Has anyone been diagnosed with Langer... - Lung Conditions C...

Lung Conditions Community Forum

56,314 members66,939 posts

Has anyone been diagnosed with LangerHans Histiocytosis cell X?

kelv37 profile image
8 Replies

I have been diagnosed with this condition after a lung biopsy.I have been told its rare and my hospital have never come across or treated it. Im now in the hands of Papworth hospital and having a lung transplant. Im having 3 day transplant assessment on Monday. /i was wondering if anyone else has this.

thanks

Written by
kelv37 profile image
kelv37
To view profiles and participate in discussions please or .
Read more about...

The ability to reply to this post has been turned off.

8 Replies

Sorry I have never heard of this There are a few member though that are on the transplant list so hopefully some one will be able to help with that, give the BLF helpline a ring on monday and they will be able to help Wishing you lots of luck on Monday

julie xxx

I haven't personally got this but the MacMillan.org.uk site seems quite helpful. I know that Papworth has an excellent reputation so I think you are in the best hands. Very best wishes. X

kelv37 profile image
kelv37 in reply to

Thanks for that. I been there before and was well looked after

x

tracey1971 profile image
tracey1971

hi kelv37 i was diagnosed with langerhans cell histeocytosis 4 years ago there is a web site you may find helpful histio.org it has lots of information. i am seen at the royal brompton every 6 months.

kelv37 profile image
kelv37 in reply totracey1971

Hi Tracey thanks for that. I did research found some sites but they was linked to America but missed that that one. What treatment are you taking. Mine deteriated after getting pneumonia 3 times this year and ended up in ICU with stage 2 resperitry failure. Strange when I go to differet hospitals and they never heard of it and they have to look it up lol

tracey1971 profile image
tracey1971

All the sites are in America for some reason,I'm not on treatment as such only inhalers and occasionally steroids. But have been told at some point I will need a transplant as it is slowly deteriorating. What treatment do you receive ?

kelv37 profile image
kelv37

Yes I just looked.I was on the same as you but mine has been 6 years and now on 3 inhalers calcium tabs carbocisteine, Omeprazole, Unipyllin, perdisone, oxygen and nebs but nothing now works and gone down hill now. Still smile and laugh though gets me through it and still work even though it very hard as Im a Plumber but lookig forward to this Monday as Im having 3 day transplant assessment .

tracey1971 profile image
tracey1971

good luck with everything keep me posted on how you get on x

The ability to reply to this post has been turned off.

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 histiocytosis

Hello everyone Iv'e been diagnosed with L C H. I wonder if anyone here has this

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

Langerhans cell histiocytotis

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

has anyone had a double lung transplant

has anyone on here actually had a double lung transplant.....i had an assessment at harefield and...

Moderation team

See all
AsthmaandLung profile image
AsthmaandLungAdministrator
moderator_AandLUK profile image
moderator_AandLUKAdministrator
Claire_ALUK profile image
Claire_ALUKAdministrator

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.