Pulmonary Langerhans cell hystiocytosis - Lung Conditions C...

Lung Conditions Community Forum

57,110 members67,655 posts

Pulmonary Langerhans cell hystiocytosis

Artybb profile image
7 Replies

I've just recently been diagnosed with this lung disease. Does anyone know anything about it?

Written by
Artybb profile image
Artybb
To view profiles and participate in discussions please or .
7 Replies
Katinka46 profile image
Katinka46

I know nothing about your disease, but I just love the painting. The courage of the colours is wonderful. And the emotional journey in it. Well done.

I shall google your disease. It is a familiar name here. I am sure there are others who will share their experiences with you.

All the best

Kate x

Artybb profile image
Artybb in reply toKatinka46

Thank you so.much Kate. My GP said he had never heard of it either and I wonder why he is receiving a doctor's salary! It's a rare disease, related to smoking and Mr Google isn't the best place to look as it s a bit overwhelming. I'm so pleased that you like my painting and this has been my saviour throughout the loneliness of lockdown. We all have things to be grateful for and this helps us to cope through adversity.

My favourite poet, Seamus Heaney said "If we can winter this one out, we can summer anywhere. "

This is my new mantra.

Warmest wishes

B

sassy59 profile image
sassy59

I also no nothing of your lung disease but hopefully someone will reply soon who has knowledge of Langerhans.

Love the painting by the way. Xx

Artybb profile image
Artybb in reply tosassy59

Thank you so much for your support and your kind words.

B

Corin1950 profile image
Corin1950

There have been a few previous posts about this disease so if you put it in the search box they will come up and you can read other people’s experiences. I looked it up online and there’s lots of info. It seems it’s primarily caused by smoking so if you are still smoking you must get some help to stop. There’s so much help available now to do this.

Take care

X

Mrsclh profile image
Mrsclh

Hi i was diagnosed with plch last year as well as a long list of other things. Iv had a complicated time of things under 8 different consultants for all sorts of issues but my rheumatologist was the only one that explained things to me which was months after leaving hospital my lung dr that found it and diagnosed me was useless.

Look forward to hearing from you

Mrsclh

2greys profile image
2greys

radiopaedia.org/articles/pu...

Not what you're looking for?

You may also like...

Langerhans cell histiocytosis

Hello I got my results from my lung biopsy yesterday An Iv'e got a rare disease Its called...

Langerhans cell histiocytotis

Hi I have been diagnosed with pulmonary langerhans cell histiocytosis last year...I now have cysts...
Sandrapez profile image

Is anyone out there with Adult Pulmonary Langerhans Cell Histiocytosis ?

Is anyone else out there with this condition Adult Pulmonary Langerhans Cell Histiocytosis. I need...
quantum66 profile image

LCH -Langerhans cell histiocytosis in jaw

hello I hope somebody can answer me .I was diagnosed with LCH 1 month ago but I have it located...
mary27bogd profile image

Has anyone been diagnosed with LangerHans Histiocytosis cell X?

I have been diagnosed with this condition after a lung biopsy.I have been told its rare and my...
kelv37 profile image

Moderation team

See all
AsthmaandLung profile image
AsthmaandLungAdministrator
moderator_AandLUK profile image
moderator_AandLUKAdministrator
AdminTeam profile image
AdminTeamAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.