I have something wrong with me that doctors can’t figure out, I’m partially bed ridden. I’ve heard it from some friends doctors and family, that it’s all in my head and I’m crazy.
@@vla8806 Thanks, I really appreciate it. My most severe symptoms are severe nerve pain from my back to my feet, bladder issues (I use the bathroom up to about 80times a day sometimes), sleep problems, hot flashes, constipation, brain fog and other cognitive problems, numbness in my arms, and others.
You can't be treated correctly that soon because no doctor wants to admit that you have Lyme. I had to beg to be tested and I was right. Half a year of antibiotics did nothing but make me very ill. Natural antimicrobials and diet changed made me well again. So glad she took her health into her own hands.
I just found out that I have had lyme disease for 3 years. Several specialists, unnecessary surgical procedures, and 3 years later, I finally have an answer. Unfortunately, unlike Avril, by the time they diagnosed it, it had already spread to my brain, my central nervous system, and even my heart. So far the treatments aren't helping, and I had to pay out of pocket $850 down, and $340 per month for the treatments so far. It's nice to see someone speaking out about this disease that has nearly killed me and destroyed my life. In a sea of hopelessness, it gives me a grain of hope. I can only continue to hope that more doctors will become more educated in lyme disease, so that it can be properly diagnosed and treated BEFORE it gets to the point that it's too late. There needs to be more awareness about this issue. I was literally told that by each specialist I went to that they had no idea what was wrong with me. Eventually, you do start to question your sanity. To feel like you're dying (because you are) and to have drs tell you they don't know what is wrong with you, they can't figure it out, and there is nothing they can do to help you, is VERY unsettling. This disease is debilitating. There has to be a better way....
Who ever asked for systems, I can tell you mine. I basically have arthritis realy bad, it makes my legs feel like there broken, my knees, my arms. It makes my body ach, I have lower energy than I would normally, I’m on pain killers so it can be really hard for me to know when my limes is acting up, I let it go nearly forgot I had it for about 3 years now, tho for months, my heart has Ben bothering me, I Evan had a stress test done, I’m 30c thankfully things looked okay. But they sure don’t feel okey. My heart/ hurts bad some days. My legs/back, some mornings it takes me hours to finaly get up. Now consider the fact I’m on f pain killers. And I prob shouldn’t feel any of this. That’s how I know it’s back. Hat Iv Ben ignoring it. And so I prey I can grab some anti biotics. Take them for a month or 2 and then maybe start to work out and feel good again. But right now life’s too hard. Daily, it’s a struggle.
One of the best tools while hiking is to use odorless permethrin that you spray on your pants, shirt, socks that is effective after multiple washings. With this applied to your clothes you can place a tick on your pants and he will die belly up. Its not to expensive either. 10 bucks will treat two outfits.
Only about 30-40% of people get the bullseye rash. I have Lyme, and never got it. No one I know who has Lyme ever got the rash. In fact, so many people go unnoticed with Lyme because they never show a rash. Then the disease progresses and so many people are misdiagnosed with serious illnesses like chronic fatigue, fibromyalgia, MS, arthritis,alzheimers, ALS, and so many more. Also, the longer you have the disease, the harder it is to treat. Sure, if you are one of the few to get diagnosed with Lyme within the first month, and get treated with antibiotics, maybe just MAYBE you will be fine. But if you are untreated within the first month or two, then you have chronic lyme, and you have it for life. Once you have Chronic Lyme, antibiotics won't cure you, or barely treat you. The normal medical world doesn't know what they are doing with Lyme, and half the doctors refuse to even believe in Lyme, let alone treat it. You will experience more symptoms than you could imagine. Extreme fatigue, joint pain, heart palpitations, rashes, brain fog, lack of focus and concentration, blurry vision, hallucinations, memory loss etc. Those are all symptoms I have experienced. There are hundreds more. Lyme is a serious disease that so many people are affected with. I hope one day people will realize this, and actually start to help people. If you would like to know more about my Lyme story, and about the disease itself, check out my TH-cam channel. I am starting a support group for kids with chronic illnesses, so less of us are alone.
I never had the classic bulls eye rash they say you have to have to have Lyme. I had thin greens circles. I asked many different Drs if they could be Lyme to be laughed at. One even saying he may as well test for prostate cancer ( I’m female )😡 Found out April 2020 after not leaving by bed for 3 years after 10 years off bad health. I missed by kids childhoods all because the Drs refuse to learn or accept Lyme 😡
It is a shame that her doctors were so resistant to testing for any health issues. I'm glad that she stood up for herself and her health until the diagnosis was made! Those early symptoms are so key in getting tested for Lyme Disease! If you have an inkling that you could be suffering from this, it's best to go get tested and rule it out before the disease progresses! Best of luck to Avril in her treatment!
I know this is old but I was diagnosed with lyme disease at about the time this came out. I had no bullseye rash; the first sign that something was wrong was a crippling headache that would just not go away. Over a couple days, I began to have strong joint pain, major fatigue, and a high fever. I eventually developed large red marks all over my body, but still not a bullseye rash. My symptoms had been going on for nearly a month before I got my diagnosis, which was ultimately six weeks after I suspect I was first exposed. This wasn't soon enough for me to completely rid myself of lyme, and I suspect I'll have this disease forever, but I am so lucky to have a doctor that believed me from the very first visit that this was something serious. Lyme disease is usually not checked for even when all the symptoms are present because it looks so much like a typical flu. Increasing awareness about the signs beyond the infamous bullseye rash could save so many people from such a devastating disease.
