Welcome Guest! The IOSH forums are a free resource to both members and non-members. Login or register to use them

IOSH Forums are closing 

The IOSH Forums will close on 5 January 2026 as part of a move to a new, more secure online community platform.

All IOSH members will be invited to join the new platform following the launch of a new member database in the New Year. You can continue to access this website until the closure date. 

For more information, please visit the IOSH website.

Postings made by forum users are personal opinions. IOSH is not responsible for the content or accuracy of any of the information contained in forum postings. Please carefully consider any advice you receive.

Notification

Icon
Error

Options
Go to last post Go to first unread
Admin  
#1 Posted : 09 August 2007 09:01:00(UTC)
Rank: Guest
Admin

Posted By Ian Dakin
Hello

I am currently looking at the risks to an office worker who has Lupus.

She is currently receiving treatment via the NHS, but still suffers from joint pain (sometimes intense) and is fatigued when she gets home from work.

She has had a DSE assessment and I have carried out an assessment of the environment she works in. All the measurements were OK.

She is being referred to an immunologist through our workplace occupational health procedures.

Does anyone have any experience of managing the H&S of a Lupus sufferer or any tips on how to proceed?

Regards
Ian Dakin
Admin  
#2 Posted : 09 August 2007 09:04:00(UTC)
Rank: Guest
Admin

Posted By Robert K Lewis
You really can only do this in conjunction with their consultant as the symptoms and their management can vary greatly between patients. I have only known 2 cases in the last 30 years and received help from their medical practitioners.

Bob
Admin  
#3 Posted : 09 August 2007 10:20:00(UTC)
Rank: Guest
Admin

Posted By Angela Oakey-Jones
Hi Ian,

A family friend of mine suffers with Lupus and spends a great deal of time as an in-patient at St Thomas' Hospital in London where there's a specialist treatment unit.

It's probably worth contacting them to learn more about the nature of Lupus (from my scant knowledge, the immune system can attack healthy tissue at almost any time, and as a condition, it can be made worse by things like sunlight.) Also there's a really helpful charity called Lupus UK (www.lupusuk.com)

If I were you I'd probably set up some kind of rolling risk assessment, akin to an ongoing assessment during pregnancy, where the person contacts you (and their boss) when they detect changes in their condition - you can't be psychic, but you should stay in touch.

Hope this helps

Angela
Users browsing this topic
Guest
You cannot post new topics in this forum.
You cannot reply to topics in this forum.
You cannot delete your posts in this forum.
You cannot edit your posts in this forum.
You cannot create polls in this forum.
You cannot vote in polls in this forum.