LOL! This egomaniac spends his life suing everyone he possibly can over frivolous things. His Healthgrades rating is a 1.7 out of 5, I wonder why that is? If you ask any one of his peers in the field of research they will tell you to avoid this man at all costs. Good luck to all of his unwitting patients out there.

Dr. Laz saved my Dad's life!

People on reddit are saying Mebendazol, Albendazol, and raw carrots work. Fenbendazol works as it cures cancer which is a fungal parasite. Natural means- Liquid Chlorophyll, Diatenaceous earth, Pumpkin seeds, Pomegranate Juice, Cayenne Pepper, Alcohol above 10%, Papaya Seeds, Black Walnut Seed Oil, Red Clover, Oregano Oil, and Echinacea. Plants use ethanol, Saponins and Flavonoids, PGG, etc against fungus

Long AIDS is what i think you should call chronic Lyme. I realize it has nothing to do with HIV, but i feel like the results are the same.

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HOW DO THE PEOPLE WHO FALL INTO THE 40% THAT THE ANTIBODIES DONT SHOW UP IN OUR BLOODWORK GET HELP?

Thank you very much Doctor, for the your* most intelligent * helpful information seen & shared, *your valued notes of how the symptoms are correlated to each,& recomendations & treatments, were eye* opening, to the major causes & issues, = So helpful to us all suffering with this delima, Bless you x Keep up the good works, to help us & to update & inform other Doctors who *lag,,to keep up ,,x cause *setbacks to patients, Amen You Answered my Prayers x Gave more infos vs other *Docs to Patients. patients

went to ophthalmologists, optometrist, and a rheumatologist going on two years with symptoms . neither schiermers test nor vital eye stain was performed by any of them . not even a check on the glands. just prescription drops, and pills . 😢 so, I am taking omega 3, cod liver oil, and OTC eye drops . and dry heat mask 2 x da

I use menthol like Vicks, near NOT in my eyes to make them water. Or Castor oil on the eyelashes.

Exercise for fatigue? What about post exertional malaise?

Why does pilocarpine take so long to work? Can't it be made in an as needed form?

If your salivary glands are not producing enough then you cant spare any for the test.

I wonder what could have become of me if you weren't the one who came to an interval in my life. Thank you for curing my Hepatitis B Infection naturally Doctor Igudia. I immensely appreciate you.

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I was diagnosed with Gjorgrens in 2010. In 2013, I had Lympoma of my left Paradid gland. I needed 17 radiation treatments. In 2018, I got Lympoma again on my right Paratid gland and only needed 2 radiation treatments. It seems like I get cancer every 6 years. I'm due. My teeth are another issue. I've had 2 root canals that failed. I tried using those dics that stick to your gums, and I think they caused my root canal fails. I do get skeleton pain all over my body and my hand swells now and then. I use Restasis for my eyes. Now, with having new drug coverage, I have to pay $192 for a 60-day supply for the generic. I'm just a mess, and I'm turning 73 soon. .

Can you run the video through any software to improve the audio?

*You Did Not Choose To Be Classified As Diabetic, But You Can Choose To Fight Back Against Diabetes* 💪

Mine started with Erosive Lichen Planus following a long dental visit. I lost so much skin in my mouth I lived on fluid and soup for nearly 18 months. I have had life long Coeliac Disease. Food allergies. Then came the dry eyes. Dry mouth. Eventually dry nose and throat. Now it has spread down into my lungs following a dose of Covid. It is terrifying. I just know, as I live in a country which has never really heard of this problem, I will not be treated. I was offered antihistmines for the allergies - really! - I took one as an experiment (I was aware that these were not suitable really) dried everything up so much I could hardly see or breath. So, it´s only steam breathing and saline nose drops that keep me going. I probably sleep only 2 hrs at a time as the dried pain in my nose and mouth wake me. I take nasal drops and a glass of water. Sometimes I manage to get back to sleep. But I am so very, very exhausted now. I know this awful syndrome is slowly killing me. And I just accept this. I will continue as long as I can have some value in life and then I will apply for assisted death.

