Tue 28 Apr 2009
little miracles
Posted by bon under coping stuff, stuff to be done
[68] Comments
with trepidation, i’m planning to send this letter later today…to the hospital where Finn was born and where i did all the bedrest with O and the legion of ultrasounds with Posey.
i’m struck every single year by the ridiculous way in which this fine institution handles its fundraising. i’m not a fan of telethons in the first place, as the emphasis on “look at the cute little hard-luck children and their miracle stories!” makes me uncomfortable in that eerie 1950 flashback way…but the annual mailout of miracle stories to a population that inevitably includes many bereaved families seems grievously insensitive, even this year when i’m feeling pretty healed and pretty equivocal.
i could use feedback – how does this come off? i want to make my point while still sounding positive and…um…uncrazy. help? please? all suggestions/constructive criticism welcome. (deep breath).
and yeh, this is the real institution – the blog has been too public to insert false anonymity now. if you’re local, please don’t consider my critique a reason NOT to support the hospital – rather, i’m hoping to inspire them to revisit their fundraising strategies so that more families can support them without being brutalized by mail every spring.
April 28th, 2009
Dear Mr. Shaw,
I received your PEI Cares Telethon newsletter/solicitation in the mail this week, and needed to write to you to explain why your institution’s fundraising efforts unintentionally but regularly raise my hackles.
Mr. Shaw, four years ago tomorrow my son Finn was born at the IWK. I’d been airlifted to Halifax a few weeks earlier, when my water broke at 24 weeks gestation. Finn was born at 26 weeks and a day. He weighed 2.2 pounds, and had brown hair and his father’s nose. He did not make it through his first night; he died in my arms early in the morning of April 30th, 2005. He was our firstborn.
I was and am incredibly grateful to the IWK for the effort expended to try to save Finn’s life, and for the care shown him and me, both then and in my subsequent pregnancies with his younger brother and sister. We – along with some family and friends – have made memorial donations to the IWK every year in Finn’s name and memory, and plan to continue to do so. I recognize that fundraising is an integral part of the ongoing operations of the hospital, and that it is a significant challenge to mobilize the necessary funds to keep the standard of care at the level of excellence Maritime families have come to rely on.
But, may I suggest that including bereaved parents in your regular fundraising mailout is insensitive and in poor taste? Last year, one of the children featured in the mailout and on the telethon was a little girl from here in PEI who was born at the exact same gestation as my son, at only ¾ his weight, on his actual due date in August 2005. We happen to know this little girl and her family personally, and celebrate with them the fact of her survival and healthy development. But it is painful nonetheless to be faced with the public spectacle of that “miracle,” particularly as part of an emotional appeal designed to raise money. It creates a discourse wherein the children who do not have the happy ending or the camera-friendly story are further negated, in a culture which already treats infant and child death as the last frontier of horror. The telethon only reinforces the isolation of bereaved parents by reinforcing the “Oh, I couldn’t possibly imagine” response.
I give in my son’s memory because he mattered to me, and because I wouldn’t want another family to go through the same grief that we did if it were at all avoidable. But I can assure you that being confronted with intentionally emotionally manipulative mailouts asking me to “imagine” the difficulty of having a child in hospital does not make me at all more generous.
If your hospital were a cardiac facility for adults, I suspect you would not solicit donations among the widows of lost patients by sending smiling pictures of happy heart attack survivors: “This is Fred. He had a massive coronary but what a precious champion – he’s a fighter and today he’s back golfing again! Fred never gave up. His wife Joyce is just so grateful to all of you who made this miracle possible through your generous gifts.” It would be understood, implicitly, that such a mass fundraising strategy would be offensive, salt in the wounds of those whose partners did not survive their heart attacks. Losing a child is no less difficult than losing a spouse. Please show me, my family, and the other bereaved families whose children have not been lucky enough to leave the IWK healthy the same respect you would accord us if our loved ones had been adults.
