targets have been identified by many other ALSresearchers
ONE FAMILY’S PASSIONATE FIGHT AGAINST NEURODEGENERATIVE One Family’s Passionate Fight Against Neurodegenerative Diseases. July 10, 2020. The Wasserman family has experienced first-hand the devastating effects of neurodegenerative diseases: Sandra Wasserman lost her beloved husband to Parkinson’s disease, and her son to glioblastoma. Now in her eighties, Sandra has friends experiencing the THE HERMSTAD LEGACY: ADVANCES IN TREATMENTS FOR ALS The Hermstad Legacy: Advances in Treatments for ALS. January 25, 2021. On February 4th, we invite you to join special guest and ALS research advocate Ben Stiller, foremost ALS clinicians, leading researchers, and dedicated patient advocates to learn how Jaci and Alex Hermstad inspired the team effort that led to the development of jacifusen THE DON'T TALK-A-THON 2021 We really, really like you! And you really, really want to silence ALS. 100% of your $250 goes directly toward raising crucial funds for ALS research. Each person who registers for the #DontTalkAThon2021 and raises $250 or more will receive a Don't Talk-a-Thon hoodie for your generous donation and special shout outs! Fundraise. AT HOME WITH REBECCA LUKER Donate Now. Thank you for joining 3-time Tony nominee Rebecca Luker for an evening of song hosted by Santino Fontana and a conversation with Katie Couric. This event is sponsored by Playbill and the Actor's Fund. Rebecca is a highly-acclaimed, multi-Tony-nominated actress and singer. Her performances in Phantom of the Opera, The Secret Garden HOME - PROJECT ALSWHO WE AREABOUT ALSOUR RESEARCHGET INVOLVEDWEBINARSERIESDONATE
Project ALS is the world’s first ALS organization to focus exclusively on research.We have raised over $100 million in 22 years to fund ALS research programs at leading academic institutions including Harvard University, Columbia University, UCSF, and the Salk Institute, and have made significant progress toward a cure for ALS. WHO WE ARE - PROJECT ALS They founded Project ALS as a non-profit 501 (c)3 in 1998, and set forth a new paradigm for ALS research. Project ALS-funded doctors and researchers were required to work together in small teams, toward a new standard of results-oriented accountability. Project ALS requires that its funded researchers communicate regularly, share data openly ABOUT ALS - PROJECT ALS ALS, also known as Lou Gehrig’s disease, is a brain disease that targets brain cells called motor neurons. Motor neurons send messages from the brain to muscles throughout the body. In ALS, as motor neurons die, a person progressively loses the ability to walk, speak, swallow, and breathe. ALS affects adults of all ages, from teens toseniors
OUR RESEARCH
Project ALS works collaboratively with its scientists to identify the most promising ALS research and, along with its Research Advisory Board (RAB), streamlines the research process with effective strategies. Project ALS assesses progress through regular meetings and reviews by the RAB. Project ALS engages in the ongoing recruitment of JOIN THE 2021 DON'T TALK-A-THON! How the Don’t Talk-a-Thon Started. Avery Niedrowski lost her Grandpa John to ALS when she was 6 years old. He was her rock. Two years later, Avery got busy. She chose to be silent for one whole day for the years her grandpa had been unable to speak due to ALS. In return, and in his honor, she asked people to donate money to Project ALSresearch.
