diary of a mom

May 1, 2009

welcome to the club

Filed under: Uncategorized — by jesswilson @ 10:47 am

My dear friend,

I am so sorry for your pain.

Don’t worry; no one else sees it, I promise. To the rest of the world, you’re fine. But when you’ve been there, you can’t miss it.

I see it in your eyes. That awful, combustible mixture of heart-wrenching pain and abject fear. God, I remember the fear.

I see it in the weight of that invisible cloak that you wear. I remember the coarseness of its fabric on my skin. Like raw wool in the middle of the desert. You see, it was mine for a time.

I never would have wanted to pass it on to you, my love. I remember so well suffocating under the weight of it, struggling for breath, fighting to throw it off while wrapping myself in its awful warmth, clutching its worn edges for dear life.

I know that it feels like it’s permanent, fixed. But one day down the line you will wake up and find that you’ve left it next to the bed. Eventually, you’ll hang it in the closet. You’ll visit it now and then. You’ll try it on for size. You’ll run your fingers over the fabric and remember when you lived in it, when it was constant, when you couldn’t take it off and leave it behind. But soon days will go by before you wear it again, then weeks, then months.

I know you are staring down what looks to be an impossibly steep learning curve. I know it looks like an immovable mountain. It is not. I know you don’t believe me, but step by step you will climb until suddenly, without warning, you will look down. You will see how far you’ve come. You’ll breathe. I promise. You might even be able to take in the view.

You will doubt yourself. You won’t trust your instincts right away. You will be afraid that you don’t have the capacity to be what your baby will need you to be. Worse, you’ll think  that you don’t even know what she needs you to be. You do. I promise. You will.

When you became a mother, you held that tiny baby girl in your arms and in an instant, she filled your heart. You were overwhelmed with love. The kind of love you never expected. The kind that knocks the wind out of you. The kind of all encompassing love that you think couldn’t possibly leave room for any other. But it did.

When your son was born, you looked into those big blue eyes and he crawled right into your heart. He made room for himself, didn’t he? He carved out a space all his own. Suddenly your heart was just bigger. And then again when your youngest was born. She made herself right at home there too.

That’s how it happens. When you need capacity you find it. Your heart expands. It just does. It’s elastic. I promise.

You are so much stronger than you think you are. Trust me. I know you. Hell, I am you.

You will find people in your life who get it and some that don’t. You’ll find some that want to get it and some that never will. You’ll find a closeness with people you never thought you had anything in common with. You’ll find comfort and relief with friends who speak your new language. You’ll find your village.

You’ll change. One day you’ll notice a shift. You’ll realize that certain words have dropped out of your lexicon. The ones you hadn’t ever thought could be hurtful. Dude, that’s retarded. Never again. You won’t laugh at vulnerability. You’ll see the world through a lens of sensitivity. The people around you will notice. You’ll change them too.

You will learn to ask for help. You’ll have to. It won’t be easy. You’ll forget sometimes. Life will remind you.

You will read more than you can process. You’ll buy books that you can’t handle reading. You’ll feel guilty that they’re sitting by the side of the bed unopened. Take small bites. The information isn’t going anywhere. Let your heart heal. It will. Breathe. You can.

You will blame yourself. You’ll think you missed signs you should have seen. You’ll be convinced that you should have known. That you should have somehow gotten help earlier. You couldn’t have known. Don’t let yourself live there for long.

You will dig deep and find reserves of energy you never would have believed you had. You will run on adrenaline and crash into dreamless sleep. But you will come through it. I swear, you will. You will find a rhythm.

You will neglect yourself. You will suddenly realize that you haven’t stopped moving. You’ve missed the gym. You’ve taken care of everyone but you. You will forget how important it is to take care of yourself. Listen to me. If you hear nothing else, hear this. You MUST take care of yourself. You are no use to anyone unless you are healthy. I mean that holistically, my friend. HEALTHY. Nourished, rested, soul-fed. Your children deserve that example.

A friend will force you to take a walk. You will go outside. You will look at the sky. Follow the clouds upward. Try to find where they end. You’ll need that. You’ll need the air. You’ll need to remember how small we all really are.

You will question your faith. Or find it. Maybe both.

