So the CDC has seen this happen enough to collect data and issue the statement below.
Good advice and may spare you precious time and energy by having a
Bad Day At The Beach
Support groups are not appropriate for everyone, and some CFS patients may find that a support group actually adds to their stress rather than relieving it. Most support groups are free, collect voluntary donations, or charge modest membership dues to cover basic expenses (e.g. refreshments at meetings or photocopying costs).
A useful support group should include:
* Both newcomers and patients who have had CFS for longer periods of time to provide a balance of perspectives for the group.
* People with whom the CFS patient feels comfortable.
* Leaders who empathize, gently draw out shy members, and keep others from dominating, and who distill discussion into useful information.
* A history indicating the group is stable and meeting the needs of its members.
Some support groups may put their own interests before those of the individual patient. Groups that engage in any of the following activities should be avoided:
* Promise sure cures and quick solutions.
* Conduct meetings that are mainly "gripe" sessions.
* Urge patients to stop prescribed treatment and recommend a single solution to their problem.
* Insist that patients reveal private or sensitive information.
* Demand allegiance to a cult-like, charismatic leader.
* Charge high fees.
* Require patients to purchase products.
Source: CDC
IHRT is a human rights team of persons from around the world who suffer with ARD. We share a common goal of protecting ourselves and others from practices not wise for persons afflicted with ARD. We address issues surrounding ARD in a public format so that those with ARD are informed in every aspect of an issue so that they can make an informed decisions about health care.
ARD, CAPPS, Adhesions and Adhesion Related Disorder , Internal Scar Tissue, Hope for those who suffer from Adhesions
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