Painting & decorating?: This is a... - Scleroderma & Ray...

Scleroderma & Raynaud's UK (SRUK)

10,987 members5,511 posts

Painting & decorating?

Geordie_Kate profile image
5 Replies

This is a crackers off the wall question but here goes. Before starting cyclophosphamide, I decided to blitz through painting all of my doors and frames. I thought I would get it out of the way before my lungs deteriorated any more (I have lung fibrosis as a result of scleroderma). To my astonishment, my breathing got easier with gloss paint fumes. Has anyone else found this or have I succeeded in melting my lungs?

Written by
Geordie_Kate profile image
Geordie_Kate
To view profiles and participate in discussions please or .
Read more about...
5 Replies
uknlv profile image
uknlv

Hi Kate

I certainly hope not lol! I have not done any decorating for some time, good on you for being able to do all this with your scleroderma! So no idea if it helps or not, I know it isnt the best to breath it even with normal lungs, but I would imagine your breathing would be much worse if it was making the condition worse! Best of luck and hope the painting turns out nice!

BevMyers profile image
BevMyers

Probably due to all the exercise you did when you were painting and decorating!! Exercise improves your life - do as much as you can (can I suggest you open the windows though next time! ;-) )

Jane18 profile image
Jane18

How are you coping with the medication? I think I could be prescribed something similar at my next appoinment at the Lung Clinic.

Geordie_Kate profile image
Geordie_Kate in reply to Jane18

Hi. I've had three lots of cyclophosphamide treatments and it seems to have stabilised my lungs. You feel a bit quesy the following day but otherwise fine.

AshtonRains profile image
AshtonRains in reply to Geordie_Kate

Hi Kate,

I'm 21 and starting Cyclophosphamide on the 6th December, and haven't been told anything about it. What side effects have you experienced? Ashton x

Not what you're looking for?

You may also like...

Mycophenolate mofetil, poss side effects.

Hi everyone, I have limited system sclerosis with raynauds and slight sjogrens symptoms, dry mouth...

Shadow on my lungs

Recently I have had 2 CT scans, one with contrast, and they have found a 'shadow' on my lungs. I am...

Poor Memory and vertigo.

Hi I was diagnosed with limited SSc & Raynaud's 3 years ago. I have all the usual symptoms, hands,...

One of the Scleroderma patients

Hi All, I am new here and I found this forum/group along the way searching for info for...

Feeling Low

I'm feeling so low at the moment , I know its all part of the Raynauds , but the cold is just too...