PROJECT ALS INTRODUCES PROSETIN It took 6 years, and over 80 versions of the compound, to get to Prosetin: a drug that rescues motor neurons in cellular and animal models of ALS, crosses the blood-brain barrier with ease, and has been safe and well-tolerated in all of our tests to date. Notably, pathways that Prosetin targets have been identified by many other ALSresearchers
ONE FAMILY’S PASSIONATE FIGHT AGAINST NEURODEGENERATIVE One Family’s Passionate Fight Against Neurodegenerative Diseases. July 10, 2020. The Wasserman family has experienced first-hand the devastating effects of neurodegenerative diseases: Sandra Wasserman lost her beloved husband to Parkinson’s disease, and her son to glioblastoma. Now in her eighties, Sandra has friends experiencing the THE HERMSTAD LEGACY: ADVANCES IN TREATMENTS FOR ALS The Hermstad Legacy: Advances in Treatments for ALS. January 25, 2021. On February 4th, we invite you to join special guest and ALS research advocate Ben Stiller, foremost ALS clinicians, leading researchers, and dedicated patient advocates to learn how Jaci and Alex Hermstad inspired the team effort that led to the development of jacifusen THE DON'T TALK-A-THON 2021 We really, really like you! And you really, really want to silence ALS. 100% of your $250 goes directly toward raising crucial funds for ALS research. Each person who registers for the #DontTalkAThon2021 and raises $250 or more will receive a Don't Talk-a-Thon hoodie for your generous donation and special shout outs! Fundraise. AT HOME WITH REBECCA LUKER Donate Now. Thank you for joining 3-time Tony nominee Rebecca Luker for an evening of song hosted by Santino Fontana and a conversation with Katie Couric. This event is sponsored by Playbill and the Actor's Fund. Rebecca is a highly-acclaimed, multi-Tony-nominated actress and singer. Her performances in Phantom of the Opera, The Secret Garden ABOUT ALS - PROJECT ALS ALS, also known as Lou Gehrig’s disease, is a brain disease that targets brain cells called motor neurons. Motor neurons send messages from the brain to muscles throughout the body. In ALS, as motor neurons die, a person progressively loses the ability to walk, speak, swallow, and breathe. ALS affects adults of all ages, from teens toseniors
GET INVOLVED
Temporary Mailing Address: 4330 Camp Kaufmann Road Huntingtown, MD 20639. 801 Riverside Drive, Suite 6G New York, NY 10032. Phone: (212) 420-7382. Fax: (646) 559-9290WEBINAR SERIES
Webinar with Richard Kind. Erin and Valerie chat with actor and long-time Project ALS supporter, Richard Kind. Richard is the host of this year’s Tomorrow is Tonight Virtual Gala, airing Thursday, October 22nd at 7:30 ET. Project ALS webinar with Senator Mike Braun and Corey Polen from Project ALS on Vimeo. JENIFER’S LEGACY LIVES ON. Jenifer’s legacy lives on. May 6, 2021. Play Video. When Project ALS co-founder Jenifer Estess was diagnosed with ALS at the age of 35, her doctor told her to max out her credit cards, eat junk food, and just wait to die. Like most who find themselves in this situation, she wasappalled.
THE HUNT FOR ALS BIOMARKERS: FAT? 2. Disease stratification biomarkers: ALS is a complicated brain disease, made more challenging to treat because of its heterogeneity. Research has identified more than 50 genes that can cause ALS, and multiple biological processes are involved. Even with research advances, it largely remains a mystery that some ALS starts in thethroat, and
VALENTINE FOR A PIONEER Jaci and her horse Bud, March 2019 “Jaci is blazing a path that hopefully will not just cure her but set a course of treatment for countless others.” – Lori Hermstad, mother. February 14th is a significant day for the Hermstad family. On this day in 2011, Alex AT HOME WITH REBECCA LUKER Thank you for joining 3-time Tony nominee Rebecca Luker for an evening of song hosted by Santino Fontana and a conversation with Katie Couric. This event is sponsored by Playbill and the Actor's Fund. Rebecca is a highly-acclaimed, multi-Tony-nominated actress andsinger. Her
FUNDRAISING FOR PROJECT ALS We are taking a vow of silence for ALS Awareness month starting on May 22nd in honor of all individuals diagnosed with ALS. DONATE TO THE DON'T TALK-A-THON 2021 Thanks for helping us silence ALS. Thank you for your donation to Project ALS research. 100% of the money you donate will go straight toward cutting-edge, aggressive ALS research that aims to silence ALS once and for all. How often would you like to donate? One-timeMonthly. Choose a
DONATE TO TEAM CHRIS COMBS Team Chris Combs. Thank you for supporting Project ALS. 100% of your donation will go to aggressive, groundbreaking Project ALS research that's working to identify the first effective treatments—and ultimately a cure—for ALS. How often would you like to donate? HOME - PROJECT ALSWHO WE AREABOUT ALSOUR RESEARCHGET INVOLVEDWEBINARSERIESDONATE
Project ALS is the world’s first ALS organization to focus exclusively on research.We have raised over $100 million in 22 years to fund ALS research programs at leading academic institutions including Harvard University, Columbia University, UCSF, and the Salk Institute, and have made significant progress toward a cure for ALS. WHO WE ARE - PROJECT ALS They founded Project ALS as a non-profit 501 (c)3 in 1998, and set forth a new paradigm for ALS research. Project ALS-funded doctors and researchers were required to work together in small teams, toward a new standard of results-oriented accountability. Project ALS requires that its funded researchers communicate regularly, share data openly ABOUT ALS - PROJECT ALS ALS, also known as Lou Gehrig’s disease, is a brain disease that targets brain cells called motor neurons. Motor neurons send messages from the brain to muscles throughout the body. In ALS, as motor neurons die, a person progressively loses the ability to walk, speak, swallow, and breathe. ALS affects adults of all ages, from teens toseniors
OUR RESEARCH
Project ALS works collaboratively with its scientists to identify the most promising ALS research and, along with its Research Advisory Board (RAB), streamlines the research process with effective strategies. Project ALS assesses progress through regular meetings and reviews by the RAB. Project ALS engages in the ongoing recruitment of JOIN THE 2021 DON'T TALK-A-THON! How the Don’t Talk-a-Thon Started. Avery Niedrowski lost her Grandpa John to ALS when she was 6 years old. He was her rock. Two years later, Avery got busy. She chose to be silent for one whole day for the years her grandpa had been unable to speak due to ALS. In return, and in his honor, she asked people to donate money to Project ALSresearch.
