ms hopeful if he cares so much why doesn’t he study bio chemistry intercellular elation, and use herbs and nature healing , to cure , not just to treat , also we shouldn’t eat beef, Europeans laugh at all these diseases
@@ADRSupport I am trying to reach Dr. MacDonald. Do you have an email contact? I am the Admin of GBM Brain Cancer Survivors to Thrivers support group. My Mom got brain cancer from Lyme, Babesia and EBV. She is an almost 4 year Survivor from treating parasites!! I have been trying to contact him as many many people with brain tumors have a history of Lyme and co infections. If you could please let me know how I can reach him? Thank you so much!!
@@katiebrookzorena3643 I wasn't able to find any information for how to reach Dr. MacDonald. My doctors thought I had MS. I had Chronic Lyme Meningitis and treated with with Ivermectin. It worked and my short term memory is getting better. No more spinal pain, neck pain or headaches. My fluctuating body temp has gone back to normal. I know someone who has been battling cancer, he's taking Ivermectin also as well as only eating whole food, nothing with sugar or refined carbs. He's getting better.
These three video's are by far the most informative video's on Lyme Disease to date, Dr. Alan MacDonald Thank You !! You are most awesome for helping us...
I have suffered, undiagnosed with what I have continually believed is Lyme disease, for nearly ten years now. My initial physician mistook me for a drug seeker who was using my "unproven" joint and muscle issues to get pain meds, which was unfortunately a prevalent issue in my southern Ohio community. (though I am a non-smoking, non-drinking, Christian individual who did, through blood tests, prove negative for drug use) This injustice occurred despite the fact that I had seen the physician previously in regard to a telltale bullseye rash which developed after I had removed a deeply embedded deer tick and was suffering with night sweats. This physician told me that "Lyme's Disease" (his pronunciation proving his Lyme Illiteracy) did not occur in Ohio and because I had not traveled out of state, it was impossible that I had contracted "Lyme's". I continued untested for sometime, my condition worsening, before I finally bullied the Dr. into testing for Lyme. Unfortunately, I showed no antibodies which only emboldened the Dr.'s suspicion that I was merely seeking pain meds, stating at one point that "guys like you might not be users but they are selling their meds to their drug addicted buddies". At that point I requested a different doctor at our (company) clinic who also insisted that I was not infected but did eventually prescribe a 21 day course of doxycycline. Little did I know (nor did my Dr. evidently) that after such a long Lyme infection that this treatment would be insufficient. Now after years of doctoring with a myriad of physicians including Rheumatologists, Internal Medicine Specialists, Infectious Disease Specialists, as well as enduring weeks of painful and futile physical therapy, I continue to suffer with nearly every symptom that I've ever heard mentioned in conjunction with Lyme disease. Even though my father was diagnosed with Lyme very recently (showing antibodies) and I was hospitalized with fever, severe joint pain, muscle pain and stiffness, symptoms very similar to those that he was suffering (we live on the same Ohio farm and were therefore subject to the same ticks) my bone and joint physician insists that I am suffering from Polymyositis and refused to test for Lyme. This diagnosis was a change from his initial finding that I was suffering from Osteoarthritis and his second diagnosis which was Fibromyalgia and Chronic Fatigue as well as another diagnosis of Polymyalgia Rhuematica given during my recent ER visit. I have for a time been uninsured which has hampered my pursuit of a proper diagnosis and cure. My current symptoms have expanded to include wild heart palpitations, head and neck pain and dramatic loss of muscle tissue and strength. I feel like I'm dying and at times wish that I could. But there is no profit in curing me, so I suppose I will just take my prednisone like a good little patient, even though it has become increasingly less effective. I will simply I ignore my unmanaged pain, as no doctor in my area has the courage to address that issue (and it is really "all in my head" anyway). Eventually my heart will stop during one of my quite possibly prednisone induced palpitations and I will no doubt be listed as just another cardiac related death. Meanwhile the pharmaceutical companies and their unwitting (or not) cronies in the "Medical" profession can propagate their bread and butter, which is symptom treatment rather than cure. At least until some smart Lyme sufferer or their bereaved family finally realizes that they should have been seeking a good attorney rather than a good doctor, because health care in America is all about profit, not good health.
