NEWS FLASH: If you missed the award winning film on the Lyme Controversy called "Under Our Skin" on PBS, you can now see it for free on Hulu HERE: huluDOTcom/watch/268761/under-our-skin
ANYONE who SUSPECTS they may have Lyme should watch this!
The Lyme spirochete looks similar to the SYPHILLIS bacteria and needs to be treated with LONG TERM IV antibiotics for relief - most in the medical profession do NOT know this!
Please be aware of suddenly coming down with a fever or flu like symptoms in the middle of summer. Followed by loss of short term memory (phone numbers, names etc). Followed by loss of breath by walking up a simple flight of stairs. And alcohol intolerance (used to be able to have 4-6 drinks but now get drunk from 1) Most people don't remember a rash or bulls-eyes so I always refer them to tangible symptoms.
This so sucks. I'm pretty sure like 99% that this is what I have. It's so frustrating. My NP is the only one who seems to care... And that's only because she knew me before I got so sick. I've just started the doxycycline and it seems to be helping. Not sure if I can convince her to give me more if one round doesn't "cure" it. I'm 39 and applying for disability. I was studying for my BScN with a 3.65 GPA. Now I'll probably not remember I posted this in the morning. God help us all. -3
I searched over the internet for people who managed to get rid of lyme disease but I still haven't found any case which worries me. everyone is sick but nobody is cured? what happens with people suffering from lyme disease? why they don't write testimonials about their curing?
Thank you for this video. VERY informative and in an "easy to read" format for people who don't understand Lyme. I suffer greatly from Chronic Lyme. I went from the most vibrant person anyone knew, to basically bedridden most of the time. I trained horses and gave lessons and worked 16 hrs a day farm labor.... now I lay here in a dark room, heartbroken that even the sound of my children laughing kills my ears due to the increased sensitivity. LYME KILLS. Spread the word!!
I am 15 and lyme disease has basically destroyed my life. I created Lyme Teens, a social network for teens with lyme to connect. Here is a link to anyone who may be interested.. lymeteens.socialgo.com/
I am 15 and struggle with late stage chronic lyme disease. I created a social network for teens with lyme so they could connect and give support. Hope to see you there! lymeteens.socialgo.com
Never had a rash....was given the initial 200 mg dose of doxy and few days later felt crappy, tick tested positive and now i'm a wreck......it's been a month now and hopeing that's still early....i'm ready to go to a mental ward....i was crying half the day......would appreciate any positive stories with people who have this and are ok
I just had a live blood analysis and saw the Lyme bacteria for myself, swimming around happily. There were at least two of them in a tiny drop of blood - now that I've had cancer and numerous tumors, the pieces are coming together. And so many doctors have all missed it regardless of hundreds of tests... just - wow.
High fatty lamb, beef dripping diet, no carbs apart from veggies, forget sugar and junk food. Fruit diet will murder you if your a lyme patient. Eat the fattiest meat available, (no constipation), read Gary taubes book, Rob Wolf, this diet will not kill you. See famously fit dot com. I am 16months into lymes, and if you want to get up and work, protect your NS & brain have LOADS of saturated fat, no veggie oil. No dairy. Only grass fed animals. I have had no antibiotics, doin it alone! luv U
thank you ! this will help explain what I've endured while I am on my way to full recovery and survivorship after 38 years of mis-diagnosis...before it was even named in 1975, I was bit boy scout camping in 1972
PLEASE PLEASE PLEASE do internet research on using SEA SALT for curing Lyme. I had it for seven months before I was diagnosed, and doxycycline only made me sicker. I took a shot of about 1/2 teaspoon of RAW SEA SALT in a small amount of water, and in only hours I felt better than I had in months! I continued this maybe three times a day for several days and it ended my Lyme. I take this "shot" every now and then just to be sure it stays gone. IT WORKS. DO RESEARCH. TELL THE PEOPLE!!
I have had it for 3 years, had a PICC-LINE for 8 months, allergic reaction for 8 months, school said I was truant, it's 3:18 right now because I can't sleep, I wake up a 12 o' clock, I haven't been to school in years, I'm on 20+ vitamins/anti-biotics a day... yeah you guys are lucky =/
I am going on 2 years battling this disease. No one understands how I feel. Thank you for posting this video. I am going to a little chapel near my house to pray. Currently I am doing a special diet called The Fat Resistance Diet for anti-inflammation and overall immune building through whole, organic foods. Plus I am on Amoxicillin and will be adding Flagyl. Does anyone know about Clindamycin. Don't give up on yourselves. Fight!