You will never, ever take progress for granted. Every milestone met, no matter what the timing, will be cause for celebration. Every baby step will be a quantum leap. You will find the people who understand that. You will revel in their support and love and shared excitement.

You will encounter people who care for your child in ways that restore your faith in humanity. You will cherish the teachers and therapists and caregivers who see past your child’s challenges and who truly understand her strengths. They will feel like family.

You will examine and re-examine every one of your own insecurities. You will recognize some of your child’s challenges as your own. You will get to know yourself as you get to know your child. You will look to the tools you have used to mitigate your own challenges. You will share them. You will both be better for it.

You will come to understand that there are gifts in all of this. Tolerance, compassion, understanding. Precious, life altering gifts.

You will worry about your other children. You will feel like you’re not giving them enough time. You will find the time. Yes, you will. No, really. You will. You will discover that the time that means something to them is not big. It’s not a trip to the circus. It doesn’t involve planning. It’s free. You will forget the dog and pony shows. Instead, you will find fifteen minutes before bed. You will close the door. You will sit on the floor. You’ll play Barbies with your daughter or Legos with your son (or vice versa). You’ll talk. You’ll listen. You’ll listen some more. You’ll start to believe they’ll be OK. And they will. You will be a better parent for all of it.

You will find the tools that you need. You will take bits and pieces of different theories and practices. You’ll talk to parents and doctors and therapists. You’ll take something from each of them. You’ll even find value in those you don’t agree with at all. Sometimes the most. From the scraps that you gather, you will start to build your child’s quilt. A little of this, a little of that, a lot of love.

You will speak hesitantly at first, but you’ll find your voice. You will come to see that no one knows your child better than you do. You will respectfully listen to the experts in each field. You will value their experience and their knowledge. But you will ultimately remember that while they are the experts in science, you are the expert in your child.

You will think you can’t handle it. You will be wrong.

This is not an easy road, but its rewards are tremendous. It’s joys are the very sweetest of life’s nectar. You will drink them in and taste and smell and feel every last drop of them.

You will be OK.

You will  help your sweet girl be far better than OK. You will show her boundless love. She will know that she is accepted and cherished and celebrated for every last morsel of who she is. She will know that her Mama’s there at every turn. She will believe in herself as you believe in her. She will astound you. Over and over and over again. She will teach you far more than you teach her. She will fly.

You will be OK.

And I will be here for you. Every step of the way.

With love,

Jess

57 Comments »

  1. Um, Hi. I just started reading your blog last week. I am a lurker…I can’t usually say much mostly because I don’t know what to say. You see… I have been at a loss for words for about two weeks.

    I know you aren’t talking to me, but you must know that you ARE talking to me. I hear you and I feel okay. I feel that what ever we are dealing with in my little family, that it is okay and it will be more than okay. I thank you for that. More than you know, your words inspire people who don’t know you and you don’t know. Thank you. Thank. You.

    Comment by Nicole — May 1, 2009 @ 11:11 am |Reply

  2. I’m speechless….

    Comment by Denise — May 1, 2009 @ 11:29 am |Reply

  3. Wow, Jess. Wow.

    Comment by pixiemama — May 1, 2009 @ 11:50 am |Reply

  4. What a fantastic letter – wow! You’ve put so much thought and feeling into it.

    Comment by Chun Wong — May 1, 2009 @ 12:01 pm |Reply

  5. That was very moving.
    A reminder
    A wake up
    all in one -

    Comment by Cathy R. — May 1, 2009 @ 12:03 pm |Reply

  6. just here.
    wanted you to know.
    this is so moving…

    Comment by karla — May 1, 2009 @ 12:27 pm |Reply

  7. Oh, Jess, this took my breath away. (Let me tell ya, crying without breathing? Not so good…)

    Such beautiful and important words —for all of us on this journey of parenting our challenged children. I’m feeling raw and vulnerable today —and ineffectual as a parent. I needed these words just as much as the mom of the newly diagnosed.

    Thank you, thank you. You forgot to tell your friend that she could well find her greatest source of comfort and support comes from people she’s never met in person. That her heart can expand even more to love the children and the families of “strangers” who share the journey, share their wisdom, their own fears and pain, and their unbridled joys.

