I do love the dedication of some doctors, but I almost believe patients see more studies because they’re always looking!!! I know more about recent polymyositis studies than my doctors… they’re like deer in the head lights when I ask them about the study, then just give me the same rx !!! Look into low weight antibiotics!!! I want to know more about this study and why it worked. Dr Paul Clayton talks about it on KZbin

There was one crawling on my shirt with 3 white dots on it anyone know what that is

I had a tick on me about 4 to 5 days on my back. It was itching and I thought it was a mosquito but the head was in my skin . My daughter took tweezers and got it out. We sprayed antibiotic spray on it . Then used the ointment but it's been itching and swelling a little for a few days and yesterday I started feeling achy. Kind of weak and tired. I think I should go see my Dr.

Lymes was created in a lab in Lymes Pennsylvania. MAN made disease that broke free and Medicals don’t want to acknowledge it! Meanwhile PEOPLE ARE DYING FROM IT! The “bulleye” rash is not a sure sign. My daughter and I and MANY others had no bite or rash and still ended up getting Lymes.

I think that was a pointless video. No answers. Call your Dr?? No. Clean the bite spot with peroxide and deeply scrub it in, is my advice. Apply antibiotic cream with bandage. I'm not a Dr.

They have all known for yrs what lyme is, what it does and what it causes and why it's a devastating persistent disease. They knew for 40 plus yrs. All this talk about research is very slim and isn't going to happen because this fed system already know it's a devastating disease causing major nuerological immune system problems. If you know something already why research and they know. Now and for decades it's a game of how long the truth can be hidden. It's a major scam operation this fed controlled medical system is pulling and its a bad dirty business practice. These universities are involved in.

I just started Dr Brooke Goldner’s hyper-nourishing protocol outlined in her book Goodbye Lupus. After only a week I’m already experiencing great improvement. I can finally sleep without the pain and burning in my feet. As a result I’m not as fatigued or mentally taxed during the day. I fully expect to go into remission.

I live in Canada and we dont have the lotions described here, I have had 3 separate ticks in the last 3mths. I have gardened over 30yrs and never before had this problem. I didnt feel the bite and since I never had one before didnt do any checking it was only when I felt the pain and got to looking I found the tick. My granddaughter pulled it out and we went to the pharmacy and she gave me 2 pills to take right away. So far this time it is 4 days ago and the pain and redness is still there.

Living with arthritis is tough, but with Planet Ayurveda's treatment, it's much more manageable. Their remedies are truly the best out there.

I didn’t feel a thing is that normal?

Nachalna muzyka

Got shingles after taking tetanus shot

I started with severe pain in my right shoulder. Lasted for days then it went away and my neck and ear started hurting and this lasted a few days. The pain in my ear got worse and I started getting blisters on my face forehead and scalp. I have suffered horribly with pain on my face and around my eye. Then I got this unbearable itching around my eye. I rubbed and scratched it so much I got a black eye. I’m still recovery and haven’t had one day without pain in 6 weeks. Worst pain ever!!!! If you knew what I know you would run to get the vaccination.

POV: you found this video after a couple days of finding a tick in you

Great work. Are you all focusing on those of us who were not diagnosed for years or decades? We don’t have a disease, we have an infection that overwhelmed our system and tucked itself away to constantly cause us symptoms. My experience is that this takes months or years of antibiotics, herbs, and bio film busters to get it under control.

This helps me understand why I have several ailments not just one. Some symptoms are not related to the other one. A lot of patients with Sjogren's do develop FM. I just do not know which one set off the other one? For years, I have stated my illness has a nerological trigger. It isn't emotional or in my case due to CA. My brain misinterpets any form of strain as a threat and responds incorrectly to it. Close to 30, a good nights sleep did not reset my pain level like it use to. Leading to constant threats of tendonitis, bursitis. It is not just all in our head though. At least for my family. Biological changes, perhaps first with the growth spurt toddlers experience, than changes in purberty, than hitting that 30 time clock. These factors were my triggers that caused my illness to advance in me. There has to be a way to counter act these problems, in our case it may just be biological. My three adult children have not reported any signs of the more serious symptoms. All have allergies. None have reported prolong bouts of common flues requiring antibiotics. Only one has vision problems. None have reported arthritis yet. None of them report tendonitis, bursitis and my eldest is reaching 40 now.

Swear to God I'm committing suicide if I can't eat red fucking meat again.. I'm done with everything

Turn up the music so I don’t have to listen to him

Agzilla?

I got a tick when I was doing quads. I D O N T H A V E T W E E Z E R S

Thank you for your video. The one off their website really sucks. I am really scared to do my very first dose still, but now I know what to expect from the pen. I used Humira before, this is a bit different

I just wanna express my gratitude to DR ALAHO OLU Search him on KZbin Channel for curing my HSV 1&2. God will bless you. He has supplements for HPV, ALS, HIV too…..

I just wanna express my gratitude to DR ALAHO OLU Search him on KZbin Channel for curing my HSV 1&2. God will bless you. He has supplements for HPV, ALS, HIV too…..