I was just told by my doctor that I have LD. Luckily, I think I have only had it for a month or two but my symptoms are still very bad. My friends do not understand how bad it is and therefore I am receiving barely any sympathy. I am awaiting the results of a second test on LD. Wish me luck.
I have been untreated for 24 years, only properly diagnosed in July this year. Both my children I passed it to congenitally. I never had the Lyme rash. However my oldest daughter has THREE times. It does not always appear in connection with a bite. We need to stay strong and raise out voices. Here in the Uk we are such a small country the word is getting our more slowly. Thankyou for videos like this that help raise awareness.
I took doxycycline for acute Lyme and am increasingly debilitated almost 7 years later. Have experienced parasthesias, stiff neck, vertigo, seizures, convulsions, joint pain, diplopia (double vision), blurry vision, heart inflammation, increased intracranial pressure, etc....I think they should offer amoxicillin for acute Lyme disease instead of doxycycline. Leading Lyme researcher Sam Donta states amoxicillin is equally efficacious as doxycycline for Lyme disease.
Thank you for the video. It portrayed everything I've been through. This is my 29th year of LD, the first 10 untreated. I'll share this with the many people who still don't understand LD.
Dr. Jeff Sutherland of 'The Frequency Foundation' has some very interesting recent research articles on Lymes disease. If you see photos of some microscopic kinds, maybe we can understand why it feels like peices of GLASS in the brain or joints, etc. at times??? My health protocols has involved 'The Hart Dietary Procedure Plan' which has U.S. Patent, and frequency work, etc. Thank you for the video, & stimulus to more research, & greater awareness on this topic.
The movie has brought much needed awareness, however, why don't you post a list of petitions,a list of political representatives that we can contact. Put the links on your page; this will make it easier for those w ho barely have the energy to move. Please
People, "Chemtrails," are killing the biological nutrients, supporting all plant life. What do you think that is doing to our immune systems, and that of bees? I have saved a sample of snow, from a storm in late December, that left my hair sticky and gluey feeling. I showered if out immediately. Does anyone know where I can get it tested? In need of one who is trustworthy.
I read a book years ago, called "Sugar Blues" by William Dufty. An absolute read. He states that during the Bubonic Plague, the rich who could afford sugars, were dropping like flies, the poor country folk who could not, faired well.
Google....."Low Dose Naltrexone Homepage." And also here on You tube..."Controlling Lyme Disease," and see the LDN videos by "TropicalDawg" here as well. I have been using LDN, for just over a week now, and feel the need to pass the buzz. This is a drug that helps with the immune system, inflammation and endorphins. Eat as if you had a yeast problem, because Lyme loves what yeast loves. And no sugars of any kind..."Including Fruit!"
this is an amazing video. THis was done by my best friend and her son, two of the sweetest people you could ever know. As sick as they are, they are still trying to educate and fight for our rights. God bless them. Please take this disease from all of us who suffer so terribly. I know things happen for a reason, and I do believe God WILL heal us. We have lost a very dear friend from this disease, it does kill. We need to make our voices heard NOW! Before we loose more wonderful people.
This has to be one of the best lyme disease videos I've even seen. It's so hard for people who don't have lyme to understand what it's like, but hopefully with enough exposure they will get the idea. It takes over everything. It's just such a debilitating and awful disease. Thank you so much for posting this video!
For those of you who think you have lyme - join a lyme support forum, they show one at the end of this video, there are many online. Patients can tell you how and where to see a Lyme literate Md and get checked through Igenex Tick Borne Specialty lab. Lyme disease is the fastest growing infectious disease in the U.S. and has surpassed AIDS by far - ticks live in your yard and are the size of a poppy seed. Get to a forum and talk w/the experts - the lyme patients. Great video covers it all.
Look online for ILADS and look for an LLMD (Lyme Literate Dr) because most mainstream conventional Drs use inaccurate tests and follow very outdated and bad guidelines when it comes to diagnosis and treatment of this. Don't go to any Dr who follows standard government or IDSA guidelines on treating this. Treatment for chronic lyme has to last for months or years not weeks.
Gainesville Florida"Home of the fighting gators. Shands @ U.F!
My son has Lyme and co-infections! I had to search the internet to get help for my child. Lost BCBS Have only MEDICAID! We were flown to CT by Angel FLight! What an experince for my child the hard way, to have to travel to another state becuase his Doctors would not help him! To be told he is faking or it's the parents fault because of DIVORICE! That's why he is in pain!It's stress!The mother is crazy! Yes! Crazy about my kids!
"PLEASE DON'T FEED THE TICKS": I was a long distance hiker but contracted Lyme disease. ER doc diagnosed 2002 (tick bite/EM rash). Positive serology. ER doc confirmed diagnosis 2007. Wikipedia Lyme page emphasizes 'no chronic Lyme' yet describes disseminated Borrelia/late stage Lyme (?!).