Thank you for the thank you. I only wish I did it sooner...it was so overdue, so needed. I salute the people who long for the truth, need the truth and seek the truth. And especially those like Dr. MacDonald who has dedicated his career AND retirement to correcting the UNtruths with facts based on science!
alan, a heartfelt thank you for doing the series of lyme/vb series of videos and to richard for videotaping this all. we are so appreciative. great room for this where it isn't distracting for those of having glare, lights, and reflection problems of background. etc. a special thanks for telling us the subject areas to be discussed; i've been copying/pasting all of this info with the links to the lyme board where i'm on. alan and wife, here's to continued good health ;) bettyg, iowa
Thank you so much Doctor! You are blessing to an ignorant medical community.Thank you for your extraordinary work, for the bravery to say the Truth about this global problem. Neverless, there is no cure out there yet, but it gives me a hope to have my life back one day. Best regards,Ruta
@15:30 - YOU ARE DAMM RIGHT, DR!.. YOU ARE DAMM RIGHT.. Everything I read on diagnosing symptoms on my own an hour ago led to the exact same conclusions. These ass clowns in white lab coats are just as fallible as the rest of us. They need to continue learning and educating themselves because the are playing strong and wrong, and then missing the proper diagnosis that ends up leaving the patient untreated, or they end up dying for lack of due care.
Thank you for sharing this valuable knowledge with us! I hope he does study those electro-magnetic frequencies as a possible treatment for Borreliosis.
Just AWESOME! Thanks to all who spent time putting these three videos together. For Dr MacDonald's honesty and easy for a layperson to understand presentation. I just got a LOW CD8-CD57 after years of being sick and getting worse with time (more systems affected, loss of 20 yr technical career due to inability to function consistently). Told for years by Drs that people in IL dont get Lyme so no testing. Last year had ELISA test Neg, did not know and apparently neither did Dr its not good test
Dr MacDonald is such a brilliant Physician and researcher,...I had only watched part one some months back,...today watched 2 and 3...such an amazing amount of info. I too think Lyme is a "lame" name to call this infection...Borreliosis sounds like a medical condition, much more so than Lyme Disease. I had no idea the EM could present with so many variations, either. Mine of about 4 or 5 years ago was like a red/blue bruise , large, ovoid..back of knee, as tho punched there, an injury. The tick was not found embedded altho a highly engorged one was found on the floor, I assumed it fell off the cat, later I realized it may have fallen off me:-( the rash followed finding that tick on the floor. CDC map for California should have a much BLACKER look,...we are endemic, here. I just think it is highly under-diagnosed, therefore under-reported. My exposure #1 ( and likely infection, numerous symptoms) came at age 5 or 6 in deer country, high grass and creek of Shasta County . I consider myself a lifer in remission, somewhat. The EM of 2010 unfolded with 5 years of symptoms but as a poor person I have not sought treatment, and one by one most issues waxed and waned. But I'm not well. Heart and eye issues scare me. I could actually feel the bacteria reach certain parts of me knee involvement first and pronounced, both knees; felt "it" pass a lymph node at top of leg, reach my bladder, travel round my lungs. scary! many many symptoms. Also heartening to hear Dr MacDonald talk about treatment failing a patient. I believe my Mom was also a life long Borrelia sufferer, and she was prescribed oral steroids for chronic COPD cough in her early eighties , the treatment just about killed her, TWICE. 2 trips to ER in a true comatose state, revived by more of the same blasted drug which I later learned should never be given to a patient with Lyme. because it can cause death. Sadly my own laypersons research into Borrelia came to late to relate to her, but made all her health issues make sense to me, due to the high levels of outdoor exposure in certain geological areas of CA and OR, BOTH parents were highly exposed, lifelong from early childhood or WOMB, to ticks, and tick bite, just like me. I would LOVE to sit down and talk with Dr M,..it would be lopsided, because I'm just a lay person, but I have hatched theories based on much reading of my own. My final thought about it: Tick disease is "total complexity", and the science of it is really is in it's infancy, understanding of it and proper treatment. I suffered recurrent tonsillitis as a child following the known tick bite, and probably was given Penicillin, rounds and rounds,for years.... I recently read Penicillin can cause Borrelia to become a resistant bacteria, nice, huh? Oddly the tonsil trouble went away in my early teens..I experimented and started smoking cigarettes... the poisons in the tobacco, nicotine...perhaps chased the bug right out of my lymph glands/throat, because the tonsilitis STOPPED. I wondered why it just went away like that, my whole life. perhaps the native Americans were self treating with tobacco and sweat lodges. Sadly, I've been re-innoculated numerous times over 50+ years. Has the tiny tick affected my family? yes, both sides all the way back to Germany, Scotland, circa the 1700s all family being farmers, and exposed to the good earth and the not so good lowly tick.
