Any body with serositis with their lupus, like me. - LUPUS UK

LUPUS UK

32,241 members28,598 posts

Any body with serositis with their lupus, like me.

willowwag profile image
8 Replies

Is there anyone here that suffers serousitis with their lupus sle, serositis inflamation of the, heart, lungs, abdomen and lining of the abdomen. Not alot of information about on this side of things x

Written by
willowwag profile image
willowwag
To view profiles and participate in discussions please or .
Read more about...
8 Replies
anbuma profile image
anbuma

hi i went to A&E yesterday (hav e lupus symptoms even tho dr denies it)with abdo /chest pain and for 1st time a dr finally gave me an explanation(at a push)said my heart was fine btu woke this morning with the hard swollen stomach so If not OC or cyst could be the stomach lining(will add this to the lsit of q's I want answers to.

willowwag profile image
willowwag

Hi there its a awfull feeling and the pain is awfull, yes get them look as this..i had the pain for 10 years before a training doc in my surgery after seeing my many a&e admissions decided to take on my case for her final year, a few specialist app later and sent to see the right people them boom i was told i had lupus, and serousitis...i have other conditions attatched also, hypermobility, raynards, vasculitus and a abdominal hernia because of it....what is your symptoms...thank you for posting back so good to find someone else who might have it also.

gazorpf profile image
gazorpf

When I was diagnosed I had all of that. I had congestive heart failure (pericarditis, pleurisy, pleural effusions), kidney failure, costochondritis, kidney failure, bone marrow failure and cerebritis. Lupus can cause inflammation anywhere and everywhere. From your question it is not clear what information you are seeking. Take your meds faithfully, work with your rheumatologist, manage stress. That's all you can do.

zebedee01 profile image
zebedee01

Yes I suffer with serositis, its horrible!

willowwag profile image
willowwag

Hi gaz, i was just woundering if anyone else was suffering with the same sort of things...it mainly seems to be information on the net about te joint pain etc that we get but not alot of in depth info on this side of things, gaz did they manage to get you serositis under control..its so difficult my eposodes make me feel like whatever next, i work and im really thinking of trying to claim pip as everyday im struggling to get thro the day x

willowwag profile image
willowwag

Hi zeb, its just terrible ive never felt in so much pain even child birth was easier than this lol! Have you found anything that helps.

zebedee01 profile image
zebedee01 in reply towillowwag

Well steroids seem to be the only thing that help it to be honest! But I am quite new to all this. It seems every time they reduce my steroids it flares back up! I have been admitted to hospital 3 times within a year :( And then when they get my steroid dose back up the pain gets better within a few days x

Eagle41 profile image
Eagle41

I had serositis last year. Long story but lots of problems led my dr to order liver biopsy. That is when it got serious. My body didn't like the "invasion". It went crazy. Within 15 min of the test I started feeling severe (and I mean really severe) pain in my chest and abdomen. I seriously thought I was dying. My husband said I kept saying that and that I was praying out loud. I don't even remember my first two days in hospital. They did lots of tests and found inflammation around lungs,heart, and intestines. Dr says the inflammation only shows if very bad. I also had pleural effusions. My sed rate and crp were very elevated. CRP was almost 300. High doses steroids and ten days later I went home. It has been 8 months. While I am better than the hospital I am still worse than when I went into the hospital. I had no idea serositis could be so bad.

Not what you're looking for?

You may also like...

Lupus sle, but now lupus has added serositis to the mix also any information welcome on it.

On meds due to my lupus sle, but consultant has now informed me my lupus is also adding in...
willowwag profile image

innoculations and lupus/ lupus like syndromes

can anyone advise me if there has ever been an research conducted into a correlation of people...
scoobydoo1 profile image

Lupus Like Syndrome?

Hi there, ive not been well for 6 years, all the usual Lupus symptoms, my rheumy says (in my last...
kazzz profile image

Lupus Fog?? Any one with tips?

Hi All! I am Canadian...I live near Ottawa, Ontario, but have found this site to be so very...
Hockeymom12 profile image

Has anyone had severe thigh pain with their lupus?

Hi, I suspect I have lupus and am endeavouring to get tested for it as I have many of the symptoms,...
Spicer21 profile image

Moderation team

See all
Debbie_kinsey profile image
Debbie_kinseyAdministrator
chelseawong profile image
chelseawongAdministrator
michaellasmith profile image
michaellasmithAdministrator

Top community tags

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.