How To Recover From Chronic Lyme And Tick Diseases
Вставка
- Опубліковано 1 чер 2024
- Lyme disease and other tick-borne diseases often go undiagnosed or are misdiagnosed. This is partially because Lyme mimics other illnesses such as the flu, manifesting as diverse symptoms including headaches, muscle aches, stomach ulcers, constipation, and joint pain, making diagnosing and treating Lyme very difficult. Left unchecked, Lyme symptoms can worsen, creating a long-running inflammatory response and autoimmune illness. Lyme disease, or borreliosis, is caused by the bacterium Borrelia burgdorferi, which can proliferate to every area in your body. The good news is that with some work and effort, you can successfully treat Lyme disease.
In this episode, Dr. Hyman sits down with Dr. Todd LePine to discuss the Functional Medicine approach to identifying and treating chronic Lyme and other tick-borne diseases.
Dr. LePine graduated from Dartmouth Medical School and is Board Certified in Internal Medicine, specializing in Integrative Functional Medicine. He is an Institute for Functional Medicine Certified Practitioner. Prior to joining The UltraWellness Center, he worked as a physician at Canyon Ranch in Lenox, MA, for 10 years. Dr. LePine’s focus at The UltraWellness Center is to help his patients achieve optimal health and vitality by restoring the natural balance to both the mind and the body. His areas of interest include optimal aging, bio-detoxification, functional gastrointestinal health, systemic inflammation, autoimmune disorders and the neurobiology of mood and cognitive disorders. Dr. LePine teaches around the world, and has given lectures to doctors and patients at American College for Advancement in Medicine (ACAM), Age Management Medicine Group (AMMG), the University of Miami Integrative Medicine Conference, The Kripalu Center in Lenox, MA, and is on the faculty for American Academy of Anti-Aging Medicine (A4M). Dr. LePine is the head of the Scientific Advisory Board for Designs for Health and a consultant for Diagnostic Solutions Laboratory. He enjoys skiing, kayaking, hiking, camping and golfing in the beautiful Berkshires, and is a fitness enthusiast.
This episode is sponsored by AirDoctor. We need clean air not only to live but to create vibrant health and protect ourselves and loved ones from toxin exposure and disease. Learn more about the AirDoctor Professional Air Purifier system at a special price at www.drhyman.com/filter
For more information visit drhyman.com/uwc
If a doctor can’t figure it out they blame the patient. I’ve experienced this
We all need to fight to have functional medicine for chronic Lyme covered. I and many other thousands of Americans have been suffering for over 30 yrs with this horrific disease
Some facility’s like Trinity health do have functional doctors.
@@vallang4832 Where is Trinity Health? In CA? Do you know a particular functional doctor who treats lyme? Thx
Ugh, all that we go through is such BS. You’re right. We do need to fight back, but whenever we do we’re shut down.
What kind of symptoms do you have?
8999
Thank you for saying Drs need to listen to their patients , I was bit by a tick and had the bullseye 4 inches diameter, The Dr gave me a 20 day prescription for antibiotic. and then Again 3 weeks later I was bit again - bullseye, etc…the same thing. My Dr was adamantly annoyed when I was concerned and asked him for another 20 days of antibiotic, (snarling at me "You’re NOT going to get Lyme disease, the antibiotics you were on will protect you.") In fact I showed the nurse practitioners photos and even a video of the tick, and her comment was thats very small for a tick, their supposed to be bigger than that." (I merely replied you’re not really experienced with ticks are you?" To which she sheepishly admitted she was not. Both times I was bitten, the ticks were fully engorged. It’s mind boggling that even the CDC ADVISES AT LEAST THAT DOSAGE, but Drs treat you like your either a drug dealer, or a hypochondriac. I live in Virginia, and it’s a real problem here trying to avoid these critters.
My son was diagnosed with MS at 27 yrs old, and months away from being in a wheelchair, we doubted the diagnose, and sent him to a highly recommended Naturopathic doctor who order blood work that was sent to Germany to test for Lyme, (he was tested in Canada, but it came back negative...twice)... it came back positive, she proceeded to send him to a clinic in Oakville Ontario that treated him naturally, it took about 1.5 years to get the Lyme out of his system, and he is feeling really good now, he does have some nerve damage in his hands and back, but everyday he is feeling a little bit better.
I’m also from Canada. What treatments did your son get?
@@andrewreimer4042 Hello, he went to a clinic called BIE in Oakville, Ontario....highly recommend, if your dealing with Lyme, it is a natural way to rid of it permanently. I believe there may be a video on UA-cam describing the procedure, odd to say the least, but they saved his life, and he has bounced back to his old self. My son was apparently one of the worst cases they had ever seen.
Could you maybe tell me where in Germany they sent the tests to? :)
@@TEKATOKiKATA I really don't know, it was done through a naturopath in Stoney Creek, Ontario. I will try to find out and get back to you. It did cost around $500.00 but at least we found out and was able to deal with it.
@@dianef298 Thank you. That would be really helpful of you. Because I live in Germany. Have a merry Christmas.
3:15 mimic 5:40 8:30 13:31 13:50 15:30 16:50 19:19 25:00 doxycycline with silver 26:26 artemisia 27:50 28:30 30:15 japanese knotweed cryptolepus cats claw 30:50 multiple protocols 32:20 32:30 mushrooms and more 37:50 stem cells 38:50 hyperbaric oxygen 39:30 hyperthermia 42:00 ozone therapy 43:23 wrap up + peptides 44:13 specific peptide 46:26 risk to benefit ratio
THANK YOU I CAME EXACTLY FOR THIS
Thank you!
Thank you very much.
Thank you!
🙏❤️
I’m eighteen and I got diagnosed with lymes about half a year ago. I was sick throughout high school getting progressively worse with awful anxiety, fatigue, bloating and more but doctors would just tell me to take Prozac or eat more protein. I’m finally getting treatment and recovering:) Thank you for educating people about this!