I recovered from Lyme disease. My symptoms: bone crushing fatigue, racing heart, night sweats, confusion, loss of balance, hallucinations, depression, nerve pain all over, frozen joints, flu like feeling, loss of body temperature regulation, sensitivity to sound, sensitivity to light, sensitivity to smell, headaches, migraines, muscle twitching, spasms, a weird electrical vibrations throughout my body, shortness of breath, insomnia. I'm sure there are other symptoms I missed. Its torture... Best way to describe itRarely anyone ever sees the rash or the tick. They make it sound like its so easy to treat. The problem is that by the time you diagnose Lyme disease, it has become chronic for most. I too am glad I went through it. I don't take my health for granted or life anymore. Every day is a blessing on earth. Mark Hogan
Please. Could you tell what kind of treatment regime you went through? How long did you have it? Some more details probably could help a lot of suffering people...
“In the fullness of time, the mainstream handling of Chronic Lyme disease will be viewed as one of the most shameful episodes in the history of medicine because elements of academic medicine, elements of government and virtually the entire insurance industry have colluded to deny a disease.” - Dr. Kenneth Liegner
***** I'm sure you are in great hands :) The quote is perfect, I quote him all over the place in order to spread awareness. Hope you're on your way to some healing!
Jess D You are absolutely 100% correct. I'm praying that some politician will be able to experience this in his/her own family. Then - perhaps - there will be change. The LDSA board will have to "pay" someday.
Thank you Dr. Liegner for your comments and TRUTH. Until our family had to personally deal with this disease, we never knew the extent of disability it causes and the unwillingness from some in medicine, etc. to understand.
BS on the "early" thing. I found the mark less than 24 hrs later and had 105 fever a few days later. Doc gave me 2-3 weeks of amoxicillen. Weak. Went dormant and came back with a vengeance and now I'm disabled. So the "early" thing is way overstated.
this is an example to all celebs out there...how THEY should deal with their health issues...if they got problems...just look to other people for support and don't give up hope. don't hide away and give into despair because that only feeds the sickness. Avril is a huge part of my life, when I was suffering from depression as a teen she got me through it, other music helped too, not just hers but she was the core I won't lie. she is me hero and idol and when I am struggling with my own ambitions in life I look to her and wonder "what would she do". the fact she fights on through stuff like this just proves my point.
I have chronic Lyme too. It's a devestating illness that claims lives. And it does not take 36 hours to get Lyme! You can get it as soon as the tick taps into your blood stream.
I feel her pain and been laughed at by Drs for years for asking if the green marks in my legs could be Lyme!! Found out April 2020 I have Lyme after not leaving my bed for 3 whole years.
oh my god, i feel so bad for her... i have lymes too, it was diaognosed late but i am doing okaish now, but i'll be stuck with it for the rest of my life because it was diaognosed late.. i have all the symptoms now but i wont die
I can't wait until Avril is better. If I have to wait for 5 years or more soI can hear new songs from her, so be it. I still LOVE her old songs, get well soon!
I'm glad she took it upon herself to find out what was wrong. Doctors do this with so many people. Seriously what the hell are they getting paid for and telling her she's just crazy. How would that help jeez. I never new about this until it popped up on my stream. Glad she's better. She's awesome 💚
And my husband's lynes came from a regular old tick. It doesn't matter what kind of tick it is anymore. All kinds of ticks from all over the continent carry lymes. And only about 30% of lymes cases present with a ring rash. Be vigilant folks!
I read on the internet that she was a heavy cigarette smoker and with her schedule she was exhausted. This could definitely be, but Lyme....very horrible. I guess even the person who doesn't smoke, drink and takes good care of themselves can still be taken down from this terrible disease. Pray for her...she's always been great.
I did survive neurolyme and got antobiotics only after one year. It was horrible. A hell. The Situation in Austria where I live is a scandal - people do not get right diagnosis and treatment. Now I am ok but my brain clearly suffered from the infection then. Hope Avril and other people affected get healthy again !!!
I agree with the mis-information this guy just gave. I got my tick bite in Longview Wa., and the bug was not imbedded 36 hours. Our doctors in the NW say I can't have Lyme because there is no lyme in the NW. I mean get real. It just takes common logic to realize that ticks ride on animals that migrate, birds, mice, deer, etc. These guys are educated dummies but do not have that common sense? Now because of them I have chronic Lyme. If they would have been educated in Lyme I could have been cured as I went to the doctor right after the bite with the rash and flu like symptoms. It took a year and half to get diagnosed. By that time I couldn't walk. I thought I was going to die with all the symptoms and pain I was in and now it's been 5 years and I am still fighting.
Oh my gosh! That is so frustrating! I live by Mount Rainier, not too far from you and have chronic Lyme disease as well. I was bit as a child, went to the doctor. They removed it I still got Lyme disease. They have found it on every continent except Antarctica and in over 80 countries. Pretty sure it’s all over the US as well.
Stefani Sebastian I have seen the documentary buy no one talks about how to get rid of it effectively. Right now am doing a documentary movie for three months in Rosarito Beach in Mexico on treating Lyme with Apitherapy. We. Will be recording the progress with several patients from Massachussetts a 19 y.old and 69 y.old I really want to spread this information to as many people as possible because I am not charging the patients in this instance therefore extending an invitation for any one with Lyme to take advantage of this temporary treatment with Apitherapy during the documentary at no charge. We as Apitherapist have more than 25 years treating all illnesses with magnificent positive results. Please tell those you know that have Lyme to take advantage of it. rubenberthaud2001@hotmail.com
I'm glad that Avril was able to figure it out before it got too late because I think it was effecting her vocal cords as well and she wasn't able to sing. In fact there were reports that she may have died from Lyme disease. But I'm glad that she's back doing what she loves to do and as a fan of hers I'm glad that she's back to where she wants to be
I've had this same rash on my arm big circle i never thought nothing of it like the symptoms i just thought it was my seizure medication doing it.. Has me wanting to go get checked now. 😐 I've always had a fear of ticks after my older brother was diagnosed with bacterial meningitis after being bitten by a Mosquito/tick docs said one of those 2 had to of bitten him while he was camping here in Ohio's Hocking Hills.
