Lymphoedema isnt reconized at work,im sitting down all day and have arranged to get up walk about every so often which has not happened there for making my condition worse
i have Lymphoedema in both legs,im reguly having time... - LSN
i have Lymphoedema in both legs,im reguly having time off work and worried ill end up getting the sack ,any idear on what are my rights
I work in the public sector and my lymphoedema covers me under the Disability Discrimination Act (DDA). I would be amazed if you were not covered by the Act as well, take it up with yoour HR, after you have familiarised yourself with the Act
If you phone acas they can offer very good advice or look them up on the internet.
I believe you can't be discriminated against for illness but you may need to ensure that you are fit to work, your employer may be able to find a more suitable position for you, it is always best to discuss it with them first. If you are a memeber of a union they will also be able to help.
hi szkoda
if you meet the legal definition of disabled - that your lymphoedema has a substantial effect on your ability to carry out everyday tasks - then you're covered under the equality act (which includes what was the disability discrimination act) & your employer has a duty to make 'reasonable adjustments' to help you do your work
getting up & walking round the office would be a very good example of that
but i agree - get good advice from your union, a local law centre or from all the info there is on the web
acas is here: acas.org.uk/index.aspx?arti...
& there's also some info on the gov website here: gov.uk/discrimination-your-...
come back & let us know how you get on
Sorry that there is such a time lapse between you asking your question and me responding. I have only just seen it. I to have Lymphodema in both legs. My employer knew my condition when I started work. It was suggested by a friend and fellow sufferer that I ask for a footstool so that I could sit in more comfort behind my desk. I work in the public sector, in an admin role in a school. I contacted HR trying to see if I could get any financial help for work to fund the footstool and as a result was referred to Health and Safety who sent someone to access my work station ergonomically. As a result of this I was supplied with a footstool, a better chair that supports my spine when you sit with your feet up, and other things to maintain good posture. Far more than I ever expected. There was an article in the last LSN magazine that looked at what employers need to do. I also am able to get up and move about when ever I need to. This is a disability not just an illness.
Hi szkoda1922. You may be eligible for an Access To Work workplace assessment done by the DWP. I arranged to have one done a few months into my job as my employers were reluctant to look into getting me a better office chair and leg rest. A foot rest is not usually sufficient. The workplace assessment is free and you receive a report which will detail what the assessor deems suitable for your lymphoedema. Depending on the size of the company, you may qualify for a full or partial grant towards the new equipment. Unfortunately I work for a large local authority and my employer was required to fund all new equipment. You don't have to use the recommended supplier they suggest. I went googling once I got the report and found the equipment I needed online at a fraction of the price which my employer was happy about. I now have a corner desk, leg rest and a more supportive chair and I can get up and about whenever I want. The link to the Access to Work and the workplace assessment info is gov.uk/access-to-work