bcb1200
Frequent Contributor (1K+ posts)
Member # 25745
posted
Hi folks:
I don't come here as often as I used to. And that is mostly because I've been doing really well the past 5 years and have been out living my life. (I still have some very mild symptoms, but have been able to manage with ongoing treatment with herbs. Fingers crossed it holds!)
Anyway, this site was such a great resource for me since first being diagnosed in 2010. There were some great moderators and other users on here that were such a huge support to me during very dark times. I am very thankful for that.
Some examples of users who helped were Sixgoofykids, TF, Lymetoo, Keebler, etc.
Sadly, I don't see many of these folks active here anymore, aside from Lymetoo (Thank you, Lymetoo!)
Does anyone know what happened to the others above? I know Sixgoofykids and TF were well and assume they are out living their life.
Also, I do know sites like this have far less traffic in recent years as many folks have switched to Facebook groups, etc.
Anyway, just wanted to say I miss those other folks and hope they are well.
Wishing everyone great health and happiness in 2022!
-------------------- Bite date ? 2/10 symptoms began 5/10 dx'd, after 3 months numerous test and doctors
IgM Igenex +/CDC + + 23/25, 30, 31, 34, 41, 83/93
Currently on:
Currently at around 95% +/- most days. Posts: 3139 | From Massachusetts | Registered: May 2010
| IP: Logged |
posted
Hey Brad its Scott I think we Go way back to the beginning of this life changing illness, I Think we met at both of our first Local Lyme meeting in Marshfield or Duxbury i think, wow these 10 plus Years have flown by I'm glad to hear your doing well I think you might remember I have been pretty much healed ever since I got the Benzo drugs out of my system about 6 or 7 years ago I do still check out the site from time to time to see how people are doing and if i can give any good input I try, heck some times i will ask questions on hear that have nothing to do with Lyme even, So yes this site is a Great resource, I hope you have a Great Holiday and New Year, Take care old friend
-------------------- LSG Scott Posts: 513 | From Boston, Cape Cod, Mass | Registered: Aug 2009
| IP: Logged |
posted
I feel the same way. I am back as I am sick again after having struggled with late stage lyme for over 20 years. Facebook is not the same. You can't follow the posts or people. The old group here used to totally support each other and go through their journey together. They offered to take others to doctors and many other things. It's a different world now.
Posts: 580 | From southern new jersey | Registered: May 2003
| IP: Logged |
posted
yes the Salt treatment was a game changer for me
-------------------- LSG Scott Posts: 513 | From Boston, Cape Cod, Mass | Registered: Aug 2009
| IP: Logged |
LisaK
Frequent Contributor (1K+ posts)
Member # 41384
posted
I was wondering about keebler too. and some others.... but so glad to have TooToo still around!!
I was told when I posted somehting similar that many went to FB. FB pages are good, but so many newbies and not enough GREAT contributors like we had here 10 years ago.
I stil tell everyone about coming here when I hear they are new to lyme and cos. who knows, things go in circles, right?
-------------------- Be thankful in all things- even difficult times and sickness and trials - because there is something GOOD to be seen Posts: 3592 | From Eastern USA | Registered: Jul 2013
| 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/
UBBFriend: Email this page to someone!
![[Smile]](smile.gif)
Printer-friendly view of this topic