Telling your employer about your Arthritis.
Interested in hearing your experiences about letting your employer know about your condition, and your thoughts on my situation if you have any.
I have Psoriatic Arthritis which has not responded yet to any treatment in New Zealand on my current Visa so I'm moving back to the UK to see if I have any better luck on the NHS. I've got a job offer starting in April. Its a desk job like my current one with a national charity who would be I hope pretty responsible employers (I've worked for some chancers in my time 🤑).
For the first time I will tell my employer that I have this condition as I'm over having to pretend to be able to carry things, not be fatigued, or make excuses at work social events etc. I put it on my equal opportunities disclosure form on the application - but who sees those forms and what do they achieve? I don't need a fancy desk yet, and I bring my own mouse and keyboard with me like a travelling IT salesman already so I'm all good in the main. Just need time for appointments etc.
When did you tell your employer? Did you wish you did this earlier, or even before your started? Should I tell them now - and if so do I tell HR or my manager do you reckon?
All the best folks - thanks for reading this far!😎
Comments
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Hi thembrown
I am sure some of our members will share their experience of telling their employer about having arthritis. I thought you might find this section of the website useful to read as well.
let us know if you have any further questions
Best Wishes
Sharon
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My diagnosis happened while i was working for my current employer. I was in a good position because i have a great manager. I kept him updated whenever i found out a little more or any of my symptoms changed or intensified.
I got a change in role (warehouse work) so i could work in the office on admin now. I also managed to get a change in hours so i can start early in the morning and finish early. (i struggle with commuting and want to avoid rush hour).
HR & OH are fully aware as well as my area manager, I've found its easier to just be honest and open about it. It's never easy explaining it, but its better they know and can support you.
Good luck in the future, if you need any more info give me a shout.
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I informed my employer but received no support, I have been currently off sick and supposed to be going back after lock down, but again my employer is saying certain jobs I need to do but allowing other staff to get support, feel I am being discriminated against
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I was off work three months in March 2016 when I first developed Rheumatoid Arthritis but from my first consultant's appointment to now my employers have been very good and they allow me time off so I can have blood tests, etc. I always found it best to be very honest and tell them how things are. I have been shielding since March at that time my Firm put me on furlough leave and when I had my recent telephone call with my office manager I was informed that this has been extended to the end of July as I am "high risk" due to my condition.
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Hi kazza. I asked the same question about extending the 12 week Sheilding. Also I wonder if we will receive a letter from the NHS to confirm this. Thanks Yellowstone0
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I informed my employer when I started a new job and they referred me to occupational health (I work for a county council). Other than recommending things that were impossible they did allow me to have a very rare and coveted parking space which has been amazing. They also made it clear they supported me going to all appointments, physio etc which was great. Employers have a legal duty of care and I would be open and honest right off the bat rather than trying to explain after the event when something goes wrong.
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Hi Everyone,
Hope you are all having a great day!
This is my first post on the website so forgive me if I say the wrong things!
I have only recently been diagnosed with rheumatoid arthritis and when I tried to tell my employer I have been advised to work from home and I have to get regular blood tests done he was so rude to me he had me in tears. He accused me of making the whole thing up, said it was convenient I had a new illness when furlough had just ended and that I have never shown symptoms despite living with pains and decreased mobility for periods of time for up to 3 years. He questioned whether I should take the medication and queried my dedication to the business. Accused me of jumping on a bandwagon with arthritis and of being a drama queen because he knows "hundreds" of people with arthritis who don't have any issues. He also said because I am only 33 the consultant must have got it wrong as only older people get it.
I am trying so hard to get a new job but there is nothing out there. I have never felt so ashamed and embarrassed in my whole life about something that I cannot control. Even my colleagues have accused me of scamming some time off when all I am doing is working at my kitchen table rather than in the office. I have actually even been working harder which upsets me more because I pride myself on my work ethic. I was always a sort of "teachers pet" and this has sort of ruined my confidence at work and really stressed me out.
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If you check out the "Work and Financial" part of the forum you will find a lot of advice about getting things sorted at work. Plus there is the Disability Law Service, go to https://dls.org.uk/our-services/employment/ they can help with employers having to make reasonable adjustments for disabled staff.
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Hi @Cazmataz
Thank you for posting about your recent, horrible experience with your employer.
You have recently been diagnosed with Rheumatoid Arthritis and have received no support from your employer. These misconceptions are exactly what we are trying at Versus Arthritis to correct.
We have lots of info on our website about work, rights etc:
We also have info on RA which you may find helpful in learning more about your condition, and it might even be an idea to show this to your employer to try to educate him on a condition that he has no understanding of:
Please come back and let us know if this was useful or how you got on with speaking to your employer. Remember our helpline is also on hand - freephone 0800 5200 520 open Monday-Fri 9am-8pm (exc bank holidays).
Best Wishes
Debbie
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Thanks Debbie :) I will have a look at this now xx
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Hi Everyone,
Hope you are all having a great day!
This is my first post on the website so forgive me if I say the wrong things!
I have only recently been diagnosed with rheumatoid arthritis and when I tried to tell my employer I have been advised to work from home and I have to get regular blood tests done he was so rude to me he had me in tears. He accused me of making the whole thing up, said it was convenient I had a new illness when furlough had just ended and that I have never shown symptoms despite living with pains and decreased mobility for periods of time for up to 3 years. He questioned whether I should take the medication and queried my dedication to the business. Accused me of jumping on a bandwagon with arthritis and of being a drama queen because he knows "hundreds" of people with arthritis who don't have any issues. He also said because I am only 33 the consultant must have got it wrong as only older people get it.