See my personal profile here for more about IDSA conflict of interest, etc.
Whitney, thanks for your post. You don't know what it means to us to know that this video helped someone to find the answer, this was our main hope..thank you. May you be well soon sweetie..take care.
If it wasnt for the internet that lead me to lymes disease i would still be seeing doctors that were no help, they always say "that im crazy, i have no pain it is just in my head" After seeing over 25 doctors, my family and i finally started searching for an answer to all my pain. i have had lymes disease since i was 5(now 14). This video is my life, it is the one i first discored about lymes, and that lead me into reading more about lymes
If it wasnt for the internet that lead me to lymes disease i would still be seeing doctors that were no help, they always say "that im crazy, i have no pain it is just in my head" After seeing over 25 doctors, my family and i finally started searching for an answer to all my pain. i have had lymes disease since i was 5(now 14). This video is my life, it is the one i first discored about lymes, and that lead me into reading more about lymes
This is the best video I have seen yet over Lyme, people now know what it is really like for us and I hope they understand and accept the way we are, big hugs.
Without the internet & self-diagnosis 6 people in my family would all be suffering still. I had an MD yell at me to stop reading the internet and let him be the doctor! Had I not been persistent in finding out what was wrong with me & listened to him I doubt I'd be here today. My Lyme doctor told me that in medical school they are not taught about Ld. So, if any Md's read this, search lyme forums, see how we suffer, contact Turn the Corner Foundation & ILADS (dot org) - get educated!
We suffer while doctors who are not lyme literate decide the CDC has all the answers. There are thousands of us who are suffering because doctors refuse to listen, learn,& see us who we are. We are human beings who are sick & deserve quality and empathtic care in the USA. There are over 100 symptoms. I have atleast 40 & was misdiagnosed for almost 3 years after seeing 20 doctors. We are crying out for help and not only have to fight the medical community but the disease too. God help us.
I hate lymes disease. I got it when i was 9 and it really messed me up good. I am 15 now i used to be able to run and run and do all kinds of stuff...
I have awfull pain every day cause of doctors who didnt give a damn!
I would no like to thank the tons of doctors ive seen by saying "YOU SUCK ASS"
and i mean that with every ounce of my self i have
i had a good life lyme disease really ruined it...
These doctors in Kentucky are just as lyme illiterate as any others, they don't believe you can get lyme disease in this state period!!! I was told this over & over even though I had the tick and the rash at the beginning of the symptoms. I'm really ticked off at some of these doctors for some of their arrogant and smart mouth remarks and I will never forget how they treated me for many misdiagnosed diseases, now that I've found a product that works I'm hoping get rid of it. NO LYME DR'S IN KY.
Thank you for your comments and ratings. LymeliterateRN I myself learned doctor's were wrong the hard way. It is an epidemic in EVERY state. Here in Calif Md's think of this as an East Coast Disease. There are so many here misdiagnosed I am sure! Jramsboy, my son is your age and has had to put off college due to LD treatment. No matter how old or young we are Lyme is a life thief, I am glad you are doing better. What seems impossible you have proven is possible, wellness! Wellness to all, TALD
Thank you. There are too many of us to be ignored any longer.
I'm a Lyme pt who saw 40+ drs over 6 yrs despite a classic onset of this illness. I'm an RN & trusted that drs were right when they insisted "we don't have Lyme in WA." WRONG. It's in every state & it's epidemic.
Their ignorance has cost me any semblance of a normal life. I could have been cured; many could have been cured. Instead we're suffering with a dz marred in controversy.
Please go to our website shown at the end of the video for literally every subject about lyme disease. It is all educational, click on stories, resources and forum and at the board index are nearly 90 articles regarding LD. We also have a lyme disease forum with educated lyme patients available to help answer any question you may have.
your not alone. i lost the best 4 years of my childhood to Lyme. throughout my 4 years of highschool i was so sick and tired all the time i would miss over 30 total days of school each year. junior year i was homebound for 6 months. i was an athlete my whole life up to 14. but during highschool i had to watch from the stands as the best years of my life ran by me. im 19 better now. at community college from missing so much school. i dream i getter better so i can join the Marines after college.
I have now forwarded this video to many people. I have been told a mother & son w/Lyme made this video? Amazing so professional. Thanks for educating people and I hope you are both well soon. God bless.
Hi everyone, yes my son and I made the video. 6 members of our family have Lyme. (Yes California..we have lyme big time!) Thanks to all kind comments here. Our goal is to help educate our world, we are hoping this is one more way of doing that. We hope you will forward the link to family and friends and they will learn more about what you are suffering & hopefully it will help people that might have LD and not even know it. Blessings and wellness to all Lyme patients.
