any experience with Dr S. in Florida

I have Lyme disease and it is easily misdiagnosed as MS. That said, I strongly urge anyone who is diagnosed with MS because they have lesions on their brain or spine to seek 2nd oppion from infectious disease Dr. (i.e: Dr. Jemsek, in Washington DC). DO NOT TAKE THE $40k medication(pill) which ultimately paralyzes you and suppresses your immune system causing havoc on your body later on. We are unfortunately in a place that is ruled by drug companies and government that seek personal gain for their self interests rather than help people heal with the simple and inexpensive use of antibiotics. I have been able to treat my Lyme lesions and make a complete recovery and so can everyone else who's untested in exploring the true and proven cure to Lyme disease and the majority of mis-diagnosed MS patients. I hardly ever post anything, anywhere, however I felt the need to share my experience and success with not having to end up in a wheel chair, in hopes of helping others
that might be in the same boat that I was in. You can get better and you can walk again if you have been Mis-diagnosed like I was. Lesions on your brain or spine DO NOT automatically signify MS! After 4 1/2 months of being on ANTIBIOTIC IV THERAPY (Ceftin, Docy, raphamtin, Manuka honey , Vit D, VSL PROBOTICS LIVE (45 billion) and a bunch of supplements) all my lesions and aliments disappeared. I hope my post help someone else's out there who's feeling lost or helpless.Don't this is just chronic infection and once you are able break through the brain blood barrier you will get better. Good luck to all! Warmly, a caring sole.

P.S. Remember you will get worse before you get better. That's a sign that you are killing the lyme spirochetes that are infesting your brain, eyes, etc. When you're on Lyme kill cycle the spirochetes release toxins When they die and that what causes you to feel so sick. You need to flush the toxins out as much as possible. I have infared Sauna and tried to drink lots of water. Long and short of my story is that it worked and I want to help as many people out there that I can . I just wish it wasn't as expensive, so hopefully my insight and experience can help someone without them having to pay as much as I did to get this info. (Program regimn). Send me a personal message if you'd like more details. Ultimately my goal is to get congress to pass the bill to treat Lyme appropriately based on my imperical evidence of a successful treatment and control of my Lyme disease. We can not continue to have CDC control our Dr's treatment routine based on their incorrect standardized treatment for Lyme that just touches the surface and doesn't allow them to profit as much as they do when there are people chasing their tales trying to figure out why they are still so sick. We can all win this fight together and be the healties, happiest and most impactful we have ever been. Hope to be part of helping you all heal.

Help is on it's way!!! There is light beyond this tunnel!

Hello friends!!

Just found this forum in another (all-too-common it seems) desperate google search for a medical provider who will treat Lyme disease and its co-infections in the Florida area. I know the original post dates back a few years, but if anyone in the thread is still active on the forum and feels like either copying and pasting what they emailed to previous members with questions or writing it again and sending it to me (and the other person who last commented on the thread earlier in October) it would be GREATLY appreciated! Thank you!!

I was diagnosed with Lyme in September 2016, but have been battling with doctors and symptoms for at least 6 years. Need to find a LLMD in my area (San Antonio, Texas), any suggestions?[

Hello All,

Anyone with experience with Dr. S in Naples, Fla, please send me a private message. I just had an introductory phone session with him and may visit him this week.

Thanks.

Thanks Girlie. Could I ask if anyone has a recommendation for an LLMD in the New Jersey area in this forum? I'm willing to travel up to 3 hours. I live in northern NJ.

Hello All,

Anyone with experience with Dr. S in Naples, Fla, please send me a private message. I just had an introductory phone session with him and may visit him this week.

Thanks.

DreamyD said...
Please let me know any and all info about Dr S

Hi, DreamyD - welcome to our community!

I don't have any info , but wanted to say "hi"

We encourage all new members take a look through the thread at the top of the page titled: "New to Lyme?...Start Here!"


Please feel free to share your 'story' wth us.

From what I saw his legal challenges were personal. It had nothing to do with his ability to practice medicine- so I need to know MORE about him. Has he fixed any of you who have seen him?? Thanks! <3

I have now at this point seen this doctor in person and he is no joke. He is helping me greatly.

Yes I second that, what tests and treatments, how'd it go? How are you? I just left a message for this guy despite his self-promotion and insane behavior and I am really worried..

Hi sailfish - welcome to our community.

dannycoho hasn't been back to the forum since that last post of his. But, I do see his email is enabled. You could send him an email.

If you want more LLMD options, you can also email me and I will send you some names in Florida.


We encourage our new members to read through the information in the thread: "New to Lyme?..Start Here!" It's packed full of useful information.

I know this is an old post, but any reviews of this dr would be appreciated.