Thankyou so much for sharing, I am suffering through this and everything you have explained is identical to my story. Loosing everything house, cars ect to try and live
I totally agree. I live in Texas in the southern part and I am suffering with this also just got diagnosed and it took 2 yrs to get diagnosed after being put thru all sorts of Drs in the past not even wanting to do testing. I am so angry but tkful for finally getting answers. I can’t tell u how I was treated by so called professionals that are supposed to be caregivers. Even called delusional. I had tons of symptoms and spent all my financial funds, It was the demise of my career after 36 yrs in the medical field. I’m gonna be an advocate for this disease. April hopefully ur better by now sure how long u replied to this.
Ugh me too. It’s awful. Sorry to hear about you 😣 so I will keep you and all the people battling this disease in my prayers as I do that daily ….. much love ❤️ Deb.
Sorry to hear this hang in there though the med bed is going to save all of us Lyme disease warriors everyone from every disease great awakening that’s a fact stay happy health is coming stay positive
My son had the same symptoms as you, doctors could not figure out what was wrong with him, we thought it was MS as well. It wasn't until we were referred to a naturopathic doctor, who sent blood work to Germany which came back positive for Lyme disease, she then referred him to another clinic in Oakville Ontario...BIE clinic. They were able to treat him naturally using some odd device to kill the Lyme...it took a few treatments but it was successful. They were also able rid of him of life long allergies to ragweed, milk and dairy products. He is recovering now, however it is still a daily battle. It will be at least another year before he makes a full recovery, as he has nerve damage from the disease. This is a very deadly disease, if not caught early.
Was the device a Rife machine? Those are very pricey and only a few companies make true Rife units. The majority on the market are crap so be sure to get a reputable one.
The odd device is ondamed..made in Germany it kills spirochetes etc very expensive machine..however with right clinician it takes years to heal with that and special tintures.reachout to me I try help
Hope you are already better, and many of us here can relate to your story. The medical establishment needs to be more on top of knowing all about Tick-Bourne Illnesses. You are a hero for putting up with this and fighting to get well again.
True! My 36 year-old son has Lyme, Babesia, and anaplasmosis, along with king Covid. We are in Michigan, and he is suffering terribly, and has been bedridden for almost a year. He’s been to the ER 4 times, and they say us nothing. We were told not to say it’s Lyme! Apparently, it’s like saying “bomb” in an airport! Sad. He’s in meds, but is suicidal because of the pain and length of this illness. It’s so sad our medical system is so broken and corrupt, they can’t face the truth!
@@Tinyteacher1111 prayers be with you and your son. There are ways to heal apparently they are kept from us because of the insurance companies unwilligness to pay for
@@Neoyorchese Thank you! Yep! We are now taking him to a group of doctors near here that all have different specialties. They treat with IVs and supplements (which a what I’d like to add to his regimen, but his dad is so controlling and thinks I’m a nut case because I study this stuff.). However, I was extremely ill for almost 13 years with breast implant illness before someone told my daughter he thought I had this. I had NO idea there was such a thing, and no one ever mentioned this to me, yet I was in and out of doctor’s offices all the time. I was getting so many autoimmune diseases, food allergies, infections of all kinds, blood work up and down, IBS, IC, ulcerated corneas, pain, etc., and then got mold toxicity. I almost died, but really, no one would have cared because they thought I was on drugs because I couldn’t think. Not so! The money I spent, the losses of friends and family (which still is going on), the loss of my teaching career, etc. broke my heart and spirit. If I hadn’t done my research and followed through with the protocol, I’d probably be dead from lymphoma. As it is, I’m still having chronic issues and horrible pain 4 years after explant and getting pseudomonas aeriginosa from the hospital. That started leg pain and it’s still here. I think that anyone who follows through and won’t take no for an answer, but will find someone who can help is a hero like no one else! It’s so hard to live like this! I give you a ton of credit and send prayers! 🙏💕💫
Dan, I’m sorry to hear about your illness. My neighbor has also been fighting Lyme for nearly seven years. He was a pilot and can no longer fly because of the negative impacts this disease causes. The tick population here in Ohio continues to become more prevalent each year. Thank you for taking the time to talk about the risks of this terrible disease brought on from tick bites. I wish you well and hope you have a speedy recovery. God bless your wife too for the sacrifices that were required to get you back to an improved condition. Your content has always been a good resource. Thank you for all the information shared.
That’s so sad! My now 36 year-old son, who was very depressed during Covid lockdown, was spending his days trying to go to online school, but breathing in countless mold spores at his father’s house, and tried to commit suicide two years ago. He started staying with me during the days, and I recognized mold toxicity in him, since I had had it before. However, the mold had lowered his immune system and several tick-borne infections manifested. It’s been two years of severe neurological and psychological problems, in addition to horrific head pressure that came up 9 months ago when he had Covid. He complains and whines constantly, has started picking, is negative and scared for his brain and his life. He has a team of great doctors that are treating him, but his mind races, he has dark, intrusive thoughts, he says he can’t stop “the loop” in his head, he’s paranoid to go outside or anywhere, wants the blinds shut all day, his negativity and anxiety are sky high, and he’s obsessed with finding a place to help him get back on his feet. Unfortunately, these places don’t exist, and although we’ve taken him to the ER 5 times to rule out a tumor, no one believes in this and his own (former) doctor told him it’s anxiety and to go hine and relax! In addition, I am in chronic pain, plus, I just fell off a ladder and broke my upper arm and can’t drive. This is not how I pictured my retirement years! However, I always wanted to do volunteer work, so I guess that’s what I’m doing. Bless all of you who are dealing with this horrendous set of symptoms and circumstances! 🙏💕💫
Thank you I wish you the best of luck just stay positive the med bed is coming and it is going to save all of us Lyme disease Warriors and everyone from every disease great awakening I promise you stay positive always
@mikecarey1990 why don't you do it then? Need special permission? Need money? How expensive is that energy? Who is providing it? Also, some testimonials of your clients that are at least 5 years symptom free would be useful. Feel free to pray for me Mike, I'll pray for you. May the Lord be blessed 🙏
Thank you for sharing your story. I was diagnosed a few months ago as I was bit by a tick 6 years ago and struggled with symptoms of and on since. especially neurological, it was very difficult to get diagnosed, I hope that people can find help faster with medicine improvements. Hope you are doing well
Thank you for sharing hang in there the med bed is going to save all of us Lyme disease warriors and everyone from every disease great awakening it’s true we will be cured in the near future I promise you stay positive always
Cannot wait to dig into this!! After 10 years of "not feeling myself" and several false negatives. I self diagnosed and went to a Lyme literate dr and am on an herb based protocol... it's been a year of up and down... it's been tough!!! Thanks for posting
You just don’t know how lucky you are that you came back positive. THE TEST STILL ARE TOTALLY UNRELIABLE. I have had chronic Lyme disease since September 5, 2009 when my first symptom was bells positive. A month later my life was ruined. I got every coinfection and every symptom after testing negative. 70% of people that have chronic Lyme disease test negative. It is unbelievable to me that we haven’t even found a proper test. I wish you only the best of luck
It's because it's a lab- manipulated bioweapon, at Plum Island, across the bay from Lyme, Ct. A bunch of kids got a 'new' disease. I suspect vaccines. Lyme is really weaponized Syphilis. It was said Lyme is a 'cousin' of syphilis. Pathologist David McDonald found 7 of 10 Alzheimer's brains post mortem had the Lyme Spirochete. No test or valid treatment training for docs, 100 possible symptoms and 60+ possible co-infections. Fatigue, brain fog and 'hard arthritis' (70% get this)and myalgia are the most basic symptoms. I had 30+ symptoms. Neural Lyme is horrid. The Spirochetes eat connective tissue. They like low oxygen areas like behind knees, chomping away until the infection and inflammation creates so much fluid it gathers in one's feet. Karen Allen, actress, suffered with headaches for a couple of years? until two friends who traveled to Costa Rica and picked up Parasites found relief at a Chiropractor who did Zapping. 4 hrs of this, and she woke the next day with no headache. She zaps if she feels any illness coming on. Many spend all the money they have looking for relief, a positive test and valid treatment. The right supplements, diet and exercise.... Very few have figured out the right doses of cycled antibiotics, but many have inept Drs. throw meds at them causing gut dysbiosis. Doxy is a threat to the organism which can throw down DNA to create more adult Spirochetes. It can invade any organ, like brain, heart, or muscles or spinal fluid, even hide in bone marrow to survive things like Barometric Chambers, etc. Dr. Cowden uses 2 herbs and custom treatment to kill 96+% of the critters. The US doesn't screen their blood for Lyme. With Covid vaccines, also, hope you never need a transfusion.
@rare1walking I'm blown away with ur knowledge of this horrible disease. This is exactly what my hubby & I've been talking about, ever since I got the symptoms of lyme. Explains why most drs won't even ACKNOWLEDGE it, let alone know anything about it. Most insurances won't even cover it. WHY?!?!🧐🤔🤫
Listen to what I am saying the med bed is going to cure all of us Lyme disease warriors and everyone from every disease including cancer great awakening I promise you research the med bed it’s 110% true and it’s coming with the great awakening. @@rimringill2772
Listen to me please, stay positive , research the med bed it is going to save all of us Lyme disease warriors and everyone from every disease including cancer great awakening . Within one or two years at the most you and I will be cured it’s coming with the great awakening stay positive and happy, health will come I promise you I promise you I promise you 😁❤ PS I know what you are going through but it WILLget better. I don’t know you but they say 1500 people a year commit suicide because of Lyme disease but it’s a lot more than that , ALot more than that😎@@rimringill2772
Thanks for sharing your story and spreading the word about Lyme disease. I’m sorry to hear what you went through and I hope the worst is behind you. Good luck and all the best to you and your family.
I have the same symptoms. Mine started a bit differently but I have no use of my right hand and neuropathy in my legs and arms, brain fog, can’t remember things, I can’t get out of bed some days because of the pain, my spine has cyst coming out both sides for the past eight months. Unfortunately I don’t have anybody to help me the people that are supposed to love and help me don’t in fact they just make things harder.
Oh my god... Its like listening to my story. Awesome that i found this video. I got diagnosed with MS 10 years ago. Up to 2020 i had the same 'trust' in doctors as you. Then i started researching on my own and came across lyme. Sent blood work to Germany and it came back positive for lyme. I start my treatment next week with hopes for the best. Thank you for sharing and i wish you all the best! 😉🤘
@@jamespak8175 if this question was meant for me i started working out quite a lot (inside the boundaryes of my body strength ). I finished a 2 month antibiotic treatment and now im rebuilding my body. Its still not certain if i have ms or lyme or both. Everyday i see small changes on what i can do. 🤘
@@Mogy10 MM got it! I think I've tried almost everything lol. but I'm not gonna give up.. Gonna be supplementing with copper sulphate. Check out Morley Robbins and Matt Blackburns podcast. Really insightful! You're gonna start to question certain things that are considered mainstream alternative health and medicines lol.. I'm not sure but are you all about Allopathic medicine?