I have never seen a video so totally complete explain in less than 5 minutes about this sickening disease. I am sure I speak for all of us w/Lyme ...thank you..I will be sure to pass this on. Perfect song from Creed too.
GREAT video! I am a chronic Lyme patient, as are my husband, neighbors, colleagues, and many students (I'm a counselor). We're getting there! May-June Psychology today has a Lyme article and quotes ILADS docs and addresses the controversy. The political denial and complicituous medical community cannot last much longer! Glad my daughter let me use her youtube account to post!
I am not a physician but you do not have to have a perfect bulls-eye rash to have Lyme disease. In fact, you do not have to have a rash at all to have it. Send me your email and I will send you a very helpful brochure. One of the Lyme specialists that helped me with this brochure is world reknown.
Wrote a Lyme disease brochure with the help of 2 Lyme disease specialists. Will email a copy to anyone interested.
ecftube 3 months ago
NEWS FLASH: If you missed the award winning film on the Lyme Controversy called "Under Our Skin" on PBS, you can now see it for free on Hulu HERE: huluDOTcom/watch/268761/under-our-skin
ANYONE who SUSPECTS they may have Lyme should watch this!
The Lyme spirochete looks similar to the SYPHILLIS bacteria and needs to be treated with LONG TERM IV antibiotics for relief - most in the medical profession do NOT know this!
Good luck & God Bless!
MzProgressive 4 months ago
This disease and others can be stopped with Colloidal Silver Atoms! True atomic size particles of silver will kill any bioweapon
precicia 5 months ago
DON"T EVER GIVE UP, FIGHT FIGHT FIGHT, THE TIMES WHEN YOU FEEL ALONE FOLLOW THE LORD. FOR HE WILL BRING YOU THROUGH.
DaniellaMelton 5 months ago
Please be aware of suddenly coming down with a fever or flu like symptoms in the middle of summer. Followed by loss of short term memory (phone numbers, names etc). Followed by loss of breath by walking up a simple flight of stairs. And alcohol intolerance (used to be able to have 4-6 drinks but now get drunk from 1) Most people don't remember a rash or bulls-eyes so I always refer them to tangible symptoms.
adamclemens 5 months ago
This so sucks. I'm pretty sure like 99% that this is what I have. It's so frustrating. My NP is the only one who seems to care... And that's only because she knew me before I got so sick. I've just started the doxycycline and it seems to be helping. Not sure if I can convince her to give me more if one round doesn't "cure" it. I'm 39 and applying for disability. I was studying for my BScN with a 3.65 GPA. Now I'll probably not remember I posted this in the morning. God help us all. -3
MissKrisNails 6 months ago
I searched over the internet for people who managed to get rid of lyme disease but I still haven't found any case which worries me. everyone is sick but nobody is cured? what happens with people suffering from lyme disease? why they don't write testimonials about their curing?
numaiunaltblog 7 months ago
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I cured myself of a deadly case of Lyme and you can too. See kokopellisearth d o t c o m
braddgood 8 months ago
This has been flagged as spam show
read this article. hopefully it will raise some awareness about lyme.
you have copy and paste the url to go to the article
socialmedia10.dwight.edu/53151649#comment
RabidMelon 8 months ago
Thank you for this video. VERY informative and in an "easy to read" format for people who don't understand Lyme. I suffer greatly from Chronic Lyme. I went from the most vibrant person anyone knew, to basically bedridden most of the time. I trained horses and gave lessons and worked 16 hrs a day farm labor.... now I lay here in a dark room, heartbroken that even the sound of my children laughing kills my ears due to the increased sensitivity. LYME KILLS. Spread the word!!
WatchMeGoDown 8 months ago
I am 15 and lyme disease has basically destroyed my life. I created Lyme Teens, a social network for teens with lyme to connect. Here is a link to anyone who may be interested.. lymeteens.socialgo.com/
LymieAwareness 9 months ago
This has been flagged as spam show
I am 15 and struggle with late stage chronic lyme disease. I created a social network for teens with lyme so they could connect and give support. Hope to see you there! lymeteens.socialgo.com
LymieAwareness 9 months ago
Never had a rash....was given the initial 200 mg dose of doxy and few days later felt crappy, tick tested positive and now i'm a wreck......it's been a month now and hopeing that's still early....i'm ready to go to a mental ward....i was crying half the day......would appreciate any positive stories with people who have this and are ok
fugazipythons 1 year ago
I just had a live blood analysis and saw the Lyme bacteria for myself, swimming around happily. There were at least two of them in a tiny drop of blood - now that I've had cancer and numerous tumors, the pieces are coming together. And so many doctors have all missed it regardless of hundreds of tests... just - wow.