What treatments have worked? Would like to hear testimonies. A lot of treatments you mentioned sound superficial or not treating the underlining issues? Just a thought...

being recommended to doctor Igudia on KZbin has being a great blessing to my family his cure for Hepatitis B Virus is a genuine one thanks for your good deed toward humanity☺️.

My heart will remain grateful Dr Igudia till forever,for the medical attention you showed me when I was battling with my Hepatitis B virus you showed care in every way,and with the help of your herbal medication I was deeply shocked to see it work.

probiotics and immunoglobulins (sbi protect , Mega IGG 2000) are saving my life. Thank you God.

My heart just keeps thanking you and thanking you Dr Igudia for all you have done for me, you gave me your words that you could heal any sickness or disease, thank you for permanently curing me of my Hepatitis B Virus you are amazing

I really do appreciate you Dr Igudia youtube,your commitment towards saving human lives is steadfast ,all the knowledge I got from you and,the help with the herbal meds, I was recently tested negative of Hepatitis B,I’m so happy thanks doc

I thought my body would never be the same again, but you fixed it. My heartiest gratitude to you Dr Igudia for helping me cure my Hepatitis B successfully.

I am here to give this review to DR. Harry herbs on KZbin for treating and curing me from Lyme disease with his Herbs medicine i order from him and the medicine cure me completely with no side effect from the herbs medicine visit for he is helpful for Lyme disease DR harry herbs on KZbin.

QQQ. Could having tzken radio active iodine for goiter have caused the Sjogren,'s by effecting the salivary glands first?

Thank you dr Igudia on KZbin for all you do, just got my test result today and am now Hepatitis B negative. I will keep letting the world know about your good work sir

My heart just keeps thanking you and thanking you Dr Igudia for all you have done for me, you gave me your words that you could heal any sickness or disease, thank you for permanently curing me of my Type 2 Diabetes you are amazing.

Why has LACRISERT been discontinued by Bausch Health since 11-2020, considering how useful it is to improve the quality of life of people with Sjögren's syndrome who have severe dry eye? LACRISERT improves up to 90% the quality of life of these people (mostly women) and there is also no generic. I attach a video in English that in a few minutes provides enough information. kzbin.info/www/bejne/kH7IkIZslJaLj7M

All thanks to God for using dr otima to cure me completly from staph MRSA for the past 4 yrs i have be battling for this deadly infection i was about given up before dr Otima came to my rescure.

Living life to the fullest option was all I ever wanted thank you dr gboya for making that come through he gave me hope when I was lost all thanks to him 😊☺️.

I want to personally take time out to appreciate Dr Igudia on his KZbin channel for the herbs medication I ordered from him in curing my type 2 diabetes completely within just three weeks of using his natural herbs supplements

Being great full to Dr osaye from all time till all time I hope you find what your heart desires just as you have put a smile on many of our faces with just your hands and herbal’s More grace to you work doctor thanks so much for the medication,it did fight the (Els) and nailed it..

The day I came across Dr Igudia KZbin channel that was the end of my Hepatitis B virus after using his natural herbal medication in curing my Hepatitis B and I now live a more comfortable life again now.

I sincerely appreciate the work of Dr Igudia on KZbin who helped me with his natural herbs medication which I used in curing my Diabetes disease once and for all.

I really can’t stop thanking and recommending Dr Igudia on KZbin who cured my type 2 Diabetes with the natural herbs medication which I got from him on his KZbin Channel.

all thanks to DR. Osaka for curing me from Lupus with his natural herbal diet.

