Andrea Gibson interviews Lyme Disease Specialist Dr. Daniel Kinderlehrer, RECOVERY FROM LYME DISEASE
Vložit
- čas přidán 25. 06. 2024
- Poet Andrea Gibson interviews their doctor --Dr Daniel Kinderlehrer, about his new book RECOVERY FROM LYME DISEASE: THE INTEGRATIVE MEDICINE GUIDE TO DIAGNOSING AND TREATING TICK-BORNE ILLNESS.
Dr. Kinderlehrer and Andrea discuss many topics including-why Lyme often goes undiagnosed, how a person can have lyme without recalling a tick bite, why going to the doctor can be an especially painful experience for marginalized folks, and Lyme’s connection to mental illness.
Dr. Kinderlehrer's new book can be purchased here: www.simonandschuster.com/book... - Zábava
“People get PTSD from going to doctors” Yes. Yes. Yes. I became extremely ill 3 years ago from an adverse reaction to a pharmaceutical and have only just recently fully woken up to the fact that the medical community is truly sociopathic. Doctors are rarely ethical, most are extremely abusive and discriminatory, held up only by privilege and an expensive college education. I wish there were more doctors like this man.
Thank you for sharing this conversation. Although I do not have Lyme, this dialogue is really supportive for me and I’ve re-listened to this a number of times 🌍
Facts
Sociopathic bastards
This is so necessary. I can't think of a single heart that wouldn't benefit from this conversation. Well done 💗
I was diagnosed a few weeks back with Lyme. I’ve had the tests for Lyme over the years and they all came back negative until now. I’ve had these symptoms since I was five years old. I’m cautiously optimistic that things will get better after 35 years of a bad life.
How are you doing now?
@@tigerspiritjourney Still bad, I need to find a doctor that understands this. I can’t think right anymore so everything is harder. I still need to get tested for a complete panel of coinfections. It’s interesting how it’s almost like I can feel my life force wanting to leave. That’s been happening for a few years now, hard to communicate that feeling.
@@esquire9445 how are you doing? Have you gotten any treatment yet? If not, can I help?
@@smsandel I’m better than I was… in fact the best I’ve felt in decades. But I still feel like there is something wrong. Doxycycline did nothing for me. I went on 28 days of ceftriaxone, while taking Biocidin, and doing hyperbaric treatments. I just got my picc line out on Tuesday. I really don’t know what to do next. Any suggestions are appreciated.
@@esquire9445 most successful treatments based on other ppls results are bee venom therapy (cheap) and sot(expensive)
The anxiety from Lyme is no joke. I was a pretty carefree, anxiety free individual for 28 years. One random day I got sick and also started suffering from anxiety and depression. Like hard-core anxiety I've never felt sober. I couldn't understand what the heck was going on. Sure enough 2 years later my new doctor suggested a Lyme test. And sure enough it popped up positive. I didn't know Lyme was also so psychological. It changed my personality even. I'm still going through it but at least I believe I'm on a path to getting better now. Stay strong friends. You can do it!
it's fucking horrifying, i almost killed myself a few times from the anxiety and depression. bee venom therapy and sot therapy are most successful treatments I've seen ppl based on their results.
@@bigshoots1181 I am so sorry to hear of your many challenges and just know that you can get through this.
@@jojow8416 ty!
25 years of this disease- only diagnosed 1.5 years ago. It's a living hell.
42 minutes in...I woke up😮 one safe person....😳 Extended family & community... PEOPLE WAKE UP
Being believed - I can see this Dr has/is struggling to help, he feels this in his deepest parts..I am going to buy this book! Thank you very much Andrea... wishing you Peace & good health
I’m suffering for 25 yrs with Lyme 5 times and most recently almost died from ehrlichia anaplasmosis bite in October a stay in ICU for 14 days I need my doctor to read this book thank you Dr and Andrea
Absolutely the greatest most informative lyme interview iv ever seen just absolutely incredible... all the reading and studying iv done in the past 25 years all answered in this interview. ❤
This was Amazing!!! My son has had this since he was 2! He has neurological Lyme. I loved this and am so hopeful! Love and Thank you! 💓💗💫
Thank you both, Andrea and Dr Kinderlehrer. To be heard and believed seems to be so rare in medicine. And now I have a lot more to think about in my own health and healing. Thank you.
