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I'm a stay at home mom of two, a wife, and a caretaker for my younger sister. I write to vent, and maybe someone else can learn something from my vent...
 
 
 
 

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The Child That Is, The Child That Isn't

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Recently, the mother of a special needs child wrote a post that went viral on the Internet. My post wasn’t triggered by the blog, but rather a follow-up comment by the author. She remarked that someone had told her she should mourn her daughter and get over it. (That’s my paraphrase.)

The Last LeafNow, her daughter didn’t die -- she was born with special needs, so to some, the word “mourn” may seem like an odd one. But when you have a child with special needs, you do mourn.

You do.

To some it may seem like self-pity. I don’t know–maybe it is. Some people might be tempted to judge me for saying what I’m going to say, but I’m only telling the truth. When, as a woman (because it’s much more difficult for a man) you decide to have a baby, plans start to form in your head. It’s silly, but you start thinking about what they might do or be, and what they might look like. Then, you find out it’s a girl. You start to think about weddings, and grandchildren.

Then at some point, all of that is over. Forever.

Never, ever think that I compare this to the actual grief of losing a child. It’s different. But it’s bad. It hurts. And what’s more, the mourning happens over and over as the years go by.

So-called experts talk about the grief process. They name the steps: denial (Maybe she’s just a little behind); anger (Why, God? What did we ever do to you? What did this helpless little baby every do?); bargaining (Whatever you want, God, okay? Kill me, whatever. Okay? OKAY?); depression (What now? How do I face this? Do I even want to try?); and acceptance (I’ll get back to you on this one).

But here’s the thing -- the grief process can’t be listed neatly into five little steps. It also implies that there is an end to grieving, and I don’t think there is. I don’t think the pain ever really goes away. It just changes, and hides, and then pops up unexpectedly over the years to hit you again. And again. And again.

Almost eleven years ago, there was a little girl who was supposed to be born. That little girl was going to blaze a trail. Super smart, independent, and ready for anything. She would get married some day and give her mommy a brood of grandchildren to fuss over.

That little girl was never born.

Instead, Evelyn was born. She’s blazing a trail in her own way, and I can’t imagine my life without her. But there are some things I had to let go of -- some things I had to mourn, and that I’m mourning still.

I’ve been through every one of those stages, and more than once. Even denial, which I’ve always thought I was immune to, has appeared over the years, usually in my obsessive quest for a diagnosis.

Most of my grief is tied in to the things I feel like she’ll miss out on. All of the nevers. She’ll never get married. Never have kids. Never go to college. Never have a boyfriend break her heart. Never, never, never. I’ve had to let each of those things go, one by one.

Sometimes, that little girl who I thought was going to be born all those years ago haunts me. She skips up and down the toy aisle at Christmas time. She’s out running with her brother on the soccer field. She talks incessantly to me like her brother does. She gets into shouting matches with him, and sings along to songs on the radio. She’s worrying about clothes, and starting to talk about boys. I catch glimpses of her sometimes, but when I turn to look at her, she’s already gone. I have to let her go again.

So you mourn. I think as the years go by, I will learn to get over all of that. Certainly I can “accept” it more now than before. But I’m a firm believer in what I said -- that pain never really goes away. You learn to live with it, and yes, even accept it. I think that’s what acceptance really means. Not that you’re okay with the way things are, but that you realize you can’t change it, and you learn to live with it.

