Planning for the financial future
I was diagnosed with MBC in June 2017 at the age of 48. Treatment has been working, and I feel hopeful. But I am not unrealistic. Currently I work full time, and I love my job. Today we had an annual staff meeting on our 401ks and planning for retirement. I know there is not a likelihood that I will be around to enjoy this retirement I have worked so hard for. This knowledge made it very difficult to sit through the meeting, although I was required to do so. If you are still working and trying to keep life as normal as possible, how do you all cope with the uncertainty and the weird mix of hope and dread that these kinds of things bring up?
Comments
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I work full time and people are not aware of my diagnosis. I am struck with an awkward feeling when people talk about things 30 years down the line or anything beyond a year or so. I receive annual grants of company stock and always wonder if I will be around to see them vest in 3 years or be around to fulfill my next 2-3 year term as a board member of another company. I chuckle when people at work make comments about me being too young to know about menopause, retirement, death issues, etc. I find myself feeling somewhat “surreal" about it. Despite it being nearly 4 years since mets dx and me being on my 5th line of treatment, I still live in the land of denial. I do still contribute to 401k. It will either go to my DH and son or I can always cash it out early due to dx based on IRS rules. Can also cash out life insurance offered through employer if it ever comes to that. I did stop making additional payments into a Roth IRA but have continued all other saving while I am able to do so. One day at a time.
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I too work full-time in the position I've had for almost 20 years. I also love my job. Some people know -- my boss, a few co-workers, the head of HR. They want to work with me when I can no longer work full-time. Very sweet of them. So I keep them up to date on how things are going. When I was first diagnosed I did things like lowering my 401k contributions. I'm not going to live 'til retirement but my heirs can use the company match money. I also read every word on the disability plans.
As for contributing to the 5-year company strategic plan, I contribute to it, even if I won't be there to see it. My perspective counts too! People leave the company all the time for new jobs. How is that different from my situation? Over time I've gotten more used to the idea. I'm a practical person to begin with so it's relatively easy to put those feelings aside and concentrate on getting my work done. I live on de-Nile.
In fact I'm now actively planning for when I can't work anymore. There's someone who is [unknownst to him] being trained to do large parts of my job. I've written documentation and told some where to find it.
I guess the bottom line is I act as if I'll be working there forever even though I know I won't. I'll be starting iv chemo sometime in the next year. I'm hoping it won't impact my ability to do my job but it probably will. There will be decisions to make. [Do I have to? Waaaah!]
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I’ve asked this same question.. I’m in my early 40s and likely will not reach normal retirement age. I save a little because with this dx, one just never knows. I’m working full time now (don’t love my job but it pays well and the insurance is good) but who knows how long that will last. I’m not married so I feel like I need to put something away so hopefully if I do have to go out on medical disability, I won’t have to eat cat food or ramen noodles
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I find it so hard planning when everything is so uncertain. I have an insurance policy I can cash in, but only when I only have 2 years left to live, how will I know when that is? I don't want to cash out early and live another 20 years (well actually that would be a nice problem to have) but I don't want to leave it too late and not be well enough to enjoy it.
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As long as you can work, put away as much as you can. And if there is a company match, make sure you get as much of that as you can!
I only stopped working about 16 months ago [oh do I miss it!], but in the seven years that I was metastatic and working I made sure to have enough saved to pay for health insurance for two full years, and then a bunch extra to cover some of the difference between disability and what I used to actually make.
No one has EVER regretted having money in the bank. If/When you apply for disability, you can then start to draw on your retirement savings without penalty to pay for some of your living expenses as needed.
Don't think of this as saving for retirement. That isn't what we will get. It is saving for your future needs
*susan*
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I met with a financial planner when I was diagnosed, because I was in the process of receiving a personal injury settlement and needed to figure out how to protect it for my sons. Talk about timing.... He advised me to quit working to get the clock rolling for Medicare. Didn't work for 3 years, and am now working PT and receiving SSDI, I am bringing home the same as I was making working FT with SSDI and working PT..I like my PT job and still have time and energy to live. I invested the settlement into a piece of property and put it in a trust for my sons. With the Medicare I have a smaller deductible and it costs less than my policy did before..I was able to be on my husbands(soon to be ex) health insurance while I was in the 2 year waiting period for Medicare. Some policies have a lifetime max that they will pay but not Medicare.
