TULIP is a brand new, exciting project helping chronic illness sufferers to cope with any issues in the workplace. Their website is live now, and will officially be able to subscribe members in the next couple of weeks.


Here is a the story behind TULIP from the Founding Member Danielle:

The idea for TULIP first came to me when I had a bad experience at work myself.
My employer began disciplinary proceedings when I had 3 absences within 6 months, all due to endo, and no longer than 2 days each.

I’d never been in any trouble at work before, I’d only been diagnosed that same year and I still didn’t really understand my illness. I couldn’t promise I’d never have another day off sick, every treatment I’d tried so far hadn’t worked and I didn’t know what was around the corner!

I tried everywhere for advice but the likes of ACAS and the CAB knew nothing about endo, although they were as friendly and helpful as they could be. Any advice I found online was vague and I couldn’t afford to pay for professional legal advice, especially when I was at risk of losing my job! I felt completely alone. I had to attend a disciplinary hearing and was told I was entitled to have either a work colleague or a trade union representative accompany me. I was no longer a member of a union as they had been unable to offer any advice in the past because they didn’t understand my condition, and I didn’t feel comfortable putting a colleague in that position, so I had no choice but to go to the hearing by myself

It was the worst mistake I ever made. There were 2 of them and they took turns in reeling off accusations and threats about my job, I hardly got chance to speak. I went in to the meeting with three A4 pages of notes, as I wanted to mention my achievements and accomplishments at work, and the fact that apart from my absence record I was a model employee, but I was never given any opportunity to defend myself or put forward my own version of events. I’m a strong person and they reduced me to tears!

I was given a written warning and told to leave the room, before being warned if I had any more absences the consequences would be very very serious. My endo is made worse by stress, and over the next month I worked myself into such a state of panic that most days I struggled to get out of bed. It was a  Catch 22 situation – I was scared of being ill, but being scared was making me ill! I used to love my job and now I dreaded going to work.

In the weeks that followed, I asked for time off for hospital appointments but my requests were always refused. I wanted to start GnRH as the treatment I was on wasn’t working, but I could never get them to agree to an unpaid couple of hours off. My health continued to deteriorate, until things came to a head one day in a meeting with a senior manager. She told me I should, at the age of 23, with no kids, “just go and have a hysterectomy”! I quit the same day as I finally realised I had to put my health first

As soon as I got back on my feet, I started planning a project that could help other people who had been in the same situation as me. TULIP was originally just going to be a helpline for advice and support on employment issues, then it occurred to me how much more help we could provide if we were a Trade Union

I can’t stress enough that we are not your average Trade Union – we won’t be going on strike or demanding higher wages! Our goal is simply to stop people with chronic illnesses being  treated unfairly in the workplace. Your monthly membership fee covers everything you could need if you were to face a dispute at work. We have legal experts on hand to offer accurate, up to date advice on employment law, your Union representative can contact your employer on your behalf if you have any problems you don’t feel comfortable addressing yourself, and we can accompany you to any meetings or hearings you may need to attend

We will also run campaigns wherever possible to raise awareness of chronic illnesses. I strongly believe if employers were educated more, there would be less discrimination, and by raising the public profile I hope to be proved right!

As we are a non profit organisation, any money left over will be re-invested in the company to improve the services we can provide for you.

There is a lot we want to do, but we are starting off small! However, one long term goal is to be able to offer financial assistance, in the form of a grant, to our members who need it most. We all know how hard it can be to cope financially when you take an extended period of time off work, for example after surgery, and we’d like to help make those hard times easier.

We are also very passionate about charity, especially the fabulous work that Endometriosis UK do, so for any endo sufferers who join us, we will donate 10% of your monthly membership fee, for life. If you have another chronic illness, please feel free to choose a charity relevant to you.

If you would like any further information please visit where you can also register for updates as soon as membership is available.


Let’s End Endo & Society6

This project all started with me (Kaye Sedgwick) wanting to just give something back to Endometriosis UK after its helpline supported me after I was diagnosed five years ago. I was scared, confused and felt so alone, but they helped me find answers and point me in the direction that has helped me move forward.

I created these illustration which where used in their teenage awareness campaign in 2012.

I am now offering these illustrations for sale from Society 6 as a large range of products, including:
art prints
tote bags
pillows and much more.


For every piece sold I shall donate $1.00 to Endometriosis UK.

Shipping costs vary depending on what you order but is available WORLDWIDE.
UK buyers, please be aware Import duties and taxes may apply (esp on orders over £15.00 or $22.67). Please contact your local customs office for more information.