Follow the money. I truly believe that the MEDICAL community is out to keep you sick so they can get more money out of you and your insurance. I dealt with so many doctors on my mother's behalf and my care, only to be redirected to other doctors and tests. Example my mom right eye needed cataract surgery but the left eye was ok fie another one year. They talked my 87 yr old mother into doing both cuz they're pretty sure she wouldn't live another year.
Anyone one watching this please also look into Rachel Zoffness and her book on pain management. She talks about how pain and sickness is ALWAYS physical and emotional. Lyme is real but enduring it can wreck you emotionally and you need to work on your mental health. Hit it from all angles!!!
Such an enlightening interview! Thank you both for sharing this with the world.
Thankyou sooooo much for acknowledging the biological infection cause of mental illness. I've been diagnosed with Schizophrenia but it is a bi-product of Lyme and Co.
Wow
Wow.... what a gem of a doctor❤❤❤
My 8 year old son was bit by a tick 12 days ago, yesterday I got results, he got lyme desease, this really is braking my heart, I took him to the ER because his knee was swollen for no reason. Today he is starting antibiotics.
Hello, how is he feeling now, after a month?
Ticks is usually brought from animals such as deers, and so on. Keep them away from your yard.
Fantastic interview. I wish I could think of a good question to ask. I guess one thing I'd note is that when I physically feel okay I'm feeling mentally okay too. I had the same sensation you had, that I knew intuitively it was connected to my health. I only found out years later that I had Lyme. I wonder, are there many things that have a similar correlation?
Props to Dr. Kinderlehrer, who is reaching out to educate professionals, a seemingly thankless task.
amazing! I was feeling so hopeless before seeing this. now I feel more hope! thank you for doing this interview
That was incredibly well done,. So good to hear you Danny.
Thank you Dr. kinderlehrer! ♥️
Thank you for sharing!!!! I’ve listened to this over and over! I can relate to everything!!! Still in my journey of recovery with naturalpathic medication ❤️
Very cool to see patient and Doctor gel in this way. Both of you want to help others and it shows.
This is wonderful interview. Thank you so much.
I am getting book for my dr.
I had bulls eye rash 40 years ago and have need for my dr to understand.(uk)
I totally feel visiting dr has exacerbated cptsd, good insight I learn from this interview.
I’m giving the book to my doctor as well. She don’t believe in lymes and tells me I’m depressed.
Thanks so much for this interview. Interviews by people who have first hand experience with the disease interviewing Lyme literate doctors are so important for bringing out the complexities of this disease. Yes to PTSD from dealing with the medical industrial complex!
Thank you so so much !!!
That was pretty good for your first interview and thank you to the doctor who’s book I’m off to buy right now.
Thank you so much for making this and sharing more of your stories. I've been working to find the right doctors to diagnose and treat what I strongly believe is Lyme disease. So far I've found many other stealth infections, so I trust I am on the right path. This interview is giving me courage to keep looking for the right help.
P.S. I was in your poetry class last fall and thsi gave me feels like that class did. I hope you will offer another class in the future.
I’m in the northern Detroit area, and was just diagnosed with a live form of Babesia Microti (not just the antibodies, and my doctor said she’s never seen this before.), one Bartonella, and 4 boriallises. I don’t feel that bad except that for the past 2 1/2 years I’ve felt fluids and had a headache. However, I’ve had mold toxicity, breast implant illness, a plethora of autoimmune diseases, infections, and I’m in constant and chronic pain. I also have a broken arm and found out about had a stroke from the mold.
I’m the caregiver for my grown son who has mold, Lyme, long Covid, and neck herniated discs. He was is in so much pain, he’s irritable and complains all day.
It’s hard on me, but all my ex says is, “When can you drive?”
He’s the one who let his house go and high levels of
mold are still in my son’s system! He’s been living at my house for two years!
We are faring for ourselves but the ex is driving him to his appointments.