Hey Emma, hope you are doing well! I personally have been dealing with a lot body pain, tingling sensations and fatigue. Did you experience the same symptoms and what did you do to recover!
Can you share your experience
@@georgelopez9517 hi, yes I did and recovery is very difficult to be honest. I’m still working on it I would recommend finding a lyme literate doctor
@@emmapemex1434 glad you're doing better. what are you taking for your recovery? What kind of test did you take that showed a positive diagnosis? Can we get some details please?
For me I am on Doxyxycline. Hope it works. I tested reactive in short term disease.
I've been dealing with this for 35 years so this all rings a lot of bells. It goes in to remission and comes back every so often. I have a good Functional Medicine doctor now because it came back after getting Covid and it's much harder to beat this time. It triggered mast cell activation and dysautonomia. I am now sensitive to salicylates which makes taking a lot of the herbs to fight it intollerable so I'm having a tough time with it. I'm now 53 so it's a tough battle. I hope everyone with this issue is getting the write help from great doctors like these two.
I don't have any money to see anyone outside md who is bad at helping me
I would love to go to the Wellness Center however it is outrageously expensive and no insurance is accepted. How can you really help people when it's too costly for most folks?
I know, I would love to go. Just can't afford it. I wish they took insurance
No reply from these jokers
Your best bet is to find an open minded ND near you, and bring up a topic that you have seen here. In the US patients have to be their own advocates. Unfortunately you have to take on this challenge while your sick. I hope you find your answers, and never give up on recovery.
The clinic does not accept insurance because it's the insurance companies that are not covering/approving proper treatments for Lyme. The only course of treatment insurance pays for are continual rounds if antibiotics for Lyme disease( which only suppresses the Lyme) and that's if you can even get diagnosed. Why? because the insurance only pays for the CHEAP (worthless) labs tests like the Alyssa or the Western Blot for Lyme which are highly unreliable. A reliable Lyme panel will run you $ 300 to a grand or more with repeated labs needed. Genex is the only company with a reliable Lyme labs and no insurance covers Genex. So stop blaming the Doctor for what the insurance companies are doing. Also it costs millions even to lease a building and buy all the appropriate medical equipment and pay all the staff to run a private practice.
Its not them babe its insurance comps
I most likely became infected with Lyme disease in Washington State and not from ticks. Then when I went to Vermont, I was exposed to ticks. However, the only infection that came out in the test was from previous exposure, not a new infection.
When I asked doctors in Washington State to test me for Lyme (because I wondered if I had it), they wouldn't test for it. So, that means I went for several years with the disease. Prior to leaving for Vermont, (a year or two prior) I was experiencing strange neurological symptoms. The doctors didn't know what was causing it. Then I read Stephen Buhner's books about Lyme and my list of symptoms showed up in his descriptions of Lyme, plus I had the positive test in Vermont.
I recently added Cryptoleptis to my protocol of Japanese knotweed, medicinal mushrooms, NAC, astragulus, cat's claw and Solomon's Seal. I also meditate, practice Reiki on myself and do my best to release stress.
Awh, I was treated for Lyme disease for a year with antibiotics even though my western blot came up negative according to the standard, I had the rash and everything, I couldn’t afford to continue treatment, I didn’t have insurance I’m still so sick and I’m in search for what is going with me,😞this was back in I think 2011. Thanks for the information, I was laughed at in ER when I tried showing my Lyme rash, gave me cream and shoved me out the door. I have tried everything natural, I’ve tried telling myself it’s in my head, as many people have told me, but I know I have something wrong with my immune system, I’m so sick of being sick, so sick of being soooooo tired and it’s so hard to just do daily tasks. I haven’t driven in at least 7-8 years it’s so draining, sorry I totally just vented here, lol thanks so much for all the information ❤️✌️😊
I had a hugh bullseye rash on my leg back in 1990. Someone told me it was a tick bite..We were camping all summer. A few months went by and my back and neck started bothering me. I asked a pharmacist if he though I might have Lyme and he asked me if I had had a fever which I didn't. Because of what he said I was doing all kinds of things to get better. I eventually called the CDC and told them about my rash in 1996. They said that any rash unknown bigger than 2 cm.s was suspicious for Lyme and that if I had the bullseye (which I did) it was a 100% diagnosis for Lyme and more accurate than any test. I then went to a infectious disease doctor and was put on a PICC line and gave myself 2 grams of an antibiotic every day for 6 weeks. I hope you see my response. The best thing to do now though is a total clean diet and try to lessen your stress. Cortisol always makes everything worse and increases inflammation. My doctor actually told me this and he was so right. Just those two things can help so much in getting better.
Don’t give up. Look at Joe Dispenzas meditation work. It is being rigorously researched work by teams at UC Davis.
I'm so sorry you felt that way, I hope you find relief soon. or find someone that take you seriously.
I know the feeling of everyone telling you "stop thinking you're sick, if it's in your head you'll believe". For me just getting the diagnosis was such a relief knowing I'm just going crazy and that I'm actually sick and my body is tired.
Hugs to you . I totally understand and hurt with you. You are a soldier fighting an enemy with little help. Hugs.
Thank you Mark for sharing, finally! Ist cousin to syphilis. After years of misdiagnosis I was finally told I had Chronic Lyme. Am suffering more as I age. Antibiotics did not work. ONLY temporary. Stem cell healing had worked for someone I know. After 17 years of suffering Lyme. Had to get help iin Mexico from physician there. In less than 1 year finally well. Age 60. When in USA will AMA finally admit it to be epidemic. I'm 78 and giving up. No where to turn on a social Security budget. So SAD for thousands of ailing seniors.
Boy, is that the truth! You have to pay to have functional medicine labs done to find this, and it’s expensive! I’ve spent thousands because my son was living in mold in his father’s house, and the mold lowered his immune system so this stealth infection of two kinds of Bartonella manifested. He’s SO sick, because it’s been going on for years as the mold got worse, because it wasn’t taken care of! I’m furious that he let this endanger his son’s health. He’s 35, and has had brain traumas as well starting with meningitis at age 7 that almost killed him.
