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örülök, hogy találkoztunk! Nekem az 1970-es években találták meg a sarcoidosis betegségemet a tüdőmön. IV-es stádiumban voltak mikor szövettannal igazolták. Magyarországon az orvosok akkor még alig ismerték, ezt a betegséget, de volt Debrecenben egy professzor, akit ha végre megtaláltak, akkor prednizolonnal kezdtek. Fél év után csípőfájdalom miatt az összes cortizon származékot kipróbálták, de a csípőimben a femur elhalt. 4 évig minden létezőt kipróbáltak, de ha elhagyták a cortizont, megint elindult a gyulladás. Aztán a saját döntésem az volt, hogy gyógyszereket nem szedek. Akkor fejlesztette dr. Béres József a Béres cseppet, ami nyomelekből ásványi anyagokból állt és stimulálta az immunrendszert. Csak ezt szedtem ezután, és 10 év alatt írta le a professzorom, hogy elmult a sarcoidózis, már csak hegek maradtak a tüdőmön. ma 45 évvel a kezdetek után szedem a Béres cseppet, a tüdőm, szívem gyengélkedik, de élek, mert sose adtam fel a reményt!

Is there a sarcoid clinic near south east Louisiana?

Is there a sarcoid clinic near south east Louisiana?

Sarcoidosis was overwhelming until I found Planet Ayurveda. Their treatment is the best solution I’ve found.

Today i just diagnosed with sarcoidosis in lung.

I like doing the plank. I might try it again at the weekend. Thank you for this advice

I have sarcoid. At this point it has mainly affected my parathyroid/hypercalcemia. No serious issues with lungs but there is granuloma. I have CKD resulting from Sarcoid/Calcium toxicity. Was on presidone for a few years. And hydroxyclorquine for four years. Got off it for fear of eye issues. Are there any new Rx alternatives for auto immune/ anti inflammatory that won't potentially ruin my eyes or liver. And of course CKD. Thanks

Very informative & nice video on Sarcoidosis! It can be a tough battle, but Channel and sir offer hope and guidance. My friend's journey with sarcoidosis took a positive turn with Planet Ayurveda's supplements. Let's raise awareness and empower each other! 🙌

Thank you so much for such an informative and educational session. Dr Raj is fantastic and I love his upbeat style. I have pulmonary sarcoidosis (in remission) and sarcoid in my eyes. I live in New Zealand and must say I am well looked after currently with yearly checkups with my pulmonary specialist (although he doesn’t seem to know or share anything other than the basics) and two monthly checkups with Uveitis specialists etc. I was diagnosed via a bronchioscopy in 2020 and put on prednisone for a year. I completely agree with Dr Raj diet exercise and a healthy lifestyle is key to staying in remission. Thanks to Life and Breath Foundation I don’t feel so alone with this illness and have learnt so much that helps me stay positive. I found magnesium really helped me. Keep up the great work I’m sure many of us around the world appreciate your dedication to helping us with what can be a very difficult disease.

Amazing information. Thank you

I have NS and it's every three- four months there's a new symptom. I have numbness, vision problems, balance issues and weakness. I volunteered to be a test patient in a study of the disease by the Ohio State University. O hope they learn something that helps cure this horrible disease

I need help. I was just diagnosed and none of my Dr's seem to know much about it. So far they have found it in my lungs eyes and mouth. My teeth are literally grumbling out of my mouth for the last 6 months but I had to quit my job so I don't have the money to get them pulled and put new teeth in. I cannot find a way to make my insurance pay to help me since it is due to my sarcoidosis. What should I do?