My doctor said that she had read an article, and so did I, that a psych hospital was tested and 90% tested positive for Lyme! Imagine going through life never knowing your symptoms are caused by an infection, which is what happened to my son. During his entire life after having meningitis at 7, he was labeled as bipolar, and various other labels. It’s awful!
They told us not to say Lyme to the hospital, because they don’t believe in it!
WHAT?!
Very disheartening!!!
Saviour
I decided to name my alter ego Andrea for oh my gosh, she is my most favorite poet of all time.
Andrea your poem that I know every word to called I do as well as the the every word of wasabi. Let me to a realisation that living is the most beautiful way of letting go of the hurt that keeps coming back.
So the next time someone calls me psychotic I'm just going to say, it's my poet in me. And I will calmly whisper Andrea.
Even though I would like to scream your name Infront of the Grand Canyon, and hear back Ana in return.
P.S. thank you Andrea Gibson. ❤️
Thank you for this interview, which describes the way the doctors of this era do not really pay attention to the patients because of the quota they have to cover… that is my experience, unfortunately. So, I congratulate Dr. Kinderlehner for sharing his experience. There is not doubt, we have to take the initiative to dig and learn what is the best way to take care of ourselves by learning from other experiences. Blessings on your way.
I bought this book while watching and listening…thank you…!!!
GREAT interview!!!
Btw thank you soooooo much for this video it has given me faith. This video should be directed towards folks with lyme disease and its co infections. I need the book and will stay close to these vids
I have a smidgen of hope.
I wish I could afford to see him. I'm wasting away being told I don't know what's wrong with you. I'm at a huge loss.
Great interview. Very hope inspiring & connective. Divine communion, really.
What an amazing Dr. and interview 💙
I am eagerly awaiting my lyme test; I was diagnosed with Fibromyalgia 4 years ago and I've always felt there's a lot going on in my body.
I have appointments since three years now...same thoughts, same feelings described in this story. Haven't been able to work since one year after I finished university.
No medicine would have worked out... Which should have worked out if it is only a psychiatric problem. They didn't worked on the symptoms ... But still, the doctors keep going saying this is just a psychiatric problem without testing any infections or autoimmune processes . I became my own doctor, reading dissertations..spending a lot on supplements. Reading studies and I hope to find a real doctor like you.
But these videos already help to keep it together and to stay strong to make more appointments at the right addresses to find the answer for the symptoms. Thanks a lot!
And still, the psychological problems are there but I think it is nearly impossible for some people to heal from that if doctors don't take look on the consequences( of for example trauma over years) for the autoimmune system or infections in the body...cause the symptoms of infections could be harder for them. They need to start thinking of the hole package and not just taking a look at one symptom and then trying to 'heal' it with one or two medicines.
This is not the place to write down long stories like that but I had to say it.
Andrea, I love poetry. Once upon a time, it loved me.
I lost my ability to write my beautiful poetry, years ago.
You give me hope though, that maybe....
You get it ! Wow! In the beginning, middle ,still stuck on Lyme rd.never heard those words and believed them 🐥
A friend of mine had a pet rat too, the sweetest, clever being.
Andrea. Thank you for so many reasons. This was wonderful. Im on the wait list for Dr K (over a year. ) While im determined to see him Im having a hard time coming up with a list of other docs that treat in such a comprehensive way. Do you happen to have a list of other docs that you could recommend while wait for the best? Thank you !
Dr. Horowitz, Dr. Steven Bock, Dr. Mast,
I have a lyme related disease which no dr will diagnose. I have no money to waste on fake tests and so I can't stand it when I'm in with pain flat out two and a half weeks that I phone for a dr phone appointment. They slam the phone down when I'm in mid sentence and then when I phone back I get another dr. The one I was trying to qvoid. She says I have gingivitis and don't look after my teeth. I say my teeth have always been perfect apart from someone smashing me in the teeth with a metal squash racket. So she offered me a phychiatrist, for my gums as they were burning away with fibres and infections. They spread to more than two thirds of the jaw. The inside of my Cheek was touching the gums so that got infected, through the cheak to the other side.