It’s something that unless u have it you can’t even begin to comprehend it and the after affects

Hey doctor I have ANCA positive. I have dark spot over all my onder leg and feet whitout kidney or lung damage. I'm always tired my stomach hurt and i lose weight 4 kg in one month. My question is,can you have ANCA vascullitis whitout kidney and lung dammeged? I have a lot pain in my head and nauseous. Fever and tinteling over my body also a burning feeling in my legs back and head. And muscle weakness all over my body. Thank you !! My doctor say probally dissease of Wegner!!

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Healing a community for 150 years, and now demanding you receive health care. Forcing employees to take an experimental drug that is NOT a vaccination. A vaccination prevents illness. With millions who have been so called "vaccinated," yet they still find themselves sick and going to the hospital. However, since UH helped create this experimental drug faster than any intended vaccination, they have something to benefit from. Just ask how much money they are getting for each covid admit. Just ask how much money they are getting for sending their employees to other parts of the hospital despite doing little to nothing. They say you need to get the vaccination to be safe, but then demand others get the vaccination so you are safe. This is not medicine and UH should be ashamed. But, it is a business and the bottom line comes first.

*Sjögren’s Syndrome is not rare, it is UNDER-diagnosed*. It’s more than just dry eyes and dry mouth! I didn’t start having those until later on in the course of my disease. I began sharing my experiences to find a community where I can talk about it, as it has been *disabling* and also to spread awareness of the connective tissue disease *Here is my story (so far):* I have primary Sjögren’s syndrome (pSS) and recently discovered cherry angiomas all over, with a new band on my upper back (the sign of Leser- Trelat is absolutely true), and bilateral, slightly indurated, erythematous, atrophic, arcuate patches on my cheeks with areas of hypopigmentation just below them, and on cigarette paper skin with some scaling around that, telangiectasiae and acneiform papules Both eyebrows have been losing hair over the superior/lateral aspect- also *highly pruritic* as well as FMF-looking patch on the lower back- all *extremely* pruritic. They recently came about with a surge of hormones (peri-menopause). I went to a dermatologist who had looked at the photos I’d sent ahead of time to my PCP and had already decided when I got to her office that I was working myself up before she even saw me because she spoke to me in her office with a patronizing attitude (which really hurt my feelings, by the way, and as soon as the visit ended, I sobbed while driving home) as she gave a quick glance at my back with a gentle swipe of her hand and then a pat on my shoulder. As an afterthought, she then glanced momentarily (and not with a dermatoscope) at my face and dismissively informed me that she wasn’t worried and that I looked “fine”. There is also a patch of spiky skin (I postulate this is also a variant of MF) near my left elbow and many subcutaneous nodules on my arms, trunk and thighs (some tethered and painful)- all of which were also not examined and were just as quickly dismissed by the doctor due to having family HX of them). Prior to seeing tiny capillary hemangiomas appear all over, I’d also been found to have a Bartholin gland cyst, axillary cyst, acrochordons, and now velvety, intertriginous patches (that I suspect to be AN). In addition to the small moles and new crop of cherry angiomas in a band across my back, there are several small, pruritic, erythematous papules on my chest, face and back, with symmetrical, confetti-type of vitiligo on my face, chest and arms. I get a photosensitive rash on my face, arms and chest (with systemic symptoms). The malar rash has always spared the nasolabial folds prior to experiencing the telangiectasiae there. The 3” follicular patch on my back has perilesional halos. There were other changes in my hair and nails, too (thinning hair, alopecia, deep longitudinal grooves, non-traumatic splinter hemorrhages, Beau’s lines, and distal nailfold dystrophy). Both sides of my family have autoimmune diseases, along with a family history of cancer (few different types- melanoma being one of them), so along with having red hair, green eyes and freckles, I’d insisted on biopsies (unfortunately, she failed to recognize the