My husband snd I are fighting full blown Lyme disease, along with mold poisoning from hurricanes Laura and Delta. Husband about 30 yrs while hunting in many different states and me 10 yrs. Luckily our drs are functional drs. There are ticks in every state. I got but 2014 in SW Louisiana by the Texas start tick. Sadly I didn’t get to a dr in time for antibiotics to work, he was off shore and I got so sick could hardly get out of bed to eat and to attend to 11 horses , 4 labs and 5 cats. Laid in bed for 5 days until he got on shore, the bulls eye was huge by then. Emergency clinic gave me antibiotics had 3 rounds too late to work. So we are now living in N E Ok and travel to KC Kansas for treatment. Ok has 2 kinds of ticks one reg and a very tiny brown tick which slept with me and bit me 7 times around my waist and left red spots at each bite. I can tell you it SUCKS. Herxing is probably the worst thing as you’re ridding your body of these parasites. We go about every 2 weeks to KC to get our blood cleansed, using a light spectrum and methylene blue and then next day vit/mineral drip. We are going to Dallas and getting a specialized MRI scan. Our Dr Cory Priest is amazing and so knowledgeable. He finds the root problems and causes and works up from there to healing. We yse to travel to Franklin Tennessee to biometrix to get those treatments 11 hour drive. Dr Todd Farney was also amazing. We eat pretty much organic but are going Keto, Paleo and Mediterranean type of diet. Fighting these types of health issues is very expensive and exhausting especially at our age of 70. Spray your shoes, socks, pant legs at least to the knee with permethrin. Ck yourself and family members before bed or often during the day. 🙏🏼for all suffering with lyme and mold poisoning. 💜
Hoping you are on the road to a good recovery. As I'm an arborist in Wales I love working with and in trees. As I've been following your channel you are a great inspiration. Keep up the good work. And thanks for sharing the book details I'm sure this will help.
I had nearly the exact same experience 2 years ago this month. I'm still fighting it but I came close to being beaten more than once. Very hard on a relationship and a family.
Really could relate to this account. Felt his fear & pain. Thankfully friend sent info about the Wahl's Protocol. Hope is so necessary when going thru this scary medical scenario. Never, never, never give up.
My entire family had Lyme and co infections. The pain is horrible. My uncle was told he had MS so no Lyme treatment, and he passed away. We got on doxycycline etc. It's so hard. God bless you. Northern California here. Dr. Stricker in San Francisco is a life saving specialist. 🙏
late to the show found your channel and have been following along for better part of a year as I teach myself climbing and treework.. was just doing some yt digging on any anecdotal experiences with chaga in lyme patients, and saw this come up, had no idea you were dealing with chronic lyme.. have been working with it for nearly a decade. thanks for sharing your experience
What a horrific disease. I feel for you and everyone else battling and trying to manage it. I feel lucky that I seem to be coping with it as well as I am.
Sorry to hear Dan but hat off to you for your positivity and raising awareness of this affliction. I always assumed us tree surgeons were unlikely to get it due to weari g ballistic trousers and with our farmer tans only having our forearms exposed. Will definately check myself over now that I am more aware of the risk. You will have prevented a lot of acute versions of lyme by this podcast alone. Best of luck to ye.
Sorry. I too came down with neurological Lyme ect...... very bad deal I didn’t want to live. If you were to tell me I would recover I would have called you a liar. A full year is what it took. I’m blessed...... you will keep getting better. Hugs
@@lindaskillett4897 thank Lord you are fine! please how do you diagnose late stage lyme and what did you take to get cured...i have two kids, 7 and 8 and i am convinced i have lyme as i have all symptoms.One of my child have similar symptoms as well....i need to live for them.What have you done to get rid of lyme?
@@whatsnewshetalks5784 Hi Sorry I just saw this. Not sure How to check msg. It just popped up watching a utube video. I have lot to say... If you want leave your number... But the truth is herbs alot of them and continuously. for a long period of time. there has been a time when I had to get things under control with a help of a lyme doctor in seattle WA Dr Marty Ross.
Several years ago I pulled a tick off my shoulder, didn't think anything of it until about three days later when I started to feel like death was setting up shop in my body. It was then that I noticed the bullseye where I had removed the tick. Went to the doc, got the antibiotics, but haven't been the same ever since. If you want to wake people up to the real problem, research the origins of the disease, then tell everyone you know.
How wonderful that you got the the rash!! I never did. I didn't know until my knees went on me and I began sleeping 14-16 hours a day. Fortunately, I found a wonderful "Infectious Disease Specialist" who I apparently need to go back to soon.
Hi Dan. I just happened upon this video. I would also at this point be dx'd as having MS. but I know whatever is going on is tickborn. Unfortunately, there is more to Lyme than Lyme. The Lyme part is in check for me for some time, but it is the coinfections that the ticks also carry that give me trouble. Diet is CRUCIAL. Microbe Formulas have some supplements that have helped me, too. Dr. Jay Davidson has some excellent guideline as well. I need to get back to doing coffee enemas because they were helpful for the liver and ridding the body of toxins. GOD IS GREATER THAN LYME! In my weakness, He is strong. Jesus bless you to know Him and love Him as He loves you.
@@Lannie74 i take phase 1 from cellcore. so i think its the step 1 from microbe. as well as all of their drops and minerals etc. im suffering from cirs aka mold illness
Thank you for sharing. I'm sorry you're having to go through this. Hope you are able to get back in the trees soon. Do you (or any other people reading this) have any recommendations of repellents to keep ticks off in the 1st place? Do you know whether there is more risk of exposure in walking through grasses & brush or up in trees? I think I read somewhere that the most common place for deer tick bites is the ankle.
Great awareness warning thank you. I train and assess for nptc in the UK and this really brings home how essential it is to push the health and safety elements that people are often so dismissive of.
I was bitten by a tick on my right leg. Not knowing what it was. Carried on as normal. Feeling unwell and very simular to you don't like going to the docs. Six months later took seriously ill affecting my central nervous system. Lost lots of weight struggling to see. Heart issues. Etc. after two lumber punchers an scans given. Still none the wiser. Sent home from hospital 3 times. Eventually I was taken back into hospital again and remained there for 6 weeks. Eventually thanks to a great specialists Lyme disease was the diagnosis. Antibiotics were administered. Thanks for sharing. 🖒
Thanks for sharing your journey. I also have Lymes, and have been reading Buhner’s book. May I respectfully point out that the resveratrol he recommends is from Japanese Knotweed. He recommends Japanese knotweed, but if you can’t find it, he said you can get resveratrol just make sure it’s made with Japanese knotweed.
I heard you talking about igenex tests. there are a lot of different test options for lyme on their website, which one did you choose? thanks, hope you are doing well
I have been watching your videos and love your channel. Just came across this one though. I'm sorry this happened to you. Hope things are going good for you. Im a climber in the southern united states in Georgia and have learned a lot from your channel. Thanks and I wish you the best.
Sorry to hear that Jim. It’s a horrible disease. I’m managing it well through diet and lifestyle, but still have lasting symptoms. Make sure your get tested at a reputable place as there are a lot of false results. I got tested at I-genex which is the best in North America apparently
@@ClimbingArborist Your story was so encouraging, and I watched it to the very end. Thank you! You are down to earth and your info is very helpful. I was on the fence about the books, but after watching your video I'm getting both books today plus Buhner's Lyme Co-infection book, as I also have Bartonella. I'm certain that I would have been diagnosed with MS as well had I not insisted to test for Lyme first. As a recently unemployed Registered Nurse (guess why?), I've had a lot of time on my hands, have been doing extensive research on Lyme-related treatments and found some up-to-date info. I hope you are okay with my sharing it here. Have you heard of phage testing and phage therapy for Lyme disease? Phage testing can tell whether or not someone has Lyme with no chance of false negatives or false positives. See RED laboratories via YT. Dr. 'T' explains in his vids how this testing works. He is the former director of clinical studies at the Pasteur Institute in Europe, so I hope this cutting edge technology to diagnose Lyme - in early or late stages - will one day be mainstream. Also, Phage therapy via energy medicine is on the horizon and is currently being tested in the US. See "New Lyme-Phage Treatment Appears to Eliminate Borrelia" and "The Effect of Antibiotics on The Phageome and Microbiome" to learn more. I'm not necessarily advocating for it but find the info compelling and am considering it for myself as an option versus months on antibiotics that I feel may not work, since I've got late stage neuro-Lyme. Just before the positive co-infections diagnosis (I tested for Lyme and co-infections separately due to out-of-pocket costs), I bought a set of 3 NIR lights (RubyLux) on Amazon (her website/blog is very helpful for those with Lyme, BTW). Now it turns out I cannot use the lights while on this next round of doxycycline (no light exposure or get skin burns) and am considering going off and using natural herbs and the lights, as I've read the lights are very effective at helping those with symptoms of Lyme. This info is a keeper - "The MOST POWERFUL Antioxidant is Melatonin, NOT Glutathione" by Dr. Berg. Note: The title is misleading - It's about light/NIR light. I learned that companies are now pouring billions into building phage factories all over the world. Is it no wonder? Phages may be the answer to antibiotic-resistant infections. A heartwarming phage success story - 'My husband squeezed my hand to say he wanted to live, then I found a way to save him.' Wishing all the best to you and others reading this who are suffering with Lyme & Co and/or any other antibiotic-resistant infections. Together we can beat this!
i have elevated lyme and my drs did nothing at all i bought doxy from india myself but i feel its too late and i have typical chronic lyme symptoms i demanded that i see a specialist recently , i am positive that morgellons is lyme related also , your talking on this subject is amazing and will make sense to a lot of people ... it is far far far more common than we are led to believe and it is not taken seriously enough at all awareness is rubbish , and most drs are rubbish too .. we have to educate ourselves about this .. thank you so much for your time talking about the seriousness of this .. there is a clinic i hear in germany where they guarantee to clear it .. have you heard about this ??? I think its v expensive though
Jill please get tested as well. In case you can catch it earlier. I am just thinking how my whole family tested positive and had it a chronic long time. I wish we could have been diagnosed earlier. Chronic pain is well horrible. Doxy and pain meds and prayers to Jesus got us through. I had just graduated from university when diagnosed. I was bit by a tick at 14 but no one else really knew when they got it. I'm all for vitamins etc. and antibiotics plus pain medication. In America you need specialists. I hope your family is doing well. I lost so much weight too and got severe anemia. It's so hard. The fatigue and pain are so hard. Doxycycline is harsh but it saved our lives.