Living with Evelyn is the easy part. She’s the joy of my life. She brings

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AmazingMom 7 pts

Wow! All I can say is thank you, thank you, thank you! You explained perfectly what I hav been living for the past 13 years- not once, but twice. My oldest daughter is now 13. She is Autistic and moderately cognitively impaired. She suffers from Crohn's Disease, but due to motorical challenges, she has difficulty with the independent-living skills we all take for granted that would make having this condition bearable (trying not to get too graphic, here). At 13, she still cannot brush her own teeth, brush her hair, put her shoes consistently on the correct feet, know where food is on her face to clean her mouth...you get the idea. She is profoundly disabled, and the dreams I had for her over the years...the faith I had at she would one day "catch up" have all but disappeared. I learned to let go of the dreams I had for her and accept her for what she is. I thought I was going to be okay. Then, 2 years ago, my husband and I gave birth to our daughter. When I was pregnant with her, I was overjoyed; it felt like a second chance to have the daughter I dreamed of having-- the one who would dance, sing, and chase her older brother around the yard. To be sure, I had an amnio performed to quell those fears. The results given to me said "normal" and I was beyond eager to meet my little girl the remaining months of my pregnancy. I had a scheduled c-section (my 3rd), so I went to the hospital anticipating her arrival. I couldn't wait! I even joked with my doctors about tying my tubes; since the test came back normal and I was approaching 40, I felt safe to say that we were done with our family. They tied my tubes. All I remember next was that my daughter had to be rushed to the NICU. She was small- under 5 lbs. The doctors began picking apart her facial features, and before 2 weeks had passes, she was diagnosed with a rare syndrome. Non-hereditary. But one that affects Herr growth and all aspects of her development. She is now 2, and she cannot sit up independently. She has a hearing loss, suffers seizures, is fed by a tube, and is not likely to walk for a long time, of ever, and is even less likely to be verbal as she grows. My dreams for my daughter were dashed again, and the grieving process is unending. I love her. I have come to accept that which I cannot change. But I cannot help but be painfully conscious of the loss of those dreams every time I see a little girl skipping down the sidewalk or carrying a baby doll...or saying "momma." I have also had moms in my "circle of special needs" tell me that it is time to stop grieving and, essentially "get over it." As they walk down this road for the first time, it might be easy for them to say and do. For me, it has been a second loss, and I cannot seem to explain why it is not that easy for me. Your post puts those reasons into words that, for the first time in a long time, reassured me that I am not alone.

SunbonnetSmart.com 1357 pts

 AmazingMom Beautiful...honors to you and yours. Much Love, Fondly, Robin

wordsandmusic365 10 pts

Your post is honest, brave, moving. Thank you for writing it.

SunbonnetSmart.com 1357 pts

 wordsandmusic365 Yes, thanks so much for sharing and writing it. Fondly, Robin

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Mommybostic 7 pts

singerj Thanks I'll check it out!

sharongreenthal 31 pts

The reason this post moved me is because of your complete honesty.

I don't have a special needs child, but I do have a child who struggles to succeed in some very serious ways. He is 19 now and very much still trying to find a way to be in the world. Though not nearly as heart-wrenching and difficult as your situation, it has challenged my husband and me to redefine what our expectations of our son should be, and we've had to let go of what we think he should be doing at this point in his life vs. what he's capable of doing.

I applaud you for sharing honestly your feelings about your daughter, who you obviously love very much.

TheBlackTortoise 30 pts

My special needs daughter is 32. Your post captures the ongoing process perfectly. Searching for a diagnosis resonates with me. My daughter has pseudo-hypo-parathyroidism. For whatever reason, knowing, helped me. I have another daughter and two sons and twelve grandchildren. Many times we don't even realize the hopes/dreams we have for our children until we are faced with simple milestones turning into stop signs. That goes for the siblings, too.

My daughter is MMI. She is "married" to a young man, who now lives with us, too. Surprise! I'm learning a new side to being a mom of a special needs person. The other day, Daughter 1 called to let me know her sister, Daughter 2, had called to just vent about her mother. "It felt good to have a real sister, for a change," Daughter 1 said. "Do you know what I mean?" Yes, I do, those are the glimpses of the daughter I expected. That is not to take away from all the delightfulness of Daughter 2. She is indeed a wonderful person.

Dr.Ann 5 pts

Thank you for sharing your story and your heart on this post. It is very moving. Many blessings to you, Evelyn, and your family in the days and years ahead.

~Ann

Mommybostic 7 pts

Thanks for all the kind words. Even those who don't really agree with me were still able to express themselves without judgement. I've always wondered about people who can't disagree with someone without tearing them down. This is a very personal post about my own feelings. Maybe I should put one of those disclaimers like they do on TV--****this post is the opinion of the writer and in no way reflects the thoughts or opinions of special needs parents as a whole.****

I write to vent my own feelings, but also try and connect with people and let them know that others sometimes feel the way they do, because that's what I get from reading other people's experiences.

Michellew_ 5 pts

I took your post as a reminder to cherish the things that I so often complain about. Incessant chatter, sibling bickering, and constant drama over clothes, boys, and what have you. I tend to get irritated by these things. Instead, I should perhaps take them as a blessing.

amlindsey 15 pts

Therapists have told me to "mourn" over my parents, who failed as parents. I do feel grief that I will never have a mother who thought to hug me when I got my first period, or even acknowledged it as a life event, a mother who would fight for me instead of moving to another state after my father won sole custody. I feel grief that I will never have the father who wanted to walk me down the aisle, who vehemently refused to come to my college graduation and my wedding because my mother would be there.