Perhaps a separate database could be established, Mr. Shaw, wherein families who’ve made memorial donations for their children could have a simple, tasteful, “We’re fundraising and would very much appreciate your continued support in memory of your child, should you feel so inclined” letter sent, instead of the standard telethon-focused “miracle” onslaught?
I genuinely want to support the good work the IWK does, and would be happy to volunteer my assistance in revising your fundraising strategy amongst bereaved families. I ask you to please consider doing so, and in the interim, to please remove me from your mailout list. I will continue to donate, but on terms that respect my son’s memory rather than erase him from view simply because he was not, in telethon terms, a “miracle.”
Yours sincerely,
Bonnie Stewart




April 28th, 2009 at 10:38 am
My god, I never knew they sent those horrible “miracle” pleas to the bereaved… I find them insensitive, I can only imagine what it must feel like for you and other babylost families.
The only thing I would say is that you should wrap up your letter with a specific request; for a reply, or a phone call, or to be removed from their current mailing database. That way you can hold them to account if you don’t get from them what you’re looking for.
I’m having an extra dessert tomorrow for my wee birthday twin Finn. I know it’ll be a hard day; I’m thinking of you.
April 28th, 2009 at 10:41 am
My only suggestion would be to leave out the part where you recommend a separate data base. I think they should make the change for all their fundraising efforts. There are other ways to make an appeal. I think your offer to help revise the campaign is a great idea.
I think the letter is very well written. You did a great job of laying out what is upsetting to you and why. You are really very positive about it all. I say send the letter.
April 28th, 2009 at 10:42 am
Oh, I just read Hannah’s comment. We must have been typing at the same time. I like her idea for a specific request.
April 28th, 2009 at 10:49 am
I think it’s just right.
April 28th, 2009 at 10:55 am
I think it’s an excellent letter. I do fear that your tone when you give the example of the heart attack victim might come off as a tad sarcastic. I think you should leave the analogy in but maybe tweak the way the quoted part is presented.
And yes, I agree that you need to imply that a response is warranted.
I very much like the way you have offered to help them create an alternative for bereaved families. You might even want to include the line “assist in developing policy in this area.”
Good luck with it.
April 28th, 2009 at 10:57 am
I actually love the analogy you used. It is sad that a letter like this actually has to be written. I would guess that you have become a number to them, a number that amounted to dollars being given in the past. That is wrong. They should offer you their apologies and they should change their habiats. I think it is fantastic that you are sending this. Hope it changes their ways.
April 28th, 2009 at 10:59 am
I think I just disturbed the neighbours with my cheers. It’s perfect, Bon.
April 28th, 2009 at 11:09 am
Good letter – to the point and non-hysterical.
Part of the problem may be that the one hand doesn’t know what the other is doing. Privacy requirements may mean that the fundraising office doesn’t have access to lists of those parents like you. However, that you’ve been making memorial gifts all along, the fundraisers ought to know better – but they probably just haven’t thought of it. Good that you’re pointing it out.
April 28th, 2009 at 11:10 am
Can I borrow some of your tact? It’s a characteristic I struggle to develop.
I think the letter is extremely respectful, well-written, and honest. If I were them, I’d jump at the chance to have you help fix the situation, especially as a volunteer.
I disagree that you should “imply” the action you want, but feel that you’ve made a specific request to be removed from their mailing list. Will you be disappointed if you get no other response than removal from the list? If so, ask directly for a personal response: “I hope to hear from you personally so we can discuss the possibilities” or “I look forward to speaking with you personally in May” or something similar. Otherwise, well done.
Having seen my mother go through the loss of a child, and now being a mother myself with children at the age of the one she lost, I *can* and do imagine, though I try not to dwell on what could be in order to preserve my rationality. I’ll be keep you and Dave in my thoughts and prayers today and tomorrow, especially.
