Hi All,
I regularly check in to the forum and read all your posts, and I would be very grateful for any advice. My mum feels I should ask on her too as I’m sure there must have been someone in my situation at one point? (I hope, I feel very worried right now)
I’m sorry for the long post, I’m just so confused and really don’t know where I stand. Thank you, thank you, thank you in advance!!!
I was diagnosed with RRMS in July 2009, aged 22 and at the peak of my career, a Deputy Manager of a Children’s Nursery.
During that time my work was very supportive- I think! Well my dad worked there too as a Caretaker and I think I was treated well because of him being there too. He retired in August this year.
Since 2009 I have been promoted to Nursery Manager, I absolutely love my job. I do struggle with my day-to-day symptoms like everyone else, but we just carry on, determined not to be beaten!
I have been on Tysabri since August 2010 and this has helped a great deal, reducing relapses from every 6 weeks to 3-4 months.
I reduced my hours in 2010 to 30 hours per week, however with having a busy job I still completed work at home and was therefore working a 39-hour week!
So I spoke to my line Manager then (who is also the director) who said that I should change my contract back to 39 hours, 30 hours a week at work, 6 hours a day, then 9 hours at home. I have done this now for well over a year and this has worked really well. It allows me time to rest but also time to complete things at home e.g. paperwork!
I had a relapse recently in August/September and was back at work on 1st October.
Each time I have been off sick in the past year it has only been for MS, not a cold etc. I have had 50 days off in the past year in total.
I was told in October at a return to work interview that I would be referred to Occupational Health. I didn’t mind this at all.
However, this Wednesday when I was at work my line Manager (who is now the Qualified Teacher that works alongside us) she asked me to meet with her to prepare the paperwork to send over to the OH ready for my appointment on Wednesday 31st October 2012.
During this meeting it was suggested to me that I need to reduce my hours, either work 5-6 weeks solid then have a week off, I asked if this would be unpaid or annual leave, she said “I don’t know, probably unpaid” she then went on to suggest maybe I do a day less at work in the week e.g. have a Wednesday off. She also said, “Well surely you receive DLA and that will help towards your finances” I couldn’t believe it, I told her that my finances are none of her business, she also said “also isn’t your partner back in work now?”
I know I should have got up and walked out, but I was just so shocked. Should she be commenting on my finances? Or about my DLA?
I do receive DLA, and that costs goes towards a cleaner around my flat, taxi to work on my “bad days”, money for my mum’s petrol to take me to and from treatment etc. Things that I can’t no longer do and need help with!
I would be grateful if anyone could advise me with them “making” me reduce my hours? Discussing my DLA?
I do my job as well as the next person and since in my Management and with the hard work of my team we have had a “good Ofsted”
I have been keeping a record as I feel that there are comments which are said to me that are unfair, she told me “I went on the MS website to find out information on how to support you and I was so surprised to hear that you can get tired from just using a pen, using a pen!!”
She also kept comparing my MS to a lady who works at the Centre who is over 60 and has arthritis.
Please would some one help me with any advice, I just don’t know what to do. I don’t want to reduce my hours while I am “well” and am more than capable to continue.
Thank you in advance for any advice