I won’t let him go back to his dad’s house, because he remediated it all wrong! Backwards, in my opinion! It will never be a safe place for him!
My son looks like death warmed over, blackened eyes, he’s paranoid, and has been through a gamut of nonsense diagnoses from psychiatrists! Bipolar is the favorite! A-holes!
I wish I could offer you a cure. He’s going through a herx reaction now and has to cut back the antibiotics he started taking.
My husband is suffering from chronic Lyme. Where in Mexico did you find the right help? We are near Guadalajara please share if you can. Thank you
Ldn?
Same here .. 61 and husband self employed, no insurance so I watch videos and try to figure out what I can do minus the dr.s
@@phreed6320 what are your symptoms and have you tryed teasel and ldn
So grateful to know that there are still docs that listen to their patients and actually practice medicine as the art it is. Empathy is key to fully understand how patients are suffering and that is not always a given. Very informative discussion and much appreciated.
Thank God for medical doctors who aren't sold out to drug companies and utilize holistic methods to treat the entire patient!
Chronic pain is no joke. It's every day waking up not knowing how you're going to feel but with the help of natural herbal medication I was free from (Lymedisease) get to know the powerful herbs man that healed me through is Facebook link facebook.com/Dr-Eromosele-herbal-roots-108749510943383/ or Whatsapp him directly +2349051812935 to sovle your pain.
Just sad that there aren't more of them. Live in a small town so no holistic options ... refuse to go to medical drs and waste my money.
Excellent talk, I’m a provider with Lyme learning how to treat muse self because 95% of MD don’t treat lyme sufficiently
I did the heat treatment almost 2 years ago in Germany, and I am still Lyme free!! I feel 100% better!!🥰 and I since have had a healthy happy baby 🥰
what is heat treatment?
@@nikisawyers7559 ua-cam.com/video/XxF4HbsIVrg/v-deo.html
How did you get it like what do I need to do to get this done
Where in Germany did you go? I am exploring this
Sauna ozone or what?
My uncle in law in Ireland was recently diagnosed with Lyme disease after fifteen years of chronic pain in the face and head, seven operations to treat symptoms. Part of his tongue removed. Saw over twenty specialists across Europe and America. German doctor diagnosed successfully just weeks ago. His luck has changed thanks to people who think like you, keep making these educational podcasts and videos!!
Which doc?
Could you please tell me what the Name of the German doctor is? :)
I was diagnosed with Lyme disease recently and I need a good doctor in Germany so please tell us the name and location of the doctor!?!?
Can we maybe get an updated video on this. Maybe something has changed in the past 2 years?
Yes updated Amen!
Alkaline diet worked for me. 85%veggies, animal protein no grains or added sweeteners. Low dairy. 18 days of Doxycycline, colostrum, fermented foods. Pre and probiotics. 2 weeks later dramatic improvement. At 70 years old my energy is a bit diminished but feeling good.
Great news Chris, I'm happy for you. However, I think recovery is vastly different for everyone, myself included.
I'm 62, and have had this life destroying disease for 14 years now, and I've tried virtually everything to get well again.
For me, my brain fog is BY FAR my worst symptom, in a series of terrible symptoms. I'm certainly exhausted, anxious, dizzy, weak, and my bones and muscles hurt. But this indescribable brain fog is on another level. I don't even feel attached to my own body. It's as if I've been walking around concussed for 14 years, and it's brought me to my knees many times, mostly because I can't describe it well enough for people to understand.
I don't know if you experienced this level of "fog", but I'm glad you are feeling better.
These people who think brain fog is just about forgetting your car keys, have no clue how far off they are.
@@094340 do you take ceftriaxone IV with silver nanoparticles?
This was easily one of the most helpful, educational, and scientific dialogues I've ever heard. This content is amazing. Please make more things like this! Thank you for making this. As someone who has struggled with Chronic Lyme for 7 years now, this video really opened up the way I've thought about these infections. Now that I think about it... I haven't had a fever above 99 in years. I'll consider doing some more infrared saunas to induce and artificial fever!
I had a tick bite that grew to the size of a quarter. I got a Band-Aid saturated it with andrographics tincture put a glob of bentonite clay saturated again with andrographics put the Band-Aid on for 24 hours, and the inflammation was down to the size of a pea. Changed the dressing every day, and within five days it was almost completely gone no symptoms. This protocol is from Stephen Buhner book “Healing Lyme” fabulous book
I been on proper human diet for 30 days!!! I finally feel like there is hope. 97 got bit. Diagnosed finally in 07. 3 years of what was to be intermittent doxy... My wonderful doctor died. He was 87. I haven't found a doctor... I tried but if the first thing they ask is HOW DO YOU KNOW YOU HAVE LYME? MY PTSD KICKS IN AND I RUN! I ONLY EAT MEAT, EGGS, BUTTER, A BIT OF CHEESE ... I CANT WAIT TILL NEXT YEAR.
This was absolutely the best thing I've watched on Lyme disease! Thank you and thankful for great minded Doctors like you two!
Yes, this dr. knows his stuff!
Japanese knotweed. Works better than antibiotics
Dr. Hyman, let your interviewee talk!!!
I’d be very very curious to know what both of these doctors think about the book BITTEN by Kris Newby who also made the documentary movie “under the skin” about Lyme.
Apparently William Bergdorfer ,the scientist credited for discovering Lyme disease, later admitted that they had been working on Weaponizing ticks on Plum Island outside of Lyme Connecticut. After he died he made sure that Kris got all of his files and she wrote this book. It was taken seriously enough for Congress to call on the Pentagon to investigate whether Lyme had been a bio weapon that got out. Of course it’s ridiculous to investigate themselves and I’m sure that the truth will never come out. But if anyone would like to hear her summarize the book she’s on many podcasts including BetterHealthGuy talking about it and she sounds very sane and very intelligent.