My wife went undiagnosed with Lyme for many years, until finally getting a diagnosis last year... but getting better seems to be the hardest part. I set up a GOFUNDME for her, because not everyone can afford the treatments. www.gofundme.com/katherinelyme Thanks to everyone who spreads the truth about this horrible disease.
THE BULL'S EYE RASH IS NOT ALWAYS PRESENT!!!! I thought that I was ok because no rash. MOST PEOPLE DON"T EVER SEE ANY SYMPTOMS EXCEPT THE PAIN!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! The night sweats!!!!! AND joint pain moths to years later.
I thought mine was a giant mosquito bite. Afterall, I'm in Texas so Lyme disease wasn't the first thing on my mind. Telling people to wear long sleeves like this reporter just won't happen in 100°F weather.
Lymes disease is terrifying . I have a friend who is struggling with it . She said the new treatment is out for it and it’s thousands of dollars . Like 23,000 I think . It’s insane . So scary . She said she can’t go through the day without loving her body . Because moving her body is the only thing to make her feel the pain a little less
I don't see how celebraties are more Important or significant than normal people. Why even bother report this on the news when there are other people who had worse cases of Lyme disease and recovered.
Perhaps, but there is no greater evil. Everyone goes through tough shit. We can only work together to prevent/treat it. Based on our society's culture, a celebrity will get more attention than the average citizen. Yet, she's at least helping those with Lyme Disease. It's not a fun one either.
Yeah I understand how you think about the celebrity thing but look at it this way. People who listen to Avril and don't know about Lymes now know about it.
I don't mean this in hate or anything, but in all honesty, Avril doesn't know what real suffering is. She got over it quickly, and made a full recovery. She is fortunate. I know someone who has been in severe debilitating pain w/ paralysis from an injury. It has been so bad she would cry and even scream from the pain, and it left her housebound, and she struggled this way for five years, with no family help or a cure. . .and she was treated very badly by doctors and nurses, although her case is legit, and had two massive surgeries. I have so much empathy and respect for her, because this is what true misery is. Thus, Avril doesn't know what it is to truly suffer; not to mention, she also milked this for quite a bit of attention she didn't deserve. I have no respect for her. I wish that the public wouldn't coddle people like her, when there are so many in much much worse conditions in this world, including the woman with pain.
You misunderstand me, and you are judging, . . . .thus, not the one to think before you speak. I think of all my words before opening my mouth. Who said anything about competition? I am talking about accurate PERSPECTIVE and accurate discernment. Your words don't really show evidence of this. Do you know what "Triage" is? It is the crucial process that wounded people go through in medical facilities to determine who gets treated first, based on whoever has the MOST severe injuries and suffering. The most severe get treated and attended to first, whereas the ones with lesser issues get treated last. If all got treated equally, this is would be injustice to those who suffered more. Avril was not sick long, and she did not have horrendous and excruciating pain, she was not financially strained, and she made a FULL recovery. Whereas my friend had a devastating spinal cord injury, permanent paralysis, 5 YEARS of crippling pain, financial hardship, and no cure. She will never run or dance again, and this was part of her dream. Based on this evidence, my friend's situation is much, much worse, and acknowledging this reality and respecting the suffering of people like her is called having correct perspective, and it is fair, and shows respect for what she and others like her have suffered. Therefore, because of this, those with the lesser issues like Avril should not be receiving equal support, respect and attention to those with much more traumatic and painful situations (like my friend). Consequently, as well, this makes Avril the one with with a sense of entitlement. THINK about this, and have some heart to hear what I am saying.
+Mysterious Night don't know where you're getting your info from but Avril spent months bedridden and she hasn't made a full recovery, no one that gets diagnosed late makes a full recovery. There is no cure if not caught right away.
What a weird stance to take on what was basically a PSA. Everyone has known someone in their life who has suffered tremendously. Everyone suffers in their unique way as well. It doesn’t mean anyone’s suffering is lesser or greater. Unless you are living their experience, there’s not a chance you understand the full story.
I went through much of the same and had to remove the sugar, gluten, dairy... Diet is key with these type of conditions mine being auto immune..... It's amazing when you start dealing with your diet, what you can be healed from which is just about everything... I take no medication from a doctor and... I refuse... I go to doctors for diagnosis then I go home and take care of it naturally... As far as I'm concerned doctors are only educated idiots ... Best wishes to Avril Lavigne... With what she is doing an absolutely no she will be fine... It's good to detox the liver and the whole body for that matter and then you can get on a semi normal diet but always keeping the gluten and the sugar and the dairy out...
When you have it you know. Doctors kept telling me I must have covid, even though I tested negative. No. It feels like nothing else. 3rd ER visit in 1 week, with Bell's Palsy, I had lost 15 lbs. in 8 days. I was dying. They admitted me & saved my life, but it's been a 2 year struggle since.
Get well avril ilove you dont die pls Well all here to support you even u dont know me im praying for wish you appreciate our efforts for you we love you
Wow!!! I just found out today I have lyme disease after 3 months. I had to withdraw from college in the Fall from it. First thing I that popped up when i typed in lymes disease was this video. Everything Avril said is dead on. Especially about the doctor's and everyone thinking your crazy. Even the brushing her teeth part! If anyone out there is suffering from it or may think they have it, hang in there and God Bless😇🙏♥️✌️✝️...
Just got diagnosed with chronic Lyme 3 months ago through my Naturopath because main stream Dr’s think it’s all in your head!!! Still in 2022!!!! 🤬🤬 He wants me to do some $5,000 treatment that isn’t guaranteed to work OR relieve my symptoms! I think I will be looking into some other all natural remedies. I have also just cut out sugar, NO FRUIT! A low histamine diet and I’m also intermittent fasting. The food sensitivities are horrible. I’m down to eating MAYBE 10 foods. I am also looking into Near Infrared sauna 3 X a week because I’ve heard great benefits in the detoxifying of your body that way. I hope I can get some relief because most days I just wanna die. This is no way to live. I’m barely surviving!
