Scared about future and money

I have been told I may have secondary, bone cancer in my hip joint/femur after having mastectomies in Aug this year. More scans and now biopsies required for further diagnosis and treatment options.

My work have reduced my pay anyway whilst I am off recovering from masts, (SSP and a small company contribution) but I need to know what I can claim (and my husband regarding carers allowance) in relation to benefits.

Can anyone point me in the right direction? My husband wants to drop his hours to maybe 2 days a week to look after me the rest of the time. I don’t know too much about benefits (DLA, Incapacity, Carers Allowance etc) Can anyone shed any light on this please?

Thanks x

I. like you haver had my pay cut and have had to claim for the first time in my life.

Yo be honest I was going to try and muddle one and then I thought about how much I have put in and have decided to claim incapacity benefit.

It is simple to do - there is a free phone or local rate number (Call 0800 055 6688 (8am - 6pm Monday to Friday)). to call the Job Centre or equivalent and it takes about 20mins over the phone - they send you the completed forms and tell you what docs certificates they need.

They were incredibly helpful and should be able to advise you on what your husband my be able to claim!

Hi Poannie

I am sorry to read that you may have developed secondary bone cancer, I understand that this must be a very difficult time for you and your husband.

Regarding financial issues and benefits, I am sure other users will be able to offer advice and information about their experiences of this, but in the meantime, I have given a couple of links here, one to the Department of Work and Pensions website which gives information about the various benefits and how to claim these and the other to Macmillan who offer lots of advice and support around financial issues.

dwp.gov.uk/lifeevent/discare/

macmillan.org.uk/Get_Support/Financial_help/Home.aspx

Please also feel free to call our helpline who will also be very happy to offer advice on this subject. They are on 0808 800 6000 and open Monday - Friday, 9am - 5pm, Saturday, 9am - 2pm

I do hope you find this information useful.

Kind regards

Louise
Moderator
Breast Cancer Care

I also like phardy had never claimed anything before but my hospice care nurse gave me the info and form and took it to the gp for signing ( Disability living allowance) I am still working and also get mobility as I am unable to do shopping on own and get very breathless if do more than2 stair steps… everyone is very helpful and make the claiming as painless as poss - the form is huge and can put people off … there are also many other types of allowance as the above have given you the links just ask and hopefully this will help you and your husband… just really sorry you have to visit here and wish you well with your treatment youwill see many of us who have been around for a long while so it is not all doom and gloom… the sun is shining this morning…

There is another thread with this info on as well

When I got my secondaries diagnosis, I got into a flat panic about money. I’d had difficulty getting permanent jobs after my primary treatment, though had, for a while, had no trouble getting well paid temporary work (which at the time,came without perks such as life cover, medical insurance etc. that was given to permanent staff). Now, staff are “protected” against being deprived of such benefits by being given rolling temporary contracts and it just made gettting work impossible! I did not feel protected.

As I’m a graduate, I responded to one of those adverts encouraging people to go one year post graduate teacher training courses (PGCE) with training bursaries. Got ill with secondaries during the course and had to drop out in the last term. Thought “What will I do now, I’m unemployable now I’m terminal?” Anyway, I’m surviving but an expert on the benefits system!

Don’t give up your current job unless you are forced to. Use Employment Law and Disability Discrimination Law to the utmost. If they really want you gone, they may bribe you with a generous augmented Early Retirement pension. Check out your usual options at this time anyway.

Although you feel bad now (most of us felt terrrible until our treatment started working) you may find in a few months you feel much better. Don’t therefore resign too quickly and don’t let your husband become your carer too quickly. Getting new jobs can be tough. Many people live for ages with bone mets and once they get pain relief from bisphosponates feel very normal. I was in severe pain when I had to drop out of my teacher training course, but after 3 months of Arimidex and Pamidronate, I felt a total fraud that I wasn’t working. I also missed the company and daily routine you get from working (as well as the money). A few years down the line, I’m no longer feeling as well as I was (have more than bone mets now) and know I can’t work. However, I’m separated and do all of the chores by myself with no carer, so it can be done.

Things to check out:
*Pension and Permanent Health Insurance options from current employer
*Incapacity Benefit (an unemployment benefit for those unable to work and below State Pension Age)
*Disability Living Allowance (there are personal care and mobility components) available to both employed and unemployed people and it is not means tested
*If your new combined income is low, Tax Credit and, if you have children in fulltime education Child Tax Credit
*Again if you have children between 16 and 19 in fulltime secondary education, check out EMA
*If you get Disability Living Allowance mobility component, the Blue Badge (from the authority who collects your Council Tax) and also car tax exemption (from DVLA)

I found out about most of these by using search engines and applied for everything by myself. Others have found their Citizens Advice Bureau or Macmillan Nurse helpful. It worries me, however, how many people just hand over all the paperwork to a Macmillan Nurse who fills in everything for them and they never see the forms again. Your signature is on the forms so you should read them and check you agree with what has been said. Keep photocopies of everything in case it gets lost in the system or you have to appeal. Get proof of posting (free) at your Post Office.

Many benefits are backdated to the date you request the forms, so applying for the paperwork quickly makes good sense. If there is likely to be any significant gap between your Statutory Sick Pay finishing and being able to begin claiming Incapacity Benefit, do claim Job Seekers Allowance. As well as the small amount of benefit, it keeps going your National Insurance records so safeguarding your rights to Incapacity Benefit when eligible and a full State Pension at State Pension Age. A while back, there was someone on the forums complaining that Benefits staff were being unhelpful and inflexible because of a broken NI record. Benefits staff have to work within the law and have little discretion, so you MUST ensure an unbroken NI record somehow, even if it means the indignity of signing on.

Well done holeybones you really are a wonderful person it really helps to get all the info I agree though about taking photocopies etc of everything so if you need to look back at anything or have to appeal… although mnine went through no probs. Although my nurse helped me she didn’t fill it in I had to do that but she knew her way around the form and it is a very long form and if you are on several benefits there is just so much paperwork… As you say keep the job you’ve got if you can , my work is only part time but they are being brilliant as they should be …

Thanks for all the info though… hope you are keeping well at the moment.

Holeybones has really set eveything out well since this is such a difficult area.

Just a note about DLA - disabled living allowance - this one isn’t backdated so apply as soon as possible. This one is also payable even if you are in work. Luckily for me my Mac Millan nurse did all the forms and I had no trouble whatsoever.

Best of luck

Ruthie