ME/CFS AUSTRALIA (SA) INC
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PO Box 28,
South Australia 5007
North Terrace House,
19 North Terrace,
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Closed over Christmas
(reopened 1 February 2017)
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.
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Chronic illness support groups transform life for sufferers
Tuesday 5 August 2014
Chronic Illness Support Groups Transform Life For Sufferers
Kotecki Vest was a broadcast journalist and political director. She stopped working after she was diagnosed with lupus.
“My immune system is so low that picking up my children at school is a danger,” she says. “So I keep my sanity with Facebook, Twitter, Instagram and wherever else we” — other lupus patients — “can all get together.”
Her online community includes a chronic-illness Facebook group, a lupus group and others. They bring her laughter, belonging, and information.
A PewResearch Internet Project reported that, as of November 2013, “One in four U.S. adults (24%) say they are living with a chronic condition. One in five (20%) are living with two or more conditions.”
Some of the most active chronic disease groups on the web are for conditions that afflict young women. According to a 2010 study done by Comscore, “Women are more engaged than men on the Internet, and they chart their own course.”
“These wired, actively engaged patients can improve the management of their chronic diseases and lead to better health outcomes.” He continues, “Paying attention matters, people who are active enough to go and read about their condition on the Internet are people who pay more attention to their condition — and the more attention they pay to it the better they do.”
Top Online Support Groups
Julie Ryan suffers from Fibromyalgia, along with migraines and cluster headaches. She has been researching and writing about Fibromyalgia since she was diagnosed with it in 2010.
According to Ryan, online support groups are a way to learn about one’s own disease process, while supporting others.
“Understanding how these disorders affect those around us influences how we treat each other. More people are being diagnosed with fatigue related disorders. By understanding these disorders we learn to be more patient with others.”
A few large listings of support groups are available, with dozens of conditions represented:
Julie Ryan has catalogued the 10 most popular online support groups for women with fibromyalgia and other conditions. The top three are:
Many support groups have also made their home either partly or entirely on Facebook. One obvious benefit of Facebook is the ease of communication and coordination via the platform, which many members use on at least a weekly basis. Among the many conditions represented are:
And yes, there’s even a support group for Facebook addiction. Its effectiveness is anyone’s guess!
Starting Your Own
If you have a rare disease with no online community, you might want to start your own. This is a chance to make a difference in the lives of other people. But be warned: this responsibility should not be taken lightly. It takes work and a real time commitment to create and run a group. Some websites offer helpful guidance:
If you have a common health issue, it might not make sense to start a new support group. There are over 12,000 “chronic pain” support groups in Yahoo’s “Health and Wellness” section. Instead, search for a group that matches your needs; you can sort groups by size or by years in existence.
Whether you join a group or start your own, remember: your support needs are what brought you here. Treat your fellow group members with the same kindness and respect that you expect for yourself.
The above originally appeared here.
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