She originally met Bergdorf her because she interviewed him for the documentary but he did not disclose the rest of the story until after he died.
Do they speak of cure in book ... it's on utube about that island ... have you also looked into telegram dirt road discussions?
Thoughts ...ivermectin?
Excellent movie and book
I can't wait to read "bitten" and see her podcasts & docu-
Movie! Thank you for your comment!
I lived on Eastern Long Island and felt strongly Plum Island was to blame. I got very ill in my 30s. I tested negative for lymes in a few tests. In my 50s I was diagnosed with babesiosis. It went untreated and my doctor told me my body fought it off so no medication could help.
Thank you for passing this info about Connecticut! I knew I’d read something referring to it a long time ago but couldn’t recall and never saw anything about it any where else.
Brilliant information… thank you both!
Great presentation -
Thank you. This is the best I've seen. 💚🙏
Excellent video, thank you.
Brilliant...so appreciative for these functional care physicians!
Glad to see smart docs talk about these issues with very good knowledge and experience
Fantastic. Best Lyme disease discussion out there by far. Thank you!
Excellent information here.😊
Great insight and valuable information on many approaches to treating chronic tick-borne illness.
This is the BEST program on Lyme disease ever! Will send it on!
I'm sending this to my ND. I will pay him to watch it if I have to! If he doesn't, I'll be contacting your clinic!
Thank you for this great video.
These guys have the most optimistic outlook on Lyme's I have seen. I thought these patients were hopeless. If youre dealing with Chronic Lyme's watch this and you'll see that their are treatments and patients can and do get much better.
I was bit by ticks in Pakistan in 1999. In 2007 one morning I woke up and my whole body was inflamed & in severe pain. I was unable to walk or use hands etc. I ws then diagnosed with rheumatoid arthritis and osteoporosis. I've been in chronic pain for the last 15 years. None of the medications work on me. I can recall pains here and there after 1999 leading up to 2007. Could I have been misdiagnosed and actually have Lyme disease? Any advise would be appreciated.
Thank you for a very informative, useful and structered conversation/video spec to Dr. Todd LePine. Many of that I already heard and some of it by used but it was very organised.
Chronic pain is no joke. It's every day waking up not knowing how you're going to feel but with the help of natural herbal medication I was free from (Lymedisease) get to know the powerful herbs man that healed me through is Facebook link facebook.com/Dr-Eromosele-herbal-roots-108749510943383/ or Whatsapp him directly +2349051812935 to sovle your pain
HBOT was a life saver when I was ill. Highly recommend.
WOWEE!! I had to get a pen and paper!!!😀 I'm so glad to hear of these treatments since I've been doing a lot of old school things to alleviate my symptoms. THANK YOU
There's a big connection between lyme - connective tissue - hypermobility. I know a lot of people who are hypermobile and experience the same symptoms and somethimes they have both which influence each other in some way.
Yes it’s awful
Why is that? I’m hyper mobile and have chronic back pain and my son is hyper mobile and has Bartonella and Babesia that was triggered by mold toxicity at his father’s house. He’s getting worse and was on two kinds of antibiotics, but the doctor thought he had herx and took him off except for clay and charcoal and an antihistamine. I’m scared because he gets worse by the day, sleeps constantly except at night and has terrible head pressure! Where can I call or take him? We live north of Detroit.
it seems people born with connective tissue disorders are more susceptible to Lyme and co. Look up RCCX theory. There’s not much out there on the subject. The question is what can be done to stop the suffering in those with these combined issues.
@@Tinyteacher1111 look up Jen Brea, Jeff Wood who both recovered from severe and disabling ME/CFS and POTS. They have websites/blogs and talk a lot about the emerging science linking EDS/hyper mobility/connective tissue disorders, spinal issues like CCI and tethered cord and complex chronic illnesses like Lyme, Mold, MCAS, POTS, ME/CFS and even Long COVID. It may give you the answers your looking for.
I didn't know that! I have EDS
Man, I've been suffering with lyme for 4 years now. 2 weeks of doxy didn't get it. Ive got the joint and muscle pain, pounding heart, brain fog, blurry vision, pressure in my eyes and head, bloating, trouble using my hands.. it's crazy. My doctor is not convinced the Lyme is still present. He perscribed an antacid for the bloating.😂 I'm very athletic, and ive just been pushing through the hard days to get out on the bike and hit my mileage targets like I always have. It seems to help. My heart will struggle sometimes for the first few miles, then most times, it finds its rhythm, and I can still go for hours. It's harder now, but it usually makes me feel better. I'm afraid it's slowly disabling me, but this gives me some hope of a recovery. I live 10 minutes from Lyme CT. If there's any Connecticut funtional medicine doctors in here that think they can take on my case, I'd love to have another go at this.
I contracted Lyme 2 years ago and it has been a roller coaster. A year after I was diagnosed I went back to the DR. since little progress was made with the symptoms of the Lyme. New bloodwork found I also have Alpha Gal Syndrome and Rocky Mountain Spotted fever. I was put back on the Doxy. 2 years later and the symptoms are worse than ever. I also had 2 weeks where I had 4 different Lone Star ticks attached to me.
This is the most informative discussion on this matter, to date. My problem now is the antibiotics have caused a candida overgrowth and (self diagnosed) a suspected biofilm issue. The only treatment that seems to work is starvation. And I also find that when I stop eating the symptoms get better, then much worse. The only relief is meditating for hours a day and the first couple of days on a fast.