April 28th, 2009 at 11:10 am
lol, Mad…i know, i know. the sad part, i lifted the sentences directly from the letter i just got this week in the mail – all i changed were the names, ailment, and sport involved. the “precious champion” and “never gave up”? that’s all them.
but perhaps i should dial it back a bit and then point out specifically how “never gave up” (underlined in the text) sort of implies offensively that MY wimpy kid did just that?
April 28th, 2009 at 11:17 am
Well said, Bon. I think you’ve done a service to the hospital, other families and yourself.
Happy Birthday, wee Finn.
April 28th, 2009 at 11:19 am
It’s a powerful letter. Two very minor things: “in my son’s memory because he mattered” may be better as “matters”, and the big paragraph could be broken into two. I also think it’s reasonable and appropriate to ask for a specific response – even if it’s just that he advises you of what plans he has to address the matter.
I hope Mr Shaw is responsive.
April 28th, 2009 at 11:20 am
Good lord, they actually used the phrase “precious champion”? I’m sorry, it sounds like the colour commentary for the Westminster Kennel Club dog show. It bloody does.
Now I’ve gone through “reeling” and straight into “seething”.
April 28th, 2009 at 11:33 am
OMG!
If it is there words exactly, then by all means use them. You might want to let them know, though, that you are using their exact wording b/c the people who read the letter may not me aware of the copy text on the brochure. That alone brought to their attention may spark editorial change if nothing else.
April 28th, 2009 at 11:37 am
An excellent letter. It is so respectful and reasonable, I imagine it will hit him like a ton of bricks. I’m guessing nobody even thought of the effect of the letters on bereaved parents, or else did not consider the fact that bereaved parents were part of the database.
April 28th, 2009 at 11:38 am
This comment is totally off-topic, but WTF? I guess I always assumed that one of the benefits of government-sponsored health care was that it was, well, government sponsored. Obviously, I have no idea how these things are generally funded in Canada, but, to a clueless outsider, it seems a little odd to be soliciting private contributions in the first place.
April 28th, 2009 at 11:41 am
perfect. i do not think you should change at all. it would weaken the letter.
April 28th, 2009 at 11:54 am
Hey Bonnie,
I think the letter makes your point strongly. Sometimes we all need a hit over the head about stuff like this. I remember lunching with a girlfriend who is in treatment for breast cancer. She felt so small compared to ’survivors’ who can speak openly or become poster-women. She always woke me up to language we use around disease where some ‘win’ the battle … so others are clearly losers.
Let me know if you ever want to have a more public radio chat about this. Take care, K
April 28th, 2009 at 12:14 pm
Excellent. I hope they sit up and take notice.
I’m sorry that you are bombarded by this thoughtlessness.
April 28th, 2009 at 12:16 pm
I wouldn’t change a thing. This is quintessential you. This is how you feel and he deserves to know exactly how you feel.
April 28th, 2009 at 12:26 pm
a beautiful letter, bonnie. perfect just the way it is.
April 28th, 2009 at 12:42 pm
I think it’s a very good letter. And I think that the hospital needs to be made aware of how insensitive their fundraising efforts are.
April 28th, 2009 at 1:01 pm
It’s perfect. Your usual eloquence and grace shines. I am in tears. How could she not recognize the truth in your words and respond to your generous offer to help. xo
April 28th, 2009 at 1:02 pm
Um, “shine.” I hate comment typos on my favorite writer’s blogs. I just ruined my own day
April 28th, 2009 at 1:03 pm
Dude, did I seriously just mis-plural-possessive in a correction comment? I’m leaving now. I might drink.
April 28th, 2009 at 1:03 pm
I LOVE this letter. The hospital where my son was born has fundraising on behalf of the Childrens’ Miracle Network and it has always bugged me – are the ones who don’t make it home not miracles? Bravo for writing this!!
April 28th, 2009 at 1:21 pm
The only bit I would change is the phrase, “It creates a discourse wherein…” The rest of the letter up to that point, especially the sentence immediately before, is very personal in tone, so those words seemed to shift into a more academically distant mode. You could even just leave those words out and keep the rest of the sentence almost exactly as is.