PROJECT ALS INTRODUCES PROSETIN It took 6 years, and over 80 versions of the compound, to get to Prosetin: a drug that rescues motor neurons in cellular and animal models of ALS, crosses the blood-brain barrier with ease, and has been safe and well-tolerated in all of our tests to date. Notably, pathways that Prosetin targets have been identified by many other ALSresearchers
ONE FAMILY’S PASSIONATE FIGHT AGAINST NEURODEGENERATIVE One Family’s Passionate Fight Against Neurodegenerative Diseases. July 10, 2020. The Wasserman family has experienced first-hand the devastating effects of neurodegenerative diseases: Sandra Wasserman lost her beloved husband to Parkinson’s disease, and her son to glioblastoma. Now in her eighties, Sandra has friends experiencing the THE HERMSTAD LEGACY: ADVANCES IN TREATMENTS FOR ALS The Hermstad Legacy: Advances in Treatments for ALS. January 25, 2021. On February 4th, we invite you to join special guest and ALS research advocate Ben Stiller, foremost ALS clinicians, leading researchers, and dedicated patient advocates to learn how Jaci and Alex Hermstad inspired the team effort that led to the development of jacifusen THE DON'T TALK-A-THON 2021 We really, really like you! And you really, really want to silence ALS. 100% of your $250 goes directly toward raising crucial funds for ALS research. Each person who registers for the #DontTalkAThon2021 and raises $250 or more will receive a Don't Talk-a-Thon hoodie for your generous donation and special shout outs! Fundraise. AT HOME WITH REBECCA LUKER Donate Now. Thank you for joining 3-time Tony nominee Rebecca Luker for an evening of song hosted by Santino Fontana and a conversation with Katie Couric. This event is sponsored by Playbill and the Actor's Fund. Rebecca is a highly-acclaimed, multi-Tony-nominated actress and singer. Her performances in Phantom of the Opera, The Secret Garden HOME - PROJECT ALSWHO WE AREABOUT ALSOUR RESEARCHGET INVOLVEDWEBINARSERIESDONATE
Project ALS is the world’s first ALS organization to focus exclusively on research.We have raised over $100 million in 22 years to fund ALS research programs at leading academic institutions including Harvard University, Columbia University, UCSF, and the Salk Institute, and have made significant progress toward a cure for ALS. WHO WE ARE - PROJECT ALS They founded Project ALS as a non-profit 501 (c)3 in 1998, and set forth a new paradigm for ALS research. Project ALS-funded doctors and researchers were required to work together in small teams, toward a new standard of results-oriented accountability. Project ALS requires that its funded researchers communicate regularly, share data openly ABOUT ALS - PROJECT ALS ALS, also known as Lou Gehrig’s disease, is a brain disease that targets brain cells called motor neurons. Motor neurons send messages from the brain to muscles throughout the body. In ALS, as motor neurons die, a person progressively loses the ability to walk, speak, swallow, and breathe. ALS affects adults of all ages, from teens toseniors
OUR RESEARCH
Project ALS works collaboratively with its scientists to identify the most promising ALS research and, along with its Research Advisory Board (RAB), streamlines the research process with effective strategies. Project ALS assesses progress through regular meetings and reviews by the RAB. Project ALS engages in the ongoing recruitment of JOIN THE 2021 DON'T TALK-A-THON! How the Don’t Talk-a-Thon Started. Avery Niedrowski lost her Grandpa John to ALS when she was 6 years old. He was her rock. Two years later, Avery got busy. She chose to be silent for one whole day for the years her grandpa had been unable to speak due to ALS. In return, and in his honor, she asked people to donate money to Project ALSresearch.