I went through a suspected MS diagnosis after horrible symptoms. They found a single lesion on my spinal cord so officially diagnosed with clinically isolated syndrome, or pre MS as my neurologist calls it. I turned down the meds I was offered. This year after continued Ill health I ordered blood tests from Germany, positive for lyme. Then the NHS tests were negative. A further private test in Belgium (phage test) picked up a different strain of borrelia. I'm convinced it's borrelia that infected my nervous system and damaged the spinal cord. One year of various treatments and I'm still struggling with it all.
I feel your pain buddy, I'm sorry you are going though this. Apparently the German testing centre is one of the 2 best in the world for Lyme. If you want to get your life back and you have the drive and determination then read this book, educate yourself on these principles and the issues foods cause the body and it will give you life back again. I can attest to that after 4 years
@@tomwebb986 I was in a really bad way and scared my life was ruined, so I went super strict on the Paleo plus version of her diet for a long time, while implementing lots of other things into my daily life, and supplementing with may herbs. I noticed very quickly my health improving and in 2-3 months I was back to about 85 % of my former self.
I take Cellcore Lyme protocol and their detox protocol.it’s expensive but it is working for me. I have three Lyme co-infections. I’ll also now take the Japanese knotweed resviratol to see if that helps as well. Thanks for doing this video. 🙏🏼✨
Hi I have loved your channel and I've become a tree climber in an animal park. This video has opened my eyes to this risk so thanks. Get well soon love to you and your family. Thanks for sharing
Yes it is hard mentally and neurological issues, I got so bad I could not force myself to stay awake sitting up, standing up. It’s very hard remembering words and speaking words, severe forgetfulness and many many other symptoms. Such as painful rheumatic symptoms, it has so many symptoms cardiac is a large one too. It in turn has financially wrecked me, was the demise of my career after 36 yrs. I’ve never even known anyone from Lyme disease. I have hopes that I will respond to treatment and get on with life.
Cindy, I understand. I got Lyme in 1996 when I was 17. I am now 43 and struggle with it still. I am having an implantable loop recorder placed soon for my arrhythmias (I never even had so much as a single missed beat until I got sick with Lyme). Fatigue, memory issues and cardiac are the worst for me. Over the past 2.5 decades I have had many many symptoms. I also got babesia as a bonus from my tick bite. I hope you are able to get well and not relapse!
@@rachellydy3367 perhaps my naturalpathic can help its been five years diagnosed here but I had symptoms for years my heart doing same thing..maybe my dr can help..via long distance I'm upstate ny..try reachout somehow..she's cheapest dr around I'm up to 11k already $ going fast try get mail to each other yt won't let me post number or mail
There is a saying that beekeeper's never become arthritic because they have been stung by the female worker bees, and specifically the worker bees that guard the entrance to the hive. Apitherapy (api = bee) is allowing yourself to be stung by a bee or bees which aided in lessening the affects of Lyme's disease. Depending on how comfortable you are holding the bee and placing the stinger near a less sensitive area ...or having a friend do it for you... this may be a less expensive modality versus taking medication, etc.
I've been sick for a very long time. Diagnosed with many different disorders and syndromes. Currently I am diagnosed with vasculitis. But I'm starting to suspect Lyme disease. The problem is that I have taken the western block test. It came back negative. My question is, can this be a false negative and can the bacteria hide from test or are there any other types of tick born bacteria that the doctors may have missed
70 percent false negatives from that test. Mine was negative also. Yes they can hide. The test they use detect lyme antibodies. So if your body isn’t producing antibodies then itll be falsely negative
Just a note . I contracted lyme disease in Pa. ( tested twice to be sure) caught it early and took a small dose of medication that completely eliminated my symptoms and have had no issue for years. I do know people that were diagnosed after a long period and have chronic problems.
I been thinking about being tested for Lyme disease. I was diagnosed with MS 2 years ago but lately I been having a tight neck and tightness in my knees and elbows. My tingling and numbness never went away completely and I also have burning sensation too.
Chris do Elisa and Western blot many times..mine showed up to late knew I got bit..antibiotics don't work unless you take them 30-45 days Doxycycline then need naturalpathic dr to get tinctures its 11k$ for me which is cheap my sister 80k sislaw over 200k 8 years.its wicked only thing covered is bloodwork..usa doesn't cover lyme drs..sickening
Hello Dan, thanks for sharing your story with us. Did you have sleeping issues, insomnia? I’m taking apo zoplicone but it doesn’t work effectively. Insomnia is killing me so pain and needles, numbness, crawling sensation, bad digestion, etc. I feel like I can’t get normal sleep anymore. I wake up and I don’t feel tiredness or sleepy anymore as before. Not sure if you went through the same thing. I wish you good health. Take care!
Thanks I'm in Illinois! I believe I have it. Worried about getting false negative. And it's wrong. What was the name of the best place to send my Lyme test? Glad you are doing well.
Hi, That's a great story of recovery. A friend of mine is having chronic Lyme now and looking for a good clinic in the US. Would you mind sharing where you got treated? thank you for sharing.
I am curious if you ever found ticks on yourself before and after your diagnosis? Depending on the tick, you do have symptoms after they “burrow“ into your skin. Their attachment and feeding cycle on your body surely must have been detected by you? When I grew up in Germany we as kids had them often and even really small ones - once they start to attach, will be noticed. I appreciate your candor and effort educating “us” through sharing of your story. My biggest question I have wrestled with is the fact that so many supplements are ineffective because our body through its absorptive organs is not design to process such concentrated and isolated compounds. I found that most fasts are more destructive than helpful. It seems eliminating sugar in its many forms and disguises is essential. Increasing ones gut ecology is profound as well as “ventilating” your body and gut through exercise is an absolute. Imagine how we evolved over millions of years - and set it in contrast what we we are doing to our bodies now! You and I are moving almost all day as arborist but most people are stationary most of the day and night - the negative health effects born from that are tremendous . As arborist we may inhale to much cellulosic compounds (especially if you work with redwoods or cedars be careful) and gasoline fumes possibly injuring ourselves. I send you my best wishes!
So you haven't taken antibiotics at all? Its for sure first thing to do with lyme chronic or not. In chronic lyme it rarely cures you but it always helps and there's a always change to be cured with antibiotics.
WOW!! You got walloped! I got extremely stressed out in 2016 becoming homeless and this critter rose up as they do and have made living in a car...... Well let your imagination run wild 🙉😫😥😨🥵 I do believe I've had this ALL my life when I look back on my life long struggles with health issues. Oh well. Glad you have someone to assist you. JESUS BLESS YOU
Can I ask you to to make a list of all the supplements and companies names / pictures. I tried to write them as you showed them but not sure I got them all and for sure did not get the companies names.
I'm now for years on from suffering from Lyme. I'm doing great and I would say that this has mainly been down to lifestyle and diet changes. I eat paleo diet, predominantly eating fruit, salads, nuts and some meat and fish. This I believe has helped above everything else. I still religiously take resveratrol, reishi mushroom, omega 3 oils, and sometimes take other things but not everyday. Apple Cider vinegar is also something I drink daily. Diet is key to a good life. I really hope this helps,
@@ClimbingArborist try carnivore diet it's heal alot of people my lyme test is in lab it's terrible I have also Hashimoto thyroiditis recently dignosed 😥😥
Thank you for this I’m feeling they exact same way I got bit in Thailand 3 years ago by a tick and got the bulls eye I went on antibiotics But seems to come back 3 years later I started getting tingles in my back Feeling super tired I’m going to try some of these supplements What supplements were your go to? How you feeling now?
I don’t know if I have Lymes disease but I have suffered sooooo much it’s unbelievable! I own a small landscaping company and worked outside all the time so I have really been suspicious that it could be Lyme. My symptoms come and go and when I’m sick I’m bedridden for at least one week and sick from anywhere from 3 weeks to 3 months. I did have a rash on my back that my husband noticed and said it was weird. It was there for a while. I don’t get pain but I get extreme fatigue and extreme muscle weakness to where I can walk a few steps and have to stop for a minute because my calves start burning. I have been to several doctors and they all tell me my blood work is normal
Go to lyme specialist and private laboratory you will see accurate results if u hve lyme it's very very complicated to diagnose and only lyme specialist u need.
@@user-hv8jw1fx7x that is fascinating because I have been highly suspicious of this! I have been taking parasite medicine because I have heard that the tests for parasites always come back negative unless you go to a special place which I don’t know. I have had basically almost all kinds of parasite medicine there is
Those are pretty clear cut symptoms.. the neck pain gives it off instantly - sounds like incompetent doctors. In central europe these kinds of things are pretty common, so when you go to the doctor in these parts, the very first thing they suspect is lime... the issue is that when fighting lime... the classic course of "just do antibiotics for 3 weeks and you are done" is laughably insufficient (according to many experts). even if you catch it early, it can lay "dormant" and stealthily just eat at you... then later down the line you dont even realise the slow progress, but you develop many "chronic" issues and nobody knows what the hell is going on
Makes me cross that you were wrongly diagnosed and initial assement was see how you feel in a couple of days rubbish. Oh well cant get anywhere on the blame route of things. I'm happy for you mate that your okay and still with us to raise awareness. It's no wonder I didn't get more ticks when i was younger playing in the new forest.
Hi, I am so glad that I came across your video. I also have a chronic lyme disease, and I happe to be taken care of a very good medical doctor. I was initially treated with antybiotics and then she introduced Buhner'd protocol which is a combination of herbs against lyme. It works wonders and I strongly recommend it to everyone who suffers from chronic lyme disease ❤
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
Actually the bacteria are using your nervous as a super highway through your body. MS is a genetical sloughing of the myelin sheath... Whereas with Lyme, the bacteria actually erode and or possibly eat the myelin sheath ... So it's MS... reduce the bacteria stops the erosion. I was infected by tick on the coast of Washington state (during the greatest hike of my lifetime, ironically) and my body is still regrating neurological damage!! The doctors and specialists were letting me Parrish and it took 6 year's to finally get diagnosed and get my disability insurance! Education is the best we do for ourselves!! I was diagnosed at stage 4 chronic Lyme from the get go!! Stay moving and thank you for the information on Paleo!! None of my idiot friends use deet!!! God bless ... No one gets it till they get it though. Lyme has stolen my life. But I struggle to learn to live with it rather than die from it! Take cre
I am now probably back to 90-95% of my pre Lyme self. I believe there will always be certain lasting effects/damage, but I feel all the changes I made in my life have hugely benefited and help my recovery. I'm not certain if I will ever be rid of Lyme
To keep ticks off your skin, wear tight woven natural fabrics that cover all your skin (long sleeves and pants), and because ticks alway crawl upward, layer your clothes so that the highest garments are tucked into the next lower garment (shirt into pants, pants into socks, etc) in this way your clothes always shunt a climbing tick outward, away from your skin. If in the woods, wear a hoodie drawn tight to your face, because ticks can sense body heat and drop down on you from the trees above. When you get back to your home or a protected indoor environment, strip your outer clothes off on a porch or other room you don't live in, and put the contaminated clothes immediately into a washing machine with plenty of soap (soap helps the water drown insects and arachnids like ticks), then take a shower and comb your exposed hair with a nit comb to make sure you don't have ticks in your hair. Once you are clean and in clean clothes, you can relax in your tick free home, assuming you don't have other creatures going outside and bringing ticks back with them, like children or pets. If ticks get brought in they can hide in your carpet or furniture, and breed and feed on all living creatures inside, and they can be very hard to eradicate.