Call me cynical, but I wouldn’t be surprised if they send heart-attack survivor brochures to the widows too.
April 28th, 2009 at 1:22 pm
My goodness. I just can’t believe you even HAVE to write this letter. I just transitioned careers to focus more on raising funds from communications and this is a basic cardinal rule. Segment your lists. In the database, they should be able to send different mailings to different people. Yes fundraising is important, but a one appeal to fit all doesn’t work.
April 28th, 2009 at 1:29 pm
I think it is WONDERFUL. Send it.
April 28th, 2009 at 1:53 pm
Niobe, public health care notwithstanding, this hospital raises millions every year through their annual telethon, and relies on the additional funds to (and here i quote the mailout) “purchase new equipment, fund innovative treatments, and attract the best doctors.” public health care has many, many positives but suffers from a perennial case of underfunding…i don’t begrudge the hospital its fundraising, just want them to reconsider their approach and adjust it to audience, a little.
right now, it appears that anyone who contributes during a telethon, even with a specifically “in memoriam” donation, gets not only all the regular telethon mailings but this year this new campaign for pre-telethon gifts, all selling the stories of “champion children” and “miracles.”
April 28th, 2009 at 2:36 pm
Thank you so much for this, so much. We’ve received two fundraising mailings from the hospital where Teddy died, both highlighting success stories, both hurtful though I know that wasn’t the hospital’s intention.
The last one came two weeks ago and I sat there in the kitchen wondering if I should send a note in the return envelope asking to remove our names from their fundraising list, just till we make it through this first year. But I didn’t have the emotional energy to spend, so I just threw the note away.
Your letter is eloquent and not the least bit mean spirited, and it makes it’s point clearly and poignantly. I’m grateful to you for taking this on, especially because some of us can’t right now.
April 28th, 2009 at 2:48 pm
Completely uncrazy. You rock! Don’t volunteer – let them pay you.
April 28th, 2009 at 2:56 pm
perfectly said.
April 28th, 2009 at 3:03 pm
Perfect as is. Since the “Fred” example comes from their own literature…I would, in the private correspondence version, use the actual wording, mention that you are quoting the hospital, and point out the implications of the “he never gave up” line. Ugh. And I think your suggestion of the separate database is a good one. As is the suggestion of another commenter that you end with the supposition that Mr. Shaw will contact you in some fashion. I hope your letter does bring you a response.
April 28th, 2009 at 3:12 pm
I support and applaud you for writing this letter – it needs to be said, and you have done it well. I hope Finns’ tree grows big and strong.
April 28th, 2009 at 4:37 pm
I actually like the comparison to the heart attack victim. I really don’t think they think this through very well when it comes to infants (just must not be around long enough, I guess). Like some above, I wouldn’t ask for another database, I would insist the MIRACLE language get thrown out entirely. I might even drive home what you perceive the antithesis of Miracle to be writ large in Finn, thanks to them.
For reference, if you or they are so inclined, Alexa at Flotsam blog read a piece on NPR a few weeks ago about how her premie (whose twin did not survive, incidentally) is not a “miracle,” but a helluva lotta hard work.
April 28th, 2009 at 5:51 pm
Perfect! Should I add that I haven’t read the other comments (no time today)?
April 28th, 2009 at 6:09 pm
Send it. And take them up on it when the ask for your help.
Bravo.
April 28th, 2009 at 6:09 pm
Just 2 things – he may sign the letter, but it’s most likely his job to send it so I’d take out the Mr. Shaw in the late para as it’s already deeply personal and honest and frank and that may make him feel a personal attack that could lead him to dismiss your words. And second, ask to be removed from the mailing list. They have to, and it’s probably one of the many mass name grabs big organisations do to send out mailers. I agree with your suggestion about the seperate database and think it’s a good, but maybe could be gently phrased, suggestion – they can and maybe should appeal directly to families with communication that shows that they do understand that your child, and all the other children that have died at their hospital, did and do matter to their families and friends and all of us. That shows that going through that with you makes a difference in them, and that shows empathy and respect. In this age they have absolutely no excuse for untargeted communications. I hope your letter helps them do this better.