EXACTLY HOW IT HAS BEEN FOR ME! HAVE TO DO EVERYTHING ALONE, DOCTORS WONT LISTEN TREATING ME LIKE AS IF I JUST WANT ATTENTION OR SOMETHING! AND NOT EVERYONE GETS THAT GODDAMN BULLSEYE RASH, OR MAYBE NOT SEE IT!
Oh my gosh, so true! The misinformation is flat out dangerous. You do not have 36 hours! It can reach the brain within 24. And even the CDC website will tell you if you have the rash, you have the disease. The test tests for antibodies, which are not present for three or four weeks. After that time, you already have chronic Lyme disease anyways…
I keep hearing this erroneous statement that this thing has to be on you for this extended period of time the one that gave me the bullseye rash and Lyme disease wasn't even on me for 24 hours
Mindbender223 When hey say it is only a tick bite that causes it, they are lying. Any vector-borrne insect can transmit the disease. Regardless of what the "doctor" says.
i had a bulls eye rash antibiotics both IV and oral ( oral several times) it has been 2 1/2 years I developed heavy metal toxicity due to depressed immune system...I am still ill...any suggestions? I also felt like I was dying! the MD's got a negative western blot test so noone takes me seriously...Can you help direct me ?? I can only work 4 days every second week and sleep the rest i take IV treatments ...I need more help... I have all the symptoms that are classic for lyme.....
The first most important thing to do is to get any mercury amalgams out of your mouth by only a holistic or biological dentist and not a conventional dentist.The mercury amalgams are the silver fillings that dentists originally said for years had no mercury in them but are made of just silver.They then admitted there is mercury in them but they don't leak any mercury out of them.Well now there is scientific fact that they constantly release mercury and other metal in the body.The university of Calgary has a video proving this theory and it is called The smoking gun.Its on You tube and the American dental association hates them for exposing the truth.
When she said doctors thought she was crazy I can so relate! That’s what happens a lot with people with autoimmune disease
I have something wrong with me that doctors can’t figure out, I’m partially bed ridden. I’ve heard it from some friends doctors and family, that it’s all in my head and I’m crazy.
@@Gobrowns123 heyy how ru doing now?
@@ananthepan2424 not good :/
@@Gobrowns123 what are your symptoms? I really hope you find answers ❤
@@vla8806 Thanks, I really appreciate it. My most severe symptoms are severe nerve pain from my back to my feet, bladder issues (I use the bathroom up to about 80times a day sometimes), sleep problems, hot flashes, constipation, brain fog and other cognitive problems, numbness in my arms, and others.
Avril, whenever we always stay with u
She repented to Jesus
You can't be treated correctly that soon because no doctor wants to admit that you have Lyme. I had to beg to be tested and I was right. Half a year of antibiotics did nothing but make me very ill. Natural antimicrobials and diet changed made me well again. So glad she took her health into her own hands.
And the test doesn't normally catch it either
+TheMoncada6 I was lucky, my doctor prescribed me antibiotics as soon as i gave her my symptoms
me too. well the part where I had to cry and beg for a test and my doc finally agreed to it God help me. hope u feel better
My daughter pulled a tick the back of her leg today. It was on her less than 24 hrs I'm sure. Should I call the doctor?
Always
I just found out that I have had lyme disease for 3 years. Several specialists, unnecessary surgical procedures, and 3 years later, I finally have an answer. Unfortunately, unlike Avril, by the time they diagnosed it, it had already spread to my brain, my central nervous system, and even my heart. So far the treatments aren't helping, and I had to pay out of pocket $850 down, and $340 per month for the treatments so far.
It's nice to see someone speaking out about this disease that has nearly killed me and destroyed my life. In a sea of hopelessness, it gives me a grain of hope. I can only continue to hope that more doctors will become more educated in lyme disease, so that it can be properly diagnosed and treated BEFORE it gets to the point that it's too late. There needs to be more awareness about this issue. I was literally told that by each specialist I went to that they had no idea what was wrong with me. Eventually, you do start to question your sanity. To feel like you're dying (because you are) and to have drs tell you they don't know what is wrong with you, they can't figure it out, and there is nothing they can do to help you, is VERY unsettling. This disease is debilitating. There has to be a better way....
What were you’re symptoms??
Good luck in your health and journey.
Who ever asked for systems, I can tell you mine. I basically have arthritis realy bad, it makes my legs feel like there broken, my knees, my arms. It makes my body ach, I have lower energy than I would normally, I’m on pain killers so it can be really hard for me to know when my limes is acting up, I let it go nearly forgot I had it for about 3 years now, tho for months, my heart has Ben bothering me, I Evan had a stress test done, I’m 30c thankfully things looked okay. But they sure don’t feel okey. My heart/ hurts bad some days. My legs/back, some mornings it takes me hours to finaly get up. Now consider the fact I’m on f pain killers. And I prob shouldn’t feel any of this. That’s how I know it’s back. Hat Iv Ben ignoring it. And so I prey I can grab some anti biotics. Take them for a month or 2 and then maybe start to work out and feel good again. But right now life’s too hard. Daily, it’s a struggle.
I’m afraid I put it off to long :(
@@anythinggoes1127 Take Ethiopian Black Seed Oil, Olive Leaf Extract, Ashwaganda
get well avril!!! keep fighting... we love you!
One of the best tools while hiking is to use odorless permethrin that you spray on your pants, shirt, socks that is effective after multiple washings. With this applied to your clothes you can place a tick on your pants and he will die belly up. Its not to expensive either. 10 bucks will treat two outfits.
