The ME / CFS Stichting Nederland is committed to strengthening the position of patients with ME / CFS (chronic fatigue syndrome). We focus on ALL ME / CFS patients. Regardless of the severity of their ...
Webmaster
Contact person
Kinga Gomoluch
#17936
Scan me or visit www.volunteer.deedmob.com/o/MECVS-Stichting-Nederland/opportunities/Webmaster/17936 to join
Summary
Do you like to keep our websites up to date and well laid out? Are you a bit creative and do you like to work with wordpress? Then read on quickly ...
Detailed description
Wij zijn op zoek naar een vrijwilliger die affiniteit heeft met webdesign en webbeheer voor het bijhouden van wijzigingen op onze website (Wordpress).
Je onderhoudt onze websites en zorgt dat ze technisch up to date zijn. Je voegt content toe en houdt de sites technisch in orde.
In principe kan je alles gwoon thuis online doen. Incidenteel kan het voorkomen dat we eens samen op kantoor in Hilversum bij elkaar komen om iets te overleggen of uit te proberen.
Je hoeft geen afgeronde opleiding in webbeheer en webdesign te hebben. Als je er maar een goede dosis verstand van hebt en het vooral leuk vindt. Dat is het meest belangrijk.
Werktijden: nader in te vullen en in overleg
Bijzondere Voorwaarden:
Inwerkmethode en begeleiding: in overleg
What volunteers need
🗣️ Native language skills
What we will provide to volunteers
💸 Reimbursement of costs
About ME/CVS Stichting Nederland
The ME / CFS Stichting Nederland is committed to strengthening the position of patients with ME / CFS (chronic fatigue syndrome). We focus on ALL ME / CFS patients. Regardless of the severity of their illness, their origin, gender or age. Young people with ME / CFS receive extra attention from us. They still have a life ahead of them and deserve extra help.
We do this by:
- Aiming for broad recognition and recognition of ME / CFS as a very serious disabling physical disease
- offering (a platform for) contact with fellow sufferers
- Contribute with progress towards the cure of ME / CFS
- as a knowledge center for ME / CFS to contribute to the sharing of information, knowledge and experience
- contribute from our network to scientific research aimed at the cure of ME / CFS.
For this we focus on ME / CFS patients, their family members and relatives, healthcare professionals and policymakers. We continuously work to achieve our goals with dedication, independence, integrity and an open attitude. We have an inclusive, positive basic attitude. We look at what can still be done and what can be improved. We are optimistic and enjoy our work. Our bottle is always half full and never half empty.
Activities
Representing interests, offering fellow sufferers contact and providing information