So answering the phychiatrist offer, I said no I'm not mentally ill, I have autism so she said that autistic people are mentally ill unfortunately.
My husband was angry she falsely accused me of neglecting my teeth.
I was in pain for more weeks. She fold me to take pain ki,legs all the time and refused me antibiotics which was what I needed badly. Anyway gingivitis doesn't produce fibers inches long.
I believe your example that a virus caused anorexia in the girl, because I have noticed that autism is caused by candida overgrowth in the fetus, and people get ocd from viruses such as turrets is caused by streptococcus. Autistic spectrum are more prone to suffering the worst of viruses when they catch them because they already have a rich breeding ground for viruses and spirochetes. An ancient times philosopher told us that all disease begin in the gut. This is no riddle, the egg came before chicken. And virus came before mental illness. Why do drs pretend it is the reverse way round. The auto immune system doesn't know which germs are a sense of self, ocd is fear of believing negative thoughts are your own and not knowingvthat it isn't the true self.
Hi Andrea, thank you so much for sharing this, is so important all that you both share. Is there a way to put Spanish captions to the video? Id like to share to the spanish speaking community with lyme. Im bilingüal so id be happy to help if there is a way.
34:00
Spot on. I'm afraid I'm going to be one of the ppl that die never seeing a Doctor that will admit they dont know so I must be crazy. My wife and I have depleted our savings trying to get help. The twist she's an Rn in the ER for the last 20 years and at first when I started not being able to hide it she thought maybe it in your head. Yes we are still married lol but she now believes me more because I've declined in health so much so. I hate this disease so much.
THANK YOU Andrea for this enlightening interview. Happily I am one of those people who had a tick bite with the bull's eye, went on a horrible round of antibiotics and for 18 years have had no symptoms. Sadly my adult son, recently started experiencing some really odd symptoms and I suspect it is Lyme Disease. He want to the infectious Disease department at a hospital in Montreal and was dismissed because he didn't have the bull's eye rash.
They didn't know, or offer an opinion on the cause of his odd symptoms (very swollen ear lob, then the swelling in the other lobe, then rash all over his torso, next a horrible migraine and then a swollen knee). He has never before even had a flu or cold and is in great physical shape cycling daily even through the winter.
I have done a lot of research to find a doctor in Montreal who treats Lyme disease and have yet to find one. If anyone who reads my comment knows of someone in Montreal, I am very grateful for your time in responding. Thank you and God Bless.
Do you know how long symptoms have been since first onset regardless I would go to private dr get treatment you would no by taking antibiotics And his response I only know drs in America.
@@JP-xs5lo His symptoms were a full month and his knee is still stiff. Sadly there are no private doctors in Canada and the doctors there are not well versed in Lyme Disease. My research continues and I have found use of a variety of herbs that have promising benefits. It seems that the treatment is very individual; one person responds well to a certain herb while another person does not improve. It seems to be trial and era and keeping the immune system strong.
Why is it our fault of this disease & why will doctors tune us out? I’ve been yelled at by a few doctors, telling me it’s in my head, while the accuracy of tests and care is sitting in my folder right in front of them? I do have PTSD with doctors, I won’t even go to the emergency any longer because now I feel this one specific doctor put notes out about me that he feels is wrong! Grateful my son heard him, my family is so upset I won’t go into doctors now, last time I ended up at the hospital, I ended up there for a month, with my lung, heart, i was so sick, yet the doctors still don’t believe?
Make sure you document everything you have, where, when, what the doctors visits were abt. I have little faith in urgent care, they're training on you. You have to be your own advocate. I tested positive for lymes and anaplasmosis, after 5 different doctors had the info over 5 months to order the lymes disease test.
@@karenclausen6724, I do, blows my mind when one goes in for help, and if they don’t “ believe “ it’s possible, after all the endless tests, visits to docs, they seem to become deaf, blind, even with the most accurate test results right in front of their own eyes. Honestly, I was holding the test results in my hand, & this doctor told me, it needs to be sent to this lab, well, guess what results I was holding in my hand!! Then, he began to cover his beliefs up more!! I honestly have no clue what more they expect from me? I have no clue how I can change results any different!! If I could, I certainly would! I wouldn’t have to go see them that doubt... it can make a person want to give up!! It’s mind blowing.