Dear God, this disease is hell. I am a survivor!!
hey! what have you done to treat them? thank you.. :)
I am survivor too! Lyme is horrible
@@EllencyOfficial you need a specialist,Doxi is the most common antibiotic used for Lyme but you will suffer all your life,Lyme is hell!
@@Gladyslm all your life? 8-o
Sign this one too.
www.lymehope.ca/lyme-petition.html
Only about 30-40% of people get the bullseye rash. I have Lyme, and never got it. No one I know who has Lyme ever got the rash. In fact, so many people go unnoticed with Lyme because they never show a rash. Then the disease progresses and so many people are misdiagnosed with serious illnesses like chronic fatigue, fibromyalgia, MS, arthritis,alzheimers, ALS, and so many more.
Also, the longer you have the disease, the harder it is to treat. Sure, if you are one of the few to get diagnosed with Lyme within the first month, and get treated with antibiotics, maybe just MAYBE you will be fine. But if you are untreated within the first month or two, then you have chronic lyme, and you have it for life. Once you have Chronic Lyme, antibiotics won't cure you, or barely treat you. The normal medical world doesn't know what they are doing with Lyme, and half the doctors refuse to even believe in Lyme, let alone treat it. You will experience more symptoms than you could imagine. Extreme fatigue, joint pain, heart palpitations, rashes, brain fog, lack of focus and concentration, blurry vision, hallucinations, memory loss etc. Those are all symptoms I have experienced. There are hundreds more. Lyme is a serious disease that so many people are affected with. I hope one day people will realize this, and actually start to help people.
If you would like to know more about my Lyme story, and about the disease itself, check out my TH-cam channel. I am starting a support group for kids with chronic illnesses, so less of us are alone.
Thanks. I'll check it out.
I never had the classic bulls eye rash they say you have to have to have Lyme. I had thin greens circles. I asked many different Drs if they could be Lyme to be laughed at. One even saying he may as well test for prostate cancer ( I’m female )😡 Found out April 2020 after not leaving by bed for 3 years after 10 years off bad health. I missed by kids childhoods all because the Drs refuse to learn or accept Lyme 😡
@@reds542 so sorry you were going through this how are you in 2022 did you found help?doctr treatment?
Take Ethiopian Black Seed Oil, Olive Leaf Extract, Ashwaganda and raw honey. Especially those. Be consistent and they will treat it.
@@reds542 Take Ethiopian Black Seed Oil, Olive Leaf Extract, Ashwaganda and raw honey. Especially those. Be consistent and they will treat it.
She's an inspirational strong warrior. I'm so proud of her
It is a shame that her doctors were so resistant to testing for any health issues. I'm glad that she stood up for herself and her health until the diagnosis was made! Those early symptoms are so key in getting tested for Lyme Disease! If you have an inkling that you could be suffering from this, it's best to go get tested and rule it out before the disease progresses! Best of luck to Avril in her treatment!
Avril, as a lymie myself I feel all of your emotions so deeply!! Stay strong we lymies 💚 need to stick together much love # lymewarriorsforlife
@FreedomandMagicdiet ,supplementing, take your health into your own hands
I know this is old but I was diagnosed with lyme disease at about the time this came out. I had no bullseye rash; the first sign that something was wrong was a crippling headache that would just not go away. Over a couple days, I began to have strong joint pain, major fatigue, and a high fever. I eventually developed large red marks all over my body, but still not a bullseye rash. My symptoms had been going on for nearly a month before I got my diagnosis, which was ultimately six weeks after I suspect I was first exposed. This wasn't soon enough for me to completely rid myself of lyme, and I suspect I'll have this disease forever, but I am so lucky to have a doctor that believed me from the very first visit that this was something serious. Lyme disease is usually not checked for even when all the symptoms are present because it looks so much like a typical flu. Increasing awareness about the signs beyond the infamous bullseye rash could save so many people from such a devastating disease.
Hang in there I have had chronic Lyme for 6 years now, it's tough.
I’m so sorry to hear that. I have it to you! Have you tried N..A.E.T.therapy or cranio biotic therapy? That is saved my life
This is one of the many reasons why people look up to Avril
Glad she's can recover! Love you QUEEN and we want you back in a 100% healthy!!
I recovered from Lyme disease. My symptoms: bone crushing fatigue, racing heart, night sweats, confusion, loss of balance, hallucinations, depression, nerve pain all over, frozen joints, flu like feeling, loss of body temperature regulation, sensitivity to sound, sensitivity to light, sensitivity to smell, headaches, migraines, muscle twitching, spasms, a weird electrical vibrations throughout my body, shortness of breath, insomnia. I'm sure there are other symptoms I missed. Its torture... Best way to describe itRarely anyone ever sees the rash or the tick. They make it sound like its so easy to treat. The problem is that by the time you diagnose Lyme disease, it has become chronic for most. I too am glad I went through it. I don't take my health for granted or life anymore. Every day is a blessing on earth. Mark Hogan
Could you please tell us, how long your journey was and what treatment you went through?
Which treatment cured you...?
Please.
Could you tell what kind of treatment regime you went through?
How long did you have it?
Some more details probably could help a lot of suffering people...
are you in the united states? ive tried to type this a couple of times and it didnt send.
are you in the united states or abroad/?
@@silberregen653 what country do you live?
“In the fullness of time, the mainstream handling of Chronic Lyme disease will be viewed as one of the most shameful episodes in the history of medicine because elements of academic medicine, elements of government and virtually the entire insurance industry have colluded to deny a disease.”
- Dr. Kenneth Liegner
I so AGREE! ... and so has the VA and the Military as well. I don't see anything changing anytime soon. Unfortunately.
***** I'm sure you are in great hands :) The quote is perfect, I quote him all over the place in order to spread awareness. Hope you're on your way to some healing!
So true
Jess D You are absolutely 100% correct. I'm praying that some politician will be able to experience this in his/her own family. Then - perhaps - there will be change. The LDSA board will have to "pay" someday.