I’m starting today but the Oregano-1 soft gel has been changed to another brand & if u look at ingredients the extra Strength Physican BRAND thru Wild Spice but the drops says p73 so I got both! Got Red light from Amazon $319 table one & im doing baths Epsen Salt & baking soda 20 min The sauna seemed to much work! Thanks im praying it works! Got the book but it’s large & I can’t constrate brain fog can’t think! Have to NOT get stressed cause Relapse & flare up! ❤
I finally found someone who experienced something similar to what I'm now going through. It's horrible, so sorry you had to endure it, however, you've confirmed what I've suspected. I had an autoimmune disorder all my life, my blood work showed that I had CREST syndrome, a sign of possible MS although I had a type of Lupus. I changed my diet 4 years ago to organic Keto/IF plus detoxing, and it was a tremendous help. 2 1/2 years ago I was in the hospital for Lyme Meningitis. After 4 weeks of antibiotics I still tested positive for Lyme. It's been a struggle. 2 weeks ago I had an MRI due to Vertigo that began on Jan. 2nd., I still have it; and was diagnosed with MS. I also found some information that shows a possible connection between Lyme and MS. Here in the State Chronic Lyme isn't recognized, however, I just learned that the 'Med Establishment' is now recognizing it as Post-Treatment Lyme Disease Syndrome, PTLDS, and said it was under diagnosed. I'm in Upstate New York where it's been an epidemic here for well over 10 years. I'm also finding that MS is an autoimmune disorder, I'm getting back on Keto/IF, but I'll absolutely get the book that you're recommending and tweak my diet. I have to question which came first, the Tick Born Disease or the MS; I think the Lyme bacteria was already in my soft tissue where it prefers to live. Blessings to you and thank you so much for sharing your story.
Hi Jacqueline, sorry to hear about everything you are going through. , I was initially diagnosed with MS, but when I read up a lot on Lyme and finally got myself tested for it, it made sense that the MS diagnosis was incorrect, as Lyme is known as the great masquerading disease as it can appear as many things. I continue to eat a paleo diet, exercise a lot , get out in nature a lot, go in cold water a lot etc etc…
@@ClimbingArborist Thank you so much. Just this morning I found videos by Alan B. MacDonald, MD. He's a Pathologist who has proven that MS is indeed caused by Lyme Borreliosis. He also worked with the doctor who discovered Lyme years ago. He has many videos on Vimeo. His info is not being told to our doctors. It lives in the spinal fluid but there isn't a blood test for it, has to be done with DNA. He believes that it actually can be healed the same way it's healed in animals who have the same symptoms of MS, with anti parasitic meds used by Veterinarians, but to do it safely, at the same time steroids need to be used. My cat gets the same antibiotic that I do, just a smaller dose, so it makes sense. We can't find help here in the States, we've become the sickest country in the world, people are just now beginning to question why, sort of forced to. (we need something to un-brainwash people LOL) I turned my tv off over 10 years ago. I'm absolutely going to tweak my diet to Paleo and everything you've mentioned. Best of luck to you on your journey. Cheers!
Jacqueline I live upstate NY too..my dr is in Clinton corners 2 hours north Manhattan.She is helping save my life..its not ms it acute lyme..my dr was paralyzed over a year.Try reachout me we try email I get you her number before she retires.
@@karenlittleton6073 Karen, thank you so much for responding. I did have another spinal tap done and it turned out to be chronic lyme meningitis. I had it for three years! I took ivermectin and the pain in my spine, neck and the horrible headaches were gone in a few days. I found a doctor up in Syracuse who said he thought it was chronic before I even mentioned it, he seems to be on the right track.
This has almost killed me 3 blood transfusions blood count 3. fake heart attack& fake COPD & they said I was bleeding inside so they order a colonoscopy & endo & the next day I woke up & my whole face was swollen lips so large I couldn’t eat! The relapse flare-up took me down again! It’s a vicious cycle!!! ❤
I am fascinated and shocked by your story. Your first symptoms are classic Lyme presenting symptoms. The steroids may have been a terrible option if you do have Lyme and not MS. Did you consider complaining about possible misdiagnosis. NHS neurologists need to hear stories like this, otherwise they wont change or understand Lyme - the Buhner protocol is cheaper than the one you follow, I think you are doing the Klinghart protocol.
Steroids suppress the immune system. I would think that would not be a good thing for someone battling lyme disease! Omg. I was misdiagnosed as well. What the hell is wrong with many of these doctors!!!!!
Hang in there bud. Got mine 1 and a half years ago. Terrible shit. Pretty much the same as our man here, could barely walk with grutches for months. Got depressed out of me mind. Now healing mine with radical diet changes supplements etc. Quit all nicotine drugs whatsoever. Getting better slowly and surely. Still feeling those electric pins and needles on all 4’s constantly especially lying on my back. Muscle spasms and pain still takes my sleep away but it surely gets better. Been a nightmare. Goodluck. Great video by the way man.
I have Lyme. The major labs don’t test for the most accurate protein markers, the test are based on very old inaccurate data. You need be tested by IGenex, a tick-borne infection specialty lab. Go to igenex.com
I have had Lyme since 1993 but didn’t know until almost 20 years. I remember having the EM rash, but I was 17 and went to the college health clinic and was told it was just ringworm and anti fungal cream was all I needed. Symptoms began & progressively my healthy teenage body, had symptoms from every system beginning with my brain and cranial nerves then to my joints and once it got into my bloodstream & lymph I had no idea how I could be so sick after being healthy up until summer of 1993
I worked at a LLMD practice and if not for that, & seeing myself in my patients charts, I still would have not have found out why I am so sick. We had all the patients use IGenex because they were the best test
It isn’t cheap, but just having a positive diagnosis gives you hope, that you now know where to focus your research. They offer tests for all the co-infections as well but it can get real pricey. Not sure if insurance reimburses now for it, but the lab only took prepayments. The kits used to be free, but I see now they charge a $20 fee but if you use the kit, they take the $20 off your amount for the tests you choose. I highly recommend all patients with any autoimmune disease, especially CFS, fibromyalgia, MS, Alzheimer’s and so many more to do this test because I am sure it is the cause of most of these disorders. Due to to the spiral shape of the bacteria, it infects every one in different places so the symptoms are so widespread. It can get into any tissue, nerve, organ, cross into the brain, live in joints and muscles and has the ability to change forms known as the “round body” form that enables it to hide from the immune system. If you do the test, make sure you are having symptoms when the blood is drawn, because if it is hiding you won’t have enough antibodies in your blood to test positive. So wait until you are feeling horrible, get the sample done and send it in.
Sounds like American Obamacare. My Dr's were like that when I injured my back. 'Instead of an CTscan let's just send you to physical therapy and see if you scream out in pain. Then we MIGHT send you to a specialist.' who cares if this is a three month process and you have to work to survive.
Thankyou so much for sharing, I am suffering through this and everything you have explained is identical to my story. Loosing everything house, cars ect to try and live
I totally agree. I live in Texas in the southern part and I am suffering with this also just got diagnosed and it took 2 yrs to get diagnosed after being put thru all sorts of Drs in the past not even wanting to do testing. I am so angry but tkful for finally getting answers. I can’t tell u how I was treated by so called professionals that are supposed to be caregivers. Even called delusional. I had tons of symptoms and spent all my financial funds, It was the demise of my career after 36 yrs in the medical field. I’m gonna be an advocate for this disease. April hopefully ur better by now sure how long u replied to this.
Ugh me too. It’s awful. Sorry to hear about you 😣 so I will keep you and all the people battling this disease in my prayers as I do that daily ….. much love ❤️ Deb.
God bless, ive had lymes for 18 years.....lost everything also, keep your head up april.
Yes, you WILL lose control of everything - guaranteed!
Sorry to hear this hang in there though the med bed is going to save all of us Lyme disease warriors everyone from every disease great awakening that’s a fact stay happy health is coming stay positive
My son had the same symptoms as you, doctors could not figure out what was wrong with him, we thought it was MS as well. It wasn't until we were referred to a naturopathic doctor, who sent blood work to Germany which came back positive for Lyme disease, she then referred him to another clinic in Oakville Ontario...BIE clinic. They were able to treat him naturally using some odd device to kill the Lyme...it took a few treatments but it was successful. They were also able rid of him of life long allergies to ragweed, milk and dairy products. He is recovering now, however it is still a daily battle. It will be at least another year before he makes a full recovery, as he has nerve damage from the disease. This is a very deadly disease, if not caught early.
Need more info on this odd device please!
Was the device a Rife machine? Those are very pricey and only a few companies make true Rife units. The majority on the market are crap so be sure to get a reputable one.
The odd device is ondamed..made in Germany it kills spirochetes etc very expensive machine..however with right clinician it takes years to heal with that and special tintures.reachout to me I try help
I can help him.
I only charge $75, but if you are not happy with the results, you don´t have to pay me. @@karenlittleton6073
Hope you are already better, and many of us here can relate to your story. The medical establishment needs to be more on top of knowing all about Tick-Bourne Illnesses. You are a hero for putting up with this and fighting to get well again.
True! My 36 year-old son has Lyme, Babesia, and anaplasmosis, along with king Covid. We are in Michigan, and he is suffering terribly, and has been bedridden for almost a year. He’s been to the ER 4 times, and they say us nothing. We were told not to say it’s Lyme!
Apparently, it’s like saying “bomb” in an airport! Sad.
He’s in meds, but is suicidal because of the pain and length of this illness. It’s so sad our medical system is so broken and corrupt, they can’t face the truth!
@@Tinyteacher1111 prayers be with you and your son. There are ways to heal apparently they are kept from us because of the insurance companies unwilligness to pay for
@@Neoyorchese Thank you!
Yep!
We are now taking him to a group of doctors near here that all have different specialties. They treat with IVs and supplements (which a what I’d like to add to his regimen, but his dad is so controlling and thinks I’m a nut case because I study this stuff.).