ExZonie 1 year ago
High fatty lamb, beef dripping diet, no carbs apart from veggies, forget sugar and junk food. Fruit diet will murder you if your a lyme patient. Eat the fattiest meat available, (no constipation), read Gary taubes book, Rob Wolf, this diet will not kill you. See famously fit dot com. I am 16months into lymes, and if you want to get up and work, protect your NS & brain have LOADS of saturated fat, no veggie oil. No dairy. Only grass fed animals. I have had no antibiotics, doin it alone! luv U
Catherine8raw 1 year ago
I was misdiagnosed 35 years ago and if i had not used the internet I would still be unaware
drcorina57 1 year ago
Misdiagnosis is HUGE in Arkansas!
Jburdo4680 1 year ago
this video is my life in a nutshell........wow.
colla16 1 year ago
this video is my life in a nutshell.
colla16 1 year ago
Awwwwwwesome! Thank you for sharing it.
babyboom58 1 year ago
thank you ! this will help explain what I've endured while I am on my way to full recovery and survivorship after 38 years of mis-diagnosis...before it was even named in 1975, I was bit boy scout camping in 1972
danlmt6 1 year ago
I dont know about other locations, but in Maine, black flies are also carriers of lyme disease.
klrathome 1 year ago
PLEASE PLEASE PLEASE do internet research on using SEA SALT for curing Lyme. I had it for seven months before I was diagnosed, and doxycycline only made me sicker. I took a shot of about 1/2 teaspoon of RAW SEA SALT in a small amount of water, and in only hours I felt better than I had in months! I continued this maybe three times a day for several days and it ended my Lyme. I take this "shot" every now and then just to be sure it stays gone. IT WORKS. DO RESEARCH. TELL THE PEOPLE!!
iLoveSydBarrett 1 year ago
The CDC is part of the government's coverup of this terrible disease.
It has stolen my life from me.
If I didn't have 3 children and a wife, I would give up and swim with the sharks (and I can't swim).
mikespikejones 1 year ago
I have had it for 3 years, had a PICC-LINE for 8 months, allergic reaction for 8 months, school said I was truant, it's 3:18 right now because I can't sleep, I wake up a 12 o' clock, I haven't been to school in years, I'm on 20+ vitamins/anti-biotics a day... yeah you guys are lucky =/
AkimboLizard 1 year ago
I am going on 2 years battling this disease. No one understands how I feel. Thank you for posting this video. I am going to a little chapel near my house to pray. Currently I am doing a special diet called The Fat Resistance Diet for anti-inflammation and overall immune building through whole, organic foods. Plus I am on Amoxicillin and will be adding Flagyl. Does anyone know about Clindamycin. Don't give up on yourselves. Fight!
Amos1010 2 years ago
I was just told by my doctor that I have LD. Luckily, I think I have only had it for a month or two but my symptoms are still very bad. My friends do not understand how bad it is and therefore I am receiving barely any sympathy. I am awaiting the results of a second test on LD. Wish me luck.
hangman9090 2 years ago
I was diagnosed two years ago. I now 13
redEQUALSgreen 2 years ago
same here, but for 3 years, I wasn't diagnosed until 6 months after the bite, I'm pretty sure I'm never gonna get better =p
AkimboLizard 1 year ago
I have been untreated for 24 years, only properly diagnosed in July this year. Both my children I passed it to congenitally. I never had the Lyme rash. However my oldest daughter has THREE times. It does not always appear in connection with a bite. We need to stay strong and raise out voices. Here in the Uk we are such a small country the word is getting our more slowly. Thankyou for videos like this that help raise awareness.
poppymoone 2 years ago 2
picc line since march w 4 diff abx,,,it;s hell
vandlent 2 years ago
Thanks for making this. Lyme is a horrid disease ! It destroys lives !
I am on Licc Pine 4 lyme
puppet show about lyme on my page
Cammster101 ..please comment and rate
thank U
Cammster101 2 years ago
Hi,
I was just published, proved chronic Lyme!!!!
I am trying my best , helping, want to do more.
i will start support group again, love you all, its the hardest battle, people do care, we are working 7 days a week.