@@mamashanshan2772 follow the money. The MEDICAL community is a BIG HUGE business. Every body part is worth money. They reallly don't care abt the person, only what money can be made off that persons body. 🤨😉
@@karenclausen6724 that's why free market healthcare is the solution. these doctors are going to have to directly compete for your money and private labs are going to take on big pharma. these crony capitalists and insurance companies are done for.
@@karenclausen6724 lol. Sorry.
Join managing morgellons channel. Brittany, shes dealing with morgellons. And the same problems with Drs.
I'm wondering if lime is morgellons.
I have an allergy to red meat and pork . Four yrs ago I tested for lime after a bullseye tick sighting. I tested negative and moved on. I purchased this book after seeing this wonderful interview two days ago. In the course of a week they have messed up just sending in the blood work three times now. How can I located an LLDD .. a literate lime disease doctor ? I live in Richmond Va.
btw I have been listening to your spoken word and I find you amazing. You are inspiring me to return to spoken word
There is a lot of tick born allergy to beef and pork here in Virginia. My nephew has it.
Getting the book
We live in Oregon and my daughter have gone undiagnosed for 10 years. Debilitating Disease. Anxious to hear what antibiotics wk the best.
What an amazing doctor. He's got so much compassion, if only doctors knew what he knows. Yes - bartonella is surely the trickiest infection.
Andrea...I'm going thru the body pains and the mental and emotional extremes. Great interview! Can you please tell me what regiments you did? And are you much mch better today? Thanks
You mentioned the there is a large difference between mortality from Covid in Western Civilization versus Third World Countries. Has anyone compared the rates of autism in Western Civilization versus Third World Countries?
Wow.
After 3 weeks Lyme treatment earlier this year, I’ve been written off with chronic fatigue or long covid with no further treatment for lyme. I have been on a gradual decline for 3 years following an insect bite - I didn’t see the insect so Lyme wasn’t suspected until this year after my 3rd hospital stay for IV. I’ve been in hospital on IV every year since the bite. Neurological symptoms continue to develop - brain fog, memory loss, pressure headaches, stress, sudden feelings of rage, hopelessness. I am not normally hopeless - I have always been a very optimistic and hopeful person. I feel like my brain is inflamed and I lie awake most nights wondering if I’m eventually going to die from whatever this is. As I watch this I feel believed and that gives me hope. If you have any connections in the uk I would be grateful to be put in contact with them. I really don’t know what the next step is to get to the root cause of all this. Thank you 🙏
Hi how r u feeling now did u get help and relief?try to change your diet is a game changer with treatment (carnivore diet)search on yt there is alot of successful stories
You have to go to the USA, Lyme not treated in the UK. Long story, as to why!
Try cats claw and skullcap herbs!
Thank you so much Andrea and Dr.Kinderlehrer. I will check out the book and also the poetry.🙂 Longtime (20 year +) Lyme ( Bartonella and Babesia ) Warrior here. Fantastic all around info , insight and Good Love transmitted. You are right, we are all heroes. Lots of Love sent from ticky and beautiful Cape Cod, MA.🥰 I will "pass it on". To all those healing up, for me the herbs ( ala Stephen Buhner Herbal Protocol) worked for me, along with some other "Angel Docs" (and other helpers) in NJ and PA. I am truly blessed to be alive and pretty well. Keep going and Never ever give up!☮❤
Hi, who did you see and get help from in PA? And also who in NJ as well? Thanks.
Hi there Andreea,
I really need help miss. It's been years of torture and suicide is on my thought for a while now due to this multi sistematic illness
can I please get a way to contact the Dr, as in my country this is "not real" and coping with life became a matter of time before I do something stupid
Very interesting since I am now looking for any information I can get to help my daughter who has Lyme and has had very little success in finding a doctor to treat her properly.
Live blood cell analysis through health food store. There's one in Fallbrook California...thats how I learned about it.
