ME/CFS AUSTRALIA (SA) INC
Registered Charity 698
PO Box 28,
South Australia 5007
North Terrace House,
19 North Terrace,
Hackney, SA, 5069
1300 128 339
ME/CFS Australia (SA) Inc supports the needs of sufferers of Myalgic Encephalomyelitis, Chronic Fatigue Syndrome and related illnesses. We do this by providing services and information to members.
ME/CFS Australia (SA) Inc aims to keep members informed of various research projects, diets, medications, therapies, news items, etc. All communication, both verbal and written, is merely to disseminate information and not to make recommendations or directives.
Unless otherwise stated, the views expressed on this Web site are not necessarily the official views of the Society or its Committee and are not simply an endorsement of products or services.
BBC Broadcaster John Darvall on ME/CFS
Friday 17 July 2015
Two weeks ago I went to see a 38 year old woman called Naomi at her home to interview her for my BBC radio programme. I don’t like doing what are known as a ‘pre-rec’ after a three hour live programme. I always feel ‘flat’ and feel I lack the ‘spark’ a live show and red ‘ON Air’ light gives me. After this interview I will never be so pathetic again.
Naomi has lived with M E, Myalgic Encephalopathy, for 25 years of her life. She went from being a bright, vibrant young girl to seriously ill in a matter of weeks. Now Naomi is barley able to get up from her bed for 20 minutes a day because of a virus and how her body reacted to it. When I knocked on the door to interview Naomi I knew little about M E. other than its dodgy reputation and the questions about whether it was actually a real illness. When I left Naomi’s parents home where she lives, having spoken to her, her mother and brother for an hour I cried.
I played the recorded interview out on my radio programme, put the video of Naomi’s story up on social media, lovingly made by her brother Tom, and thought that was it. I was wrong.
I am not a big fan of social media. It seems to be little more than a platform of inanity and fantasy. At it’s worst it is a vehicle of anger, hatred and allows those who delight at taking offense at anything to hide behind their made up names and say hurtful, stupid and ill-informed things without real consequence or responsibility. This is not to be confused with free speech. Free speech is saying what you feel or believe and having the courage to be seen standing up to say it. At its very worst social media is full of narcissists and the delusional with a worrying need ‘followers’ or ‘friends’, a mob of cowardly, unidentifiable cockwombles hiding, carping and hating.
Social media can also be a huge force for good; a force for change and it can give voice to those who don’t have one. Naomi’s story on the radio and Naomi’s video story has revealed thousands like her who are suffering, thanks to social media.
I never knew how big a problem M E is. It is only through Naomi’s courage in giving what little energy she had in telling her story and allowing me to share her story that others now have a voice too. Thanks to Naomi others can get help and have hope. This includes my own stepsister who I never knew has M E until this week.
I will now do more to help others with this condition. M E is dreadful, debilitating illness that when it takes hold it never lets go. For Naomi, for all those living with chronic pain and M E, I will do more while I can. I will also use social media too because I can finally see what it can do rather than what it seems all too capable of doing now.
The above, with comments, originally appeared here.
blog comments powered by Disqus