Thank you Dr. Liegner for your comments and TRUTH. Until our family had to personally deal with this disease, we never knew the extent of disability it causes and the unwillingness from some in medicine, etc. to understand.
BS on the "early" thing. I found the mark less than 24 hrs later and had 105 fever a few days later. Doc gave me 2-3 weeks of amoxicillen. Weak. Went dormant and came back with a vengeance and now I'm disabled. So the "early" thing is way overstated.
this is an example to all celebs out there...how THEY should deal with their health issues...if they got problems...just look to other people for support and don't give up hope. don't hide away and give into despair because that only feeds the sickness. Avril is a huge part of my life, when I was suffering from depression as a teen she got me through it, other music helped too, not just hers but she was the core I won't lie. she is me hero and idol and when I am struggling with my own ambitions in life I look to her and wonder "what would she do". the fact she fights on through stuff like this just proves my point.
The girl I have feelings for has Lyme. I had no idea how awful it was. I have a newfound respect for her and what she goes through.
I have chronic Lyme too. It's a devestating illness that claims lives. And it does not take 36 hours to get Lyme! You can get it as soon as the tick taps into your blood stream.
I feel her pain and been laughed at by Drs for years for asking if the green marks in my legs could be Lyme!! Found out April 2020 I have Lyme after not leaving my bed for 3 whole years.
Avril has been my hero and role model since I was a little girl. She inspires me every day and most definitely when I was younger
I KNOW AVRIL CAN DO THIS!!! FIGHT THIS DISEASE AVRIL! WE LOVE YOU. STAY STRONG!
my bestie and I literally reflecting this together and it's still resonates us! Avril did amazing and is a fighter!
Lyme disease is definitely not fake. I've had it since I was 21 n I'm 38 now. n like has been hell.
Has it got better for you?
No just worse and worse. 22 major surgeries to keep me alive and lots more to go through. On 28 diff meds a day. Its literally hell.
I'm sorry. I'm suffering too, but not nearly as bad you. I have more neuro symptoms and memory loss.
Oh wow. I'm sorry to hear that. It has effected that way as well. Prayers to u hun. N tyvm.
Thank you I appreciate it. Hope you get well to.
oh my god, i feel so bad for her... i have lymes too, it was diaognosed late but i am doing okaish now, but i'll be stuck with it for the rest of my life because it was diaognosed late.. i have all the symptoms now but i wont die
I can't wait until Avril is better. If I have to wait for 5 years or more soI can hear new songs from her, so be it. I still LOVE her old songs, get well soon!
So I ***
I'm glad she took it upon herself to find out what was wrong. Doctors do this with so many people. Seriously what the hell are they getting paid for and telling her she's just crazy. How would that help jeez. I never new about this until it popped up on my stream. Glad she's better. She's awesome 💚
And my husband's lynes came from a regular old tick. It doesn't matter what kind of tick it is anymore. All kinds of ticks from all over the continent carry lymes. And only about 30% of lymes cases present with a ring rash.
Be vigilant folks!
Omg, Avril is my biggest idol evR, so glad she's feeling better
Best wish for her to get well soon. I really like her
I've had Lyme disease for 38 years. I was misdiagnosed for 27 years and I had a bullseye rash. I am in Late stage Lyme.
she is such a huge voice to the voiceless :)
Keep Holding On Avril !
I read on the internet that she was a heavy cigarette smoker and with her schedule she was exhausted. This could definitely be, but Lyme....very horrible. I guess even the person who doesn't smoke, drink and takes good care of themselves can still be taken down from this terrible disease. Pray for her...she's always been great.
We are here for you Avril!
Good snapshot of Avril Lavigne’s struggle with Lyme but the discussion at the end is lacking.
I did survive neurolyme and got antobiotics only after one year. It was horrible. A hell. The Situation in Austria where I live is a scandal - people do not get right diagnosis and treatment. Now I am ok but my brain clearly suffered from the infection then. Hope Avril and other people affected get healthy again !!!
GETWELL AVRIL ♥ We are here .
I agree with the mis-information this guy just gave. I got my tick bite in Longview Wa., and the bug was not imbedded 36 hours. Our doctors in the NW say I can't have Lyme because there is no lyme in the NW. I mean get real. It just takes common logic to realize that ticks ride on animals that migrate, birds, mice, deer, etc. These guys are educated dummies but do not have that common sense? Now because of them I have chronic Lyme. If they would have been educated in Lyme I could have been cured as I went to the doctor right after the bite with the rash and flu like symptoms. It took a year and half to get diagnosed. By that time I couldn't walk. I thought I was going to die with all the symptoms and pain I was in and now it's been 5 years and I am still fighting.
You don't even have to get the rash to still be infected, that's what happend to me 24years ago. Keep fighting, I will, for the rest of my life!
Oh my gosh! That is so frustrating! I live by Mount Rainier, not too far from you and have chronic Lyme disease as well. I was bit as a child, went to the doctor. They removed it I still got Lyme disease. They have found it on every continent except Antarctica and in over 80 countries. Pretty sure it’s all over the US as well.
I love avril lavigne!!!!!!
Stefani Sebastian
I have seen the documentary buy no one talks about how to get rid of it effectively. Right now am doing a documentary movie for three months in Rosarito Beach in Mexico on treating Lyme with Apitherapy. We. Will be recording the progress with several patients from Massachussetts a 19 y.old and 69 y.old I really want to spread this information to as many people as possible because I am not charging the patients in this instance therefore extending an invitation for any one with Lyme to take advantage of this temporary treatment with Apitherapy during the documentary at no charge. We as Apitherapist have more than 25 years treating all illnesses with magnificent positive results. Please tell those you know that have Lyme to take advantage of it. rubenberthaud2001@hotmail.com
Stefani Sebastian same
So scary to think a little tick can cause so much problems. Everyone please be careful. Prayers go out to you.