I am trying so hard to get a new job but there is nothing out there. I have never felt so ashamed and embarrassed in my whole life about something that I cannot control. Even my colleagues have accused me of scamming some time off when all I am doing is working at my kitchen table rather than in the office. I have actually even been working harder which upsets me more because I pride myself on my work ethic. I was always a sort of "teachers pet" and this has sort of ruined my confidence at work and really stressed me out.
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I work for the NHS as a stores person in the theatres I've been there for 11 years now I've had osteoarthritis now for the past five years in my thumbs now over the last six weeks I have it in my neck reading some of the posts on here I think it depends on your line manager and employer having been to hr to try and get help with my role I was giving tests to do lifting etc to see if was capable of doing my job the outcome was yes I was OK to lift 20kg plus day in day out with now support whatsoever from them so I got an independent assessor in to help me along with my union rep eventually things have got easier at work with most of the heavy lifting jobs taken off me, so even though I work for the NHS people don't get support with arthritis as some people may think for those out there who struggle from day to day keep fighting for your rights don't be ignored!!0
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Apologies for the hijack thembrown.
I just wanted to welcome @Mart to our online Community.
Pain in the neck is really tough to cope with you have my sympathy. I'm sure you probably already know most of this but here is some information about neck pain:
I am very sorry to read your struggle to get support from your employer. Well done though for keeping at it because working is so good for us if we can possibly keep going. I hope you will be able to keep your job a good while longer now.
Thank you for sharing your story
Ellen
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Hi All,
New to the forum and currently surviving RA for the last 10 years. A real pleasure to meet you all, hope you're all doing well given current affairs.
I am one of those fortunate enough to have one of those extremely rare supportive employers. They have been nothing short of amazing for the entire time I've been there.
I told my current employer, who I've been with for 6 years now, at the time I went along to the interview for the position. After getting the job, the Director of HR said she spent a couple of weeks learning about my condition and has done everything she could to support me. They've won awards for their industry-leading supportive attitude and proactive approach to dealing with disability, mental health and wellbeing. I have regular meetings to discuss how I'm getting on and they're constantly asking if they can be doing anything different to better support me. My line of work is such that they've given me freedom to choose when I want to work, as long as I do my 38 hours in the week, they don't care when I do them - which has been so refreshing and has meant I can work around the chronic fatigue that dogs me every step. I honestly count my blessings every day that I found such a warm, welcoming and understanding place. I never ever thought I would get to a point when I would actually look forward to going to work but I do.
My previous employer wasn't such a delight to be at but, I have always felt it best to be upfront and honest about what this illness was doing for me. At the end of the day, neither they nor I have any control over what my illness is about, I'm as much along for the ride as they were. Unfortunately, they kept seeing me as being uncooperative, despite the fact I did everything that was expected of me and more. Even when they could see how swollen my hands were at times, they still claimed I was putting it on, and claimed the letter my RC wrote to outline a few facts for them was fake.
It did teach me to not be so accepting of my situation and to change the things that I can control. To be more selective and heavily research employers and ask leading questions during interviews to reveal insights they're hiding. The best decision I ever made was to leave that place and, with my current employer being what they are, I've never looked back and certainly don't miss the old place.
The only down side about my current employer was that I ended up having to move from one end of the country to the other, leaving a lot of my friends and family behind. It was a hard decision but, given where I am today, I think it was the right one - at least that's what I keep telling myself :)
Steve
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Hi Stabbedbadger,
Welcome to the Online Community Forum.
It sounds like you have very understandable employers. Hope you continue to join in with other discussions and topics on the forums.
Take Care and Stay Safe
AJ_x
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My employers have been really brilliant to me when I explained that my OA had also moved to my hips and knees. They allow me to work from home and have paid for my taxi to work.
i have been working in the same organisation for over 14 years.
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I have only been in my job for four weeks and got the OA diagnosis yesterday.
I work in construction in an all male environment, I am in the office , I don’t feel I can tell anyone about this.
I am hoping once they get my pain under control I will manage. The consultant has recommended a pain patch , has anyone else got one ?
I have been on various different painkillers for the last year and nothing has helped
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I understand your predicament new to the job, new to the diagnosis and a supposed macho environment. You could be pleasantly surprised. I worked in the head office of a major contractor for seven years and whist there had an angina attack. They could not have been more supportive.
If they do prove to be awkward, is it the sort of place you would want to work long term?
Good luck.
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Hi @Vanessajayne , I don’t work for a contractor, but am closely involved with the construction industry and work with builders of all varieties. I’ve been pleasantly surprised how supportive they’ve been over my severe OA in my hip and recent hip replacement. Arthritis appears to be quite common in builders and other tradesmen and their families, so even the most macho know how painful and debilitating this can be.I hope you’ll find understanding and support with your colleagues.
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Thank you I may pluck up the courage to tell them
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Hi all,
Thank you for the varied comments and opinions since I started this thread. @Cazmataz your situation sounded horrible and I hope you have sorted it now.
I have since started at a second employer since I wrote the post, and following the advice on here I have made them aware after the offer, but before accepting the job that I have the condition. They are a small company with 5 people and so I feel like there will be no-where to hide. This would be my recommended time to approach a company however, as you hopefully will see their true colours right away.
In my own case I seem to be perennially tied to a desk these days and its the inactivity which is hard for me. So I make sure that they know now and then that fatigue is ongoing, and more or less invisible - as are most of my symptoms. Luckily I have had bosses that listen when I say this though there is definitely an element of 'proving myself' which I do first just to show that I can handle stuff before making any complaints, or bringing up symptoms. This shouldn't be the case, but I find it helps just smooth things over.
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