LymeReality 2 years ago 3
Wrote a Lyme disease brochure with the help of 2 Lyme specialists. Will email to anyone interested.
ecftube 2 years ago 5
I am interested in you e-mailing the Lyme brochure! Had it for 35 yrs. IV's not enough. On Doxycycline 3 mos. 10 more to go.
txsherrie 2 years ago
@txsherrie im so happy to here there are people goiong throigh the sme stuff im not CRAZY
DnRsledparts 1 year ago
@DnRsledparts YOu aren't crazy & you are not alone!
babyboom58 1 year ago
@ecftube please email me what you have. thanks terrystreehouse@yahoo.com
terrystreehouse13 1 year ago
This has been flagged as spam show
I took doxycycline for acute Lyme and am increasingly debilitated almost 7 years later. Have experienced parasthesias, stiff neck, vertigo, seizures, convulsions, joint pain, diplopia (double vision), blurry vision, heart inflammation, increased intracranial pressure, etc....I think they should offer amoxicillin for acute Lyme disease instead of doxycycline. Leading Lyme researcher Sam Donta states amoxicillin is equally efficacious as doxycycline for Lyme disease.
Azorka82 2 years ago
Thank you for the video. It portrayed everything I've been through. This is my 29th year of LD, the first 10 untreated. I'll share this with the many people who still don't understand LD.
znoodlelady 2 years ago 2
Dr. Jeff Sutherland of 'The Frequency Foundation' has some very interesting recent research articles on Lymes disease. If you see photos of some microscopic kinds, maybe we can understand why it feels like peices of GLASS in the brain or joints, etc. at times??? My health protocols has involved 'The Hart Dietary Procedure Plan' which has U.S. Patent, and frequency work, etc. Thank you for the video, & stimulus to more research, & greater awareness on this topic.
tigr7170 2 years ago
Comment removed
ecftube 2 years ago
The ONLY problem with this video is that it doesn't elaborate on the FACT that only a SMALL percentage of Lyme patients ever had a rash!
igspal 2 years ago 8
This is true - studies now show as few as 15% may see a rash. Thanks for bringing up an important point.
TruthAboutLD 2 years ago
This has been flagged as spam show
"melikerns" idea to openeyepictures
The movie has brought much needed awareness, however, why don't you post a list of petitions,a list of political representatives that we can contact. Put the links on your page; this will make it easier for those w ho barely have the energy to move. Please
Prethenie 2 years ago
This has been flagged as spam show
People, "Chemtrails," are killing the biological nutrients, supporting all plant life. What do you think that is doing to our immune systems, and that of bees? I have saved a sample of snow, from a storm in late December, that left my hair sticky and gluey feeling. I showered if out immediately. Does anyone know where I can get it tested? In need of one who is trustworthy.
Prethenie 2 years ago
This has been flagged as spam show
I read a book years ago, called "Sugar Blues" by William Dufty. An absolute read. He states that during the Bubonic Plague, the rich who could afford sugars, were dropping like flies, the poor country folk who could not, faired well.
Prethenie 2 years ago
This has been flagged as spam show
Google....."Low Dose Naltrexone Homepage." And also here on You tube..."Controlling Lyme Disease," and see the LDN videos by "TropicalDawg" here as well. I have been using LDN, for just over a week now, and feel the need to pass the buzz. This is a drug that helps with the immune system, inflammation and endorphins. Eat as if you had a yeast problem, because Lyme loves what yeast loves. And no sugars of any kind..."Including Fruit!"
Prethenie 2 years ago
Wrote a Lyme Disease Brochure with the help of 2 Lyme specialists. Will be happy to email to anyone.
Elaine in VA
ecftube 3 years ago
ive been living with it for 9 years.
the doctors did a echo and found water around my heart.
i hate u lyme disease! i wont let u beat me
fastgirl321 3 years ago 2
this is an amazing video. THis was done by my best friend and her son, two of the sweetest people you could ever know. As sick as they are, they are still trying to educate and fight for our rights. God bless them. Please take this disease from all of us who suffer so terribly. I know things happen for a reason, and I do believe God WILL heal us. We have lost a very dear friend from this disease, it does kill. We need to make our voices heard NOW! Before we loose more wonderful people.
lymefighter30 3 years ago 2
This has to be one of the best lyme disease videos I've even seen. It's so hard for people who don't have lyme to understand what it's like, but hopefully with enough exposure they will get the idea. It takes over everything. It's just such a debilitating and awful disease. Thank you so much for posting this video!
awarenessdaytributes 3 years ago 2
This is one of the best. Not asking for money, not selling books, not selling bogus cures. Thank you, M.
melkerns 3 years ago 4
For those of you who think you have lyme - join a lyme support forum, they show one at the end of this video, there are many online. Patients can tell you how and where to see a Lyme literate Md and get checked through Igenex Tick Borne Specialty lab. Lyme disease is the fastest growing infectious disease in the U.S. and has surpassed AIDS by far - ticks live in your yard and are the size of a poppy seed. Get to a forum and talk w/the experts - the lyme patients. Great video covers it all.
lymelights 3 years ago 8
where can i get check holly shit i might have lymes
imduch 3 years ago
Look online for ILADS and look for an LLMD (Lyme Literate Dr) because most mainstream conventional Drs use inaccurate tests and follow very outdated and bad guidelines when it comes to diagnosis and treatment of this. Don't go to any Dr who follows standard government or IDSA guidelines on treating this. Treatment for chronic lyme has to last for months or years not weeks.
neelubird 3 years ago 2
wow i have a lot of symptoms scary
imduch 3 years ago
Gainesville Florida"Home of the fighting gators. Shands @ U.F!