Where is Dr. Raj located - I', in Houston, TX and I'm on a wait list to see a Pulmonogist based on lung CTs and bronch EBUS MD Anderson ruled out cancer and said Sarcoidosis is what they think

For a change I have to admit , I like this pulmonologist Dr Raj. First & foremost I like his expertise , second to his apparent sarcoid & pulmonary expertise, would be his personality and sense of humor, which I’ll tell you , is hard to find. I would love to see or have this doctor as my pulmonologist. Too bad he’s not on the east coast near NJ/NYC area. I will say , I did consult back in 2016 with Dr Morganthau in NYC. I’ve had pulmonary sarcoid since 2004, thankfully I’m not on prednisone , which can do more havoc on the body/organs , than the sarcoidosis itself. I like Dr Raj’s demeanor and his seemingly prudent and conservative approach on whether to even treat those of us with sarcoid. He admits that sarcoid can mimic several other conditions/diseases, as most of us proactive sarcoid patients already know. That’s why I think a Dr’s choice of therapy for sarcoid becomes a paramount decision by any specialist the sarcoid patient might see. Bottom line, Drs. need to rule OUT multiple symptoms a sarcoid patient might present with “BEFORE” initiating ANY of these treatments mentioned in this webinar. Would hope to see this particular Dr do another webinar , preferably ,an interactive zoom with Audio/Video so patients can asks him questions directly.

Your life will turn upside down with Sarcoidosis. I was denoised with Sarcoidosis in 2005 with my lungs. Now it spread to my skin. This disease is no joke so take it seriously. Bug your doctor as often as often as you need to. This is your life so do what can you do to get better. I am 61 so, I am scared of what don't know what is go on in my body.

Living with sarcoidosis presents its challenges, but discovering Planet Ayurveda has been a blessing. Their treatment and medicine are amazing, offering hope and a path to better health for those with this condition.

hey dr Harris, i am a obs/gynae doctor, want to write you on your email

Very useful & healthy food tips for Sarcoidosis! Big thanks to this channel and Doctor for addressing sarcoidosis! 🌿 Dealing with this condition can be overwhelming, but Planet Ayurveda's herbal remedies have been a game-changer for me. My neighbor, who also struggled with sarcoidosis, found relief with their supplements. Don't let sarcoidosis dictate your life; give Planet Ayurveda a try!

I have CBD for sarcoidosis and it helps a lot to sleep and get rid of nerve pains

Dr Burg has been a huge help with taking prednisone The Dangers and the alternatives

D3 with K2 50000 IU a day or more is what I’m taking

I've tried countless treatments for sarcoidosis, but Planet Ayurveda's approach is by far the most effective for me.

Best doctor I have ever had, because of the way he relates to the patient in wording, response to concerns, research, it feels like he actually cares about my life in general which i am not used to because we were taught to smile and say we feel fine at doctors because we don’t want to be impolite and take up their time.

When doing the straw breath practice, is it small increments of continuous inhalations until you fill only the lower part of the lungs before the exhalations? The first few inhalations go to the lower lungs, my diaphragm expands, then I seem to fill the upper part which causes me to suck my stomach in. Does this mean I'm using the upper chest, and I should stop beore I get to that?

So grateful I found this. Thank you for sharing your journeys. I recently was diagnosed with neuro sarcoidosis. I related to the last testimony. I’m alittle overwhelmed & scared but coming across this video has brought some peace of mind for the future. Thanks again and how can I get connected?

Thank you both for your support ❤

Dr. Harris you are speaking on measurements of Vitamin D level and PTH; if we do not have the tools how can this be checked? It’s extremely expensive to go to a Doctor and ask for a check of these different requirements. They only check for what they want to check not what the patient recommends. If we get well they lose money…

Dona walk in nyc!

Erica what are the side effects from?

This is so helpful 🙏🏽. Thank you

I first want to thank my Lord and Savior Jesus Christ,I first heard about sarcoidosis were at the age 26. I’m a singer but noticed that I was having problems with breathing so went to my doctor. My doctor told me after X-ray I had Granuloma. And he told that I would after get older it would change to sarcoidosis. In fourties’ I started getting pneumonia a lot until I had two headaches because my oxygen was 60 low. I was diagnosed I had sarcoidosis and it effecting my lungs. 2006-2008 I flare up with my skin and joints and I couldn’t walk sitting everything cause pain. And now I’m 71 years old and I’m having flare up a whole lot. I take steroids for the flare ups. Thanks you Doctor there are not many people understand sarcoidosis.