I mourn the relationships I will never know, even though I still love the parents I have. I would be shocked if you did not mourn for the relationship you dreamed of with your daughter. I don't see any conflict with your love for the daughter you have.

xina143 11 pts

I get it. I have five boys, and in a way I mourned for the daughter we would never have. I adore my boys, but there is a small part of me that mourns the daughter my husband and I won't ever have. I think you are very brave for posting this, and I enjoyed reading it.

Audrey @Mom Drop Box 14 pts

Wow, your post gave me chills! I can't say I know what you're going through, but I imagine that if I were the parent of a special needs child, I would have those same feelings. Thanks for sharing your perspective.

wantapeanut 8 pts

My son is autistic, and although I have experienced grief, I haven't mourned. I think there is a difference. To me "mourning" does imply death, and having lost a brother to cancer, I feel quite starkly the difference. But replace "mourn" with "grieve" (and maybe it's just semantics), and I understand what you are saying. It is possible to both love the life and the child you have, and grieve the life you imagined. I'd recommend Susan Walton's piece, which I disagreed with but provides an interesting counter point to this post: http://blog.sfgate.com/lshumaker/2011/09/08/grieving-autism-not-so-much/

Cheryld 8 pts

Hugs. Beautiful post! It is a mourning process. Anyone who has been through it knows.

Tarasview 7 pts

that was beautifully said. I have a special needs son and I totally get it. I'll just sit here and bawl for awhile longer but thanks so much for your post :)

janey jay 5 pts

Change "Evelyn" to "Will" and you have completely and precisely expressed me, my feelings and my life. I take comfort in knowing that I'm not the only special needs mama who feels this way. And the advice about getting out of your own head = spot on. It's ok to mourn what won't be as long as you take time to celebrate what is. Thanks for speaking for me ;-)

edavis 229 pts

Nice and honest and feelings shared by many others who don't have the words to express them. Thanks.

Forever 17 125 pts

I can completely relate to everything you have written, I too have a special needs daughter and she is a huge blessing and I too struggle with what she "wont" do but the best advice I can give is just try to deal with each issue individually as it arises or you will drive yourself nuts. You should check out some of my posts I think you might find you are not alone :) Thanks for sharing, Great post!

Mommybostic 7 pts

Forever 17 Thank you. I think you hit the nail on the head--you drive yourself nuts. That's the biggest challenge. Getting out of your own mind. Thanks for reading, and I will absolutely check out your posts!

Conversation from Twitter

RoundRockGal
RoundRockGal

Mommybostic I discovered you thru Blogher & can relate to your post about Evelyn. I will leave a comment on blog - but wanted to say hello!

Conversation from Facebook

Pamela Cytrynbaum
Pamela Cytrynbaum

If you feel you need to grieve, then you do. If not, then don't. Nobody gets to judge or decide.

Pamela Cytrynbaum
Pamela Cytrynbaum

http://www.blogher.com/bill-rights-grief-and-loss-dont-tell-me-how-mourn

Mama Be Good
Mama Be Good

I feel for Mommybostic. It sounds like she's in pain. But I wished she would not have spoken for all us moms. Not everyone mourns. I didn't. We just come from different places.

Terri Patillo
Terri Patillo

Mourninmg is for death and loss. So, for me, it would not be appropriate. Our oldest was born with Spina Bifida (her Mother didn't take a single pre-natal vitamin). She's had almost 20 ops. There are more to come. BUT, she's a brilliant young woman, she walks (yes, with a grave limp), talks, drives, lives, loves, and laughs. Her needs are many but we celebrate her live every single solitary day. We don't mourn her disabilities -- we overcome them.

Stephanie Guittard Scigliano
Stephanie Guittard Scigliano

beautifully written. thank you for your honesty.

Christine Sheffield
Christine Sheffield

we do not always mourn.

Robin Jones Hill
Robin Jones Hill

Beautifully written! I couldn't have said it better myself! My daughter is "graduating" this year and I think this stage has hit me worse than any other (except when we finally realized that she would never "catch up"). {{{{{HUGS}}}}}} to you and your precious family!

Nelle Douville
Nelle Douville

As a parent of a now young woman with Type I diabetes, I wish she did not contend with this disease. Yet she is so much else that makes me burst with love and joy, so intelligent, approachable and friendly, with a good idea of her future direction, yet who also knows when to stand her ground... these things overpower diabetes and shine. She has to contend with its effects, but does so with a grace that was and remains an example to me.

Michele Morris Cohen
Michele Morris Cohen

I totally get that. It hits you when you don't expect it. My worst Christmas was the one when my niece, who is 9 months younger than my son, got a bike. My son can do a lot, but he can't ride a bike.