I work part time , I am trying to find a leaflet for my employers who seem ignorant to my condition , I love my job but feel they are taking advantage .
Any info would be much appreciated
I work part time , I am trying to find a leaflet for my employers who seem ignorant to my condition , I love my job but feel they are taking advantage .
Any info would be much appreciated
if you go onto FibroAction web the have some information you could print of. I also found the NHS wed explaination sheets really well written and I have given these out before to help others understand, if it would help I can send as an attachment to an email, hope this is usual hugs xx
thanku tess10 ,,, x
I went on an American website and printed out the information along with the NHS information, didn't make a jot of difference but at least I tried. I have lost job after job due to time off sick or brain fog making me make huge mistakes so now work for myself as I am the best boss I could have xx
Hi
If u go on the gov website or type in DDA into Google it will come up. There's lots of useful info on there, particularly if uve become disabled whilst at work (my fibro came on suddenly in March 2003) or if u are disabled whn u apply for a job etc. Whn i mean disabled i mean u hv a long-term chronic condition which gives u disability rights at work and youre entitled to reasonable adjustments too. Also DDA is part of the Equality Act now. I can send u more info to an email address. Mine is mimiweeks99@aol.com
thanku mimimdm ,,,i am being sent for an assessment to ERCC something to do with ergonomics ...work are still asking for full availability on a 16 hr contract yet 6 days to them aint enuff when I have asked for sundays off as a rest day ,,,will update outcome ,,,have spoke to usdaw and they are finding me some information too ...x