I'd love to recommend this to my hubby, but he still thinks I don't have lyme..
But just on the way OFF chance.. I will email him this link.
How does one "ask to join?" and how can you tell if they are the spouse only?
Just wondering.. kw
-------------------- KentuckyWoman tired of medical run-arounds
Two roads diverged in a wood, and I, I took the one less traveled by, And that has made all the difference. ~ ~ Robert Frost Posts: 221 | From Kentucky | Registered: Sep 2012
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Honored Contributor (25K+ posts)
Member # 12673
- Not sure anyone can ever tell on ANY website, even here, if people are always who they present themselves to be.
Most are though, still, it's best to never, ever share certain specific personal details on any website.
Most sites have suggested guidelines regarding posting - for personal security.
Even with safety measures in not sharing any specific personal detail that could be recognized by a friend, neighbor, coworker (or a stalker or a thief), there is still so much of value that can be discussed. -
Posts: 48021 | From Tree House | Registered: Jul 2007
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Ohh dude, it has been freaking 7 years since 2013. However i would like to tell you that i was a member of a facebook group also related and dedicated to the spouses of the Lyme patients. So those guys have actually helped me a lot. I mean they gave me so many great advice, they recommended me a great doctor in my area. I was really grateful to those people, however i felt really bad that the group was closed, because they also had a group on instagram and it was banned due to the fact that they had to buy followers worldwide for instagram, and their facebook account was connected to the instagram one.