My main gripe is all indicators point these symptoms are the medical community repeating a protocol that does little for the people suffering from a chronic/long term issue. One protocol and if it does not work, then go see a shrink, because we followed the same lame and ineffective treatments. In other words: It is in your mind and your gut issues are a side effect of the treatment. I had to beg to get the initial test because I never had a bullseye. The initial visit was prefaced on the idea the medical literature is accurate and all encompassing. The medical community nowadays relies on Google. I have seen NP's search Google for answers, all the while ignoring the patient. This is another form of EGO and only causes more suffering. And intelligence does not start with a degree. In fact, the thought of intellectual superiority from the medical community is actually its greatest impediment. A degree earned is an indication of conformity. Dr. Mark Hyman was brace enough to fight the Establishment with his work and recommendations on sugar intake. This work has provided comfort to the suffering masses and uncovers an established system working against the best interests for human development. The proof is in the intakes we are offered as a society. Much Love and a prayer of healing to all suffering from these symptoms. Thank you for posting this video, some of us have given up on cures and this may prevent future suffers to be more optimistic.
fisheydaddy, Good post.
fisheyedaddy, Did you bring the tick to the Dr to get tested for Lyme disease?
Fisheyedaddy-try cats claw,oregano oil ,black walnut /wormwood,Monolauren,andrographis-do some reading on each of these things,start slow with one and see if it help’s-most of these have helped me -consider a probiotic,and a product called pepzin/gi -again do some reading on it-good luck to you 👍
Wow I have never read a comment in it’s entirety that is this long, but glad I did! You are absolutely correct and I have also witnessed providers searching Google for answers with me right there. 🤦🏻♀️
I have just been diagnosed with chronic Lyme from my Naturopath yesterday, August 11, 2022. He gave me 3 options for treatment.
• Lyme-N the most expensive at $4,000 for the 3 month treatment in the form of a nebulizer.
• Antibiotics combined with herbals.
• Herbals alone.
My husband laughed at the Lyme-N because of the cost. I know it’s ridiculous but my gut health is already in the toilet and I really don’t want to go down the antibiotic road again. I’ve been on SO many antibiotics in the past that it’s probably partly due to the havoc it wreaked on my gut!
Willing to pay $8,000 for a boob job then I’m sure half that for my health, well being and most of all my SANITY is not too much to ask! 😡😒
Strong balanced thc/cbd cannabis from a medicinal supplier. Use an authorized dealer if possible. Ditto for the vaporizer. Start low & go slow. Pulse the dose, that is to say, dose every other day.
thank you doctor. ive had this for 18 years.
Live blood cell analysis helped me visually see the spirochetes when my white blood cells were so low I couldn’t make antibodies to be detected.
Is that what the test is called?
@@KikitheBarber Look up DARK-FIELD MICROSCOPY IN LYME BORRELIOSIS
Super interesting thank you 🙏🏻🌷
Chronic pain is no joke. It's every day waking up not knowing how you're going to feel but with the help of natural herbal medication I was free from (Lymedisease) get to know the powerful herbs man that healed me through is Facebook link facebook.com/Dr-Eromosele-herbal-roots-108749510943383/ or Whatsapp him directly +2349051812935 to sovle your pain
I was bit my tick had bullseye, went to dermatologist took biopsy said no tick parts left, refused test, now 3 years later, vision, heart, skin, fatigue, cramps in feet, back pain, headaches and the medical profession is gaslighting me and over 10 ct and 10 X-rays showing full body arthritis! Please help!
So helpful🙏🏼
Chronic pain is no joke. It's every day waking up not knowing how you're going to feel but with the help of natural herbal medication I was free from (Lymedisease) get to know the powerful herbs man that healed me through is Facebook link facebook.com/Dr-Eromosele-herbal-roots-108749510943383/ or Whatsapp him directly +2349051812935 to sovle your pain
Thank you Dr Hyman💕
Chronic pain is no joke. It's every day waking up not knowing how you're going to feel but with the help of natural herbal medication I was free from (Lymedisease) get to know the powerful herbs man that healed me through is Facebook link facebook.com/Dr-Eromosele-herbal-roots-108749510943383/ or Whatsapp him directly +2349051812935 to sovle your pain
I don't know where these guys practice but one of them said his patient couldn't afford treatment makes me think they're in a private practice that demand cash. If you need treatment go to the Spaulding rehab in Boston they have a lime clinic they'll accept your insurance and they're very comprehensive. It's one of the best places to go anywhere.
I’ve had Lyme since I was 19… the compromised medical system is directly to blame for ruining my life… now I’m 45 unemployed.. still sick … no wife no family no future
Look into CIRS
@@holylabsdoes Lyme cause CIRS?
I'm sorry 😞😞 and am also experiencing the same thing. It can turn your life Inside down and outside down. Lyme is very bad disease and it is hard to treat. This thing too causing chaos for me imagine am in university and can miss classes because of this thing. It can make you discomfort when you around people. I think 🤔 WHO needs to see about this because it really causing disaster for people. I'm from Africa and am experiencing this.
Just some suggestions. Very low/no carb and regular fasting with aip diet, cut out any hydrogenated and seed oils, take minimum 20kiu d3, k2, magnesium daily (jeff bowles). Iodine and selenium (lynn farrows) get some sun daily, try grounded sleep to ground rod outside window with bedsheet. Researh americas undiagnosed parasite problem (and how to allows lyme to persist) and if youre feeling really desperate and bold, join an mms chlorine dioxide forum. You dont have to believe it, im still undecided, but if you talk to enough people that have used it and understand the corruption in biopharma complex maybe it will open your mind. Theres a lot of lyme testimonials from that crowd.
@@KMx108 It can definitely activate the genes if you test positive for them. But what those doctors are finding out is that most Lyme patients really have CIRS. I have studied this for a while now. Been mis diagnosed for Lyme and have test to back that conclusion up which makes all the difference in ones peace of mind they are tackling the right issues.
thanks for this podcast. very interesting. I found out that antibacterial apple coder vinegar eradicates mrsa & e. coli. this was reported in nature magazine. Could it help to eradicate lyme bacteria too? Love & peace to all.
After a month of doxycycline, a Silver I.V. helped with Ehrlichea and it's brain fog. You are right. I have never had a fever even years since the tick bite giving me Erhlichea. My blood samples after malaria like symptoms showed only 20% platelets and white blood cells and was diving. Two weeks later the Lyme test came back Negative yet I would have died.