Inexpensive. Only about $60.00
Then went to a naturopath and spent thousands in testing only to get the same results...although nothing about these parasites entering the cell walls.
Huge waste of money and time.
Where are you located?
Testing - -what about DNA Connexions? Positive and my western blot only showed 1 band - negative. You are so right, positive at specialty labs and negative at regular labs. How can I get some help?
This is very interesting. I don't think that chronic infections existed before 40 years ago, roughly?
How do I book an appointment with Dr K?
28 years of suffering and finally diagnosed. I suffered panic attackes that didnt go away causing severe high state anxiety. I was put on so many drugs and drs convinced me i was biopolar. Now that ive lost everything and inhave no money dor treatment what options don't have? Do you have any recommendations
Hi
I was just looking for answers and I found you.
I have a lot of problems with my intestines. Can I have an appointment with the dr?
Where are you guys located
Would love to know Dr.K's thoughts on the Johns Hopkins herbal study for Lyme disease!
May I recommend the audiobook by Kris Newby: BITTEN: The Secret History of Lyme Disease and Biological Weapons.
Namaskar Dear Ones:)):)):))
@Missy22 I was JUST wondering about this! Something was just pulling at my thoughts that "THEY" did this...what better way to feed the big pharma monster & all their other sinister agendas?
Thanks for the book reference. 🌻
i have lyme. i have 2 kids alone. i live in alberta, canada and theres absolutely no help. at all.
I hope you can get antibiotics. A Canadian doctor moved to New York to
Help more people. Get a hold of her. I can't remember her name
Im in small town sask. 3 ppl in my town that i know who've been properly tested have chronic Lyme. I can't wait for our healthcare to collapse, the amount we pay in tax dollars is ridiculous. We have universal drug dealers.
Did you both also had derealization and depersonalization?
All is like a dream - I have no emotions, no soul, no link to reality.
It’s more than just BrainFog - I can’t recognize myself In the mirror, forgot about my past. It’s horror, agony 24/7.
Not to speak from the debilitating headache and pain all over.
I also have permanent eye pain and blurry vision
Sorry to hear this. My good friend is dealing with the same things. Have you tried any dietary changes or protocols by any chance?
You r absolutely right try to change your diet to for carnivore diet it's heal alot I believe see about carnivore diet success stories there is alot diet play a major role because food is medicine I wish you and pray you for your recovery
Are you going outside I mean driving a car,house work,etc?sorry to ask I am house bound I have also same symptoms but no pain I started carnivore diet but still need treatment
Do you have lyme and co infections
@@donaldpasserelli3529 i am not sure
Theory: The US has “neglected” parasitic infections by labeling it as a hygiene problem that is found mainly in 3rd world countries.. patients with Borrelia have high levels of biofilm in the stool. The testing that we do to check for parasites doesn’t work when biofilm is present In the 3rd world they only have microscopes.. You can see the organisms using microscopes. But in the US we have the CDC recommending I direct testing that has high false negative results for Lyme disease. So maybe it is that in the US we have high levels of undiagnosed Lyme disease as well as undiagnosed or false negative parasites. Perhaps this is why the mortality rate in the US is so high.
i have lived in the woods all my life had several tick bites. back in 1990 i got diagnosed w cfs, depression, anxiety, panic attacks put me on xanax then a couple yrs late i was diagnosed w fibro, low thyroid, bladder problems now im having major fatique, muscles are painful, hand hurt very bad. been checked for ra they said it was low factor but cant tell me whats going on soo many things seem to me its one thing causing all this. my dr will not test me n says if i never had the bulls eye rash so blames it all on thyriod and fibro. i hear most come back negative but would like to find help
I read somewhere in a medical revieuw, that the bullseye is not allways present. Also...
Not only ticks cause lyme. Mosquitos, other insect bites too.
I just got diagnosed with Lyme originally diagnosed with health anexity in I’m on all kind of psychiatric meds I’m so done with doctors
❤
Hey guys, anyone from Romania who got sick of being sick and tired of talking to doctors ? I really need to talk about it with someone who gets it
Are you ok?