What a pity this wonderful man is retired. What I wouldn't give to talk to him awhile. He literally said everything I've been trying for three years for my doctor to hear. She won't treat me I have been covered with lesions for 3 years and much biofilm. I'm going to die and no one cares. My quality of life is zero.
I agree with everything you say sir...but the quality of what is required for a physician regarding CME is no longer adequate. When you have a 3x board certified Emergency Medicine physician who has worked in a level I trauma center for 24 years needing to "Pump on Annie's Chest" as a requirement to retain hospital privileges, CME is not working as it was intended.
I salute you dear sir and would love to hug your neck. I have two different kinds of Spirochetes. One causing Lyme and the other Morgellons. As well bartnella. On top of that mycoplasma and the Epstein Barr virus. I was infected with all of those on the same day working in my yard. I wasn't bit by a tick. Although I was by mites. The hell I've been through this last year and half has truly been just that, HELL. Mostly due to all the so called doctors I've seen. It took a natural path to identify all those. I was failed by the medical industry. label delusional and laughed at. If only those doctors put in a quarter of your care and effort I wouldn't be still suffering and dieing today. I thank you for all of us out here. May GOD bless u for ur work.
sorry to hear this kristy.please never give up.alternative medicine is vital I believe in fighting this .am looking at shungite on behalf of someone dear to me with lyme and co infections. perhaps its worth a shot,plenty usa sights sell same. bless you.
@@dubinatub1 thank you. I'm trying not to give up. I also have Lyme titters but u know how that goes. With a few co infections. The Morgellons is what seems to be the hardest to keep under control. Now everyone around me is coming down with this evil mess. And none of us have been bitten by a tick.
doc, i live in ct, 35 minutes from lyme, suffering for over 9 years, and i can't find a good doctor within 150 miles of here!!! Hell many don't even believe in lyme disease, been on iv antibiotics, done revolving antibiotics, etc... many different types and times and am still suffering. If you or anyone can give me some new suggestions and realistic affordable suggestions to getting treatment and help i would gladly listen!!!! Thank you though for this very informative video and please continue to fight for us!!!!
Scoot Caseau Might want to private message that user who is seeking a doctor and remove this comment with the doctor's name. It's generally unsafe for ILADS-certified LLMDs to have their names made public due to lawsuits.
Is there a diagnosis code for Borelliosis? I love his reco to stop calling it Lyme so patients not discriminated due to medical politics. I am just starting to educate myself about this disease and this was the best start.
ok when you have tested positive twice now.....now what? I got two weeks of antibiotics.... I have been denied life insurance and have a form stating Lyme is the preexisting condition as the reason, yet I dont have it.
2 weeks of Doxycycline will not kill Lyme bacteria which has a 4 week life cycle! Can only kill it during the growth phase, and so treatment must bracket multiple life cycles.. Hoping you have sought treatment by an ILADS TRAINED LYME LITERATE MD BY NOW!!!!!!!!!!!!!!!!!!!!!
This man is such a gift to humanity
PLEASE dr MacDonald...come to the UK and educate our doctors and government!
He truly cares! You hear it in his voice!
Thank you for this!
ms hopeful if he cares so much why doesn’t he study bio chemistry intercellular elation, and use herbs and nature healing , to cure , not just to treat , also we shouldn’t eat beef, Europeans laugh at all these diseases
What a clever man. Sir, I award you my Nobel prize ! Amazing talk.
These videos have so much information that we aren't told when we get diagnosed. Priceless. Thank you.
Thanks so much. Let me know if you need help. :)
@@ADRSupport I am trying to reach Dr. MacDonald. Do you have an email contact? I am the Admin of GBM Brain Cancer Survivors to Thrivers support group. My Mom got brain cancer from Lyme, Babesia and EBV. She is an almost 4 year Survivor from treating parasites!! I have been trying to contact him as many many people with brain tumors have a history of Lyme and co infections. If you could please let me know how I can reach him? Thank you so much!!
@@ADRSupport katiebzorena@gmail.com
@@katiebrookzorena3643 I wasn't able to find any information for how to reach Dr. MacDonald. My doctors thought I had MS. I had Chronic Lyme Meningitis and treated with with Ivermectin. It worked and my short term memory is getting better. No more spinal pain, neck pain or headaches. My fluctuating body temp has gone back to normal. I know someone who has been battling cancer, he's taking Ivermectin also as well as only eating whole food, nothing with sugar or refined carbs. He's getting better.