Where did you go to get your silver IV, etc.? Was there a doctor that helped cure you?
This is fantastic. I started seeing a functional medicine doctor in Toronto and began Ozone treatment so it was great to hear that it can be beneficial, as a lot of medical backed articles state that it’s ineffective. At the steep cost for treatment I fear reports of that nature. I am however concerned that I haven’t been prescribed antibiotics with a 2 year chronic stage 3 case of Lyme disease. I may have MCAS which is perhaps why…but it’s hard to get answers as to the logic of avoiding this. The last thing I want is to go down the holistic ‘magic wand’ rabbit hole where pragmatic treatment protocols are overlooked. Bringing both traditional and alternative treatments together is essential.
Great video thank you
we watched this from a hyperbaric oxygen tank in bali :) great talk! Wish I heard this 2 years ago... you managed to put the best things Ive gathered into 1 talk and more! Going to up my garlic and get some nano silver
I was a body builder and a farrier. Lyme has stolen my life. Help may be out there, but it is financially out of reach for most chronic lyme people. We have not been able to work, so we are financially drained. I avoid doctors now because they have nearly killed me trying to treat symptoms.
Lyme is a cruel disease. People look at you and say " you look fine". Lyme related suicide is much higher than people realize. When you suffer for years with no answers, you start to beg for death.
You are so right. But there are some effective for most low cost things that may help you. Make sure you are not low B 12 or not processing it this is common for people with lyme. This can be self tested by just low cost SUBLINGUAL B 12 drops, double dose for two weeks. That helps with the brain fog, fatigue, nerve damage issues. If you feel better you need to continue at the regular dose. OSHA root supplement helps people as well who are very sick with lyme but it is not as hard on the body and organs as the parasite killers commonly used. There are more and more is discovered all the time. Best wishes to you. I know how hard it is from personal experience.
That's absolutely right suicide is always linked to chronic neuroborreliosis
Hyperthermia, hypobaric oxygen therapy, intravenous ceftriaxone with silver nanoparticles, herbs, all that good stuff costs quite a bit of money.
Such a complex illness and so debilitating!! No acknowledgement or support by main stream. My son and I both have dysautonomia, extreme fatigue, pain, and many co-infections.
Very interesting!
I was diagnosed with APL leukemia several yrs ago, and when I was admitted into the hosp., one of the first questions asked, was have I had any tick bites. I told them the ticks bite me all the time. I was immediately treated for lyme disease before they could treat the leukemia. I have had autoimmune disease for yrs. Still to this day I have all over itchy rashes, headaches, high BP, tired all the time, my hair falls out, and many other symptoms.
Crazy I haven’t had a fever for at least 20 years
I have been doing scans with a frequency scanner on myself. I am using frequency to heal myself and my health seems to be improving a lot. On my scans Lyme and other tick born illnesses showed up very strong. I have been bitten by several ticks over the years I never had a rash or any over whelming symptoms but over the years I have been aware that my health is not as robust as I would like for it to be.
Being a natural healer I have tried many different things to try an revive my health. I am very interested in polarity therapy and frequency therapy and have been studying both for decades. I own two types of frequency devises. The last one I bought just recently is the one that the Lyme and other tick born illnesses frequency show up on the scan. Naturally I have been running the frequencies that are known to treat these diseases. There are many videos on youtube using frequencies for Lyme. The comment sections are full of tips and experiences using the specific frequencies. I suggest that if you do tune into the frequency videos that you tape a good pair of ear buds to the pulse spots (as though it is electrodes) on your wrist one bud for each wrist instead of listening to them with headphones. Don't over do it this method. Start out slow. Pay attention to your body. Any new thing I try with my body I also take half the recommended dosage just to see if I feel it is going to do some good or if I might have a bad reaction to it. Some times less is more.
Would love to watch a video using frequency to help Lyme. Would you have a video to copy here? I have recently been learning a bit about this but would love to also get a device to help. Thank you!
@@sandyharmon874 "Lyme frequency" put that into the search bar
OMy gosh, I so need you guys.
My last dog had lime disease, he was put on antibiotics. When he got older, I think maybe 13, he ended up having something wrong with his brain. He kept walking in a circle day and night. It got so bad he just cried while he did this. I couldn’t even stop it by holding him. Vet didn’t know what was wrong. I had him put him down , his life became a nightmare. Could someone tell me what caused this.
Wonderful! But the fees are extremely expensive, otherwise I would make an appointment.
Sad.
Yes, it is sad. So many of us poor people are left out in the cold, to suffer horribly and go to an early grave, because we cannot afford to get help from functional medicine doctors. We are left having to deal with traditional medical doctors who often dismiss natural things like vitamins and supplements, and frown upon alternative medicine such as nano-silver or ozone therapy. And then they often just push drugs on us that they get kickbacks for prescribing(drugs they often would not take themselves due to dangerous side effects). They often do not really care about us, they just care about the money and the kickbacks.
Wow my 40 yr old daughter had cronic lymws with her2nd pregnancy the maternal transmission has alway made me wonder a out this.i am watching the grandaughter closely so far she seems fine but if any problems arise I'll have the Elizaspot test and put and also bring this video a d you to my daughyets attention.thank you for averything.i will keep up on all yo uh r wonderful info
In Australia a young female scientist came down the south coast of New South Wales and collected a whole heap of ticks. She tested them and what she found was a whole heap of new unidentified bacteria’s and viruses…
Hyperthermia is great, though I think one should be asking why the immune system isn’t mounting a fever on its own in the first place. Often times, spinal issues like tethered cord syndrome and CCI or C1/C2 misalignments disrupt the autonomic nervous system which suppress natural killer cells and a healthy robust immune response that is needed for a fever.
Jen Brea who recovered from ME, Mold sensitivity and POTS also got her first fever in years after correcting her CCI and tethered cord which shows her immune system was back to normal.