My son has Lyme and co-infections! I had to search the internet to get help for my child. Lost BCBS Have only MEDICAID! We were flown to CT by Angel FLight! What an experince for my child the hard way, to have to travel to another state becuase his Doctors would not help him! To be told he is faking or it's the parents fault because of DIVORICE! That's why he is in pain!It's stress!The mother is crazy! Yes! Crazy about my kids!
gatorlyme 3 years ago 3
This has been flagged as spam show
"PLEASE DON'T FEED THE TICKS": I was a long distance hiker but contracted Lyme disease. ER doc diagnosed 2002 (tick bite/EM rash). Positive serology. ER doc confirmed diagnosis 2007. Wikipedia Lyme page emphasizes 'no chronic Lyme' yet describes disseminated Borrelia/late stage Lyme (?!).
See my personal profile here for more about IDSA conflict of interest, etc.
Azorka82 3 years ago 2
Whitney, thanks for your post. You don't know what it means to us to know that this video helped someone to find the answer, this was our main hope..thank you. May you be well soon sweetie..take care.
TruthAboutLD 3 years ago
If it wasnt for the internet that lead me to lymes disease i would still be seeing doctors that were no help, they always say "that im crazy, i have no pain it is just in my head" After seeing over 25 doctors, my family and i finally started searching for an answer to all my pain. i have had lymes disease since i was 5(now 14). This video is my life, it is the one i first discored about lymes, and that lead me into reading more about lymes
thank you so much
whitney
synchrogirl21 3 years ago 3
If it wasnt for the internet that lead me to lymes disease i would still be seeing doctors that were no help, they always say "that im crazy, i have no pain it is just in my head" After seeing over 25 doctors, my family and i finally started searching for an answer to all my pain. i have had lymes disease since i was 5(now 14). This video is my life, it is the one i first discored about lymes, and that lead me into reading more about lymes
thank you so much
whitney
synchrogirl21 3 years ago 4
This is the best video I have seen yet over Lyme, people now know what it is really like for us and I hope they understand and accept the way we are, big hugs.
DaisyDenHaag 3 years ago 3
Without the internet & self-diagnosis 6 people in my family would all be suffering still. I had an MD yell at me to stop reading the internet and let him be the doctor! Had I not been persistent in finding out what was wrong with me & listened to him I doubt I'd be here today. My Lyme doctor told me that in medical school they are not taught about Ld. So, if any Md's read this, search lyme forums, see how we suffer, contact Turn the Corner Foundation & ILADS (dot org) - get educated!
TruthAboutLD 3 years ago 3
2:37 could not describe these 5 years any better. Internet became the most valuable resource to lead to the diagnosis
purefire47 3 years ago 2
Fabulous.
LYMIES ROCK! ;)
AmyPW8 3 years ago 2
We suffer while doctors who are not lyme literate decide the CDC has all the answers. There are thousands of us who are suffering because doctors refuse to listen, learn,& see us who we are. We are human beings who are sick & deserve quality and empathtic care in the USA. There are over 100 symptoms. I have atleast 40 & was misdiagnosed for almost 3 years after seeing 20 doctors. We are crying out for help and not only have to fight the medical community but the disease too. God help us.
MsMaddyAddie 3 years ago 3
Great video! When i saw over 100 symptoms, I felt like someone did really understand me!!!
HCritelli 3 years ago
I hate lymes disease. I got it when i was 9 and it really messed me up good. I am 15 now i used to be able to run and run and do all kinds of stuff...
I have awfull pain every day cause of doctors who didnt give a damn!