Thank you implicitly for all you do Dr Alan MacDonald a true hero and pioneer 💚
Thank you for your work and wonderful lectures, Dr. MacDonald.
God Bless you, Dr. MacDonald
wishing you all the best from Ireland.
These three video's are by far the most informative video's on Lyme Disease to date, Dr. Alan MacDonald Thank You !! You are most awesome for helping us...
I have suffered, undiagnosed with what I have continually believed is Lyme disease, for nearly ten years now. My initial physician mistook me for a drug seeker who was using my "unproven" joint and muscle issues to get pain meds, which was unfortunately a prevalent issue in my southern Ohio community. (though I am a non-smoking, non-drinking, Christian individual who did, through blood tests, prove negative for drug use)
This injustice occurred despite the fact that I had seen the physician previously in regard to a telltale bullseye rash which developed after I had removed a deeply embedded deer tick and was suffering with night sweats. This physician told me that "Lyme's Disease" (his pronunciation proving his Lyme Illiteracy) did not occur in Ohio and because I had not traveled out of state, it was impossible that I had contracted "Lyme's".
I continued untested for sometime, my condition worsening, before I finally bullied the Dr. into testing for Lyme. Unfortunately, I showed no antibodies which only emboldened the Dr.'s suspicion that I was merely seeking pain meds, stating at one point that "guys like you might not be users but they are selling their meds to their drug addicted buddies". At that point I requested a different doctor at our (company) clinic who also insisted that I was not infected but did eventually prescribe a 21 day course of doxycycline. Little did I know (nor did my Dr. evidently) that after such a long Lyme infection that this treatment would be insufficient.
Now after years of doctoring with a myriad of physicians including Rheumatologists, Internal Medicine Specialists, Infectious Disease Specialists, as well as enduring weeks of painful and futile physical therapy, I continue to suffer with nearly every symptom that I've ever heard mentioned in conjunction with Lyme disease. Even though my father was diagnosed with Lyme very recently (showing antibodies) and I was hospitalized with fever, severe joint pain, muscle pain and stiffness, symptoms very similar to those that he was suffering (we live on the same Ohio farm and were therefore subject to the same ticks) my bone and joint physician insists that I am suffering from Polymyositis and refused to test for Lyme. This diagnosis was a change from his initial finding that I was suffering from Osteoarthritis and his second diagnosis which was Fibromyalgia and Chronic Fatigue as well as another diagnosis of Polymyalgia Rhuematica given during my recent ER visit.
I have for a time been uninsured which has hampered my pursuit of a proper diagnosis and cure. My current symptoms have expanded to include wild heart palpitations, head and neck pain and dramatic loss of muscle tissue and strength. I feel like I'm dying and at times wish that I could.
But there is no profit in curing me, so I suppose I will just take my prednisone like a good little patient, even though it has become increasingly less effective. I will simply I ignore my unmanaged pain, as no doctor in my area has the courage to address that issue (and it is really "all in my head" anyway). Eventually my heart will stop during one of my quite possibly prednisone induced palpitations and I will no doubt be listed as just another cardiac related death. Meanwhile the pharmaceutical companies and their unwitting (or not) cronies in the "Medical" profession can propagate their bread and butter, which is symptom treatment rather than cure. At least until some smart Lyme sufferer or their bereaved family finally realizes that they should have been seeking a good attorney rather than a good doctor, because health care in America is all about profit, not good health.
Thank you for the thank you. I only wish I did it sooner...it was so overdue, so needed. I salute the people who long for the truth, need the truth and seek the truth. And especially those like Dr. MacDonald who has dedicated his career AND retirement to correcting the UNtruths with facts based on science!
Dr. MacDonald, thank you very much for and ADR Support for this series of videos.
alan, a heartfelt thank you for doing the series of lyme/vb series of videos and to richard for videotaping this all. we are so appreciative.
great room for this where it isn't distracting for those of having glare, lights, and reflection problems of background. etc.
a special thanks for telling us the subject areas to be discussed; i've been copying/pasting all of this info with the links to the lyme board where i'm on.
alan and wife, here's to continued good health ;)
bettyg, iowa
Thank you so much Doctor! You are blessing to an ignorant medical community.Thank you for your extraordinary work, for the bravery to say the Truth about this global problem. Neverless, there is no cure out there yet, but it gives me a hope to have my life back one day. Best regards,Ruta
Wow - what a lucid and comprehensive explanation. Thank you so much for this!