CCI and tethered cord are extremely common in those with EDS and hyper mobility due to ligament laxity from weak collagen impacting musculoskeletal structures, which would explain the link between these conditions with Lyme. Long COVID is also being linked to CCI because they reckon the collagen degradation from COVID destroys the ligaments in the neck resulting in CCI and resulting ME/chronic fatigue and POTS in many patients.
As plenty of bone broth colestrum.first
@@tomsale5142 where do you buy or make ..how much ??
What are things that can help
@@tomsale5142 what else can you recommend if post covid
@@joanneclark8256 around 20 of pounds a month you mean ldn?
Lynn Margulis wrote a paper about Spirochetes. Has it been published?
Great movie! How come IDSA and many more does not get it? I did not catch - how did you 2 docs recover? Chronic Lyme is by WHO ICD11 recognized inderectly.
Thanks.
Dr. Hyman continually interrupting Dr. LePine and not allowing him to fully answer the questions was most frustrating.
It's a discussion more than a presentation.
Very interesting! But a lot of the terminology was over my head.
Wondering.. can hep c. also be gotten from the Lyme tick ?
hello ty for this informative video 😊
do u think fasting can help with lyme
?
A ray of hope.... looking back to 1989..
2023 A ray of hope....thank you
I was diagnosed with Rocky Mountain Spotted Fever last year. It has been a very difficult year. I was hospitalized 4 days with sepsis from this tick born illness.
Chronic pain is no joke. It's every day waking up not knowing how you're going to feel but with the help of natural herbal medication I was free from (Lymedisease) get to know the powerful herbs man that healed me through is Facebook link facebook.com/Dr-Eromosele-herbal-roots-108749510943383/ or Whatsapp him directly +2349051812935 to sovle your pain
Chronic pain is no joke. It's every day waking up not knowing how you're going to feel but with the help of natural herbal medication I was free from (Lymedisease) get to know the powerful herbs man that healed me through is Facebook link facebook.com/Dr-Eromosele-herbal-roots-108749510943383/ or Whatsapp him directly +2349051812935 to sovle your pain.
@@GiangNguyen-lh1zs I have been taking moringa and turmeric for more than 6 months and have no chronic pain. Flare up maybe for few hours before major storm and that is it. Never know about energy level. I still only have 1-2 hours daily.
@@vixxcottage how do you use turmeric? It needs fat so I use dairy milk🥛 but would use another method if possible
@@rkuehhas I take a capsule with breakfast every morning. Also 2 moringa capsules at the same time.
Got AFIB from Lyme, thanks Lyme .
Good to hear about garlic (destroys biofilms).. i succeeded with my garlic growing experiment. Its so delicious i ve been munching raw garlic gloves like all day long 😅 (i ve got lyme etc +mold, garlic also is very good antifungal. Maybe garlic is pretty much anti-anything-pathogenic🤔)
Garlic also keeps nasty human creeps from getting too close to your face
I was told garlic works in the body like antibiotic. Did you consume garlic verses antibiotic for lymes?
@@mariaa.bryson8126 since im very antimedicine, i never concidered antibiotics in the first place. Specially since most of the best lyme doctors (for example Klinghardt) do NOT recommend antibiotics... I personally have found that homeopathy has yeilded me the best results, hands down. Also different kinds of energy healing have been very helpful. Dr Garrett Smith (nutrition detective) also has the best detox and nutrition program ever invented: helps lyme as well any health problem. Hope this helps 😊
@@tiarianamanna973 i was just told that if you are newly diagnosed with lymes and do not take the antibiotics in the early stages it can be much harmful later in regards to the progression. It is so very upsetting because it's not like you will have all the answers right away to help slow the progression. Questions like where do I begin and what do I take to help this from happening all these questions are certainly not preventing the lymes from spreading while you are navigating your best and healthiest options. It really is so very upsetting. 😢
@@mariaa.bryson8126 i totally get you! And most of us dont even get the diagnosis correct until after a good while. But i whole heartedly recommend homeopathy and garrett smith, because those things WORK, no matter what is the diagnosis 😌 and just like you said about the antibiotics.. it might slow the lyme. But not stop it. And it will make your own body weaker. And it will make the lyme burrow deeper, which will later on, cause only more serious problems. But homeopathy can fully uproot your illnesses, as can this nutrition detective, because these methods dont "fight" against the disease. They instead will repair your body, and when the body is repaired it doesnt matter what bugs come on your way, because your system will function fully and autocorrect any problems 🙏
Please look into these things, they DO work, and i know you can be fully healed ✨🌞✨
A very helpfull program. the strange thing about lyme disease it is that it just sitz in your body and its true i did not have a feever within 25 Years. But the symtoms are still gruesome.
My mom has had chronic Lyme disease for 13 years now. there are some day's that her whole body hurts that she can't even get out of bed.i always wish I could do something for her.
Stem cell is only answer if you can find a physician in USA. Otherwise Mexico and other Countries will help.
Look up Ritchie shoemaker. These guys worked off his discoveries and give no credit.
Krystal there is hope, keep searching 💕💕. 5 years in severe pain and I am now much better. 🙏🏻
@@sarah29880 hi im so hsppy for you. Please tell me how did you recover/ keep it under control? My partner is suffering so so bad.. mentally and physically
@@ookipuki so i have done many many treatments of antibiotics and colloidal silver, herbs, HBOT, AIP diet etc
I have done something called nutritional balancing with dr. L Wilson
Some things with nutritional balancing involve coffee enemas, infrared saunas, a diet based on meat and a ton of veggies, etc. I did not get better till these things. It’s a long road, but can be done. A lot of herx but then much relief. Email me and we can chat! I would hate anyone to suffer like I did. The mental till is the worst. Flytz2980@sbcglobal.net.
is there any correlation between having lyme and tick borne illnesses and developing celiac disease spontaneously in mid life?
Is the ELISpot test the same test that Igenix does? Does that test also detect the co-infections like Babesia, Ehrichia, etc?