However, I was extremely ill for almost 13 years with breast implant illness before someone told my daughter he thought I had this. I had NO idea there was such a thing, and no one ever mentioned this to me, yet I was in and out of doctor’s offices all the time. I was getting so many autoimmune diseases, food allergies, infections of all kinds, blood work up and down, IBS, IC, ulcerated corneas, pain, etc., and then got mold toxicity. I almost died, but really, no one would have cared because they thought I was on drugs because I couldn’t think. Not so!
The money I spent, the losses of friends and family (which still is going on), the loss of my teaching career, etc. broke my heart and spirit.
If I hadn’t done my research and followed through with the protocol, I’d probably be dead from lymphoma. As it is, I’m still having chronic issues and horrible pain 4 years after explant and getting pseudomonas aeriginosa from the hospital. That started leg pain and it’s still here.
I think that anyone who follows through and won’t take no for an answer, but will find someone who can help is a hero like no one else! It’s so hard to live like this!
I give you a ton of credit and send prayers! 🙏💕💫
These videos bring the rest of us hope when the doctors don’t have any answers. Many thanks for posting this.
Dan, I’m sorry to hear about your illness. My neighbor has also been fighting Lyme for nearly seven years. He was a pilot and can no longer fly because of the negative impacts this disease causes. The tick population here in Ohio continues to become more prevalent each year. Thank you for taking the time to talk about the risks of this terrible disease brought on from tick bites. I wish you well and hope you have a speedy recovery. God bless your wife too for the sacrifices that were required to get you back to an improved condition. Your content has always been a good resource. Thank you for all the information shared.
That’s so sad! My now 36 year-old son, who was very depressed during Covid lockdown, was spending his days trying to go to online school, but breathing in countless mold spores at his father’s house, and tried to commit suicide two years ago. He started staying with me during the days, and I recognized mold toxicity in him, since I had had it before.
However, the mold had lowered his immune system and several tick-borne infections manifested. It’s been two years of severe neurological and psychological problems, in addition to horrific head pressure that came up 9 months ago when he had Covid. He complains and whines constantly, has started picking, is negative and scared for his brain and his life. He has a team of great doctors that are treating him, but his mind races, he has dark, intrusive thoughts, he says he can’t stop “the loop” in his head, he’s paranoid to go outside or anywhere, wants the blinds shut all day, his negativity and anxiety are sky high, and he’s obsessed with finding a place to help him get back on his feet. Unfortunately, these places don’t exist, and although we’ve taken him to the ER 5 times to rule out a tumor, no one believes in this and his own (former) doctor told him it’s anxiety and to go hine and relax!
In addition, I am in chronic pain, plus, I just fell off a ladder and broke my upper arm and can’t drive.
This is not how I pictured my retirement years! However, I always wanted to do volunteer work, so I guess that’s what I’m doing.
Bless all of you who are dealing with this horrendous set of symptoms and circumstances! 🙏💕💫
As an energy healer, I am able to eliminate Lyme in less than an hour, and have done it hundreds of times.
Thank you I wish you the best of luck just stay positive the med bed is coming and it is going to save all of us Lyme disease Warriors and everyone from every disease great awakening I promise you stay positive always
@mikecarey1990 why don't you do it then? Need special permission? Need money? How expensive is that energy? Who is providing it? Also, some testimonials of your clients that are at least 5 years symptom free would be useful.
Feel free to pray for me Mike, I'll pray for you.
May the Lord be blessed 🙏
Thank you for sharing your story. I was diagnosed a few months ago as I was bit by a tick 6 years ago and struggled with symptoms of and on since. especially neurological, it was very difficult to get diagnosed, I hope that people can find help faster with medicine improvements. Hope you are doing well
Thank you for sharing hang in there the med bed is going to save all of us Lyme disease warriors and everyone from every disease great awakening it’s true we will be cured in the near future I promise you stay positive always
Cannot wait to dig into this!! After 10 years of "not feeling myself" and several false negatives. I self diagnosed and went to a Lyme literate dr and am on an herb based protocol... it's been a year of up and down... it's been tough!!! Thanks for posting
You just don’t know how lucky you are that you came back positive. THE TEST STILL ARE TOTALLY UNRELIABLE. I have had chronic Lyme disease since September 5, 2009 when my first symptom was bells positive. A month later my life was ruined. I got every coinfection and every symptom after testing negative. 70% of people that have chronic Lyme disease test negative. It is unbelievable to me that we haven’t even found a proper test. I wish you only the best of luck
It's because it's a lab- manipulated bioweapon, at Plum Island, across the bay from Lyme, Ct. A bunch of kids got a 'new' disease. I suspect vaccines. Lyme is really weaponized Syphilis. It was said Lyme is a 'cousin' of syphilis.
Pathologist David McDonald found 7 of 10 Alzheimer's brains post mortem had the Lyme Spirochete.
No test or valid treatment training for docs, 100 possible symptoms and 60+ possible co-infections. Fatigue, brain fog and 'hard arthritis' (70% get this)and myalgia are the most basic symptoms. I had 30+ symptoms. Neural Lyme is horrid. The Spirochetes eat connective tissue. They like low oxygen areas like behind knees, chomping away until the infection and inflammation creates so much fluid it gathers in one's feet.
Karen Allen, actress, suffered with headaches for a couple of years? until two friends who traveled to Costa Rica and picked up Parasites found relief at a Chiropractor who did Zapping. 4 hrs of this, and she woke the next day with no headache. She zaps if she feels any illness coming on.
Many spend all the money they have looking for relief, a positive test and valid treatment.
The right supplements, diet and exercise....
Very few have figured out the right doses of cycled antibiotics, but many have inept Drs. throw meds at them causing gut dysbiosis.
Doxy is a threat to the organism which can throw down DNA to create more adult Spirochetes. It can invade any organ, like brain, heart, or muscles or spinal fluid, even hide in bone marrow to survive things like Barometric Chambers, etc.
Dr. Cowden uses 2 herbs and custom treatment to kill 96+% of the critters.
The US doesn't screen their blood for Lyme. With Covid vaccines, also, hope you never need a transfusion.
@rare1walking I'm blown away with ur knowledge of this horrible disease. This is exactly what my hubby & I've been talking about, ever since I got the symptoms of lyme. Explains why most drs won't even ACKNOWLEDGE it, let alone know anything about it. Most insurances won't even cover it. WHY?!?!🧐🤔🤫
Listen to what I am saying the med bed is going to cure all of us Lyme disease warriors and everyone from every disease including cancer great awakening I promise you research the med bed it’s 110% true and it’s coming with the great awakening. @@rimringill2772
Listen to me please, stay positive , research the med bed it is going to save all of us Lyme disease warriors and everyone from every disease including cancer great awakening . Within one or two years at the most you and I will be cured it’s coming with the great awakening stay positive and happy, health will come I promise you I promise you I promise you 😁❤ PS I know what you are going through but it WILLget better. I don’t know you but they say 1500 people a year commit suicide because of Lyme disease but it’s a lot more than that , ALot more than that😎@@rimringill2772
Sorry to hear about your illness, praying for your recovery. Wish you and your family the best. Love your videos, you have taught me a lot.
Thanks for sharing your story and spreading the word about Lyme disease. I’m sorry to hear what you went through and I hope the worst is behind you. Good luck and all the best to you and your family.
Thanks for sharing Dan. I wish you and your family all the best for the future. You're a great teacher, thanks. Cheers, John
Yeah Dan, thanks for the advice.
...dont have words to thank u anough for this report!!!
I have the same symptoms. Mine started a bit differently but I have no use of my right hand and neuropathy in my legs and arms, brain fog, can’t remember things, I can’t get out of bed some days because of the pain, my spine has cyst coming out both sides for the past eight months. Unfortunately I don’t have anybody to help me the people that are supposed to love and help me don’t in fact they just make things harder.
Tiffany, I am praying for you.
Oh my god... Its like listening to my story. Awesome that i found this video. I got diagnosed with MS 10 years ago. Up to 2020 i had the same 'trust' in doctors as you. Then i started researching on my own and came across lyme. Sent blood work to Germany and it came back positive for lyme. I start my treatment next week with hopes for the best. Thank you for sharing and i wish you all the best! 😉🤘
Good luck, wishing you good health and happiness, research about nutrition, have a diet and good lifestyle and your body will take care of the rest.
If you don't mind can you tell us what you are doing to take care of the illness??
@@jamespak8175 if this question was meant for me i started working out quite a lot (inside the boundaryes of my body strength ). I finished a 2 month antibiotic treatment and now im rebuilding my body. Its still not certain if i have ms or lyme or both. Everyday i see small changes on what i can do. 🤘
how is your treatment going?
@@Mogy10 MM got it! I think I've tried almost everything lol. but I'm not gonna give up.. Gonna be supplementing with copper sulphate. Check out Morley Robbins and Matt Blackburns podcast. Really insightful! You're gonna start to question certain things that are considered mainstream alternative health and medicines lol.. I'm not sure but are you all about Allopathic medicine?
My husband snd I are fighting full blown Lyme disease, along with mold poisoning from hurricanes Laura and Delta. Husband about 30 yrs while hunting in many different states and me 10 yrs. Luckily our drs are functional drs. There are ticks in every state. I got but 2014 in SW Louisiana by the Texas start tick. Sadly I didn’t get to a dr in time for antibiotics to work, he was off shore and I got so sick could hardly get out of bed to eat and to attend to 11 horses , 4 labs and 5 cats. Laid in bed for 5 days until he got on shore, the bulls eye was huge by then. Emergency clinic gave me antibiotics had 3 rounds too late to work. So we are now living in N E Ok and travel to KC Kansas for treatment. Ok has 2 kinds of ticks one reg and a very tiny brown tick which slept with me and bit me 7 times around my waist and left red spots at each bite. I can tell you it SUCKS. Herxing is probably the worst thing as you’re ridding your body of these parasites. We go about every 2 weeks to KC to get our blood cleansed, using a light spectrum and methylene blue and then next day vit/mineral drip. We are going to Dallas and getting a specialized MRI scan. Our Dr Cory Priest is amazing and so knowledgeable. He finds the root problems and causes and works up from there to healing. We yse to travel to Franklin Tennessee to biometrix to get those treatments 11 hour drive. Dr Todd Farney was also amazing. We eat pretty much organic but are going Keto, Paleo and Mediterranean type of diet. Fighting these types of health issues is very expensive and exhausting especially at our age of 70. Spray your shoes, socks, pant legs at least to the knee with permethrin. Ck yourself and family members before bed or often during the day. 🙏🏼for all suffering with lyme and mold poisoning. 💜
Hoping you are on the road to a good recovery. As I'm an arborist in Wales I love working with and in trees. As I've been following your channel you are a great inspiration. Keep up the good work. And thanks for sharing the book details I'm sure this will help.
