Topic: Lymenet protocol if you think someone is in danger!
Kudzuslipper
Frequent Contributor (1K+ posts)
Member # 31915
posted
I guess this is to the moderators to answer.
Is there a protocol if you feel someone is in such dire straights that they are in danger of hurting themselves? Is there a way to notify someone?
I know we are mostly anonymous-- some have made connections, I have not made any personal connections where I know more than what is posted. But there are times (and I know we all feel this) that I have felt worried for posters safety.
Is there a protocol to help? or is that the safety and danger of an online board or this nature?
Posts: 1728 | From USA | Registered: May 2011
| IP: Logged |
posted
We ran into this a few weeks ago. There is nothing we can do unless we have a phone number or an address. If the person who is in danger doesn't have someone here that has their phone number, then we can't help them.
Perhaps this is a lesson for all of us!
-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96222 | From Texas | Registered: Feb 2001
| IP: Logged |
Tracy9
Frequent Contributor (1K+ posts)
Member # 7521
posted
I am a moderator of several forums, but one in particular on Facebook is called Lymie 24/7 and it's main purpose is to be a place for those with Lyme to turn if they are feeling hopeless, depressed, or suicidal. It is designed so that there is always someone online to talk to.
We have had many close calls where people were acutely suicidal, and tried to figure out a way to keep them safe. There just isn't any way. We tried to institute a data bank where we collected people's contact info and stored it, but of course it was voluntary.
The bottom line is, no internet forum can save someone who wants to remain anonymous. We've been really fortunate in our group to have been able to contact the police and they have found people in emergency situations with what we could get from their Facebook pages, but it's no guarantee.
The best we can do is reach out and be there for people, which is what everyone on Lymenet already does, as well as Lyme Friends, and the Facebook groups. So, so many lives have been saved by everyone here, and will continue to be.
13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG. Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/