Great podcast, Daniel is very informative. Only thing that could have been left off was the “Woke” spin she had to keep throwing in. I am a Regular Indian/white guy and I lost count of the docs who appeared to take pleasure at blowing me off despite such obvious total health collapse I was (am still in). This has cost me over a decade of my life and I still haven’t found help. FYI, I live in a super “woke” community here and believe me, there is not a damn ounce more compassion or desire to help in this community versus the “regular non-wokish” type docs. No difference whatsoever……. If your looking for “oppression or discrimination” then you most certainly will find it. And there is a very good reason why, but if you don’t know why then your probably never going to know why……
The reason third world countries had exponentially lower Covid death rates is because they were treating EARLY rather than sending people home to get sicker, and they were not killing them in the hospitals with remdesivir, which causes organ failiure, and ventilators.
9:50 I agree it's harder to plan a lyme future and rebuild the highschool and puberty that would have happened than dealing with the disease itself(rationalizing laziness can't get up for school) the shame of missing out and not having that career and having that memory of that Dr who seemed to know but kept avoiding the diagnosis due to cdc fear
Feels like adam sandler going back to jr high when everything went wrong
I have a problem trying new medicines. I've had lyme for about 12 years. I think I have covid syndrom too on top of lyme. I'm supposed to try japanese knotweed today but I'm nervous. Has anyone ever tried it? Thanks!
How did this work out?
@@C3mito3 I took the Japanese knotweed for one day. It agreed with me ok. It gave me alot of shivers, and more pressure in my head which means it's doing something. I am going to try it again later for a longer period of time. I am waiting for modified citrus pectin to come in the mail. I have read alot about it. It sounds really good. It's good for lyme. It Inhibits the growth of cancer, binds to heavy metals and mold. It may help with covid too. The lady I talked to on the phone said they did have some testimonies of it helping with covid. I have to wait2-7 days to get it. I'm going to take this for at least a few days. I will keep you posted on how it works.
@@hilarymurray7800 awesome thank you, yeah I'm currently trying hbot hyper bariac oxygen, just recently did my first dive many say it helped for lyme/ covid /chronic illnesses ima give it a try for couple months might want to give it a try if the herbs don't work. I'll give u an update aswell!
@@C3mito3 I've heard that it's really good! People with even stroke and brain damage have improvements with it. Let me know how it's working!
@@C3mito3 how is it working out for you? I did hyperbaric oxygen chamber myself, extremely expensive.
My naturopath put my on h2O IV's he said its better than hyperbaric oxygen chamber. 10 sessions once a week along with glutathione push.
Personally I can't believe he didn't do chelation therapy. Getting those heavy metals out is important.
I did alot of ionic foot baths and highly recommended them
Dr. Klinghardt has a protocol too. He is in Seattle area. He got sick himself and is extremely knowledgeable.
Please update us...
Best wishes
I began using IV heroin in 2015 and shared needles with one who had lyme and hep c
I am worried now that I have lyme because of my symptoms. I know I have hep c . Has anyone heard of lyme transfer from shared needles?
No, seems impossible to transmit like this!
Yes cause it a bacteria as well as a virus can be transferred from surfaces,needles,etc.
Oh god I have tick attachments everyday
I have have it so long my house is infested now what do I do I can’t move or rip out my carpet ticks do t come off clothes either in wash I pick them off after out of dryer
I’m in a nightmare
They got in your house?
What are best antibiotics for lyme?
Doxycycline
@@MISSMONA2007 maybe for the first month lol 😂
Work with your knowledgable doctor IF you decide to go the antibiotic route. There are many antibiotics which may be effective for different bacteria at different times, alone or in combination. There is no best antibiotic, so please don’t just ask for a prescription.
Andrea I'm suffering from Lyme Disease, (Babesia and Rocky Mountain Spotted Fever are gone)
Now have a new Bartonella infection with Lyme and Long Covid. I really heard myself in your words.
I related to everything you said.
I'm not getting better.
I believe that your environment has a lot to do with the healing.
What State are you both in?
Thanks.