April 28th, 2009 at 8:27 pm
Perfectly said Bon, I would not change a thing. In fact I’d like to borrow this myself to send to the big children’s hospital here in Melbourne. I’ve had the same thoughts buzzing away in my head for weeks, as their big annual telethon every year is on Good Friday. For weeks leading up to it, the papers were filled with stories on those miracle babies. Those “survivors”. My 40+ week stillborn baby does not count. Did not take a breath, so she does not count. But she was a miracle, as all children are.
Keep us posted with any response you get.
I think you’re fabulous, Bon.
And to echo what someone else said, Finn “matters”.
April 28th, 2009 at 9:20 pm
It sounds great Bon. Definitely send it.
April 28th, 2009 at 9:26 pm
thanks, to all of you. it is sent. minor changes, made at your suggestion.
and a chance to talk about it on CBC as well, perhaps. which is a wonderful opportunity and also a terrifying prospect, given that PEI loves its telethons and i don’t wanna be the hater making people all uncomfortable and alienating fine folks who just want to help. yet i do think language matters.
thoughts on how to do this gracefully, should i get the chance to take it to air?
April 28th, 2009 at 9:46 pm
You will be graceful if you are on the air – that is who you are. I saw someone on campus the other day who reminded me of you, somehow, and it made me miss the non-virtual version and wish you (or I) lived closer.
April 28th, 2009 at 10:26 pm
You should talk about it on CBC, if given the chance. Just be your usual calm and lovely self; speak from your heart about your own experience and about Finn, and you’ll be fine.
And remember that there will ALWAYS be critics, but there will be lots of folks cheering for you, too.
April 29th, 2009 at 1:39 am
Oh I would have gone a BOATLOAD more crazy than that, Bon. You handled it with wonderful tact.
April 29th, 2009 at 2:42 am
I usually just lurk, but thank you so much for writing this letter. It is beautiful and SO relevant even beyond baby loss. Society in general portrays those who survive ordeals as being infinitely stronger than those who don’t and even those who survive but do not get better. As someone with a progressive illness, it gets pretty painful when people continually laud those who recover, etc., as being herculean while those of us who lose function and may eventually not survive just must not be trying as hard. It doesn’t have anything to do with being stronger or weaker – it’s all about being lucky enough to have the physical capacity to improve/survive.
I truly ache for your loss, Bon, and I KNOW that your sweet Finn was every bit as strong and every bit as much a fighter as the children they talk about in those newsletters. I’m so sorry things turned out this way, and I’m even sorrier that you continually have to be confronted with things like this.
April 29th, 2009 at 12:46 pm
This took my breath away. In words that were so succinct and clear and crisp, you managed to capture the complexities of your emotions (and in a manner that reflects all families who have faced the loss of a child) — while making a very direct complaint to their marketing strategies. How did you do this? It would have taken me months of stewing and fuming to make this happen… to get out my feelings from the issue and figure out how to express it all clearly. You are amazing.
My only thought is that the database suggestion seems to take away from your overall point?
April 30th, 2009 at 10:07 pm
I’m sorry but I have to delurk to point out something none of the commenters (or the writer) seems to even consider…that perhaps the organization is very familiar with the delicate line it walks in its stratagies and, dare I suggest, actually does its very best NOT to offend any donor segment, many of whom have very personal and painful reasons for being donors. As much as I hate to point this out, I suggest to you that the donor has a responsibilit to specify what types of mailings/appeals they wish to receive, because foundations like these DO NOT have access to personal files and therefore DO NOT know anything about a donor’s wishes unless it is specified in writing.
Sorry to highjack this post…it is just very frustrating to see so many people suggest that this would come as a surprise to an organization as senstive and aware of this. They live it every single day.