PROJECT ALS INTRODUCES PROSETIN It took 6 years, and over 80 versions of the compound, to get to Prosetin: a drug that rescues motor neurons in cellular and animal models of ALS, crosses the blood-brain barrier with ease, and has been safe and well-tolerated in all of our tests to date. Notably, pathways that Prosetin targets have been identified by many other ALSresearchers
ONE FAMILY’S PASSIONATE FIGHT AGAINST NEURODEGENERATIVE One Family’s Passionate Fight Against Neurodegenerative Diseases. July 10, 2020. The Wasserman family has experienced first-hand the devastating effects of neurodegenerative diseases: Sandra Wasserman lost her beloved husband to Parkinson’s disease, and her son to glioblastoma. Now in her eighties, Sandra has friends experiencing the THE HERMSTAD LEGACY: ADVANCES IN TREATMENTS FOR ALS The Hermstad Legacy: Advances in Treatments for ALS. January 25, 2021. On February 4th, we invite you to join special guest and ALS research advocate Ben Stiller, foremost ALS clinicians, leading researchers, and dedicated patient advocates to learn how Jaci and Alex Hermstad inspired the team effort that led to the development of jacifusen THE DON'T TALK-A-THON 2021 We really, really like you! And you really, really want to silence ALS. 100% of your $250 goes directly toward raising crucial funds for ALS research. Each person who registers for the #DontTalkAThon2021 and raises $250 or more will receive a Don't Talk-a-Thon hoodie for your generous donation and special shout outs! Fundraise. AT HOME WITH REBECCA LUKER Donate Now. Thank you for joining 3-time Tony nominee Rebecca Luker for an evening of song hosted by Santino Fontana and a conversation with Katie Couric. This event is sponsored by Playbill and the Actor's Fund. Rebecca is a highly-acclaimed, multi-Tony-nominated actress and singer. Her performances in Phantom of the Opera, The Secret Garden ABOUT ALS - PROJECT ALS ALS, also known as Lou Gehrig’s disease, is a brain disease that targets brain cells called motor neurons. Motor neurons send messages from the brain to muscles throughout the body. In ALS, as motor neurons die, a person progressively loses the ability to walk, speak, swallow, and breathe. ALS affects adults of all ages, from teens toseniors
GET INVOLVED
Support Project ALS Research by Drinking ONEHOPE Wine. ONEHOPE is a charity-based wine company that gives back with every purchase. If you buy ONEHOPE wine via this link, 10% of of your purchase will go. Trivia Night! February 25th. Join us in teams ONE FAMILY’S PASSIONATE FIGHT AGAINST NEURODEGENERATIVE One Family’s Passionate Fight Against Neurodegenerative Diseases. July 10, 2020. The Wasserman family has experienced first-hand the devastating effects of neurodegenerative diseases: Sandra Wasserman lost her beloved husband to Parkinson’s disease, and her son to glioblastoma. Now in her eighties, Sandra has friends experiencing theWEBINAR SERIES
Webinar with Richard Kind. Erin and Valerie chat with actor and long-time Project ALS supporter, Richard Kind. Richard is the host of this year’s Tomorrow is Tonight Virtual Gala, airing Thursday, October 22nd at 7:30 ET. Project ALS webinar with Senator Mike Braun and Corey Polen from Project ALS on Vimeo. JENIFER’S LEGACY LIVES ON. Jenifer’s legacy lives on. May 6, 2021. Play Video. When Project ALS co-founder Jenifer Estess was diagnosed with ALS at the age of 35, her doctor told her to max out her credit cards, eat junk food, and just wait to die. Like most who find themselves in this situation, she wasappalled.
