I have asthma, bronchiecstasis and ILD, as well as rheumatoid arthritis. The RA was diagnosed 20 years ago, the asthma and bronchiecstasis 12 years ago, and the ILD earlier this year, and at a rheumatology appointment this week, I was told that my ILD was caused by the RA. Is anyone else in the same situation?
lung disease related to RA. - Lung Conditions C...
lung disease related to RA.
Hi Helen. Me 🙋. My lung disease was caused by RA too. 🙁 Interstitial lung disease is an umbrella term for so many conditions, has your been identified?
Love,
Cas xx ❤
It hasn’t yet, or I haven’t been told. I was supposed to be being discussed at the October multidisciplinary meeting. My brother has IPF but doesn’t have RA.
I have ra related ild , pulmonary fibrosis , there are drugs which help slow down the progression ,I'm under brompton who are the best .. all the best
You’ve had two good replies so far Helen with more to come perhaps. Thinking of you and sending good wishes.
Carole xxx❤️🤗
I have RA and bronchiectasis, but no-one has ever said they're related.
My gp told me when first diagnosed that heart and lung problems come with r.a. sadly she has now left the practice, I feel she would have looked after me better x
I’ve known from the beginning that I may get related heart and lung issues, also that RA is life shortening, which I didn’t really want to know!
Hi Helen. I was diagnosed with RA 25 years ago. Following Covid my immune system was so compromised that I now have two severe lung infections- Nocardia and TB! I was put on very strong antibiotics, which have subsequently seriously affected my liver and kidneys (not certain what's worse!)Unfortunately RA is one of those conditions that does compromise your entire immune system, particularly as we get older (I'm now in my mid 70's).
I wish your husband well and hope he receives the treatment he needs. Best wishes
I have read articles with it linked to Vasculitis. I think so many of our conditions link into these lung and heart issues. I often wonder if in many decades to come there might be one particular link to it all. Good luck and take care. xx
I think so too Dottie11.howre u feeling now x
I am now weight stable which is good. I have a visit to Endocrinologist coming up and will know more then. My dentist has written another letter to the hospital. He has never seen anyone take as long to heal before. Three months and still little progress. He is very experienced and has decades of work under his belt. I am concentrating on nutrition, rest, meditation, graded exercise as so weak. But most importantly trying to keep a sinus issue from going to my lungs. So far so good. Thank you for asking. How are you ? xx
Gd to hear you've made some progress.i hope yr mouth heals soon,it's dragged on 4u.i hope yr endo are gd & can help. Ive had the hardest yr of my life, with severity of AI+ no professional input whatsoever : (Family put foot down+been given 1st endocrinology appointment nxt week 🤞🙏 ,11mths aft sst showed I've no cortisol! I'm cautiously optimistic+ hopeful
I hope ucan get sinuses clear.i use steroid nose spray,antihistamines+ sterimar,+ decongestants at times.my sister was given a mometasone spray recently + it cleared her sinusitis.ive not tried that 1 x
mometasone spray -I have used in the past but sometimes makes my nose very dry and bleeds. Wishing you the very best for your Endo appointment. I really understand your comments re professional input , agree 100%. Deserve better and it seem to always come down to having to keep pushing for help. xx