Now we know. Stay strong Avril. We love you!
I'm glad that Avril was able to figure it out before it got too late because I think it was effecting her vocal cords as well and she wasn't able to sing. In fact there were reports that she may have died from Lyme disease. But I'm glad that she's back doing what she loves to do and as a fan of hers I'm glad that she's back to where she wants to be
Incredible how even the top doctors won't do shit.
Get well soon Avril!!
Prayers honey hope you are feeling better
I've had this same rash on my arm big circle i never thought nothing of it like the symptoms i just thought it was my seizure medication doing it.. Has me wanting to go get checked now. 😐 I've always had a fear of ticks after my older brother was diagnosed with bacterial meningitis after being bitten by a Mosquito/tick docs said one of those 2 had to of bitten him while he was camping here in Ohio's Hocking Hills.
You are all experts on your own body. Only YOU know when something doesn't feel right.
My wife went undiagnosed with Lyme for many years, until finally getting a diagnosis last year... but getting better seems to be the hardest part. I set up a GOFUNDME for her, because not everyone can afford the treatments.
www.gofundme.com/katherinelyme
Thanks to everyone who spreads the truth about this horrible disease.
THE BULL'S EYE RASH IS NOT ALWAYS PRESENT!!!! I thought that I was ok because no rash. MOST PEOPLE DON"T EVER SEE ANY SYMPTOMS EXCEPT THE PAIN!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! The night sweats!!!!! AND joint pain moths to years later.
I thought mine was a giant mosquito bite. Afterall, I'm in Texas so Lyme disease wasn't the first thing on my mind. Telling people to wear long sleeves like this reporter just won't happen in 100°F weather.
36 hours? That's quite a bit past the true inoculation period. I would say 1-2 hours actually...
Wish you the best Avril, we love you.
Avril Lavigne.... please get well soon... i will pray for you everday ;(
She is so brave she fought with this 💙
I am your fan Avril and I am here for you. Get well soon!
I've had it for 35 years. Just diagnosed a month ago finally.
What were your symptoms?
I’m so glad she is healthy and back🤘🎸💆♀️
I'll pray for you get well soon.
Your awareness is awesome, stay strong ❤
avril ily
Lymes disease is terrifying . I have a friend who is struggling with it . She said the new treatment is out for it and it’s thousands of dollars . Like 23,000 I think . It’s insane . So scary . She said she can’t go through the day without loving her body . Because moving her body is the only thing to make her feel the pain a little less
What's the treatment? I have chronic lyme
Unfortunately, they aren't giving the entire story.
thanks for sharing Soko Shoko
I don't see how celebraties are more
Important or significant than normal people. Why even bother report this on the news when there are other people who had worse cases of Lyme disease and recovered.
Perhaps, but there is no greater evil. Everyone goes through tough shit. We can only work together to prevent/treat it. Based on our society's culture, a celebrity will get more attention than the average citizen. Yet, she's at least helping those with Lyme Disease. It's not a fun one either.
Anonymous Male I guess
Julia Binarystar Stop complaining and be happy that a celebrity is spreading the word.
Julia Binarystar Maybe because no one reads MY diary entries on living with Lyme.
Yeah I understand how you think about the celebrity thing but look at it this way. People who listen to Avril and don't know about Lymes now know about it.
My mom might have it . I’m so afraid. I’m praying 😢
I don't mean this in hate or anything, but in all honesty, Avril doesn't know what real suffering is. She got over it quickly, and made a full recovery. She is fortunate.
I know someone who has been in severe debilitating pain w/ paralysis from an injury. It has been so bad she would cry and even scream from the pain, and it left her housebound, and she struggled this way for five years, with no family help or a cure. . .and she was treated very badly by doctors and nurses, although her case is legit, and had two massive surgeries.
I have so much empathy and respect for her, because this is what true misery is.
Thus, Avril doesn't know what it is to truly suffer; not to mention, she also milked this for quite a bit of attention she didn't deserve. I have no respect for her. I wish that the public wouldn't coddle people like her, when there are so many in much much worse conditions in this world, including the woman with pain.
You misunderstand me, and you are judging, . . . .thus, not the one to think before you speak. I think of all my words before opening my mouth.
Who said anything about competition? I am talking about accurate PERSPECTIVE and accurate discernment. Your words don't really show evidence of this.
Do you know what "Triage" is?
It is the crucial process that wounded people go through in medical facilities to determine who gets treated first, based on whoever has the MOST severe injuries and suffering. The most severe get treated and attended to first, whereas the ones with lesser issues get treated last. If all got treated equally, this is would be injustice to those who suffered more.
Avril was not sick long, and she did not have horrendous and excruciating pain, she was not financially strained, and she made a FULL recovery.
Whereas my friend had a devastating spinal cord injury, permanent paralysis, 5 YEARS of crippling pain, financial hardship, and no cure. She will never run or dance again, and this was part of her dream.
Based on this evidence, my friend's situation is much, much worse, and acknowledging this reality and respecting the suffering of people like her is called having correct perspective, and it is fair, and shows respect for what she and others like her have suffered.
Therefore, because of this, those with the lesser issues like Avril should not be receiving equal support, respect and attention to those with much more traumatic and painful situations (like my friend).
Consequently, as well, this makes Avril the one with with a sense of entitlement.
THINK about this, and have some heart to hear what I am saying.
+Mysterious Night don't know where you're getting your info from but Avril spent months bedridden and she hasn't made a full recovery, no one that gets diagnosed late makes a full recovery. There is no cure if not caught right away.
What a weird stance to take on what was basically a PSA.
Everyone has known someone in their life who has suffered tremendously.
Everyone suffers in their unique way as well. It doesn’t mean anyone’s suffering is lesser or greater.