follicular patch, and did not take a punch of it, but took one nearby, instead). Again, unfortunately for me, she’d sent the biopsies (3 in total) to a pathologist who was not a dermatopathologist and the results came back as you would suspect for early (misdiagnosed) FMF. The dermatologist did not mention that FMF was in the differential to the pathologist, even though I told her that FMF is a concern. CBC and CMP with AI panel with UA showed a small decrease in lymphocytes, anemia (chronic), low lipase (chronic), mild protienuria, slight increase in eosinophils, along with zinc and vitamin D deficiency, but on the whole, WNLs (with the exception of weakly positive ANA by IIF and +SS-A; these had been repeated three times with exact same results). I have had 20 doctors so far (specialists, not including my PCP) and have had to fight tooth and nail for every test I’ve had. I’ve been made to feel like everything is due to anxiety or else they want to say it’s all GERD (which I do not have and was proven by EGD and took every type of PPI for months with no effect) or some kind of GI issue (they always want to say I have Crohn’s with no signs or symptoms except occasional steatorrhea, which coincides with chronic pancreatitis). Other signs and symptoms of pSS which I regularly experience are polyarthralgia, polyneuropathy, polymyopathy, asthma with recurrent bronchitis, unstable angina, previous SCAD episode, HTN and TIAs, neurological decline (mental fog, word substitution, memory impairment, etc.), BPPV, bilateral Frank’s sign, nephrocalcinosis, xerosis, oral aphthae, nasal aphthae, chronic dry cough, Raynaud’s, xerostomia, xerophthalmia, dysphagia (difficulty swallowing due to progressive esophageal narrowing), night sweats, random low-grade fevers, hyper/hypoglycemic episodes (not unlike HHS), palpitations, widespread, (tetany-like) muscle cramping, bilateral flank pain (bilateral nephrocalcinosis), epigastric pain with nausea and diaphoresis (chronic pancreatitis), tendinosis, fasciitis, bone spurs, dental caries, jaw pain, and chronic, burning lower back pain (both mechanical and referred). I also have an adrenal adenoma (which is currently being tested for pheochromocytoma), overactive bladder and obstructive sleep apnea. Having pSS complicates everything because none of my doctors are knowledgeable about the syndrome and have all- except my neurologist and nephrologist- have no answer, give no diagnosis, and subsequently, no treatment (with the exception of HTN, OAB and OSA, along with opioids for joint pain). I’m in pain all the time and cannot work due to the widespread pain and debilitating fatigue, along with hypersensitivity to everything (as soon as I get stressed out- physically or emotionally), I get hives, a malar rash, Raynaud’s symptoms, puffy eyes and am overall, just miserable. I’m not the type to be anxious or depressed, but after all of these tests and health problems, and knowing deep down that something is very wrong, it is starting to really depress me. I’m writing to any and all of the specialists that I know to find help so that the FMF does not progress, or so chronic pancreatitis does not turn into pancreatic cancer, and to find a good rheumatologist (I’ve already dismissed two due to their refusal to diagnose me based on clinical evidence, weakly positive ANAs and +SS-A). After researching all of these issues I’d been experiencing on my own, I am finding that my case is very similar to other people with Sjögren’s syndrome. They also attest how difficult it has been for them to finally get diagnosed (properly).

This is a great video‼We have a clinic that treats Sjogren's Syndrome naturally prior to glandular damage. I hope we can all continue to help the large majority of Sjogren's patients that are suffering.

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Nice video on Sjögren's syndrome. There is a very beneficial medical product for people with this pathology, called "LACRISERT" that is not currently manufactured. We call on the manufacturer BAUSCH HEALTH USA to resume supply. kzbin.info/www/bejne/kH7IkIZslJaLj7M 6.-DRY EYE: WITHOUT.LACRISERT.SPAIN SINCE 11- 2020-SJÖGREN'S SYND.

A very big appreciation goes to Dr IGUDIA on his KZbin channel who cured my type 2 Diabetes with his natural herbs medication and I now live a more comfortable life again.

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Remarkably Thank you

Thank you for the video. I want to thank Dr IGUDIA on KZbin who cured my type 1 Diabetes with his natural herbs medication