posted
It's been difficult to come back here to Lymenet. It was once a home. I once "knew" each person on here: their struggles, their favorite advice, their victories, their defeats, I mourned their their losses and cheered them on. I tried to give some advice myself, once in a while.
But, little did I know, I was just about to rise from the ashes.
Three months after that post. I updated my situation. So much better. Using herbs, changing diet. Then I went on with my life. After that, my family and I continued to get better and make more and more progress. I committed to formally studying herbalism and a whole new world opened up to me. We are all feeling better than ever. I have more vitality and zest for life than I ever had. And I am thankful for every minute of it .
I can now honestly say I have so much gratitude for having Lyme. Going down this path not only shifted my life direction, it gave me my whole self back. It required me to make difficult decisions, on my darkest days. Alone, on the floor, in tears. It taught me to follow my instincts. Do my research. Listen to my body. Search for the unknown.
I wrote my whole Lyme story out here, in case you want to read it. It needs some editing. But, you'll forgive me - I know. http://bruntil.com/wp/mystory/
(In one of my earlier, more hopeful days on LymeNet, I saw a post asking, "Does Anyone Ever Get Better?" The only responses were a handful of people saying yeah, people probably do but they go on living their lives and don't come back. I vowed then, if I ever got better I would come back. I may not be doing it as often as I had hoped, but I'm back (happy to see there is a Facebook presence, I'll join and perhaps help share my info there more regularly))
Posts: 274 | From United States | Registered: Feb 2012
| IP: Logged |
posted
Hi welcome back . Glad to hear doing well. Myself I agree with you on. I can now honestly say I have so much gratitude for having Lyme. Going down this path not only shifted my life direction, it gave me my whole self back.
It required me to make difficult decisions, on my darkest days. Alone, on the floor, in tears. It taught me to follow my instincts. Do my research. Listen to my body. Search for the unknown.
I have been in remission for a while now, and do make my presence known at lyme support groups still.
Whether sharing different protocols or just listening to them . Or if they want to hear my story, and to see smiles on their faces. Wow it can end and
That their is a light at end of tunnel and sharing and understanding what others are going through .
I think it's important to still speak out for those who can't whether signing petitions , rally , and other useful ideas like a specific letter writing campaign but I won't go into details on that one on the forums.
emailing or speaking with your local congress men getting lyme pamphlets bring them to work or just have some handy .
The forum's are good but seeing people in person is just so much better.
And to know when to keep quiet when you hear someone has another diagnosis but it could and more likely lyme and another tick borne illnesses.
That sort of bothers me but if they are satisfied with their diagnosis that lyme mimics .
I can't change that, you can lead a horse to water , but can't make it drink.
Posts: 238 | From Where | Registered: Aug 2012
| IP: Logged |
surprise
Frequent Contributor (1K+ posts)
Member # 34987
posted
Just lovely. Thank you, both.
-------------------- Lyme positive PCR blood, and positive Bartonella henselae Igenex, 2011. low positive Fry biofilm test, 2012. Update 7/16- After extensive treatments, doing okay! Posts: 2518 | From USA | Registered: Nov 2011
| IP: Logged |
LisaK
Frequent Contributor (1K+ posts)
Member # 41384
posted
thank you
-------------------- Be thankful in all things- even difficult times and sickness and trials - because there is something GOOD to be seen Posts: 3558 | 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/
Topic Closed
![[Smile]](smile.gif)
Printer-friendly view of this topic