The most important aspect of all this is that the engineer by putting red label on tv will have improved his first time fix and will have much improved figures

Thanks for info much appreciated

I have been put in Support group ESA with a 13 week sick line , Question is after 13 weeks do i send in another or do DWP contact my GP

Thanks for replies .I am sure savings will soon depreciate ie 100 pounds utility bills 200 council tax etc

I have just been made redundant health issues.I am higher rate dla and wife on carers allowance.Sent away Ea50 form with sick line was told should go to support group. I was advised to claim contributory based esa is this correct and how much would i recieve .With redundancy and wages etc i have 11k in bank .I know this wil effect claim but would i be better claiming income based esa Help appreciated

Thanks for reply as i said still going through another year of chemo as am still classed as terminal illness

Thanks for reply but i have been 8 years with firm and pension has been wound up afew years ago and moved yo private insurance firm not based on final salary

Sorry main question is whether they will take dla of me Death in benefit is just throw away line .On lots of medication for pain stess etc

recieved letter from dla on extent of my condition metastatic pancreatic cancer was given higher rate of dla on 2006 special rules . fortunetly im still alive but not in good health going through year of chemo .originaly had chemo for year 2006 . had scans for bone cancer also scans behind eye mentioned small lesion which could turn into secondarys as having headaches just out of hospital spending week in just before xmas , im still holding down job although shorter hours ,, want to get 4 times anual salary on death for my family. dla obviously want to take it of me but if took mobility car would have to resign from work 25 miles away 2 trains and over 2mile walk not fit enough to make it in any advice would be gratefull feel like benefit cheat because im still living

yes

I paid back 400 to pensions uk to buy smallpension for her'Only source of income except her Spanish husbands oap pension Many thanks for reply

Sister lives on small uk pension 25pounds a week .Spanish stroke wheelchair husband has small pension ,family has to conytinually help out .I know its a bit rich with austerityprogramme but any info would be gratefull thanks

My notes from 2005 say most likely a pancreatic adenocarcinoma 3 years later its a well defined neuroendocryne tumour seems most likely is a common phrase

my friend has been made redundant from currys after23 years along with a lot of other technicians this is probably to blame

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check out cancer missdiagnosis thread given months to live in 2005

thank you for all posts i would be gratefull for comments on medical notes as follows july 2005 endoscopic ultrasound of pancreas demonstrated a 5 cm mass in tail of panc with adjacent lymphadenopathy the splenic vein was occluded with multiple venous collaterals the mass is most likely a panc adenocarcinoma Mr...(EDITED NAME) may end up needing a staging laparoscopy possible proceeding to a distal pancreatomy and splenectomy it would be best to vaccinate him preoperatively other hospital appointment sept 2005 panc adenocarcinoma with confirmedmetastatic lympth node involvement and vascular encasement the tumour is inoperable if you could see him with a view to pallative chemo sept 2005 at oncology mr...(EDITED NAME) is devastated at news he has inoperable met panc we discussed marginal benefits of pallative chemo he has agreed to attend cru for phase 2 study mr and mrs...(EDITED NAME) are both clearly struggling with his devastating news july 2008 surgical unit as you know this gentleman was admitted to ae with bleed into neuroendocryne tumour of panc core biopsy confirmed nature of this we did radical resection tail spleen and diaphragm pathology confirmed a neuroendocryne tumour all quotes from notes is it normal practice to act on most likely a carcinoma many thanks please excuse grammer etc

read last sentence first post

i hate to sound condescending but cancer was never ever aggressive it was im led to believe a carcinoma of the neuroendocryne gland of pancreas i have no medical knowledge and i am a bit of a luddite regarding computers the 38 chemos and TRIAL DRUG had to be stopped after 1 yea r to quote docs damaging organs that would prove more debillating the chemo was also certainly not a breeze and have been told if any further problems i will not be treated with chemo

check out cancer missdiagnose 3years before they got it right

original told cancer had spread lymph nodes stomach etc could not operate ffwwd 2008 other doctors said its less aggresive neuroendocryne if it grows any bigger we couldnt operate also said 38 chemo and trial were not suitable for type of cancer nb 2 diff hospitals 2 diff opinions do you think someone got wrong

the tumour had grown 5times original size since original diag scan every 2months paid by drug company confirmed the prof said if he hadnt op 2008 it would nt been able to operate sugg you google panc cancer

i was diagnosed with pancreatic cancer july 2005 given 3 months to live advised to trial phase2 m200 and chemo every mon for 1year 38 chemos later still working fulltime stopped ffwwd july2008 went to western ae dept massive bleed in tumor same symptons as 2005 4pts blood biopsyx2 then they said could operate it neuroendocryne cancer 6 weeks later tumor out bloods ok ctscan ok 3d nuclear scan ok no cancer cells in body maby someone got it wrong