Cleo: Mi Esclerosis Múltiple

Living with multiple sclerosis presents unique challenges that others don't typically face on a daily basis. Meet Cleo, your digital Multiple Sclerosis companion. Cleo was designed to help you while living with MS. With Cleo, you'll have access to information, inspiration, support, and a variety of tools, conveniently accessible in one app. Our goal is to provide a valuable app to help you, your support team, and your healthcare team. We're here to support you on your journey. Live a life of greatness!

Cleo is built on three key features:
* Personalized content to find tips, inspiration, and news related to multiple sclerosis
* A personal journal to track your health, visualize your data, and share reports with your healthcare team
* Wellness programs designed by healthcare professionals tailored to your specific needs

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

PERSONAL JOURNAL
When your healthcare team better understands what's happening to you between appointments, you can make better decisions together. Cleo can help you track your moods, symptoms, physical activities, and more. Link Cleo to Health Connect to track steps and distance. Then, create reports to share and discuss with your healthcare team. Cleo is also there to help provide reminders throughout the day. Set appointment and medication notifications based on the schedules discussed with your healthcare team.

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

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