Update Cleo en krijg toegang tot nieuwe functies:
- Stel je afspraakherinneringen in.
- Toegang tot to-do lijsten en notities voor je afspraken. Met spraakherkenning kun je aantekeningen maken terwijl de app geopend is.
- Sla de gegevens van je zorgteam op, deel rapporten met hen en bekijk gemakkelijk je afspraken.
- Exporteer afspraakdetails naar je telefoonagenda.
Je hoeft geen notitieboekje mee te nemen!
Living with Multiple Sclerosis can be challenging every day. Meet Cleo, the app that can help you cope better with your life with MS. In the Cleo app you will find a lot of information, inspiration, tips and various tools that can support your daily life with MS. Your life counts!
The 3 main features of Cleo:
* Tailored content for tips, inspiration and news about MS.
* A personal diary to track your health and symptoms, make the data easily visible and share the reports with your healthcare providers.
* Wellness programs designed by professionals and adapted to your specific needs.
CUSTOMIZED CONTENT
Discover articles and videos with tips for coping with MS, ideas for improving your well-being, and information on MS-related topics. Adjust the content to your own interests and personal preferences.
DIARY
When your caregivers have a better understanding of how you are doing between appointments, you can make better decisions together. Cleo can help you easily track your mood, symptoms and physical activity, among other things. Connect Cleo to your Google Fit to keep track of the number of steps and distance covered, for example. You can create reports from the data to share and discuss with your healthcare providers. Cleo can also send you reminders during the day. Set appointments and medication notifications based on schedules discussed with your healthcare providers.
WELLNESS PROGRAMS
Cleo offers access to wellness programs specially developed for people with MS by MS experts and rehabilitation specialists. You can choose from different intensity levels based on your ability and interest, in consultation with your healthcare providers. Remember that everyone's experience with MS is different and your doctor and/or nurse will always be the primary source of information regarding your MS.