April 30th, 2009 at 10:44 pm
actually, Nancy, i got a very thoughtful and positive response from the IWK today suggesting that maybe they haven’t given thought to this in the past…and my donations have all been specifically tagged “in memoriam” but still received the generic mailout in response. they do not appear to have a separate strategy targeting different audiences whatsoever, actually, at this point.
many other institutions and organizations who do similar work very specifically separate their bereaved donors from their mass appeal donors, so my Glow in the Woods colleagues were kind enough to inform me, precisely because the narrative and language used in the mass appeals is the antithesis of the way they wish to approach memorial donors. the separation is simply good business, in addition to being considerate.
and there are so many places where our culture already puts the onus on the grieving to make others comfortable…is it really necessary to suggest that the same be done with solicitations for money?
May 1st, 2009 at 3:20 pm
Bon, I’m so happy this worked out!
Feel free to tell them to send it to Sick Kids as well and other Canadian hospitals, because some are good, and some are terrible.
They will definitely have serious problems with privacy legislation, but there are lots of ways around that, and if you want to email me, I am happy to chat about it more. Privacy legislation really is used improperly constantly and ends up hurting patients and it drives me nuts!
May 2nd, 2009 at 9:03 am
I’m sorry I missed the deadline Bon, but I wouldn’t have changed anything anyway. I’m glad you got a response – are you going to go on tv to discuss it?
May 3rd, 2009 at 4:33 pm
I am very glad you got a response. Part of the problem often arises as fundraisers , successful professional ones anyway, move from place to place so are not necessarily invested in the organisation that is paying this year’s wage. This is why they make such mistakes and they really, really shouldn’t.
May 4th, 2009 at 3:12 am
Great letter. And an education.
May 5th, 2009 at 7:38 am
the story was on CBC this morning, and my only regret – other than the fact that hearing myself makes the perfectionist in me cringe – is that the IWK`s positive response nonetheless focused mostly on the privacy laws that prevent them from identifying which families are bereaved.
i`m well aware of this. my suggestion, directly to the CEO of the Foundation, was simply that they create a separate listing of donors who tag their donations in Memoriam. i don`t believe that impacts privacy laws whatsoever, since it`s self-identifying.
i wish the story had taken up that option.
May 5th, 2009 at 7:50 am
Hi Bonnie,
Just listened to the interviews on CBC – it is great to know you have opened a dialogue with the IWK Foundation. Good luck with it.
I was also pleased to hear Mr. Shaw point out what I tried to articulate above – that Cdn hospitals are prevented from approaching families while they are patients, or from accessing any info about them. Foundations can only solicit from donors or general publics.
He also implied they do not have any information suggesting you are a bereaved parent. “In memorium” does not mean the same thing. You may have made the donations in honour of Finn, however if your file is marked in memorium, it could be a donation on behalf a child, a friend’s mother, a staff member or former volunteer who has indicated in an obituary they would like the IWK to receive donations.
Finally, Mr. Shaw also talked about the vast difference between Canada and the U.S. He was right about that. In the U.S. you can walk into a patient’s room and ask for money!
Anyhow, I hope you do get to meet Mr. Shaw and he can show you how complex it is.
I also believe it is not fair to use the analogy about an adult facility – they would and do absolutely send appeals to many segments without knowing whether they are bereaved. Not intentionally, but it happens. They just don’t have the information they need to tell them not too.
All the best,
Nanc
May 5th, 2009 at 8:28 am
hi Nancy,
no, i realize that “in memoriam” doesn’t indicate nearly enough info. it offers the beginning of a self-ID process, however, which could be the trigger for a simple checklist mailing or email asking donors to indicate what mailouts they’d prefer to receive. one extra step.
which is very different from putting all the onus on people who already feel profoundly exposed to have to make the first move saying “geez, this feels in poor taste.” it took me four years to get up the courage to do that. i’m still actually shaky imagining the barrage of “oh stop whining” that i imagine may come forth from the story. it’s not actually that i’m such a flower that the mailout crushes me, but it does feel like a pretty thoughtless slap each time – especially in the context of actually asking me for money – and i think the hospital can do better. i’m grateful that they agree.
with the CCU analogy, it’s the poor taste thing i’m trying to explain. yes, solicit me. but we use images and language around children in these telethon situations that most would instinctively recoil from and question if they were used in an adult context. the “what a precious miracle!” language, etc.
anyhoo, we’ll see what comes of this. i’m sure i’ll learn a great deal in the process. thanks very much for following the story.
