Siste kommentarer
-
Kategorier
- April 2024
- March 2024
- February 2024
- January 2024
- December 2023
- November 2023
- October 2023
- September 2023
- July 2023
- May 2023
- April 2023
- March 2023
- February 2023
- December 2022
- November 2022
- October 2022
- September 2022
- August 2022
- July 2022
- June 2022
- May 2022
- April 2022
- February 2022
- January 2022
- December 2021
- November 2021
- July 2021
- May 2021
- March 2021
- February 2021
- December 2020
- November 2020
- September 2020
- July 2020
- June 2020
- May 2020
- April 2020
- March 2020
- February 2020
- January 2020
- December 2019
- November 2019
- September 2019
- August 2019
- June 2019
- May 2019
- April 2019
- March 2019
- February 2019
- December 2018
- November 2018
- September 2018
- August 2018
- July 2018
- June 2018
- May 2018
- April 2018
- March 2018
- February 2018
- January 2018
- December 2017
- November 2017
- August 2017
- July 2017
- June 2017
- May 2017
- April 2017
- March 2017
- February 2017
- January 2017
- December 2016
- November 2016
- October 2016
- September 2016
- August 2016
- July 2016
- June 2016
- May 2016
- April 2016
- March 2016
- February 2016
- January 2016
- December 2015
- November 2015
- October 2015
- September 2015
- August 2015
- July 2015
- June 2015
- May 2015
- April 2015
- March 2015
- February 2015
- January 2015
- December 2014
- November 2014
- October 2014
- September 2014
- August 2014
- July 2014
- June 2014
- May 2014
- April 2014
- March 2014
- February 2014
- January 2014
- December 2013
- November 2013
- October 2013
Tag Archives: aksjon
ME-syke Madeleine og morens appeller
Madeleine og Hege holdt begge appeller på arrangementet Millions Missing i Oslo. Millions Missing hadde tilsvarende arrangementer i byer over hele verden. Tusen takk til disse flotte jentene, og til arrangøren som viser oss hvem som mangler i den norske … Continue reading →
Posted in Barn og unge med ME, Fra ungdom, ME
|
Tagged aksjon, ME-foreldre, ME-mamma, millionsmissing, Myalgisk encefalopati, pårørende, Ungdom med ME, Ungdom om ME
|
Leave a comment