Cleo, mi aplicación para la EM

An app for people with MS. Reminders, Cleo nurse and much more!

Living with Multiple Sclerosis (MS) presents unique challenges that others do not typically face on a daily basis. Meet Cleo, your digital companion in MS. Cleo was designed to help you live with MS. With Cleo, you'll have access to information, inspiration, support and a variety of tools, conveniently accessible in a single app. Our goal is to provide a valuable app to help you, your support people, and your healthcare team. We are here to help you on your journey. Live a special life!

Cleo is based on 3 key features:

* Content tailored to find tips, inspiration and news related to multiple sclerosis.

* A personal journal to track your health, view your data, and share reports with your healthcare team.

* Wellness programs designed by health professionals and tailored to your specific needs.

PERSONALIZED CONTENT

Explore articles and videos with tips for living with MS, tips to improve your well-being, information about common MS symptoms, and education about the disease. Tailor the type of content you're interested in viewing for a more personalized experience.

PERSONAL DIARY

The better your healthcare team understands what is happening, the better you can make decisions together. Cleo can help you track your moods, symptoms, physical activities, and more. Link Cleo to your Apple HealthKit to track steps and distance traveled. Then create reports to share and discuss with your healthcare team. Cleo is also there to help provide you with reminders throughout the day. Set appointment and treatment notifications based on schedules agreed upon with your healthcare team.

WELLBEING PROGRAMS

Access wellness programs designed by MS experts and rehabilitation specialists specifically for people living with MS. We work with healthcare professionals to create tailored programs with people with MS in mind. After speaking with your healthcare team, you can choose from different intensity levels based on your ability and comfort level. Remember, everyone's experience with MS is different, and your healthcare team should always be your primary source of information about your MS.

Biogen-203863 March 2023