Thank you so much. May God bless you with health for a long and productive life. Thank you for your service.
@15:30 - YOU ARE DAMM RIGHT, DR!.. YOU ARE DAMM RIGHT.. Everything I read on diagnosing symptoms on my own an hour ago led to the exact same conclusions. These ass clowns in white lab coats are just as fallible as the rest of us. They need to continue learning and educating themselves because the are playing strong and wrong, and then missing the proper diagnosis that ends up leaving the patient untreated, or they end up dying for lack of due care.
Thank you for sharing this valuable knowledge with us! I hope he does study those electro-magnetic frequencies as a possible treatment for Borreliosis.
Bless you, Dr.MacDonald
Thank You Doctor McDonald I Love You !!!
awesome series... so glad I spend the time to watch!!! NJ Bow Hunter
This Doctor gives the best overview I've heard in years. Concerning Borreliosis...Lack of proof is not proof of absence!
Just AWESOME! Thanks to all who spent time putting these three videos together. For Dr MacDonald's honesty and easy for a layperson to understand presentation. I just got a LOW CD8-CD57 after years of being sick and getting worse with time (more systems affected, loss of 20 yr technical career due to inability to function consistently). Told for years by Drs that people in IL dont get Lyme so no testing. Last year had ELISA test Neg, did not know and apparently neither did Dr its not good test
Could you tell me the name of the scientist working on the electromagnetic technique to bust biofilms? Does he have a paper you could point me to?
Thank you! A wonderful series and a wealth of information.
Read LAB 257 Google it is in PDF format. Be ready for the shock
On Lyme.
We were under the 3rd Reich probably before Project Paperclip. I don't think anyone can even question that now.
Dr MacDonald is such a brilliant Physician and researcher,...I had only watched part one some months back,...today watched 2 and 3...such an amazing amount of info. I too think Lyme is a "lame" name to call this infection...Borreliosis sounds like a medical condition, much more so than Lyme Disease. I had no idea the EM could present with so many variations, either. Mine of about 4 or 5 years ago was like a red/blue bruise , large, ovoid..back of knee, as tho punched there, an injury. The tick was not found embedded altho a highly engorged one was found on the floor, I assumed it fell off the cat, later I realized it may have fallen off me:-( the rash followed finding that tick on the floor. CDC map for California should have a much BLACKER look,...we are endemic, here. I just think it is highly under-diagnosed, therefore under-reported. My exposure #1 ( and likely infection, numerous symptoms) came at age 5 or 6 in deer country, high grass and creek of Shasta County . I consider myself a lifer in remission, somewhat. The EM of 2010 unfolded with 5 years of symptoms but as a poor person I have not sought treatment, and one by one most issues waxed and waned. But I'm not well. Heart and eye issues scare me. I could actually feel the bacteria reach certain parts of me knee involvement first and pronounced, both knees; felt "it" pass a lymph node at top of leg, reach my bladder, travel round my lungs. scary! many many symptoms. Also heartening to hear Dr MacDonald talk about treatment failing a patient. I believe my Mom was also a life long Borrelia sufferer, and she was prescribed oral steroids for chronic COPD cough in her early eighties , the treatment just about killed her, TWICE. 2 trips to ER in a true comatose state, revived by more of the same blasted drug which I later learned should never be given to a patient with Lyme. because it can cause death. Sadly my own laypersons research into Borrelia came to late to relate to her, but made all her health issues make sense to me, due to the high levels of outdoor exposure in certain geological areas of CA and OR, BOTH parents were highly exposed, lifelong from early childhood or WOMB, to ticks, and tick bite, just like me. I would LOVE to sit down and talk with Dr M,..it would be lopsided, because I'm just a lay person, but I have hatched theories based on much reading of my own. My final thought about it: Tick disease is "total complexity", and the science of it is really is in it's infancy, understanding of it and proper treatment. I suffered recurrent tonsillitis as a child following the known tick bite, and probably was given Penicillin, rounds and rounds,for years.... I recently read Penicillin can cause Borrelia to become a resistant bacteria, nice, huh? Oddly the tonsil trouble went away in my early teens..I experimented and started smoking cigarettes... the poisons in the tobacco, nicotine...perhaps chased the bug right out of my lymph glands/throat, because the tonsilitis STOPPED. I wondered why it just went away like that, my whole life. perhaps the native Americans were self treating with tobacco and sweat lodges. Sadly, I've been re-innoculated numerous times over 50+ years. Has the tiny tick affected my family? yes, both sides all the way back to Germany, Scotland, circa the 1700s all family being farmers, and exposed to the good earth and the not so good lowly tick.