Unless you are living their experience, there’s not a chance you understand the full story.
I went through much of the same and had to remove the sugar, gluten, dairy... Diet is key with these type of conditions mine being auto immune..... It's amazing when you start dealing with your diet, what you can be healed from which is just about everything... I take no medication from a doctor and... I refuse... I go to doctors for diagnosis then I go home and take care of it naturally... As far as I'm concerned doctors are only educated idiots ... Best wishes to Avril Lavigne... With what she is doing an absolutely no she will be fine... It's good to detox the liver and the whole body for that matter and then you can get on a semi normal diet but always keeping the gluten and the sugar and the dairy out...
Hey.. It's been so long since ur msg.. But can u suggest a diet for healthy living?
When you have it you know. Doctors kept telling me I must have covid, even though I tested negative. No. It feels like nothing else. 3rd ER visit in 1 week, with Bell's Palsy, I had lost 15 lbs. in 8 days. I was dying. They admitted me & saved my life, but it's been a 2 year struggle since.
She is so beautiful inside and out. Chad is a lucky ducky
you must feel better Avril :(!!! i have so much things need to tell you :(
Don't blindly rely on doctors rather do research by yourself before any treatment.
All my support to her
So so sad. I pray to the Lord she recovers100%?
I asked my mom who is a doctor if there is any reason why they wouldn't test her for Lyme disease and she said there is no reason not to
No antibiotic will help you if you've had it for a long time. It is absolutely the hardest thing to get rid of if it ever even can be gotten rid of
Rife machine can get rid of it
NOOOO AVRIL CUT OUT HER FAVORITE FOOD! PIZZZZAAA!
Oh my god I love Avril so much :(
you are right Jess B
Get well avril ilove you dont die pls
Well all here to support you even u dont know me im praying for wish you appreciate our efforts for you we love you
Hi, does someone know who is the doctor here on this show ? Thanks a lot.
I'm going to the doctor tomorrow to check for that
Wow!!! I just found out today I have lyme disease after 3 months. I had to withdraw from college in the Fall from it. First thing I that popped up when i typed in lymes disease was this video. Everything Avril said is dead on. Especially about the doctor's and everyone thinking your crazy. Even the brushing her teeth part! If anyone out there is suffering from it or may think they have it, hang in there and God Bless😇🙏♥️✌️✝️...
Just got diagnosed with chronic Lyme 3 months ago through my Naturopath because main stream Dr’s think it’s all in your head!!! Still in 2022!!!! 🤬🤬
He wants me to do some $5,000 treatment that isn’t guaranteed to work OR relieve my symptoms! I think I will be looking into some other all natural remedies. I have also just cut out sugar, NO FRUIT! A low histamine diet and I’m also intermittent fasting. The food sensitivities are horrible. I’m down to eating MAYBE 10 foods. I am also looking into Near Infrared sauna 3 X a week because I’ve heard great benefits in the detoxifying of your body that way. I hope I can get some relief because most days I just wanna die. This is no way to live. I’m barely surviving!
The bullseye rash is bullsht, stop it! Lyme needs to be diagnosed thru a spinal tap no matter how vague the symptoms may be.
Omg how sad I am as her diehard fan
EXACTLY HOW IT HAS BEEN FOR ME! HAVE TO DO EVERYTHING ALONE, DOCTORS WONT LISTEN TREATING ME LIKE AS IF I JUST WANT ATTENTION OR SOMETHING! AND NOT EVERYONE GETS THAT GODDAMN BULLSEYE RASH, OR MAYBE NOT SEE IT!
Wow. That guy at the end is irritatingly misinformed.
Oh my gosh, so true! The misinformation is flat out dangerous. You do not have 36 hours! It can reach the brain within 24. And even the CDC website will tell you if you have the rash, you have the disease. The test tests for antibodies, which are not present for three or four weeks. After that time, you already have chronic Lyme disease anyways…
“Take the antibiotics in the first month and you’ll be fine.”
Tell that to the biofilm.
Exactly
avril be healthy!
youre always in our hearts
hope all my comments are not erased again
Stay strong avril
Avril has always been a warrior in my eyes 💫🥰💪🏾🌹4:11 he was thinking of his genitals 👍🏾
I keep hearing this erroneous statement that this thing has to be on you for this extended period of time the one that gave me the bullseye rash and Lyme disease wasn't even on me for 24 hours
Tick bite or Mosquito bite or Flea bite?
Mindbender223 When hey say it is only a tick bite that causes it, they are lying. Any vector-borrne insect can transmit the disease. Regardless of what the "doctor" says.
+Mindbender223 I'm inclined to agree
+Mindbender223 that is most probably not true
May04bwu Why not?
+Mindbender223 no comment?
I am 99% sure I have it but my doctors refuse to take me seriously. I don't know where to go next.
i will pray foryou avril
RFK is going to make it all better.
I LOVE YOU AVRIL
Did anyone catch the Freudian slip at 4:08?
i had a bulls eye rash antibiotics both IV and oral ( oral several times) it has been 2 1/2 years I developed heavy metal toxicity due to depressed immune system...I am still ill...any suggestions? I also felt like I was dying! the MD's got a negative western blot test so noone takes me seriously...Can you help direct me ??
I can only work 4 days every second week and sleep the rest i take IV treatments ...I need more help... I have all the symptoms that are classic for lyme.....
sharon witzu - go to the sponagle wellness clinic
The first most important thing to do is to get any mercury amalgams out of your mouth by only a holistic or biological dentist and not a conventional dentist.The mercury amalgams are the silver fillings that dentists originally said for years had no mercury in them but are made of just silver.They then admitted there is mercury in them but they don't leak any mercury out of them.Well now there is scientific fact that they constantly release mercury and other metal in the body.The university of Calgary has a video proving this theory and it is called The smoking gun.Its on You tube and the American dental association hates them for exposing the truth.