Lyme Clinic Mexico in Puerto Vallarta

Hi LymeMomCO - welcome to our community!

I don't know of any members who have gone to that clinic.

Are you currently treating with a LLMD?


There will be more members on tomorrow so this will get a lot of views then.

I don't know about this clinic but do know of someone who got some kind of treatments in Mexico. You can read her story here: www.realfoodrebel.com

You can email her and ask if that's the same place she went and see what she can tell you about it. From her blog, sounds like she lives part time in Mexico.

It is my daughter that has Chronic Lyme....yes we have been working with a LLDR. We are looking outside USA as no one that I can find is doing the type of treatments together like this Lyme Clinic in Mexico and also spending concentrated time instead of just quick office visits or 2 week clinic. (Yes, I know there are some but nothing I see as better.) I blame the CDC and IDSA for forcing us outside the USA by their guidelines. We did notice that Dr. O M is speaking at the ILADS 2017 Conference in Boston which gives us encouragement that Lyme Clinic Mexico is a real clinic/hospital situation and not just a gimmick. After spending days/months researching I am still very confused about treatments and what works for what type of Lyme bacteria/paracite. I think that might be the problem as what works for one may or may not work for another. We know nothing is a sure bet but I DO know that I am not really convinced about using muscle testing to determine how to best individually treat Lyme.

Post Edited By Moderator (Girlie) : 12/28/2017 9:24:49 PM (GMT-7)

Hi LymeMomCO

I considered going to the clinic one year ago and had a 30-minute phone consult with the doctor. He was very thorough and I was impressed. Treatment, however, was very expensive and invasive. As the clinic wasnt very established at that time I decided to go to St George Klinik in Germany. After treatment in St George I actually deteriorated further rather than improved (Thats not to say it wouldn't work for some people but it didnt for me). I then went for treatment in a clinic in Cyprus (NeoMed Institute) which has ozone treatments and I went from being at 10% (mostly bedbound) to 40%. After 2 months I jumped to 60% and have maintained 60% for the last 6 months. I cannot recommend that clinic enough.

No Problem at all PeteZa!!.


The clinic is in Cyprus (and I am now in Ireland) so I have not been back. Patients go through a 4 week program. I ended up staying for 7 weeks as I was very ill and had noticed improvements after week 4 so I extented. I am considering returning in 6 months for another 4 weeks of treatment as I hope to make the jump to 100% after the treatment. For me it was ozone treatments (which this clinic specialise in) that made all the difference. I had done 1 & 1/2 year of antibiotics, cryotherapy, hyperbaric chamber, kinesiology, accuptuture, bio resonance, bio magnetisim, and then the 3 weeks of treatment in Germanys St George Klinik which included Iv antibiotics and Hyperthermia, and Plasmapheresis. However, I simply wasn't getting better with any of these treatment or even seeing minimal improvments. Consistent ozone treatments was what worked for me. ( Its different for everyone so please don't think I'm criticising the treatments I did previously- they just didn't work for me- Ozone was what worked for me-- different for everyone as we know!)

I met Dr O M when he was in chicago in august and he spoke at a Global Lyme Alliance fundraiser. I spoke with him at length about his treatment protocol. And I've talked to a couple of people who went to his clinic for treatment and are doing better. He is very thorough and very knowledgeable. I think he does get a number of people to improve. But, with any treatment and with any clinic, some people improve and others don't. Because I've been seeking treatment for both myself and my 11 year old daughter, I ultimately decided on treatment somewhere else. But I can say with confidence that Dr M is a stand up doctor who is getting some people better.

Post Edited By Moderator (Girlie) : 12/28/2017 9:27:26 PM (GMT-7)

Thanks Girlie. Sorry!! I totally spaced out when I wrote his full name!! I know we are not supposed to do that in order to protect our MDs

Hi! after reading all your post has anyone gone to Lyme Mx Cl, I heard from some one that it worked for her but she did not had neuro lyme.I have done some reasearch but could not find any info on the clinic /md Does anyone know anything since the last post back on 2017.

Sheekster said...

MCaro said...
Hi! after reading all your post has anyone gone to Lyme Mx Cl, I heard from some one that it worked for her but she did not had neuro lyme.I have done some reasearch but could not find any info on the clinic /md Does anyone know anything since the last post back on 2017.

I have been interested in this clinic for a couple years due to the integrative and unique procedures they do. Like plasma exchange, red cell exchange, hyperthermia, etc. The doctor seems very intelligent and you can schedule a free phone consultation with him through their website. The cost is much cheaper since it is in Mexico, but I believe it is still a safe facility for treatment from what I have heard. Here is an interesting video about some of their treatments:

http://lymemexico.com/about/dr-morales/

I haven't been myself, but if I was to go to a clinic, this would be it. It is important to note that I have already been to the Sierra Integrative Medical Center clinic in Reno, NV and I have a close friend who has been to St. George in Germany. SIMC did not put me into remission and I no longer recommend it. St. George helped my friend, but he isn't in remission either and is now about to have his first appointment at the JSC in WA DC.

Well I been doing some research on LCMx and still does not fulfill the expetations, some things are not clear. The Md is a great person he knows a lot.
What was your experience on Sierra Integrative Med Center?, the remission takes some time, how long did you attend Sierra?, I need info.

@MCash, I am putting my deposit down today for PV clinic. I have high hopes after 1.5 yrs of unsuccessful treatment and 20+ years of declining health. I am only 38. My neuro symptoms are the worst as well as vision. If you would like to chat I think I have my email listed in my profile. If not let me know.

I wish us all healing. This is such a horrible illness and way to live.
Sincerely
Sarah

AudreyW said...
Sarah, can you please share how much they quoted you for the cost?

Hi AudreyW - welcome to our forum.

Hope you find this to be a supportive and knowledgeable group here.

bumping this up-- if the next dr I am trying doesnt work I may need to find a clinic. what is an actual good one?