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I totally get the challenge of planning under these circumstances. I’m 56, no kids, no husband so doing it mostly on my own. I still work full time at a job that I enjoy but must admit that more and more I think about stepping back a bit. While I like what I do, the challenge is carving out “me time” when my plate is so full.
In terms of finances, I do have a strategy. I am fortunate in that I am eligible for LTD and have good extended health. Retirement is likely not in the cards but then, financially, it doesn’t make much sense. I’ll bring in more on LTD than with my pension and they continue to pay into the plan until I’m 65 plus I keep the premium extended health. So, I will keep plugging away until I feel it’s time to slow down.
The planner in me (project manager - sorry) had me take care of the eventualities. I updated my will in the spring, reassigning my pension, my estate and RRSPs to charity. If I live longer great. If not, it will go to causes that mean something to me. The final piece of the puzzle is getting rid of a lifetime of accumulation (my mom was into antiques). Again, I have a plan. Some things go to charity outright (warm weather gear, back packs, sleeping bags etc. for the homeless). I list things for sale and will drop the price but only so far. Once I get to a certain point, again, it goes to charity as I refuse to give things to folks who are just trying to take advantage.
I do pay close attention to the various plans and entitlements. While it may be wishful thinking, I’m looking into options to continue my health coverage past 65. The retirement plan sucks! Big issue is the lifetime cap which, as we all know, we can blow through in a couple of months! Ibrance at $7500 a pop comes to mind!
Sorry, feel like I am rambling. All this to say that I do still plan ahead. There are times when I have trouble relating with concerns about the future but, in my own way, I am able to still think ahead.
Pat.
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What have you guys done to protect your children's (possible) inheritance? My feared scenario is that I die from this stupid cancer, and after a suitable period of mourning, my darling spouse marries again. Of course he will, he's the total package. I try not to think about it.
But, the woman he marries has children too. Time passes. My beloved spouse develops senility and prepares a will where he leaves everything to second wife, knowing that she will be fair to my kid in her will.
Aaaaaaand, I've never seen that happen. Usually, the second wife just leaves everything to her kids - at least, in my family.
So, I'd like to prepare some sort of trust thingie with my 1/2 of our assets for our kid. I haven't consulted a lawyer yet because that makes it real. It's not that I don't trust spouse. I do. I don't trust the future.
Am I an awful person?
Jennifer
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Of course you're not, Jennifer. You love your children and you're smart to take steps now that will ensure your wishes are respected. Consult a lawyer and do it!
Tina
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Jennifer, your wishes are paramount. Consult a lawyer. You can set up a trust where your husband is the trustee and handles the money. Your child gets the money at age 18, 25, 30, whenever you like. Maybe on your husband's death. It would be nice if your husband is on board with the plan but in the end that's not necessary. See my first sentence. You are NOT an awful person.
I have no children but I have grandchildren, thanks to my step-son. My will is set up so there is a carve-out sum for each child. It goes into a trust and can be used to pay for college, etc. It's enough money to get them a start in life but not enough for them to live off of. [Most of it will be used to pay for college] My husband and their parents are the initial trustees. In this case it's not that I don't trust anyone, it's just that I want the kids to have money of their own.
This cost a little but was entirely worth it. Please give yourself peace of mind.
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Blainejennifer, you could consult with a financial advisor before seeing a lawyer. The FA can go over options. Dh and I saw a great one this year and I put it all out there. He said, yes, you can control your money from the grave.
I don’t think you are awful in any way. Why would you want to work your whole life, accumulate wealth along with your dh, regardless if its much or little, only for it to go to someone else’s children who never even knew you? Your thought process is excellent critical thinking, picturing scenarios you hope to avoid. Feel good about being smart like that.
Take small steps but take action. Ask around to find a good FA. Make an appointment. Take it from there. Or make a lawyer appointment. Get things in place so you can forget about them.
Dh and I have a lawyer appt this week. Its not something I feel like doing, but I told the FA I did not want our house to go to a nursing home if dh and I both end up there. He said we could get a life estate deed, so we are going to talk to the lawyer about it. The house can go to who we want on our passing with this type deed.
I told dh I don’t care if he gets married the day after I’m gone, or how much sympathy sex he tries to go after. I said just make sure our money goes to our kids. I said, if you don’t, I will come back and haunt you. I am very serious about that and I don’t feel one shred of awful for feeling that way.
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Cinloo, I don’t know how old you are, or when you were dx with mbc and what type and where its spread. But I’m glad you found us.
