A few years’ in the making….Finally the data is official 🙂 The journal Neuromuscular Disorders has reviewed, accepted and published the data of the wonderful young people and their families who participated in this study. THANK YOU.
We looked at published research measuring quality of life and wellbeing in youth with NMD. The scientific process to evaluate and summarise published research is called a systematic review. This work is now publicly available through the journal Archives of Physical Medicine and Rehabilitation. Thank you to the librarians and to Jenny, Shane, Andrew and Gail for all the help to write up what we found:
Living with severe muscle weakness no doubt impacts on health. In our study, 47 young people living with NMD have described their health and wellbeing. Interestingly, the results for those who use a wheelchair and breathing support compared with those who can walk may not be what able-bodied people may expect. Watch this space for more info as our statistical analysis unfolds….
Eleven participants shared their insights about health and healthcare engagement in interviews with the researcher. These young people were picked from all MyLifeMyVoice study participants to represent diversity in age, gender and the different experiences they noted in their questionnaire answers.
THANK YOU to the research participants for your generous time and openness.
Thank you to all who have completed the questionnaire. We are in the process of analysing all the data. If I have not yet given you a call, I may be in touch soon to double check things if needed.
We are learning SO MUCH from young people and their families. If you would like to share something that was not asked in the questionnaire, or have another thought prompted by the questionnaire, please let me know and I’ll include it in the data. firstname.lastname@example.org
Thank you to all who have completed the questionnaire!!! If you have not yet completed your questionnaire, and would like some help, text 0415 301 635 and we can finish it together over the phone.
We will end questionnaire collection after the July school holidays.
We are learning very valuable insights from young people with NMD and their families. We’ll be able to share the combined data by end 2016. Here is the June 13th 2016 picture showing the count of 14-21 year olds involved in this study.