The Live Now Foundation provides comprehensive support to people with ALS (amyotrophic lateral sclerosis) throughout Russia. ALS, better known as Stephen Hawking’s disease, is a rare incurable disease affecting motor neurons that transmit the information to the muscles. A patient with ALS gradually loses the ability to move, speak, swallow and breathe independently. There are 12-15 thousand people with ALS living in Russia.
Join our Annual Conference
The largest Russian event on Neuromuscular Diseases for the patient community, doctors, and anyone interested in the topic, with international participation
The media of the Foundation als-info.ru
Tough issues on ALS
Our new media als-help.ru provides families with variable information how to cope with ALS and get support
We don’t know
how powerful we are
until it’s the only option
In our Foundation, people with ALS can find support and professional help. ALS is a path that no one should walk alone.
How we started
The first Service for helping people with ALS in Russia was launched in 2012 at the Mercy medical center of the Marfo-Mariinsky Convent. In 2015, this team held the first ALC conference in Moscow. At the conference, people with ALS and their caregivers decided to start a charity foundation that will defend their interests in the country. Its name – “Live Now” – was invented by people with ALS themselves and their relatives — those who learned the hard way not to put the most important things off and find hope.
Since 2015, the Live Now Foundation has been providing comprehensive support to people with ALS. The Foundation has helped more than 3000 patients and their families with medical, social and psychological counseling, equipment and training materials. The Foundation also works with health authorities on regions, helps patients receive the necessary rehabilitation and medical devices, primarily for respiratory support at home.
Corporate Support options
We want to thank everyone who is ready to share their resources and support us in our mission. When it comes to helping people with ALS, we need all the help we can get – people who are ready to share their expertise, make donations, provide materials and draw society’s attention.
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