I had nearly the exact same experience 2 years ago this month. I'm still fighting it but I came close to being beaten more than once. Very hard on a relationship and a family.
Sorry to hear that brother, it’s very tough on family, wishing you strength and good health dude 🤙🤙
How are you doing now 2 years on? Hoping there's light at the end of the tunnel 👍
prayers to You. Thank You so much
Really could relate to this account. Felt his fear & pain. Thankfully friend sent info about the Wahl's Protocol. Hope is so necessary when going thru this scary medical scenario. Never, never, never give up.
You’re a great bloke Dan. All the best with your recovery. And thanks for all your videos helping safety and skill in our industry
My entire family had Lyme and co infections. The pain is horrible. My uncle was told he had MS so no Lyme treatment, and he passed away. We got on doxycycline etc. It's so hard. God bless you. Northern California here. Dr. Stricker in San Francisco is a life saving specialist. 🙏
Do you have hypomobility I've lost my mum.to severe ms heds to I have fybromyalgia after help to find cause
late to the show
found your channel and have been following along for better part of a year as I teach myself climbing and treework..
was just doing some yt digging on any anecdotal experiences with chaga in lyme patients, and saw this come up, had no idea you were dealing with chronic lyme.. have been working with it for nearly a decade.
thanks for sharing your experience
What a horrific disease. I feel for you and everyone else battling and trying to manage it. I feel lucky that I seem to be coping with it as well as I am.
Sorry to hear Dan but hat off to you for your positivity and raising awareness of this affliction. I always assumed us tree surgeons were unlikely to get it due to weari g ballistic trousers and with our farmer tans only having our forearms exposed. Will definately check myself over now that I am more aware of the risk. You will have prevented a lot of acute versions of lyme by this podcast alone. Best of luck to ye.
Sorry. I too came down with neurological Lyme ect...... very bad deal I didn’t want to live. If you were to tell me I would recover I would have called you a liar. A full year is what it took. I’m blessed...... you will keep getting better. Hugs
@@lindaskillett4897 thank Lord you are fine! please how do you diagnose late stage lyme and what did you take to get cured...i have two kids, 7 and 8 and i am convinced i have lyme as i have all symptoms.One of my child have similar symptoms as well....i need to live for them.What have you done to get rid of lyme?
@@whatsnewshetalks5784 Hi Sorry I just saw this. Not sure How to check msg. It just popped up watching a utube video. I have lot to say... If you want leave your number... But the truth is herbs alot of them and continuously. for a long period of time. there has been a time when I had to get things under control with a help of a lyme doctor in seattle WA Dr Marty Ross.
@@lindaskillett4897 so nice, what is your email so we can exchange numbers
Several years ago I pulled a tick off my shoulder, didn't think anything of it until about three days later when I started to feel like death was setting up shop in my body. It was then that I noticed the bullseye where I had removed the tick. Went to the doc, got the antibiotics, but haven't been the same ever since. If you want to wake people up to the real problem, research the origins of the disease, then tell everyone you know.
How wonderful that you got the the rash!! I never did. I didn't know until my knees went on me and I began sleeping 14-16 hours a day. Fortunately, I found a wonderful "Infectious Disease Specialist" who I apparently need to go back to soon.
@@suenetteedwards5965 do u mind telling which state and their name please. I’m n California
How are you today ? I pray you reply back
@@Deb_3 Still alive.
@@Studio55FRG So happy to see this !!!!!!!!
Hi Dan. I just happened upon this video. I would also at this point be dx'd as having MS. but I know whatever is going on is tickborn. Unfortunately, there is more to Lyme than Lyme. The Lyme part is in check for me for some time, but it is the coinfections that the ticks also carry that give me trouble. Diet is CRUCIAL. Microbe Formulas have some supplements that have helped me, too. Dr. Jay Davidson has some excellent guideline as well. I need to get back to doing coffee enemas because they were helpful for the liver and ridding the body of toxins. GOD IS GREATER THAN LYME! In my weakness, He is strong. Jesus bless you to know Him and love Him as He loves you.
I also use Microbe Formulas. Which supplements do you take? I am very interested in cleaning my liver
@@Lannie74 i take phase 1 from cellcore. so i think its the step 1 from microbe. as well as all of their drops and minerals etc. im suffering from cirs aka mold illness
No evil formed against us will prosper.
Co-infections?
Amen. God healed lyme once and I have it again for last 5 years. Its really frustrating
Thank you for sharing. I'm sorry you're having to go through this. Hope you are able to get back in the trees soon. Do you (or any other people reading this) have any recommendations of repellents to keep ticks off in the 1st place? Do you know whether there is more risk of exposure in walking through grasses & brush or up in trees? I think I read somewhere that the most common place for deer tick bites is the ankle.
Great awareness warning thank you. I train and assess for nptc in the UK and this really brings home how essential it is to push the health and safety elements that people are often so dismissive of.
Thanks for sharing. It’s a struggle.
I was bitten by a tick on my right leg. Not knowing what it was. Carried on as normal. Feeling unwell and very simular to you don't like going to the docs. Six months later took seriously ill affecting my central nervous system. Lost lots of weight struggling to see. Heart issues. Etc. after two lumber punchers an scans given. Still none the wiser. Sent home from hospital 3 times. Eventually I was taken back into hospital again and remained there for 6 weeks. Eventually thanks to a great specialists Lyme disease was the diagnosis. Antibiotics were administered. Thanks for sharing. 🖒
Was it cured?
I was misdiagnosed for 10 years with rheumatoid arthritis but I have chronic Lyme I feel his pain
Thanks for sharing your journey. I also have Lymes, and have been reading Buhner’s book. May I respectfully point out that the resveratrol he recommends is from Japanese Knotweed. He recommends Japanese knotweed, but if you can’t find it, he said you can get resveratrol just make sure it’s made with Japanese knotweed.
Did it cure you ? 1 year on are you healed now ?
I heard you talking about igenex tests. there are a lot of different test options for lyme on their website, which one did you choose? thanks, hope you are doing well
I have been watching your videos and love your channel. Just came across this one though. I'm sorry this happened to you. Hope things are going good for you. Im a climber in the southern united states in Georgia and have learned a lot from your channel. Thanks and I wish you the best.
Thank you Dan, I appreciate you putting up this video. How are you now? I hope well. I am getting tested soon.
Sorry to hear that Jim. It’s a horrible disease. I’m managing it well through diet and lifestyle, but still have lasting symptoms. Make sure your get tested at a reputable place as there are a lot of false results. I got tested at I-genex which is the best in North America apparently
@@ClimbingArborist Your story was so encouraging, and I watched it to the very end. Thank you! You are down to earth and your info is very helpful. I was on the fence about the books, but after watching your video I'm getting both books today plus Buhner's Lyme Co-infection book, as I also have Bartonella. I'm certain that I would have been diagnosed with MS as well had I not insisted to test for Lyme first. As a recently unemployed Registered Nurse (guess why?), I've had a lot of time on my hands, have been doing extensive research on Lyme-related treatments and found some up-to-date info. I hope you are okay with my sharing it here.
Have you heard of phage testing and phage therapy for Lyme disease? Phage testing can tell whether or not someone has Lyme with no chance of false negatives or false positives. See RED laboratories via YT. Dr. 'T' explains in his vids how this testing works. He is the former director of clinical studies at the Pasteur Institute in Europe, so I hope this cutting edge technology to diagnose Lyme - in early or late stages - will one day be mainstream. Also, Phage therapy via energy medicine is on the horizon and is currently being tested in the US. See "New Lyme-Phage Treatment Appears to Eliminate Borrelia" and "The Effect of Antibiotics on The Phageome and Microbiome" to learn more. I'm not necessarily advocating for it but find the info compelling and am considering it for myself as an option versus months on antibiotics that I feel may not work, since I've got late stage neuro-Lyme.
Just before the positive co-infections diagnosis (I tested for Lyme and co-infections separately due to out-of-pocket costs), I bought a set of 3 NIR lights (RubyLux) on Amazon (her website/blog is very helpful for those with Lyme, BTW). Now it turns out I cannot use the lights while on this next round of doxycycline (no light exposure or get skin burns) and am considering going off and using natural herbs and the lights, as I've read the lights are very effective at helping those with symptoms of Lyme. This info is a keeper - "The MOST POWERFUL Antioxidant is Melatonin, NOT Glutathione" by Dr. Berg. Note: The title is misleading - It's about light/NIR light.
I learned that companies are now pouring billions into building phage factories all over the world. Is it no wonder? Phages may be the answer to antibiotic-resistant infections. A heartwarming phage success story - 'My husband squeezed my hand to say he wanted to live, then I found a way to save him.' Wishing all the best to you and others reading this who are suffering with Lyme & Co and/or any other antibiotic-resistant infections. Together we can beat this!
I learned a lot about climbing from you. And I thank you for that. I hope you keep feeling better. My prayers are with you.
i have elevated lyme and my drs did nothing at all i bought doxy from india myself but i feel its too late and i have typical chronic lyme symptoms i demanded that i see a specialist recently , i am positive that morgellons is lyme related also , your talking on this subject is amazing and will make sense to a lot of people ... it is far far far more common than we are led to believe and it is not taken seriously enough at all awareness is rubbish , and most drs are rubbish too .. we have to educate ourselves about this .. thank you so much for your time talking about the seriousness of this .. there is a clinic i hear in germany where they guarantee to clear it .. have you heard about this ??? I think its v expensive though
Jill please get tested as well. In case you can catch it earlier. I am just thinking how my whole family tested positive and had it a chronic long time. I wish we could have been diagnosed earlier. Chronic pain is well horrible. Doxy and pain meds and prayers to Jesus got us through. I had just graduated from university when diagnosed. I was bit by a tick at 14 but no one else really knew when they got it. I'm all for vitamins etc. and antibiotics plus pain medication. In America you need specialists. I hope your family is doing well. I lost so much weight too and got severe anemia. It's so hard. The fatigue and pain are so hard. Doxycycline is harsh but it saved our lives.
Lyme Disease and Ticks are all over the place here in Ontario. Terrible, useless bug. best of luck on your recovery Dan.
Luckily, it seems that a lot of people are aware of it here.
I went through a suspected MS diagnosis after horrible symptoms. They found a single lesion on my spinal cord so officially diagnosed with clinically isolated syndrome, or pre MS as my neurologist calls it. I turned down the meds I was offered. This year after continued Ill health I ordered blood tests from Germany, positive for lyme. Then the NHS tests were negative. A further private test in Belgium (phage test) picked up a different strain of borrelia. I'm convinced it's borrelia that infected my nervous system and damaged the spinal cord. One year of various treatments and I'm still struggling with it all.