VALENTINE FOR A PIONEER Jaci and her horse Bud, March 2019 “Jaci is blazing a path that hopefully will not just cure her but set a course of treatment for countless others.” – Lori Hermstad, mother. February 14th is a significant day for the Hermstad family. On this day in 2011, Alex FUNDRAISING FOR PROJECT ALS We are taking a vow of silence for ALS Awareness month starting on May 22nd in honor of all individuals diagnosed with ALS. PROSETIN - HOME - PROJECT ALS Prosetin. Prosetin has raised USD0 out of their goal of USD1500000. USD0 Raised. USD1500000 Goal. Become a Fundraiser Donate Now. At Project ALS, we believe in Prosetin—and we believe we can get Prosetin to people with ALS more quickly, responsibly, and humanely than any drug company. But we DONATE TO AT HOME WITH REBECCA LUKER Thank you for joining 3-time Tony nominee Rebecca Luker for an evening of song hosted by Santino Fontana and a conversation with Katie Couric. This event is sponsored by Playbill and the Actor's Fund. Rebecca is a highly-acclaimed, multi-Tony-nominated actress andsinger. Her
DONATE TO TEAM CHRIS COMBS Team Chris Combs. Thank you for supporting Project ALS. 100% of your donation will go to aggressive, groundbreaking Project ALS research that's working to identify the first effective treatments—and ultimately a cure—for ALS. How often would you like to donate? HOME - PROJECT ALSWHO WE AREABOUT ALSOUR RESEARCHGET INVOLVEDWEBINARSERIESDONATE
Project ALS is the world’s first ALS organization to focus exclusively on research.We have raised over $100 million in 22 years to fund ALS research programs at leading academic institutions including Harvard University, Columbia University, UCSF, and the Salk Institute, and have made significant progress toward a cure for ALS. WHO WE ARE - PROJECT ALSALS CURE PROJECTPOSSIBLE CURE FOR ALSIS THEREA CURE FOR ALS
They founded Project ALS as a non-profit 501 (c)3 in 1998, and set forth a new paradigm for ALS research. Project ALS-funded doctors and researchers were required to work together in small teams, toward a new standard of results-oriented accountability. Project ALS requires that its funded researchers communicate regularly, share data openly ABOUT ALS - PROJECT ALSCURE FOR ALS DISEASEPROJECT ALS NYCPROSETIN ALSCURE FOR ALS FOUND ALS, also known as Lou Gehrig’s disease, is a brain disease that targets brain cells called motor neurons. Motor neurons send messages from the brain to muscles throughout the body. In ALS, as motor neurons die, a person progressively loses the ability to walk, speak, swallow, and breathe. ALS affects adults of all ages, from teens toseniors
JOIN THE 2021 DON'T TALK-A-THON! How the Don’t Talk-a-Thon Started. Avery Niedrowski lost her Grandpa John to ALS when she was 6 years old. He was her rock. Two years later, Avery got busy. She chose to be silent for one whole day for the years her grandpa had been unable to speak due to ALS. In return, and in his honor, she asked people to donate money to Project ALSresearch.
ONE FAMILY’S PASSIONATE FIGHT AGAINST NEURODEGENERATIVE One Family’s Passionate Fight Against Neurodegenerative Diseases. July 10, 2020. The Wasserman family has experienced first-hand the devastating effects of neurodegenerative diseases: Sandra Wasserman lost her beloved husband to Parkinson’s disease, and her son to glioblastoma. Now in her eighties, Sandra has friends experiencing the PROJECT ALS INTRODUCES PROSETIN It took 6 years, and over 80 versions of the compound, to get to Prosetin: a drug that rescues motor neurons in cellular and animal models of ALS, crosses the blood-brain barrier with ease, and has been safe and well-tolerated in all of our tests to date. Notably, pathways that Prosetin targets have been identified by many other ALSresearchers
THE DON'T TALK-A-THON 2021 We really, really like you! And you really, really want to silence ALS. 100% of your $250 goes directly toward raising crucial funds for ALS research. Each person who registers for the #DontTalkAThon2021 and raises $250 or more will receive a Don't Talk-a-Thon hoodie for your generous donation and special shout outs! Fundraise. VALENTINE FOR A PIONEER Jaci and her horse Bud, March 2019 “Jaci is blazing a path that hopefully will not just cure her but set a course of treatment for countless others.” – Lori Hermstad, mother. February 14th is a significant day for the Hermstad family. On this day in 2011, Alex AT HOME WITH REBECCA LUKER Donate Now. Thank you