When being considered for ill,health early retirement this week, the assessor concluded that I suffer from 'fatigue', he blatantly ignored the myriad of other physical symptoms that are a part of my everyday life. He claimed to have difficulty reaching a decision as he feels uncertain whether I will still be 'tired' in 10 years from now. He therefore postponed making an award/decision regarding my pension as he would like stats on how many people suffer fatigue in the long term. Does anybody know where I may find this info (if it exists that us). Thanks in advance.
Need statistics for fatigue?: When being considered... - LUPUS UK
Need statistics for fatigue?
what a prat! Does he actually know anything about lupus?
I still get fatigue/exhaustion despite medication (plaquenil is stated to help fatigue but it has not really done so with me) and I was diagnosed in 2003
When I was retired due to ill health at first I had to wait 6 month for plaquenil to have effect. Then I had to appeal a decision that turned me down (on grounds that they were not sure how long term I would be affected), so your postponment may be part and parcle of that
In order to win my appeal I had to provide "evidence" that my symptoms were "long-term" (ie would last until I reached "normal retirement age" (60 yrs old for my case) so I got my drs to write letters for me - Could your consultant and GP back up your case by writing a letter for you that spells out your symptoms and likelyhood of permenance?
perhaps Lupus UK could also help lupusuk.org.uk/
Many thanks for the advice, whilst I didn't expect the application to be straight forward, I rather hoped the assessor may have some insight into lupus. Thanks, I will contact consultant again and maybe lupus UK.
I'm sure Lupus UK could give you figures, or point you to someone who could. And maybe St Thomas hospital lupus unit, too.
Good luck slowmo. X
The Lupus UK website, states fatigue as one of the two main SLE symptoms. Good luck Sebitha
How awful and unbelievable. Get the info you need from your doctor, consultant and lupus UK. Try not to. let it stress you out to much and I hope it gets sorted for you soon. Best of luck ; ) x
Thanks to all who replied, I will contact the relevant people and hopefully ease my stress.