I would no like to thank the tons of doctors ive seen by saying "YOU SUCK ASS"
and i mean that with every ounce of my self i have
i had a good life lyme disease really ruined it...
fastgirl321 3 years ago 3
These doctors in Kentucky are just as lyme illiterate as any others, they don't believe you can get lyme disease in this state period!!! I was told this over & over even though I had the tick and the rash at the beginning of the symptoms. I'm really ticked off at some of these doctors for some of their arrogant and smart mouth remarks and I will never forget how they treated me for many misdiagnosed diseases, now that I've found a product that works I'm hoping get rid of it. NO LYME DR'S IN KY.
whistlepighunter 3 years ago 2
Thank you for your comments and ratings. LymeliterateRN I myself learned doctor's were wrong the hard way. It is an epidemic in EVERY state. Here in Calif Md's think of this as an East Coast Disease. There are so many here misdiagnosed I am sure! Jramsboy, my son is your age and has had to put off college due to LD treatment. No matter how old or young we are Lyme is a life thief, I am glad you are doing better. What seems impossible you have proven is possible, wellness! Wellness to all, TALD
TruthAboutLD 3 years ago
Thank you. There are too many of us to be ignored any longer.
I'm a Lyme pt who saw 40+ drs over 6 yrs despite a classic onset of this illness. I'm an RN & trusted that drs were right when they insisted "we don't have Lyme in WA." WRONG. It's in every state & it's epidemic.
Their ignorance has cost me any semblance of a normal life. I could have been cured; many could have been cured. Instead we're suffering with a dz marred in controversy.
We're in the millions. Enough is enough.
lymeliterateRN 3 years ago
Please go to our website shown at the end of the video for literally every subject about lyme disease. It is all educational, click on stories, resources and forum and at the board index are nearly 90 articles regarding LD. We also have a lyme disease forum with educated lyme patients available to help answer any question you may have.
TruthAboutLD 3 years ago
your not alone. i lost the best 4 years of my childhood to Lyme. throughout my 4 years of highschool i was so sick and tired all the time i would miss over 30 total days of school each year. junior year i was homebound for 6 months. i was an athlete my whole life up to 14. but during highschool i had to watch from the stands as the best years of my life ran by me. im 19 better now. at community college from missing so much school. i dream i getter better so i can join the Marines after college.
jramsboy89 3 years ago 2
AMAZING, PROFESSIONAL JOB! Video covers it all. This seriously deserves an award. Music fits perfectly, just a great job all round! Wow! is right!
gwhmnd 3 years ago
Wow
jcarreraaj 3 years ago
I have now forwarded this video to many people. I have been told a mother & son w/Lyme made this video? Amazing so professional. Thanks for educating people and I hope you are both well soon. God bless.
cotmh 3 years ago
Hi everyone, yes my son and I made the video. 6 members of our family have Lyme. (Yes California..we have lyme big time!) Thanks to all kind comments here. Our goal is to help educate our world, we are hoping this is one more way of doing that. We hope you will forward the link to family and friends and they will learn more about what you are suffering & hopefully it will help people that might have LD and not even know it. Blessings and wellness to all Lyme patients.
TruthAboutLymeDisease
TruthAboutLD 3 years ago
Great video. Straight to the point and accurate. Everyone should see this!
nawdik 3 years ago
I have never seen a video so totally complete explain in less than 5 minutes about this sickening disease. I am sure I speak for all of us w/Lyme ...thank you..I will be sure to pass this on. Perfect song from Creed too.
lymelights 3 years ago 2
GREAT video! I am a chronic Lyme patient, as are my husband, neighbors, colleagues, and many students (I'm a counselor). We're getting there! May-June Psychology today has a Lyme article and quotes ILADS docs and addresses the controversy. The political denial and complicituous medical community cannot last much longer! Glad my daughter let me use her youtube account to post!
baumsy18 3 years ago 3
Hi there,
I am a Lyme patient that wrote a brochure with the help of 2 Lyme specialists.
Would be happy to email anyone a copy.
Elaine in Virginia
ecftube 3 years ago
i have weird rashes i think might be lyme could i email them to u....
lennonlegend0909 3 years ago
I am not a physician but you do not have to have a perfect bulls-eye rash to have Lyme disease. In fact, you do not have to have a rash at all to have it. Send me your email and I will send you a very helpful brochure. One of the Lyme specialists that helped me with this brochure is world reknown.
Elaine in VA
ecftube 3 years ago
I would love one Elaine.
Amy
AmyPW8 3 years ago
What is your email address AmyPW8 ?
ecftube 3 years ago
Excellent job!!
Dawn Irons, Editor
Public Health Alert
gratefulwife2brad 3 years ago 3
Very well done -- 5 stars! Thanks for giving those of us with Lyme Disease a voice.
MrsMozart 3 years ago 3
:D
ilmb!
zxoxmissyxoxz 3 years ago
Great job, luv the song :-)
destiny4mee 3 years ago 3
awesome video! Good job. Love the song too.
rorocigio 3 years ago 3
AWESOME - BEST LD VIDEO HERE!! WOW!!
cotmh 3 years ago 2