for joining 3-time Tony nominee Rebecca Luker for an evening of song hosted by Santino Fontana and a conversation with Katie Couric. This event is sponsored by Playbill and the Actor's Fund. Rebecca is a highly-acclaimed, multi-Tony-nominated actress and singer. Her performances in Phantom of the Opera, The Secret Garden DONATE TO TEAM CHRIS COMBS Team Chris Combs. Thank you for supporting Project ALS. 100% of your donation will go to aggressive, groundbreaking Project ALS research that's working to identify the first effective treatments—and ultimately a cure—for ALS. How often would you like to donate? HOME - PROJECT ALSWHO WE AREABOUT ALSOUR RESEARCHGET INVOLVEDWEBINARSERIESDONATE
Project ALS is the world’s first ALS organization to focus exclusively on research.We have raised over $100 million in 22 years to fund ALS research programs at leading academic institutions including Harvard University, Columbia University, UCSF, and the Salk Institute, and have made significant progress toward a cure for ALS. WHO WE ARE - PROJECT ALSALS CURE PROJECTPOSSIBLE CURE FOR ALSIS THEREA CURE FOR ALS
They founded Project ALS as a non-profit 501 (c)3 in 1998, and set forth a new paradigm for ALS research. Project ALS-funded doctors and researchers were required to work together in small teams, toward a new standard of results-oriented accountability. Project ALS requires that its funded researchers communicate regularly, share data openly ABOUT ALS - PROJECT ALSCURE FOR ALS DISEASEPROJECT ALS NYCPROSETIN ALSCURE FOR ALS FOUND ALS, also known as Lou Gehrig’s disease, is a brain disease that targets brain cells called motor neurons. Motor neurons send messages from the brain to muscles throughout the body. In ALS, as motor neurons die, a person progressively loses the ability to walk, speak, swallow, and breathe. ALS affects adults of all ages, from teens toseniors
JOIN THE 2021 DON'T TALK-A-THON! How the Don’t Talk-a-Thon Started. Avery Niedrowski lost her Grandpa John to ALS when she was 6 years old. He was her rock. Two years later, Avery got busy. She chose to be silent for one whole day for the years her grandpa had been unable to speak due to ALS. In return, and in his honor, she asked people to donate money to Project ALSresearch.
ONE FAMILY’S PASSIONATE FIGHT AGAINST NEURODEGENERATIVE One Family’s Passionate Fight Against Neurodegenerative Diseases. July 10, 2020. The Wasserman family has experienced first-hand the devastating effects of neurodegenerative diseases: Sandra Wasserman lost her beloved husband to Parkinson’s disease, and her son to glioblastoma. Now in her eighties, Sandra has friends experiencing the PROJECT ALS INTRODUCES PROSETIN It took 6 years, and over 80 versions of the compound, to get to Prosetin: a drug that rescues motor neurons in cellular and animal models of ALS, crosses the blood-brain barrier with ease, and has been safe and well-tolerated in all of our tests to date. Notably, pathways that Prosetin targets have been identified by many other ALSresearchers
THE DON'T TALK-A-THON 2021 We really, really like you! And you really, really want to silence ALS. 100% of your $250 goes directly toward raising crucial funds for ALS research. Each person who registers for the #DontTalkAThon2021 and raises $250 or more will receive a Don't Talk-a-Thon hoodie for your generous donation and special shout outs! Fundraise. VALENTINE FOR A PIONEER Jaci and her horse Bud, March 2019 “Jaci is blazing a path that hopefully will not just cure her but set a course of treatment for countless others.” – Lori Hermstad, mother. February 14th is a significant day for the Hermstad family. On this day in 2011, Alex AT HOME WITH REBECCA LUKER Donate Now. Thank you for joining 3-time Tony nominee Rebecca Luker for an evening of song hosted by Santino Fontana and a conversation with Katie Couric. This event is sponsored by Playbill and the Actor's Fund. Rebecca is a highly-acclaimed, multi-Tony-nominated actress and singer. Her performances in Phantom of the Opera, The Secret Garden DONATE TO TEAM CHRIS COMBS Team Chris Combs. Thank you for supporting Project ALS. 100% of your donation will go to aggressive, groundbreaking Project ALS research that's working to identify the first effective treatments—and ultimately a cure—for ALS. How often would you like to donate?OUR RESEARCH
