Great news waffles. I found the mobility component a surprise as I answered all the questions honestly and was not bad when I applied. Not bad now either actually! All I can think is that it is a stock response to secondaries xxx
Can anyone let me know where the PIP thread is hidden please?!
Waffles it reallyis worth applying. I look at it as six months if I wasn't treated and gp was happy to sign the ds15000. It really has helped to take the pressure off. Have a look on the PIP thread. xxx
Hi Waffles, I'm no expert but I think that everyone with a secondary diagnosis can claim PIP. Like you, I heard about it on this forum but didn't think I would qualify so left it for a few years. Just recently I started on a clinical trial where there was a nurse practitioner. She told me that life has dealt us an unlucky card and we were entitled to these payments.
I thought about it and, with the rationale that I won't be claiming state retirement in the future, decided to go for it. It makes a difference! I was lucky because my hospital has a welfare officer that made the claim for me but I think a GP can do it? Someone more knowledgeable might add to this. Good luck!
At the moment I'm using mine to cover the upfront costs of the clinical trial as petrol and parking costs are high. I do get these reimbursed a month later. We also have little treats like a meal out. My darling hubby has been supporting me for 21 years with my cancer roller coaster, he deserves a little spoiling!!
I was diagnosed with secondary bone mets in May and was awarded the higher rate of pip. This enabled me to get a motability car plus blue badge and I've also applied for a bus pass. This will help enormously and I'm very grateful to get this help albeit I wish I wasn't in the position to get it!!
I was earning decent money as a teacher 3 days a week and had to go on sick leave while I had mx and first two types of chemo, both of which made me really worn out. Being able to claim ESA when my sick pay dropped was really helpful as I am nowhere near pension age and we had moved house about six weeks before my secondary DX so had the mortgage to worry about. I was encouraged to claim for PIP which I did, and was granted higher payment and mobility. I also got a blue badge which has saved me a fortune in hospital parking and means I can drive when I'm too tired to walk into town like I used to.
I later was forced out of my job so knowing I had that income was really reassuring. I now work part time as a teaching assistant so don't get ESA any more but having PIP meant I could take a lower paid job which is far less stressful and demanding.
Hi, I've just been awarded Pip too. I'll probably use it towards getting a cleaner as my house is a mess and gets me down. So to have this is a big relief.
I've just been granted full PIP. It is equivalent to the money I have been earning having a lodger. The lodger moved out recently and I am relieved that now I don't have to have one. Lovely as she was, when you are feeling rough and want to wander about undisturbed in your nightie, and even have a cry, you know you will have complete privacy. Helen
I have been debating all week if
I should finish work, its early days for me with secondary in hips, ribs axilla effecting use of arm, and unknown in one lung. I finished work after mast 6 years ago and took my pension then, retruning to work for 3 days, i have been on sick leave fro 3 weeks after radiotherapy. cannot see how i could get back to normal for work, hope I do as I am 6 years away from state penshion.
Thank you for this thread It is very informative.
keep well all .
Getting motability car (even though I don't drive, my partner is my nominated driver) has been really helpful. I can get to appointments more easily, it also means we can go out as I find public transport difficult.
The money means that I don't have to worry so much about things I might need or like to make my life more comfortable .For example I had my toilet replaced with a higher seated one which is easier for me. I get very hot and don't worry so much about the cost of using an electric fan .... these small things make a big difference.
My partner who ha become my carer is having an operation, some of my Benefit money will pay for a cleaner during that period.
Without the Benefit money I would be able to do less, be more isolated and would worry more about being able to afford things
I have secondary and receive Attendance Allowance. This is very helpful and it allows me to pay someone to clean for me and I dont have to worry about parking charges for hospital visits. I can also get a taxi when needed.
Welcome to our forum. You have entered the wrong thread you need to be in the Bone mets-please join in. You will find lots of ladies to give you support in this thread. Look forward to seeing you there.xxx
Hi, i used to come here when i first got breast cancer in 2007, just over two years ago i developed lung nodules, and last week found out that a recent scan has shown up marks on my left hip, so, its into the bones now.
So a big hello from me, and i look forward to joining in the threads.
I am able to now afford to buy extra equipments to enable me to get around better creams and treatments to help with side effects and most of all therapies to help with self esteem.
I hope this helps
Thank you Scratch
Hi everyone thanks so much for your responses, I really appreciate it. I was wondering if any of you could tell me if, and how much, being able to claim benefits has made a difference to your daily life living with secondary breast cancer? For example, has it relieved any worry, or helped you continue to do things you need or enjoy doing?
CNS Secondary Breast Cancer BCC
I have MS and applied for motability when I could no longer walk very far and I was awarded the full rate indefinitely.I was refused Disability Living Allowance because I could do most things for myself.
When I found myself with secondary cancer everyone was saying I should apply for P.I.P it took me 2 years to apply. That was June 2015 I then recieved a letter from ATOS Healthcare informing me that I would have to be seen by an assessor.August I had a letter to say someone would be coming to see me in September.
When she came she was quite nice she was an x-nurse. I answered the questions as honest as I could as it was I was feeling quite well at that time not as bad as I had previously.
October I was awarded my full motabilty until 2018 and Personal Independence Allowance at standard rate from November payable in December.I will be reassessed in October 2016
I felt guilty very claiming
I was retired on health grounds several years ago (non BC related). I was awardeded Incapacity Benefit, this later changed and I had to apply to transfer to ESA which I got, am in the Support group so don't have to go and 'sign-on'.
When I got my Secondary dx a Macmillan nurse suggested applying for DLA (Disability Living Allowance), I wasn't sure, particularly when she suggested appling under 'Special Rules' (form DS1500) which basically says you are expected to live for 6 months or less!! She explained that this was just an arbitrary figure and didn't mean I was actually going to die (well nearly six years on, I'm still here!)
I did apply under 'special Rules' which also meant I didn't have to fil lout the second half of a very long form. I was awarded the benefit at it's highest level so have been able to use the Motability scheme using the mobility component of my benefit to pay for a leased car.
Just before Christmas 2015 I had a ltter saying DLA was stopping and I'd need to reply for transfer to PIP (Personal Independence Payment),. I contacted the benefits advisor at Maggies's online who calmed m down and 'talked me through it. Basically I had to get my GP to do another DS1500 and ring the PIP office telling them I wanted to claim under Special Rules, they then asked me several questions about mobility etc. This acted as my appliction. In the New Year I got confirmation that PIP had been granted at the same rate as my old benefit (Phew!), for some reason for a shorter period than the usual three years, but at least I got it - i know they have tightned up and it's harder to get than DLA was.
That's my experience, hope i helps.
It was suggested I applied for PIP as its not means tested and they give special allowance if you are terminally ill.
I havent been granted it but I think that is the first port of call for allowances etc.
I am the Nurse Specialist for Secondary Breast Cancer here at BCC.
I wondered if I might pop in to ask a question. We are writing an article about benefits and finances for our next Vita magazine. I wondered if any of you have claimed and feel it has had a positive impact/helped in your daily life? When we do the articles I always feel its more personable if there is a quote from someone who has/is experiencing the same as the reader. Would anyone be able to give me a quote to help?