I've been on hadmila started in November.. it's making me fat.

Is it true that Cimzia causes lymph cancer? Could you give information? Thank you!

😨😨 SO many things to say… if the vial says single dose… that does NOT always mean take the whole vial. It just means do NOT reuse/repuncture after pulling the dose the doctor prescribed you… Not sure where it was on the list when this video came out but as of today Methotrexate is labeled as HIGH RISK. that does NOT mean don’t take it, stop taking it or be afraid of it, it just means be careful and respect it. That said you should do it in a clean ventilated location away from others. You need the medication in your system, they do NOT. (If a friend is assisting you that’s fine, just be safe). Avoid cross contamination when wearing gloves. DONT forget to decontaminate properly and dispose of it safely. It should not be going in regular trash. You don’t HAVE to listen to me, feel free to do your research. Not a nurse, I’m just the one in the hospital licensed to handle and draw up the dose for them to give. I’ve actively only been in the pharmacy profession 8 years but I’ve done enough to have a bit of experience at least prepping it for your health and safety. 🤷‍♀️🤷‍♀️

Thank you!! 😅

And how do I lose weight again with arthritis?

Appreciated 👍🏻

I have been on methotrexate for two years. It just does not work at all.

Cosentyx can cause this symptoms?

Late diagnosed lyme disease does something to your whole body. Doctors don't believe you, people don't believe you. I have never been the same even after 5 years of treatment. Fatigue is the worst; I also have brain fog. I had two years of unusual fatigue before they tested me for lyme. The test came back positive .

Through a bunch of research I've done. I've determined that I am too sick to handle biological monoclonal antibodies. You need a certain amount of good health to be able to handle this stuff. Some of my conditions are brutal headaches, itchy, nearly zero appetite, full body rashes that I've been to many dermatologists for and every one of them has failed me. The only thing that seems to help reduce the rashes is organic coconut oil from the supermarket.. and I don't hesitate to go on top of my head all the way to my feet with this stuff.. then I have to hide from my dog because he'll try to lick me clean. And then there's the can't get out of bed zero energy or ambition weeks at a time. If not for months.. there was only one of them that worked a little bit and that was remicade. When I had a flare up on remicade and they put Imran on me on top of the remicade and that was the end of that it blew my whole body up into a rash that was so bad that at night time I didn't realize but I was scratching throughout the night to the point where I was bleeding everywhere in bed.. the worst areas are generally my shins my face forehead and around my eyes, however it's the entire body those are just the worst areas..

I've tried 6 or 7 different biological monoclonal antibodies for Crohn's in every last one of them either does nothing at all or destroys me. Strangely enough the worst one was the last one I tried and was stelara. That left me with no energy and bed bound for weeks at a time for almost 9 months. I think I took it three times.

I think I have Lyme disease now because I got bit by a tick today at 4 and the tick head is still in my skin

Thank you!! This is so straightforward and helpful.

Is granuloma annular ? Part of rheumatoid arthritis?

Got it as a teen. Through the years, can see medical results show its progression, got the celiac test back positive, then I noticed a down hill side after the age of 25. I was 245 best shape of my life healthy, going to school, tons of hobbies, over the years of stress, and surgeries, I've been on a steep slide down hill, then got the fybromyalgia diagnosis, then I got the positive lyme, more stress and surgeries, then a cte diagnosis, now I've applied for aish disability twice, denied, I can see a Dr where I live that is a lyme specialist, but I have to personally pay for it. I'm on welfare , 1000$ a month but homeless. I'm again going in for surgery soon. The lyme bugs luv the lil bit of antibiotics I'm now feeding them. It is in my Brian and neurological system. Lyme disease is the new aids. It can be transmitted through blood and sex. Until we can get this out there, we need to speak up. There's a pandemic out there but it's not what u think k it really is. Its too late now to stop it.

Thank u

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I'm 53 and I just got shingles very painful no fun at all. Can't wait to get rid of this pain!! I still go to work everyday, I'm stronger!!

I was bitten by ticks when I was a child, over 60 years ago. I was not diagnosed nor treated for Lyme. It was not until 2005 that I was told I have Lyme infection.

My doctor miss diagnosed my shingles rash for bed bug bites and I didn't get treatment for a week later, when I went to a mentally competent doctor at the emergency room. Although the receptionist diagnosed me with shingles when she seen the rash. Over 65-year-old man sees a doctor with a painful rash you would think the doctor would know that it was shingles. I didn't know but the doctor should know more than me. I'm pissed that I didn't get diagnosed earlier. Now I may have permanent nerve damage. What really amazes me is I called several dermatologists and it would take weeks or even months to get in to see one. By that time shingles would have been all over my body. The healthcare system in the United States sucks. And the doctors are even worse.

I take 12mg Ivermectin tablets once a month, to kick the s*** out of everything that's trying to kill me. 😊

quit reading the damn prompter. makes you look amateurish, and ill informed. stop and redo

What are the symptoms of??

Very informative for newbies like me.❤

Thank you for the information❤

Thank God I found this video and channel.❤

What about HSV infection ??