Project ALS works collaboratively with its scientists to identify the most promising ALS research and, along with its Research Advisory Board (RAB), streamlines the research process with effective strategies. Project ALS assesses progress through regular meetings and reviews by the RAB. Project ALS engages in the ongoing recruitment of PROJECT ALS ENDORSES NEW ALS LEGISLATION Project ALS Endorses New ALS Legislation. June 5, 2020. Project ALS is encouraged by the introduction of two bills that aim to provide people with ALS faster, more robust access to experimental therapies. These bills are significant for specific, substantive reasons detailed below. Perhaps as importantly, they represent a sea change in ALSGET INVOLVED
Temporary Mailing Address: 4330 Camp Kaufmann Road Huntingtown, MD 20639. 801 Riverside Drive, Suite 6G New York, NY 10032. Phone: (212) 420-7382. Fax: (646) 559-9290WEBINAR SERIES
Webinar with Richard Kind. Erin and Valerie chat with actor and long-time Project ALS supporter, Richard Kind. Richard is the host of this year’s Tomorrow is Tonight Virtual Gala, airing Thursday, October 22nd at 7:30 ET. Project ALS webinar with Senator Mike Braun and Corey Polen from Project ALS on Vimeo. FUNDRAISING FOR PROJECT ALS We are taking a vow of silence for ALS Awareness month starting on May 22nd in honor of all individuals diagnosed with ALS. AT HOME WITH REBECCA LUKER Thank you for joining 3-time Tony nominee Rebecca Luker for an evening of song hosted by Santino Fontana and a conversation with Katie Couric. This event is sponsored by Playbill and the Actor's Fund. Rebecca is a highly-acclaimed, multi-Tony-nominated actress andsinger. Her
DONATE TO THE DON'T TALK-A-THON 2021 Thanks for helping us silence ALS. Thank you for your donation to Project ALS research. 100% of the money you donate will go straight toward cutting-edge, aggressive ALS research that aims to silence ALS once and for all. How often would you like to donate? One-timeMonthly. Choose a
PROSETIN - HOME - PROJECT ALS Prosetin. Prosetin has raised USD0 out of their goal of USD1500000. USD0 Raised. USD1500000 Goal. Become a Fundraiser Donate Now. At Project ALS, we believe in Prosetin—and we believe we can get Prosetin to people with ALS more quickly, responsibly, and humanely than any drug company. But we CHECK OUT DR. DOUG'S TEAM FUNDRAISING PAGE FOR PROJECT ALS We are taking a vow of silence on May 22nd in honor of YOUR LOVED ONE, who suffers from ALS CHECK OUT JACK’S CATTLE HANDS' TEAM FUNDRAISING PAGE FOR We are taking a vow of silence on May 22nd in honor of Jack Hooker, who suffered from ALS. Want to join in? Please share! Pick an hour, any hour, on May 22nd.__
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THE PROJECT ALS MISSION PROJECT ALS identifies and funds the most promising scientific research that will lead to the first effective treatments and a cure for ALS. We recruit the world’s best scientists and doctors to work together—rationally and aggressively—to develop a better understanding of the ALS disease process and, in parallel, better therapeutic strategies. PROJECT ALS is the world’s first ALS organization to focus exclusively on research. We have raised over $100 million in 22 years to fund ALS research programs at leading academic institutions including Harvard University, Columbia University, UCSF, and the Salk Institute, and have made significant progress toward a cure for ALS.Make a Donation
READ ABOUT THE LATEST UPDATES AND BREAKTHROUGHS IN ALS RESEARCH, AND SEE THE PROJECT ALS RESEARCH PHILOSOPHY – SOMETHING WE’RE PROUD TO SAY HAS ACCELERATED THE PACE OF RESEARCH.Our Research
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This year, the Project ALS family feels an even stronger urgency to beat ALS down as we move closer to the first ef… twitter.com/i/web/status/13323… Yesterday at 5:01 PM*
Register for next week's webinar featuring two of our amazing Board members and dear friends: Staci Kirchhoff and C… twitter.com/i/web/status/13316… Nov 25, 2020 3:01 PM*
2020 has brought extraordinary challenges, but the Project ALS Family has met them. The Kleiner Family Initiative s… twitter.com/i/web/status/13312… Nov 24, 2020 4:53 PM FINDING & FUNDING A CUREMake a Donation
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Temporary Mailing Address: 4330 Camp Kaufmann Road Huntingtown, MD 20639 801 Riverside Drive, Suite 6GNew York, NY 10032
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PALS Celebrating 20 Years Final WEB from Project ALS on Vimeo.
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