It is hard to listen to others make those futuristic plans. It kind of sucks. I also have family members who sometimes go on endlessly about it as numerous relatives are approaching those retirement years.
One thing I must say, tho, is who knows how this disease will play out in each of our lives. I am 7+ years now with mbc, still stable. There was no way to know at the beginning what was going to happen. So don't count yourself out, any of you. Take it a day at a time. There’s some great advice on this thread on how to approach finances.
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Thanks for your words, DivineMrsM. I have a lot of hope (and some reason to believe) that I will be around a while. I am glad I found you all too. I left a Facebook group recently because anyone who posted hopeful notes like yours was bombarded with messaging about "being realistic" and admonishments about "being in denial." I am not in denial, but I also think that there is no harm in hoping for the best. For me, living my life to its fullest means still making plans for the future. It brings me joy to think ahead about all the wonderful things life will hopefully bring. Is it so wrong to want to find camaraderie with people with similar dx who foster some hope? I am 49 now, and am open to the idea that I may live quite a few more years. I am so glad to hear you are 7-plus years out and stable. I hit the one year mark in July. I have made it through 61 rounds of chemo and have more ahead. You inspire me to keep going! I am ready! And you're right - a lot of good financial advice in this thread! Thank you!
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BlaineJennifer: You are not an awful person. I lay awake with a stage 4 dx for the last nine years worrying about my family's money and how I was going to insure that it is still there for our kids to go to college. Not only does my husband have every right to live out his old age with a new partner, he just has no common sense about money. Like you said, it's not about not trusting him, but not trusting the future. I would never expect he would do anything deceitful, but just careless. And I fear that the new woman could easily be a lot smarter about money, and could manipulate the situation so that it is not in my kids' favor. Luckily, my father outlined for me in his aging feeble years how he established a trust that will make sure that while his money will take care of my stepmother while she lives, any remaining will pass to HIS children. Get a lawyer, spend the money, make it happen. Emphasize to the lawyer that your interest is in protecting your children. It's not uncommon. I first met with the lawyer to describe what I needed 15 months ago, and just met to finalize the paperwork last month. A few eyebrows were raised when my husband was not in attendance at the meetings, but when I clearly outlined how I had planned for him to maintain his standard of living while EVERYTHING ELSE is kept in trust for our children-the lawyer was completely on board. I sleep more easily knowing this is done.
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Hi KSkier,
So glad that you're feeling well and able to work. I stopped working/went on disability, following my MBC diagnosis, but I still have some thoughts for you that might help...
...I was always very engaged with managing my finances, doing planning, etc., and this has only increased since my diagnosis. The questions are still the same....given a live expectancy of "X" (which has certainly changed), and a reasonable range around that of + or - "Y", what can I do now and in the future to ensure that my money is working for me and toward my goals....
....you had every reason to be in that meeting, paying close attention. Your 401K can become your income when you decide to stop working, which might be sooner than you think, i.e. while you are feeling well. As someone with MBC, you pretty much automatically qualify for SSDI. You've paid into this system for years, presumably, and you may not be around to collect on the SSI retirement benefit, but you can at least collect the SSDI benefit (which, at least in my case, was larger than my expected SSI retirement benefit..). As someone who is disabled/metastatic, you can withdraw from your 401k without paying the pre-591/2 penalty. Again, this is in recognition of the situation where you are unlikely to have the typical retirement. So you might decide now to put even more into your 401k, perhaps to allow you to retire soon and enjoy life a bit more.
...also, another consideration. Whatever you put into your 401k can be transferred with no tax and no penalty to an IRA when you leave your job. This IRA can be passed along to your children, spouse, etc, as an inheritance. I'm not 100% certain how it would work with a spouse, but I do know that you can pass this along to your children and they can either withdraw it all at once -- and pay lots of taxes -- or opt to do only the "required minimum distributions" (RMD, aka "stretch"), which is based on their life expectancy, as per actuarial tables. If they do the latter, they will continue to benefit from and accrue to the pre-tax contributions that you have made in your 401k savings and pay tax only on what is withdrawn each year. You can find online calculators (IRA RMD) to see how far your savings will go toward providing a life-long source of income for your beneficiaries. This can be the source for a small extravagance, an annual vacation, or a significant income cushion.
So, my point is, your 401k is possibly even more important to you today than it was before your diagnosis. I, personally, derive great happiness knowing that my savings can do wonderful things for me or for those I love, especially in light of my prognosis.
Just wanted to share my perspective! Be well!
Lynn
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