I believe this dr is in Colorado hope you get well and find effective treatment
I believe this dr is in Colorado hope you get well and find effective treatment
I believe this dr is in Colorado hope you get well and find effective treatment
I believe this dr is in Colorado hope you get well and find effective treatment
I believe this dr is in Colorado hope you get well and find effective treatment
Look up Herbal Relief of Lyme Disease on you tube Wyoming PBS Channel
How many teenagers try offing themselves...on vacation..........in Florida....................at 15............at Disney World???
This ONE did. That was the 2nd to 3rd attempt.
From there, they grew to too many to recall.
The suicide thing is what I am telling myself every day too, pretty sad.
Don’t give up.
@@gemmasmith26 thank you for your kind words, lyme is just a real living nightmare.
@@Afura33 I know, but it’s possible to get better just like the doctor and the lovely person interviewing him, there is hope :-)
Do you have lyme disease
@@gemmasmith26 I have tried 2 different lyme doctors, we have tried a lot of different antibiotics, anti parasite meds, treating the coinfections, supplements, herbs, diet change, heavy metal detox and so on. I have also tried tons of alternative stuff, I stopped counting. Nothing helped that I tried the last 17 years, I am out of money now and I can't work anymore.
When you get a personal relationship with God. Jesus Christ forgives or sins. ask for forgiveness it helps
John3;16.
@drisiborherbalhome
I live in AZ and I know I have it my house is infested in ticks my 2 dogs a I can’t keep tick free red mountain ticks breed from mar-oct and words can’t describe how tired and sick I feel my son comes from CA to hep with house and dogs I moved dogs to a friends house to get them out of my environment not any pet medicine has ever worked
I’m desperate to help them I can’t afford myself because I called a Lyme clinic omg 10 k $ I’ve got every system there is I’m probably going to die from this I’m not in n early stage I will buy your book today isn’t there a way to treat myself and my dogs
Veterinarians use microscopes and diagnose things that way… and they use objective science rather than subjective interviews.
My veterinarian printed up hundreds of pages of information for me.
My discovery came from live blood cell analysis which showed parasites in the blood. I fought like crazy to eradicate it. Went back for another update and the parasites moved into the cell walls.
@@raptureready5004 how did you eradicate it?
@@esquire9445 3 days before the full moon para cleanse from natures sunshine is a 10 day protocol of herbs..the parasites come out of the cell walls to procreate and thats when you go for the kill.
I used it the first time and they blew right through my skin..it was a horror show.
That is extremely important.
Please screen shot or write it down because when I share this it gets removed fast.
Nonetheless the battle is brutal
I did another series about 5 months in a row in 2022..didn't have that extreme reaction.
Heavy metals keep them in there.
Ionic foot baths.
Chelation therapy with a naturopath would probably be a good idea.
Tons of other modalities
But I got Morgellons too so that's over the top nightmare.
Happy to share more later if you need the information.
Nature's Sunshine can be ordered online with a huge discount something like 40% off..I would stock up.
What an incredible company, pioneers in herbal healing.
My live blood cell analyst told me that people with these parasites in their blood has skyrocketed from maybe 3% to now around 50%...and that was 10 years ago.
Best wishes
@@esquire9445 also look up herbal relief of lyme disease on you tube Wyoming PBS
The Indians have healing modalities and absolutely important information
Great podcast, Daniel is very informative. Only thing that could have been left off was the “Woke” spin she had to keep throwing in. I am a Regular Indian/white guy and I lost count of the docs who appeared to take pleasure at blowing me off despite such obvious total health collapse I was (am still in). This has cost me over a decade of my life and I still haven’t found help. FYI, I live in a super “woke” community here and believe me, there is not a damn ounce more compassion or desire to help in this community versus the “regular non-wokish” type docs. No difference whatsoever……. If your looking for “oppression or discrimination” then you most certainly will find it. And there is a very good reason why, but if you don’t know why then your probably never going to know why……
I found the opposite getting Lyme disease all I saw were woke drs completely brainwashed from med school and programmed to follow and not practice medicine whatsoever just follow directions. Why do you think Fox News was one of the only main stream news media reporting on this Lyme and reasons