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What You Should Know – revisited

Posted on: June 7, 2022 | Posted by: Emma Pearson

Main image by Aron Visuals on Unsplash

Italicised Section from Megan Devine:

I was talking the other day about the realities of the second and third years of grief. We have this erroneous (and stupid) cultural idea that grief will be over, or at least appreciably better, by the end of the first year. Eighteen months, at most. We all know that’s a lie. 

But it’s weird to talk with a person in those early months of grief and tell them that year two will be “worse” than what they’re living now. That doesn’t seem fair or helpful, either.

The problem with not telling the truth about the longer-term nature of grief is that people pass those magical one year, eighteen month, dates, and think there’s something wrong with them that they feel….. even worse.
​
This week, writers, let’s write letters to people who enter the grief world behind us. If you could tell them anything about the road ahead, what would you say? I won’t give you a passage from another writer for this one. Just go with your gut. Don’t try to make it pretty, or “writerly.” Just write what you feel. A love letter, of sorts, to the people yet to join our shores.

Image by Volodymyr Hryshchenko on Unsplash

I haven’t written into a Megan Devine prompt for a while, but this one pulls me in. It’s a prompt similar to one she uses very early in the 30 day Writing Your Grief programme – “What you don’t know … What doesn’t show… about Grief…”.  I have written into that prompt three times over the years, but not for over two years. But it’s not an easy prompt to write about.

I notice I feel reluctant to write about “what it’s really like”, because:

My losses are multiple and all way too close to the heart and bone

My losses happened fast and furiously – still reeling from the first when the second, then third, then fourth came, each one bigger and harder than the previous one

I have had to reorder, recreate my way of living so many times – and it’s still ongoing, and I realise it always will be

I have new identities that are hard for me to fashion into a coherent whole – one of five kids? Widowed but in a new relationship? Mother of three?
I have stories core to my life and experience that people simply don’t want to hear about – that at best, they bounce off of, back into the safety of their own lives and stories

I do have a beautiful new love. I still say “new” after almost 3 years. I wonder when I will drop that adjective. Perhaps never. Perhaps my love with Medjool will always feel new. Surprising. Unexpected. Unplanned for. A new love I didn’t contemplate in my life because I thought I would have Mike.

So many caveats before being able to get into what it’s really like, in years 2, 3, 4, 5….

And yet, even the people who are a bit more “like me” – I have met a few now through my Multiple Losses group for people who have lost a spouse and a child – well, of course we are all different too. We all have different experiences of the losses, different orders, different ages and years, different illnesses and accidents, different crises and traumas, different baseline characters and skillsets, different levels of support and levels of holding around us in our lives…

So with all of that, I can only express my own perspective and experience. No generalisations possible.

Year one sucks – it is mostly shock, numbness, coping, functioning.

Year two sucks – reality sets in deeper, consequences and implications are felt more vividly, extending out into the future like ripples on a lake that you couldn’t at first see because of the crater made by the boulder that crashed the surface in year one.

Year three sucks – It’s easier to talk about the person/people who has/have died to people, SO LONG AS it’s not about missing them… just bittersweet stories allowed that people can nod their heads at – nothing too uncomfortable please.

Year four sucks – because I have more and more experiences without you, that I can’t share with you, that I have no-one in my life who can “get it” like you can. There is more of me that no-one sees, knows about, witnesses.

Year five sucks – because there is more extraordinariness in the two surviving children that stops me in my tracks that I am so proud of, that I want to discuss and explore and dissect with someone who knows them as well as I do.

The gap between life before and life now ever increasing.

The topics, the experiences I don’t talk about multiplying.

The parts of me not known by another – though known deeply by myself – expanding.

The questions, issues, challenges in my life that I don’t bounce off with anyone because I am on my own such a lot.

The newly-gained capacity of spending an entire week with a bunch of new people, and at the end of it, perhaps one or two people know something of my life.

In year one and two I blurted it all out anytime I had to spend any length of time with people. Or any time I was flooded emotionally. I explained my behaviour over and over. Particularly to sales people and customer service people in shops and organisations.

So no – it doesn’t get easier.

Some parts – many parts – do get harder.

But most of all, it gets different.

New stuff, issues, challenges come up that need to be absorbed.

The early stuff that was overwhelming – some of that goes away, some of that becomes routine, and strategies are devised to cope and accommodate.

New questions emerge, unresolvable. (Where will I be living, five years from now – assuming I live five more years? I have no clue. But if Mike were alive, I would know – at least more clearly).

What I do know –

I will always be one of five kids.

I will always be married – and widowed – to Mike.

I will always have three kids.

And I will keep practising loving what I have, and what I have had, in this precious life.

Categories: Child Loss, Widowed, Widowed and Healing, Widowed and New Love, Widowed Milestones, Widowed by Illness, Multiple Losses

About Emma Pearson

My life is a whirling mix of swishy strands, dark and glowing brightly, rough and silky smooth – all attempting to be seen, felt and integrated at once. Here are some of my themes.

I am British and now recently also French (because of Brexit), and I have lived in France for the past 21 years. I am 54 and sometimes feel to be an “older widow”, and yet I feel so young. I lost my best male friend Don to bowel cancer in September 2015, my brother Edward to glioblastoma in January 2016, my husband Mike to pancreatic cancer in April 2017, and my sweet youngest child, Julia, to grief-related suicide, in July 2019. And I met a new love (let’s call him Medjool, after my favourite kind of date), off one single meeting on a dating website. Our relationship has exploded into blossom as of June 2019.

I am widowed and I am in a new relationship. I have lost a best friend, a sweet brother, a beloved husband and a precious child, and I still have both parents who are alive and well. I live my days with my grief wrapped in love and my love wrapped in grief. I no longer even try to make sense of anything. I just hope to keep on loving and living for as long as I can, while grieving the losses of loves that are no longer breathing by my side.

I suspect my writing here will be a complex mish-mash of love and sorrow. I also write on http://www.widowingemptynests.com/.

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