The master speaks!
Thank you SO MUCH.
Fascinating, thank you so much. Thanks also for the excuse to head back to Norway!
Norway is not safe.
Thank you for this informative video series!
What a pity this wonderful man is retired. What I wouldn't give to talk to him awhile. He literally said everything I've been trying for three years for my doctor to hear. She won't treat me I have been covered with lesions for 3 years and much biofilm. I'm going to die and no one cares. My quality of life is zero.
Debbie Wilson. He went to UK to do research I think?
Thank you.
I agree with everything you say sir...but the quality of what is required for a physician regarding CME is no longer adequate. When you have a 3x board certified Emergency Medicine physician who has worked in a level I trauma center for 24 years needing to "Pump on Annie's Chest" as a requirement to retain hospital privileges, CME is not working as it was intended.
Again thanks so much
I salute you dear sir and would love to hug your neck. I have two different kinds of Spirochetes. One causing Lyme and the other Morgellons. As well bartnella. On top of that mycoplasma and the Epstein Barr virus. I was infected with all of those on the same day working in my yard. I wasn't bit by a tick. Although I was by mites. The hell I've been through this last year and half has truly been just that, HELL. Mostly due to all the so called doctors I've seen. It took a natural path to identify all those. I was failed by the medical industry. label delusional and laughed at. If only those doctors put in a quarter of your care and effort I wouldn't be still suffering and dieing today. I thank you for all of us out here. May GOD bless u for ur work.
sorry to hear this kristy.please never give up.alternative medicine is vital I believe in fighting this .am looking at shungite on behalf of someone dear to me with lyme and co infections.
perhaps its worth a shot,plenty usa sights sell same.
bless you.
@@dubinatub1 thank you. I'm trying not to give up. I also have Lyme titters but u know how that goes. With a few co infections. The Morgellons is what seems to be the hardest to keep under control. Now everyone around me is coming down with this evil mess. And none of us have been bitten by a tick.
@@KristyW72 evil is right.blessings to you.
@@dubinatub1 thank you Sweetheart. U aswell, GOD bless.
doc, i live in ct, 35 minutes from lyme, suffering for over 9 years, and i can't find a good doctor within 150 miles of here!!! Hell many don't even believe in lyme disease, been on iv antibiotics, done revolving antibiotics, etc... many different types and times and am still suffering. If you or anyone can give me some new suggestions and realistic affordable suggestions to getting treatment and help i would gladly listen!!!! Thank you though for this very informative video and please continue to fight for us!!!!
Scoot Caseau
Might want to private message that user who is seeking a doctor and remove this comment with the doctor's name. It's generally unsafe for ILADS-certified LLMDs to have their names made public due to lawsuits.
www.ilads.org/patient-care/provider-search/
www.ilads.org/patient-care/provider-search/
Is there a diagnosis code for Borelliosis? I love his reco to stop calling it Lyme so patients not discriminated due to medical politics. I am just starting to educate myself about this disease and this was the best start.
Can LYme (borellasis ) be transmitted by body fluid, I will assume yes since it can be pass onto the children from the Mother.
What a brilliant idea the application of FREQUENCY? And it could be generated by HUMAN itself who has reached a state of Consciouseness.
Does anyone have with a swollen tongue with Chronic Lyme? I need to know.
Medical treatment is one of the leading causes of death. Thank you Dr. MacDonald for your honesty.
ok when you have tested positive twice now.....now what? I got two weeks of antibiotics....
I have been denied life insurance and have a form stating Lyme is the preexisting condition as the reason, yet I dont have it.
what has happened since then?
2 weeks of Doxycycline will not kill Lyme bacteria which has a 4 week life cycle! Can only kill it during the growth phase, and so treatment must bracket multiple life cycles.. Hoping you have sought treatment by an ILADS TRAINED LYME LITERATE MD BY NOW!!!!!!!!!!!!!!!!!!!!!
What test(s) should be taken to test for Lyme?
What is the treatment to rid/control Lyme?
Igenex.com
Yo where are this smart docs when u need them
He means well perhaps, and yes I've learned a bit here. But the solutions are still lacking
He is a pathologist not a treating dr
Rox600601 asked is there a diagnosis code for Lyme d. YES THERE SURE IS 088.81.
💯❤
Need to call it MickeyDees Disease....