May 5th, 2009 at 8:39 pm
You are an amazing lady. Thank you Bon.
May 5th, 2009 at 8:54 pm
I have followed you only very recently on Twitter. Had not yet settled down & read your blog.
Now I have, and I understand why you posted this & the CBC comparison.
Well done, I admire the courage it takes to muster even a response, let alone such an articulate one.
The letter is excellent. I applaud its grace and even handedness, especially in the face of all that you have no doubt had to encounter and endure and manage to somehow keep on facing up to.
Inevitably there is insensitivity and an inability of many to even cope with the scope of what your family has gone through. People say incredibly stupid things. But letters of this nature should not. And I think you are absolutely right right to explain why they need to examine their “ask” & they ways they choose to do so.
The letter is exceptional because not everyone can do so in such a measured and thoughtful fashion.
May 5th, 2009 at 9:44 pm
Very reasonable, and very reasoned. good for you for speaking up.
May 5th, 2009 at 11:39 pm
I tried to post at the CBC site but for some reason I can’t log in. I’m astounded by the rancour & stupidity of some of those comments. I regularly follow autism stories in the media so I guess I should be hardened to this kind of trollery by now. But I’m just not.
What does it cost these people to exercise a small bit of compassion? How damaged are they?
Thank you for doing what you did, Bon. Every time someone like you reminds us that we need to look out for each other, they are serving all of us.
May 6th, 2009 at 1:45 am
WOW! Bon, this letter is stunning. You said it perfectly. Thank you.
May 6th, 2009 at 1:47 pm
A lovely, thoughtful letter, Bonnie. As one who has lost an infant many years ago, I always endured those campaigns – more or less incorporated it into the overall pain burden. I never took the opportunity to do what you’ve done, actually force the Institution to rethink some of their basic fundraising suppositions. Good on you!
May 6th, 2009 at 4:53 pm
I completely agree with you. Perfect letter, Bon.
May 7th, 2009 at 12:41 am
Just seeing this since I’m mostly detatched from online lately. Good on you girl. I still remember the crap like this we got after Mom died…
May 8th, 2009 at 8:15 pm
I also found this very upsetting. Our family spent many months at the IWK over several years and lost a son. Thanks for speaking out on this matter.
May 30th, 2009 at 10:30 am
This is a great letter, and one that I want copy, replace “hospital” with “Church” and send to my place of worship.
May 31st, 2009 at 8:01 pm
I also think it is perfect. Very well written and with excellent points and analogies. I feel like saying “every year”, (because it feels like I’ve received so many of these letters from the IWK, when really it hasn’t even been a year)that we receive a “miracle” story, I feel sick to my stomach, and I never really knew why until now. I never really thought about it, because I am grateful to the IWK for the care they provided both my girls and especially my living twin. However, reading the miracle stories, makes me feel like my dead baby was a failure, and that she wasn’t strong or good enough to be a miracle. That really pisses me off, so thank you for opening my eyes and making me realize why I hated those letters so much.
February 4th, 2010 at 3:08 pm
My husband and I lost our daughter 5 years ago next week! I found myself just looking around at bereavement articles and came across your letter! I say good for you! I live in the Halifax area and during the big IWK fund raising time I hide out even still. Everywhere you go people are talking of what great things happen there! And every year we are forgotten the families that things did not turn out so well for! Since we lost Jocelyn we have had two more children both wonderful blessings. We as well are grateful for the IWK even though our story did not end the way anyone wants. I hope the IWK can see how this hurts and try to make some changes!
Good for you great letter!