I feel your pain buddy, I'm sorry you are going though this. Apparently the German testing centre is one of the 2 best in the world for Lyme. If you want to get your life back and you have the drive and determination then read this book, educate yourself on these principles and the issues foods cause the body and it will give you life back again. I can attest to that after 4 years
terrywahls.com/the-wahls-protocol/
Thanks mate, I have picked up one of her books before. How long before you saw improvement?
@@tomwebb986 I was in a really bad way and scared my life was ruined, so I went super strict on the Paleo plus version of her diet for a long time, while implementing lots of other things into my daily life, and supplementing with may herbs. I noticed very quickly my health improving and in 2-3 months I was back to about 85 % of my former self.
@@ClimbingArborist thanks for the inspiration. Do you still see any doctors about MS?
I take Cellcore Lyme protocol and their detox protocol.it’s expensive but it is working for me.
I have three Lyme co-infections.
I’ll also now take the Japanese knotweed resviratol to see if that helps as well.
Thanks for doing this video. 🙏🏼✨
Hi I have loved your channel and I've become a tree climber in an animal park. This video has opened my eyes to this risk so thanks. Get well soon love to you and your family. Thanks for sharing
Glad you're on the mend, Dan. My TH-cam feed has been missing you greatly!
I feel for you I have Lyme and know your struggles. God bless you. I am the one percent who is allergic to deoxycyline and it's a very mental illness
Yes it is hard mentally and neurological issues, I got so bad I could not force myself to stay awake sitting up, standing up. It’s very hard remembering words and speaking words, severe forgetfulness and many many other symptoms. Such as painful rheumatic symptoms, it has so many symptoms cardiac is a large one too. It in turn has financially wrecked me, was the demise of my career after 36 yrs. I’ve never even known anyone from Lyme disease. I have hopes that I will respond to treatment and get on with life.
Cindy, I understand. I got Lyme in 1996 when I was 17. I am now 43 and struggle with it still. I am having an implantable loop recorder placed soon for my arrhythmias (I never even had so much as a single missed beat until I got sick with Lyme). Fatigue, memory issues and cardiac are the worst for me. Over the past 2.5 decades I have had many many symptoms. I also got babesia as a bonus from my tick bite.
I hope you are able to get well and not relapse!
@@rachellydy3367 perhaps my naturalpathic can help its been five years diagnosed here but I had symptoms for years my heart doing same thing..maybe my dr can help..via long distance I'm upstate ny..try reachout somehow..she's cheapest dr around I'm up to 11k already $ going fast try get mail to each other yt won't let me post number or mail
There is a saying that beekeeper's never become arthritic because they have been stung by the female worker bees, and specifically the worker bees that guard the entrance to the hive. Apitherapy (api = bee) is allowing yourself to be stung by a bee or bees which aided in lessening the affects of Lyme's disease. Depending on how comfortable you are holding the bee and placing the stinger near a less sensitive area ...or having a friend do it for you... this may be a less expensive modality versus taking medication, etc.
How are you doing now? I had to go antibiotic, herbal route. It’s a bloody nightmare tbh. Had a year of wellness and I’m treating again.
I've been sick for a very long time. Diagnosed with many different disorders and syndromes. Currently I am diagnosed with vasculitis. But I'm starting to suspect Lyme disease. The problem is that I have taken the western block test. It came back negative. My question is, can this be a false negative and can the bacteria hide from test or are there any other types of tick born bacteria that the doctors may have missed
You need a better test. The test you took is in accurate garbage. You need to see a dr that will send the test to igenex. You most likely have lyme
70 percent false negatives from that test. Mine was negative also. Yes they can hide. The test they use detect lyme antibodies. So if your body isn’t producing antibodies then itll be falsely negative
Hey are you in remission now?
Just a note . I contracted lyme disease in Pa. ( tested twice to be sure) caught it early and took a small dose of medication that completely eliminated my symptoms and have had no issue for years. I do know people that were diagnosed after a long period and have chronic problems.
I been thinking about being tested for Lyme disease. I was diagnosed with MS 2 years ago but lately I been having a tight neck and tightness in my knees and elbows. My tingling and numbness never went away completely and I also have burning sensation too.
Did you get tested ?
Chris do Elisa and Western blot many times..mine showed up to late knew I got bit..antibiotics don't work unless you take them 30-45 days Doxycycline then need naturalpathic dr to get tinctures its 11k$ for me which is cheap my sister 80k sislaw over 200k 8 years.its wicked only thing covered is bloodwork..usa doesn't cover lyme drs..sickening
what says ur MRI?
Had contracted Lyme in 1992.
Caught it quick (2 months) and was treated with antibiotics.
Thank you!
You bet!
Hello Dan, thanks for sharing your story with us. Did you have sleeping issues, insomnia? I’m taking apo zoplicone but it doesn’t work effectively. Insomnia is killing me so pain and needles, numbness, crawling sensation, bad digestion, etc. I feel like I can’t get normal sleep anymore. I wake up and I don’t feel tiredness or sleepy anymore as before. Not sure if you went through the same thing. I wish you good health. Take care!
Thanks I'm in Illinois! I believe I have it. Worried about getting false negative. And it's wrong. What was the name of the best place to send my Lyme test? Glad you are doing well.
Have you made and progress with lyme disease treatment. I am suffering and would like to get help
Hey man did you recover?
Hi, That's a great story of recovery. A friend of mine is having chronic Lyme now and looking for a good clinic in the US. Would you mind sharing where you got treated? thank you for sharing.
Lyme laser in andover Massachusetts
How are you doing now ? Do you have any new videos about your health update. I can’t find it
soryy to hear this Dan .... hope things improve for you .
thank you
I am curious if you ever found ticks on yourself before and after your diagnosis? Depending on the tick, you do have symptoms after they “burrow“ into your skin. Their attachment and feeding cycle on your body surely must have been detected by you? When I grew up in Germany we as kids had them often and even really small ones - once they start to attach, will be noticed. I appreciate your candor and effort educating “us” through sharing of your story. My biggest question I have wrestled with is the fact that so many supplements are ineffective because our body through its absorptive organs is not design to process such concentrated and isolated compounds. I found that most fasts are more destructive than helpful. It seems eliminating sugar in its many forms and disguises is essential. Increasing ones gut ecology is profound as well as “ventilating” your body and gut through exercise is an absolute. Imagine how we evolved over millions of years - and set it in contrast what we we are doing to our bodies now! You and I are moving almost all day as arborist but most people are stationary most of the day and night - the negative health effects born from that are tremendous . As arborist we may inhale to much cellulosic compounds (especially if you work with redwoods or cedars be careful) and gasoline fumes possibly injuring ourselves. I send you my best wishes!
Awesome story, how are you doing today man?
Doing really well thank you 🙏
What tablets for metals ?
Just hope you'll find fine. Incredible god information you share with us. From Barcelona¡¡¡¡¡¡¡
So you haven't taken antibiotics at all? Its for sure first thing to do with lyme chronic or not. In chronic lyme it rarely cures you but it always helps and there's a always change to be cured with antibiotics.
WOW!! You got walloped! I got extremely stressed out in 2016 becoming homeless and this critter rose up as they do and have made living in a car...... Well let your imagination run wild 🙉😫😥😨🥵
I do believe I've had this ALL my life when I look back on my life long struggles with health issues. Oh well. Glad you have someone to assist you. JESUS BLESS YOU
metoo
Can I ask you to to make a list of all the supplements and companies names / pictures. I tried to write them as you showed them but not sure I got them all and for sure did not get the companies names.
I'm now for years on from suffering from Lyme. I'm doing great and I would say that this has mainly been down to lifestyle and diet changes. I eat paleo diet, predominantly eating fruit, salads, nuts and some meat and fish. This I believe has helped above everything else. I still religiously take resveratrol, reishi mushroom, omega 3 oils, and sometimes take other things but not everyday. Apple Cider vinegar is also something I drink daily. Diet is key to a good life. I really hope this helps,
@@ClimbingArborist try carnivore diet it's heal alot of people my lyme test is in lab it's terrible I have also Hashimoto thyroiditis recently dignosed 😥😥
@@ClimbingArborist did you continue working with your naturopathic doc or did you find an integrative/functional medicine doctor who works with lyme?
Great video, thank you so much...!
Are you s still doing good?
Thank you for this
I’m feeling they exact same way
I got bit in Thailand 3 years ago by a tick and got the bulls eye
I went on antibiotics
But seems to come back 3 years later
I started getting tingles in my back
Feeling super tired
I’m going to try some of these supplements
What supplements were your go to?
How you feeling now?
Has anyone tried japanese knotweed?
I don’t know if I have Lymes disease but I have suffered sooooo much it’s unbelievable! I own a small landscaping company and worked outside all the time so I have really been suspicious that it could be Lyme. My symptoms come and go and when I’m sick I’m bedridden for at least one week and sick from anywhere from 3 weeks to 3 months. I did have a rash on my back that my husband noticed and said it was weird. It was there for a while. I don’t get pain but I get extreme fatigue and extreme muscle weakness to where I can walk a few steps and have to stop for a minute because my calves start burning. I have been to several doctors and they all tell me my blood work is normal
Go to lyme specialist and private laboratory you will see accurate results if u hve lyme it's very very complicated to diagnose and only lyme specialist u need.
sounds like parasites to me. go to a local functional medicine doctor so they can run some special labs on you
@@user-hv8jw1fx7x that is fascinating because I have been highly suspicious of this! I have been taking parasite medicine because I have heard that the tests for parasites always come back negative unless you go to a special place which I don’t know. I have had basically almost all kinds of parasite medicine there is
have to go to a llmd or naturopath for the private lab testing like armin or vibrant. cdc is inaccurate and corrupt
Those are pretty clear cut symptoms.. the neck pain gives it off instantly - sounds like incompetent doctors.
In central europe these kinds of things are pretty common, so when you go to the doctor in these parts, the very first thing they suspect is lime...
the issue is that when fighting lime... the classic course of "just do antibiotics for 3 weeks and you are done" is laughably insufficient (according to many experts).
even if you catch it early, it can lay "dormant" and stealthily just eat at you... then later down the line you dont even realise the slow progress, but you develop many "chronic" issues and nobody knows what the hell is going on
Makes me cross that you were wrongly diagnosed and initial assement was see how you feel in a couple of days rubbish. Oh well cant get anywhere on the blame route of things. I'm happy for you mate that your okay and still with us to raise awareness. It's no wonder I didn't get more ticks when i was younger playing in the new forest.
Please research teasel tincture as treatment of lyme
How are you doing now?