Did you sought the test ime want to find the best test
For anyone struggling with chronic Lyme or if they might think they have it. Please reply to my comment
I haven't heard anything about how tick borne illness affects the adrenals, cortisol, and thyroid, although it seems obvious that an illness like this would greatly alter all these. Does reverse T3 go up with long symptoms?
Thank you for sone hope! My 35 year old son, whom I am taking care of, has two kinds of Bartonella and Babesia caused by his lowered immune system from mold toxicity at his father’s house. He has a doctor who put him in some antibiotics, but he got worse, and she thought he had herx, so he’s only in pain relievers, charcoal and clay, and has horrible head pressure. He hurts all over and hasn’t left the house in weeks. I’m at a loss, so I’m researching this stuff and have been up all night.
I’m so scared and I don’t know what to do now. She said to go to the hospital of his head pressure is that bad, but I’m afraid to take him there and I doubt it will be helpful. I will take him ANYWHERE if I have to! Please give me a suggestion!
Dr. Hyman said he does virtual visits. Have you tried to reach out? I use seaweed and other foods with iodine to help. Coconut oil, hemp oil may help with the pressure in his head. Does he have tinitus?
Antihistamines?
Anti histamine and switch to Keto Carnivore dieet.
Any updates on his situation? Hoping for a speedy recovery for your son.
There's hope and a cure. Danny on Dirt Road Discussions had the same as your son and is healed. He is on Telegram and is live Wednesdays and testimonies on Sundays. God bless!
No insurance not sure how to work live in garage almost homeless would give anything for help no disability was cdc positive im dying untreated. Do some of us really fall into zero help? Literally everyone around me thinks I am not sick. Is my begging for help keeping help from happening.
You should be able to use the documentation from your positive Lyme diagnosis to apply for state- run medical care since you have no income. You may be able to qualify for Medicare if you are diagnosed as disabled y a medical doctor due to the lyme. Find out if there are any community or free clinics in your zip code.
@@jycfrnkl sadly I've applied 5yrs ago, continuing denial even had an attorney. It doesn't make sense. Denied medicaid. When last had insurance, not one doctor took this disease serious. It baffles me on an concerning level. I'm almost broken,, and becoming numb to the pain and downfall, this is degrading and humiliating. I know im not the only one. Thank you for responding ♡ ...there has to be something?
@@alicexx6260 Is there maybe someone who can help you out in order to get antibiotics? A clean, simple diet is also helpful in order to fight this disease.
@Badbhex Hex I am sorry about your condition. My son was diagnosed finally in January with lyme and it is a horrible disease. He is now on three antibiotics and has had trouble with herx. We are thinking about doing SOT therapy. Been on a group on fb. Seems like it works for alot of people. A little expensive. I think the antibiotics are working for him just gonna be a very long road. Hope u find some help
@@dutyofcall7659 a lot of fish need same things and get a lot of same issues as humans it’s crazy
I think the reason why a subset of people don’t make full recovery after treatment is because of the HLA DR/DQ genetic mutation. Which is the same reason why some people develop cirs ( chronic inflammatory response syndrome) surprised this isnt mentioned
Just curious. If ticks can carry such microorganisms, why can't fleas? Also, northern New York is in dire need of a functional medicine Doctor.
I also live in Northern New York and just googled to find only one in Champlain.
What type of dr do I see for Lyme?
Dr.s in South Dakota claim lyme does not occur here. Smart ticks when they get close to the border they turn around and go back to Minnisota.
How many people who have Fibromyalgia and Chronic pain have chronic Lyme disease?
My husband was bitten by a dog tick in Colorado. He developed an unidentifiable high CRP of 120 with rheumatoid arthritis symptoms and other symptoms. I raised the issue of Rocky Mountain Spotted Fever. The doctor said that the bone marrow biopsy would have revealed that bacteria :Rickettsia... When he was bitten, he was not treated with doxycycline, but for an 'infection". Would the bone marrow biopsy reveal this bacteria as the doctor said,?
I am so scared of being diagnosed with Lyme or MS Lupus being I have Hashimoto's thyrotoxicosis CKD STG 3, 3 POLYNECTOMIES, 2 VICTRECTOMIES BOTH EYES and cataracts, than detached plars gas exchg with silicone than IDC early stage tubular that spread to nodes...,
I am deathly scared of dementia MS Lupus 🙏
I'm in pain head to toe wrist back and ankles ...
But, still thinking God for all my great times, friends, parents. I hope I get to see 70.
I'll take 65.
I did an ELISA test for Lyme and the IGG and IGM came back saying "Not Detected" with The Australian Rikkestial Reference Lab in Geelong. I then did the CLIA Lyme test with The Royal North Shore Hospital testing for IGG which said "BORDERLINE" and IGM saying Negative. I then the WESTERN BLOT test with the IGG saying not detected but the IGM said "Detected" for bands 39 & 41. My Doctor said I have a false positive result and that I don't have Lyme. From what I know in order to be diagnosed with Lyme Disease a patient must have a positive ELISA test and a positive WESTERN BLOT according to the CDC. If however the ELISA test is an old, out dated, non specific and low sensitive test, then does the WESTERN BLOT Lyme test become a better Gold Standard test for Australian Labs? Still undiagnosed after 3 years of being super ill
Holy crap. I'm so sorry about your diagnostic issues. But I wonder how is it possible for doctor to see positive tests with patient with Lyme symptoms and say it's false positive? It's inhumane. How are you feeling today?
How do I find a chronic Lyme literate doctor in my area?
Do u find people with certain blood types get it more
Yeah great info on how to treat physically, “matter to matter”. But inaccessible for the person of average financial means. Thank God for Gary Blier, Joe Disprnza and others who practice energy medicine. Highly effective, much less costly.
Energy medicine..like homeopathy?
@@Goated12348 no using the mind
Unfortunately you have to try to get rich with brain fog to afford treatment
Where would you get the PEPTIDES?