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I'm going through it im so scared of all that is happening to me and not much help I and so deficient in vitamin D and can't take it its taking a toll on me so bad i don't know what to do I feel like I'm dying in my own body I just need 1 person to care about me just a little to help me smh

New diagnosis here😢😢😢

Wow, very impressive! THANKS!

Is there a Sarcoidosis specialist in Mesa, AZ Area? Or do you treat long distance? Also interested in your findings on environmental impact. Could changing the diet help?

I have sarcodosis of my lungs 🫁

I have type 2 diabetes as well as pulmonary sarcoidosis,which has bone involvement,going for a heart mri to see if thats involved..it is so fustrating when no one understands it.

The CDC has been involved, also only in Africa .im 1/2white, 1/2 mexican american.. i have other medical problems. jaceel... .

Thank you.

Yeah so I have zero trust in pharmaceuticals, not to mention that most doctors have zero information on proper nutrition and no direction as far as any holistic or natural healing it’s all poisonous steroids and chemo, i’m trying to be nice but I’ve been suffering with this for years sure could use some help

How do I get in contact with you? I’m in New Zealand. Are there any supports you know of down here?

My left arm has huge clumpy masses and now the lumps are presenting all over my legs

I have ocular sarcoid. Lost vision in right eye due to scarring. Trying to left eye going. I go to Cleveland Clinic. In my left eye i have a blue and yellow checkerboard floater, it sits at about nine o'clock, in my eye, have had this for a little over a year, it wont go way. Any thoughts?

Sarcoidosis for me is chronic, seldom goes in remission. Living with for 21 years.

My husband had a very small crusty spot on his cheek that I kept annoying him to go get removed. He finally did and it came back positive for sarcoidosis. Of course we had never heard of it and were surprised to learn it mostly affects black women in their 30’s - he was white and in his early 60’s. He has gone in annually for the 8 or 9 years to get pulmonary function tests and occasionally a CT. His lungs test better than average and the CT shows small nodules on some lymph glands. But for the last few months he has had one joint after another become incredibly painful. At first they thought, Achilles, and then torn meniscus, but then it went to his shoulder, so obviously something to do with arthritis…? He has a number of doctors - the latest tests show pretty bad osteoporosis of his hip, which we were very surprised about, as well as very high calcium in his 24 hour urine collection. Serum calcium is normal. He was on prednisone but that’s not the best for long term - switched to methotrexate which helped but still some symptoms. Now he’s on Humera. Seems to be helping but early to say. It’s not nearly as bad as it was a few months back. The doctor believes he has arthritis - possibly reactive arthritis, but now I’m wondering if it could be the sarcoidosis? He’s always been healthy and active, never overweight, used to do a lot of cycling and eats pretty well. Just wondering how I can help him.

Any one know a sarcoidosis specialist I could go to in the Carolina's

Yup, told lung cancer & lymphoma until AFTER the biopsy of my chest lymph.

I had the pleasure of seeing Dr. Barreras a couple of times with my kids as her patients at John’s Hopkins many years ago. Wish I still lived on that side of country as I’m trying to deal with my Sjogren’s and now possible Sarcoidosis. 💜

Hi this is been tough. I have a lot of support from partner but not from basically anyone else.

I’m too nervous to hear this 😂 I’ll come back to it.

What a good doctor. So appreciated. Thank you.

Vigorously is hard for me

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…