Hi, I am so glad that I came across your video. I also have a chronic lyme disease, and I happe to be taken care of a very good medical doctor. I was initially treated with antybiotics and then she introduced Buhner'd protocol which is a combination of herbs against lyme. It works wonders and I strongly recommend it to everyone who suffers from chronic lyme disease ❤
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
Actually the bacteria are using your nervous as a super highway through your body. MS is a genetical sloughing of the myelin sheath... Whereas with Lyme, the bacteria actually erode and or possibly eat the myelin sheath ... So it's MS... reduce the bacteria stops the erosion. I was infected by tick on the coast of Washington state (during the greatest hike of my lifetime, ironically) and my body is still regrating neurological damage!!
The doctors and specialists were letting me Parrish and it took 6 year's to finally get diagnosed and get my disability insurance!
Education is the best we do for ourselves!! I was diagnosed at stage 4 chronic Lyme from the get go!! Stay moving and thank you for the information on Paleo!! None of my idiot friends use deet!!! God bless ... No one gets it till they get it though. Lyme has stolen my life. But I struggle to learn to live with it rather than die from it! Take cre
Thank you for your words, it is greatly appreciated
Your only option: NEVER GIVE UP. BE BETTER LYME FREN
With the huge prevalence of this disease,have you ever heard of any effort to irradicate thet tick?
What did you take? I have lyme
Im in Florida & contracted Lyme
Are you better now? Did you take antibiotics? You seem great in your latest video.
I am now probably back to 90-95% of my pre Lyme self. I believe there will always be certain lasting effects/damage, but I feel all the changes I made in my life have hugely benefited and help my recovery. I'm not certain if I will ever be rid of Lyme
We never hear anything about killing & eliminating the flipping ticks.
To keep ticks off your skin, wear tight woven natural fabrics that cover all your skin (long sleeves and pants), and because ticks alway crawl upward, layer your clothes so that the highest garments are tucked into the next lower garment (shirt into pants, pants into socks, etc) in this way your clothes always shunt a climbing tick outward, away from your skin. If in the woods, wear a hoodie drawn tight to your face, because ticks can sense body heat and drop down on you from the trees above. When you get back to your home or a protected indoor environment, strip your outer clothes off on a porch or other room you don't live in, and put the contaminated clothes immediately into a washing machine with plenty of soap (soap helps the water drown insects and arachnids like ticks), then take a shower and comb your exposed hair with a nit comb to make sure you don't have ticks in your hair. Once you are clean and in clean clothes, you can relax in your tick free home, assuming you don't have other creatures going outside and bringing ticks back with them, like children or pets. If ticks get brought in they can hide in your carpet or furniture, and breed and feed on all living creatures inside, and they can be very hard to eradicate.
How do you keep weight up on diet x
I’m starting today but the Oregano-1 soft gel has been changed to another brand & if u look at ingredients the extra Strength Physican BRAND thru Wild Spice but the drops says p73 so I got both! Got Red light from Amazon $319 table one & im doing baths Epsen Salt & baking soda 20 min The sauna seemed to much work! Thanks im praying it works! Got the book but it’s large & I can’t constrate brain fog can’t think! Have to NOT get stressed cause Relapse & flare up! ❤
I hope you are doing better now. 🙏
I finally found someone who experienced something similar to what I'm now going through. It's horrible, so sorry you had to endure it, however, you've confirmed what I've suspected. I had an autoimmune disorder all my life, my blood work showed that I had CREST syndrome, a sign of possible MS although I had a type of Lupus. I changed my diet 4 years ago to organic Keto/IF plus detoxing, and it was a tremendous help. 2 1/2 years ago I was in the hospital for Lyme Meningitis. After 4 weeks of antibiotics I still tested positive for Lyme. It's been a struggle. 2 weeks ago I had an MRI due to Vertigo that began on Jan. 2nd., I still have it; and was diagnosed with MS. I also found some information that shows a possible connection between Lyme and MS. Here in the State Chronic Lyme isn't recognized, however, I just learned that the 'Med Establishment' is now recognizing it as Post-Treatment Lyme Disease Syndrome, PTLDS, and said it was under diagnosed. I'm in Upstate New York where it's been an epidemic here for well over 10 years. I'm also finding that MS is an autoimmune disorder, I'm getting back on Keto/IF, but I'll absolutely get the book that you're recommending and tweak my diet. I have to question which came first, the Tick Born Disease or the MS; I think the Lyme bacteria was already in my soft tissue where it prefers to live. Blessings to you and thank you so much for sharing your story.
Hi Jacqueline, sorry to hear about everything you are going through.
, I was initially diagnosed with MS, but when I read up a lot on Lyme and finally got myself tested for it, it made sense that the MS diagnosis was incorrect, as Lyme is known as the great masquerading disease as it can appear as many things.
I continue to eat a paleo diet, exercise a lot , get out in nature a lot, go in cold water a lot etc etc…
@@ClimbingArborist Thank you so much. Just this morning I found videos by Alan B. MacDonald, MD. He's a Pathologist who has proven that MS is indeed caused by Lyme Borreliosis. He also worked with the doctor who discovered Lyme years ago. He has many videos on Vimeo. His info is not being told to our doctors. It lives in the spinal fluid but there isn't a blood test for it, has to be done with DNA. He believes that it actually can be healed the same way it's healed in animals who have the same symptoms of MS, with anti parasitic meds used by Veterinarians, but to do it safely, at the same time steroids need to be used. My cat gets the same antibiotic that I do, just a smaller dose, so it makes sense. We can't find help here in the States, we've become the sickest country in the world, people are just now beginning to question why, sort of forced to. (we need something to un-brainwash people LOL) I turned my tv off over 10 years ago. I'm absolutely going to tweak my diet to Paleo and everything you've mentioned. Best of luck to you on your journey. Cheers!
Jacqueline I live upstate NY too..my dr is in Clinton corners 2 hours north Manhattan.She is helping save my life..its not ms it acute lyme..my dr was paralyzed over a year.Try reachout me we try email I get you her number before she retires.
@@karenlittleton6073 Karen, thank you so much for responding. I did have another spinal tap done and it turned out to be chronic lyme meningitis. I had it for three years! I took ivermectin and the pain in my spine, neck and the horrible headaches were gone in a few days. I found a doctor up in Syracuse who said he thought it was chronic before I even mentioned it, he seems to be on the right track.
This has almost killed me 3 blood transfusions blood count 3. fake heart attack& fake COPD & they said I was bleeding inside so they order a colonoscopy & endo & the next day I woke up & my whole face was swollen lips so large I couldn’t eat! The relapse flare-up took me down again! It’s a vicious cycle!!! ❤
Sounds horrific
I am fascinated and shocked by your story. Your first symptoms are classic Lyme presenting symptoms. The steroids may have been a terrible option if you do have Lyme and not MS. Did you consider complaining about possible misdiagnosis. NHS neurologists need to hear stories like this, otherwise they wont change or understand Lyme
- the Buhner protocol is cheaper than the one you follow, I think you are doing the Klinghart protocol.
> NHS neurologists need to hear stories like this, otherwise they wont change or understand Lyme
Very true.
Steroids suppress the immune system. I would think that would not be a good thing for someone battling lyme disease! Omg. I was misdiagnosed as well. What the hell is wrong with many of these doctors!!!!!
I was misdiagnosed too with mild self limiting Guillaine Barre syndrome.. I'm now on my second round of antibiotic treatment 🙏
ivermectin cheaper, five bucks a tube for a bunch of doses....
I’m on daily b12 and b complex shots. It will rebuild the nerves
Wait so did you never take any antibiotics at all?
No
Would you say your back too 100%?
did you contract Lyme in Vancouver? I believe I picked mine up in Squamish
It's not yours it's the devil's.
Hi please can you tell me where you got your test from for lyme?
I think it was called i-Genex lab in California
37:30 herbs
How is your lyme now mate? Its destroyed my life ...brutal
Things are going well, I’ve changed my lifestyle dramatically that has helped me achieve a good level of health.
Read the ‘ Wahl’s Protocol’
@@ClimbingArborist OK thanks for update. I will check it out. I'm sick as hell lost my job health home wife etc. Need to try something
Hang in there bud. Got mine 1 and a half years ago. Terrible shit. Pretty much the same as our man here, could barely walk with grutches for months. Got depressed out of me mind. Now healing mine with radical diet changes supplements etc. Quit all nicotine drugs whatsoever. Getting better slowly and surely. Still feeling those electric pins and needles on all 4’s constantly especially lying on my back. Muscle spasms and pain still takes my sleep away but it surely gets better. Been a nightmare. Goodluck.
Great video by the way man.
@@xtiki1000 same mate for 6 years I was sure I had MS and Docs must be wrong. Just tested positive for lyme . You think your losing you mind
Name the test u did
Look into Chaga tea ! Stay away from caffeine !!
Hey bro do you get fast heart 150 180 cant work out cant sleep @@! Help how do you get test @@! What the best test??
I have Lyme. The major labs don’t test for the most accurate protein markers, the test are based on very old inaccurate data. You need be tested by IGenex, a tick-borne infection specialty lab. Go to igenex.com
I have had Lyme since 1993 but didn’t know until almost 20 years. I remember having the EM rash, but I was 17 and went to the college health clinic and was told it was just ringworm and anti fungal cream was all I needed. Symptoms began & progressively my healthy teenage body, had symptoms from every system beginning with my brain and cranial nerves then to my joints and once it got into my bloodstream & lymph I had no idea how I could be so sick after being healthy up until summer of 1993
I worked at a LLMD practice and if not for that, & seeing myself in my patients charts, I still would have not have found out why I am so sick. We had all the patients use IGenex because they were the best test
Back then they didn’t offer as many tests. I had the ELISA & Western Blots done which came back positive
It isn’t cheap, but just having a positive diagnosis gives you hope, that you now know where to focus your research. They offer tests for all the co-infections as well but it can get real pricey. Not sure if insurance reimburses now for it, but the lab only took prepayments. The kits used to be free, but I see now they charge a $20 fee but if you use the kit, they take the $20 off your amount for the tests you choose. I highly recommend all patients with any autoimmune disease, especially CFS, fibromyalgia, MS, Alzheimer’s and so many more to do this test because I am sure it is the cause of most of these disorders. Due to to the spiral shape of the bacteria, it infects every one in different places so the symptoms are so widespread. It can get into any tissue, nerve, organ, cross into the brain, live in joints and muscles and has the ability to change forms known as the “round body” form that enables it to hide from the immune system. If you do the test, make sure you are having symptoms when the blood is drawn, because if it is hiding you won’t have enough antibodies in your blood to test positive. So wait until you are feeling horrible, get the sample done and send it in.
Cut out sugar grains seed oils try a clove of garlic peal and eat 3times a day garlic acts like an antibiotic
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Sounds like American Obamacare. My Dr's were like that when I injured my back. 'Instead of an CTscan let's just send you to physical therapy and see if you scream out in pain. Then we MIGHT send you to a specialist.' who cares if this is a three month process and you have to work to survive.