I have a persistent cough from 2017 then 2 yrs later I was told I will need AVR. Then in Sept. 2022 I had the AVR, then a year later I had 3 failed attempts at getting lymph node samples for biopsy tests. The 4th attempt was a day surgery and I was told a month after that I had a non necrotizing granuloma - sarcoidosis. I have noticed inffrequent joint pain with the knees, mostly in connection with riding a bike.

Is it okay for a sarcoidosis patient okay to take vitamin k2 50000. Because my vitamin level was 16 l

I am being investigated my bro has neuro and my mum pulmonary

I just got diagnosed with this disease and I’m trying to get a better understanding on what it means for me

Is brown rice good

I love the work you do. I am not sure if you even realize how valuable these presentations are for us patients who often feel helpless.

Hi I have breathing n cough symptom I'm going for ECO want to know more information Shireen South Africa thank you

This really doesn't fully address the core issue of potential hypercalcemia in Sarcoidosis patients. Large doses of D3 can be very effective as an immunomodulating agent. I'd like to see someone try therapy along the lines of the Coimbra protocol, presumably combined with a reduced calcium diet or a calcium-blocking substance.

This is THE topic since I got diagnosed with sarcoidosis and osteopenia. Some say "you have to take it" , others say "never ever, it will destroy your kidneys". And as the illness itself was not already stressing, this different opinions make it even worse.

Diagnosed in 2007. I have Pulmonary and Cardiac Sarcoidosis via a biopsy and have a pacemaker. It’s in my eyes, on my skin. Arthritis in my hips( 2 replacement, Both knees both replaced, Awaiting Spinal lumbar fusion. PTSD & TBI. It’s a nightmare.

Thank you Dr. Harris! I missed a great discussion on Stress! I had NO idea about the information on stress I did not know! Thank you for the recording!

Thank you Sean! I am grateful for your organization and the medical experts who so graciously share their knowledge and how to treat this disorder. God Bless you all!

I developed Sarcoidosis in 2009, initial diagnosis was Hodgkin cancer. Later after biopsies it was confirmed to be GI, stomach and lymph nodes sarcoidosis. Later throughout the years, it has spread to liver, kidneys, lungs, around my heart and eyes. I’m searching for support and guidance on getting this under control without medication.

What about copper ?

Thank you, Dr. Harris, for all this amazing information. I haven't been diagnosed yet; I will be going for testing. I've had lung issues my whole life and at age 52 received a pacemaker for heart block and chronotropic incompetency. My new cardiologist says it's unheard of for someone that age to develop heart block without ischemia, and so he suggested it might be sarcoidosis. He may have put two and two together after seeing countless other cardiologists and pulmonary specialists, we shall see. Googling, I discovered a study that found a common infectious agent in sarcoid patients: P. acne. Then I found another study that found thyme to be extremely effective against that pathogen, at least in vitro. Since thyme is essentially food, safe for the most part, I took two drops of thyme oil in a glass of water. I had a rather marked Herxheimer reaction, so something's getting killed off. I will continue my experiment (two drops a day is about what I can currently handle, herxing wise) in hopes of killing off whatever my immune system is trying to wall off with the granulomas. Note that oregano oil and cat's claw did not give me the same herx reaction, so thyme is the one working for me. Should be an interesting ride. I'll take corticosteroids if I have to, of course, but I'm excited to try to get rid of this infectious agent in a safe way.

I was diagnosed with Sarcoidosis 3 years ago from bioposy. I have it in the heart lymph nodes lacrimal gland, skin, saliva gland, right bicep , left shoulder,both lower leg muscles. On 20ng methotrexate injections weekly abd humira 60mg fortnightly. I have dual full thickness cornea transplants due to kerecotonous 20 years ago. Approx 5 years ago my right cornea rejected for the first time, DMEK done and has rejected another 6 times, with DMEK being completed for each rejection. Both left and right rejected Late last year. My question is, is it possible sarcoidosis has caused the rejections.??

My Father has cancer. I was listening to a too oncologist from the UK and he said Vit d would be the first supplement he’d recommend to someone with cancer. My father also has sarcoidosis. What do I do?

Does stress contribute to the condition

Thank you all involved in this video 🎉