Doctor ur number one in UA-cam but u need to enhance the exhibit of your slides to get professional I would like to thank u lot u helped my wife we are seeing u from Africa
I need help understanding my Adult Pulmonary Langerhans Cell Hystoidcytosis. I was diagnosed in 2014. I had a small snipped of my lung taken and sent to the Mayo Clinic and they initially as well as Kaiser Permanente pathologist not diagnose me. I then had lung surgery and they determined that I have APLCH. With COVID-19 I am considered as a vulnerable part of the population and have stayed home due to being afraid of the consequences. Has there been any research pertaining to how this affects those of us who have APLCH? I am being asked to go back to the office but am scared so bad of being exposed.
As someone who had LCH at 15 and a relapse at 22. I've been 18 years "free of it". There was no lymph node, bone or bone marrow involvement. As it turns out, I'm type O-, can I safely donate blood?
I love your videos and I love u more . But please dr ; we need to understand what is the exact pathophysiology for each symptoms not just in this video (since as u said ; it is poorly understood) but in all videos. I can not keep the clinical features without deep knowledge from where these features are come . Thank u again
Ahmed AbdSam there’s plenty of research and Dr’s who know plenty about this and shouldn’t be speaking like this Dr. I had it and half of what he said is incorrect! www.histio.org
I had Langerhans Cell Histiocytosis and there isn’t a Dr. out there that doesn’t need to know what it is. We’re misdiagnosed and half of us are dead before you all figure it out! I was really unlucky with it and had MDS, Monosomy 7 as well. But, luckily i’m in Northern Va. and Hopkins saved my life. I suggest you look into the research Kettering and TX Children’s is doing. I didn’t do 12 months of chemo for 3 years straight for something that is small. Then the MDS. Please do yourself a favor and research it. I’m not a Dr. and I know more than you!
its good to see you uploading dr bolin, you are the best
Doctor ur number one in UA-cam but u need to enhance the exhibit of your slides to get professional
I would like to thank u lot u helped my wife we are seeing u from Africa
Thank you Dr
great video!
I have the Langerhans cell sarcoma
thank you
Nice video sir
what resource is best for reading medical case studies , from the most common conditions to some interesting ones ?
Dr Bolin, please do one on ectopic pregnancy 😊
I need help understanding my Adult Pulmonary Langerhans Cell Hystoidcytosis. I was diagnosed in 2014. I had a small snipped of my lung taken and sent to the Mayo Clinic and they initially as well as Kaiser Permanente pathologist not diagnose me. I then had lung surgery and they determined that I have APLCH.
With COVID-19 I am considered as a vulnerable part of the population and have stayed home due to being afraid of the consequences.
Has there been any research pertaining to how this affects those of us who have APLCH? I am being asked to go back to the office but am scared so bad of being exposed.
I had histiocytosis x as a child. I was diagnosed at just a few weeks old back in 1970. I have a large dent in my skull as a result of this disease.
what is the diagnosis process ?
As someone who had LCH at 15 and a relapse at 22. I've been 18 years "free of it". There was no lymph node, bone or bone marrow involvement. As it turns out, I'm type O-, can I safely donate blood?
You sound like a young doctor. Langahans cell is german terminology. And I suffered with this when I was 14 in my jaw x
I love your videos and I love u more .
But please dr ; we need to understand what is the exact pathophysiology for each symptoms not just in this video (since as u said ; it is poorly understood) but in all videos.
I can not keep the clinical features without deep knowledge from where these features are come .
Thank u again
Ahmed AbdSam there’s plenty of research and Dr’s who know plenty about this and shouldn’t be speaking like this Dr. I had it and half of what he said is incorrect!
www.histio.org
Ty for sharing. This disease got me at age 34, it is attacking my skins an both lungs. It took a lung biopsy to diagnose it from Mayo Clinic
I'm Maninder singh, from India. I'm LCH patient since 2013
Hi maninder ! Can I able to contact you? I'm also from India
Hello Maninder,Saranya can I contact you?
@@ManinderSingh-dt4gi Can you please share your contact number, I am also diagnosed with LCH, want to discuss with you. Thank you
@@rittwikghosh7309 Hi please share your contact details, I am diagnosed with LCH, want to discuss. Thank you
I had Langerhans Cell Histiocytosis and there isn’t a Dr. out there that doesn’t need to know what it is. We’re misdiagnosed and half of us are dead before you all figure it out! I was really unlucky with it and had MDS, Monosomy 7 as well. But, luckily i’m in Northern Va. and Hopkins saved my life. I suggest you look into the research Kettering and TX Children’s is doing. I didn’t do 12 months of chemo for 3 years straight for something that is small. Then the MDS.
Please do yourself a favor and research it. I’m not a Dr. and I know more than you!
Yo i wanna talk to you about lch reply
@@YoungFlashWade3 okay?
@@cdenton9484 where did Lch affect you
@@YoungFlashWade3 head to toe! Is there an easier way for you to communicate about this?
@@cdenton9484 do You have Instagram