**Anyone w/Chronic Lyme Disease?**🇺🇸

Question

If so, how long have you had it and did you ever receive successful treatment??👩🏻‍🔬🆘
I’ve been struggling with chronic Lyme disease since i was 8 years old. I’m now turning 21 in November. It’s a major struggle in my life and I could use a huge help trying to find a doctor that will help and actually believes in the disease!!🆘
🆘👨🏻‍🔬👩🏻‍🔬DOCTOR RECOMMENDATIONS👩🏻‍🔬👨🏻‍🔬 🆘

Answer

Yes! 💚 Probably had it 20-25 years along with Bartonella. Been in treatment now about 18 months....its HELL but thankgod I found a doctor who specializes in it...it's not cheap. Its been a nightmare and there's no magic pill. I truly feel like I wasted a lot of precious years of my life getting multiple misdiagnosis from mainstream ignorant doctors, unfortunately in the Lyme community  that's nothing new to us! The older I get the more scared I am becoming. Too many what ifs and unknowns. Its so hard to stay positive. Just gotta have belief , hope and prayer. 💚

Answer

I don’t have Lyme’s but Mayo Clinic is a reputable facility that handles a variety of health issues, many of which are lesser known or complex. I went there for a second opinion and if I decide to have surgery, I will have it done there.

Answer

Yes, I’ve had chronic Lyme for approximately 8 years. As I’m sure you know, there is so much controversy within the medical community about this... I’ve found it very difficult to get help from traditional doctors. I dealt with chronic migraines for years and ended up seeing an acupuncturist (which was the first time in years I ever temporarily experienced a complete removal of pain), and after several sessions, he told me that my pulse had a lot of similarities to other patients he has had with chronic Lyme (I really trust my acupuncturist— he does pulse diagnosis, which is based on using the strength/depth/etc of your pulse to identify what’s wrong with the body... at my first appointment, I didn’t tell him what was wrong with me, yet he correctly determined that I had chronic migraines, chronic fatigue, and ovarian cysts). My acupuncturist referred me to a doctor who uses a method called LymeStop, and the testimonials are pretty astounding. I’ve actually met several other people randomly who have gone to him, and he’s removed their extreme symptoms including Bells Paulsy. I went to him, and although I’m still trying to figure out how much stock I put into his methodology, I cannot deny that my chronic fatigue got drastically better after seeing him. He uses muscle testing to identify the location of the Lyme and Lyme coinfections (including erlichia and many other tick-related infections that often go hand in hand with Lyme), then works to train the immune system to attack these infections (which often “hide” in the body). I had a good experience and would recommend seeking out a doctor who does the LymeStop technique, especially since you’ve been battling a his for so long (I saw Dr. Erlandson in western Wisconsin). I understand how hard the struggle with chronic Lyme is... stay strong ❤️

Answer

How is everyone doing?  It sucks being ill and on top of everything going through a pandemic. It feels all the more depressing with the unknown.

Answer

I’m sending prayers your way. I’ve been fighting this disease all my life. There is barely any doctors that can treat us. Many lost their License or retired.  CDC bases their opinion of Lyme on a test that is 50/50 accurate. So many people get misdiagnosed and get denied treatment. The doctor I am seeing now is retiring.. before he can finish curing me. It’s very depressing, but I pray you find someone.

Answer

My niece has Lyme disease and my sister was telling me how amazing her doctor is. She travels to Washington D.C. to see him

Anyone w/Chronic Lyme Disease?🇺🇸

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