    Love.

    Comment by Niksmom — May 1, 2009 @ 12:28 pm |Reply

  8. Wow. That was astonishing and wonderful.

    You ARE me, or we are all each other, or something.

    Thank you.

    Comment by JoyMama — May 1, 2009 @ 12:41 pm |Reply

  9. Beautiful and true. You and your writing. You put into words things I want to say, but never could articulate. Thank you.

    Comment by rhemashope — May 1, 2009 @ 2:22 pm |Reply

  10. Thank you.

    Comment by Meredith — May 1, 2009 @ 3:44 pm |Reply

  11. So beautiful Jess. I wish I’d had someone write me something like this seven years ago. What a gift you are.

    Comment by Michelle O'Neil — May 1, 2009 @ 3:59 pm |Reply

  12. Oh, yes. This is what I needed when I felt so dark and alone so many years ago. No one told me that it would be okay! It’s different, and often times very difficult, but it’s okay. But my favorite part? “You’ll find your village.” I’m so glad you’re part of my village, Jess. Thank you. And, love. xoxo

    Comment by Tanya Savko — May 1, 2009 @ 5:13 pm |Reply

  13. Thank you! You are a blessing to me. Our kids will and/do fly in their own way and time.

    I am going to print this out and copy it to give to parents of recently diagnosed!

    Comment by Jenn Ethirveerasingam — May 1, 2009 @ 6:33 pm |Reply

  14. Wow! I don’t know how you do it with such perfection…the words are perfect every time. This is so important to hear!

    Comment by Stacy — May 1, 2009 @ 6:42 pm |Reply

  15. You’ll discover unexpected ways to use the untapped gifts you once thought you would never, ever find use for…

    like the way you’ve discovered to comfort us all with your beautiful writing Jess. This is definitely something I will share with those new to the club…

    Thank you for taking time to share your gift. You’re making the world a better place.

    Comment by Autismville — May 1, 2009 @ 8:49 pm |Reply

  16. Simply one of the best pieces of writing I have ever read. There aren’t enough adjectives to describe how powerful this post is.

    Comment by Betty and Boo's Mommy — May 1, 2009 @ 10:03 pm |Reply

  17. what a beautiful beautiful love letter, heart letter, soul letter. xxx

    Comment by kyraanderson — May 2, 2009 @ 8:23 am |Reply

  18. Amen. My favorite part? The quilt analogy. I’m envisioning each of our kids with these beautiful patchwork cloaks, no two alike yet woven with similar threads. Amazing.

    Comment by Audra — May 2, 2009 @ 8:49 am |Reply

  19. LOVE!!!!!

    Comment by devon — May 3, 2009 @ 12:07 am |Reply

  20. On a weekend where I found myself feeling hopeless, even helpless….because I had to give one of my angels medication….because we just couldn’t see him run all the time…because we were just worn out….because I feel like I failed, and I don’t know if I did the right thing…Thank you for reminding me that maybe tomorrow I may feel a little better. Thank you because you are all of us rolled into one, sometimes picking us up, and sometimes saying the right thing to help us keep going when we don’t think we can live do it anymore Bless you.

    Comment by TwinMom — May 3, 2009 @ 8:58 am |Reply

  21. Can’t talk now, gotta send this to everyone in my support group.

    You nailed the secret recipe: A little of this, a little of that, a lot of love.

    love.

    Comment by Carrie Link — May 3, 2009 @ 10:53 am |Reply

  22. well, i think you’re a gifted writer, so it makes sense you would generate gifts for others. over time, this is going to printed out, taped on walls next to computers, many times over.

    Comment by M — May 4, 2009 @ 8:39 am |Reply

  23. Okay. Required reading. REQUIRED.

    Can they just give this to every diagnostician and tell them, “Oh, after the parent falls on the floor, make sure they have this?”

    Might save everyone a lot of heartache.

    Snarkiness aside, this is simply perfection.

    Comment by drama mama — May 4, 2009 @ 9:05 am |Reply

  24. Wow… until this minute I did not realize how far I had come – from suffocating fear to faith and hope. Thank you for putting our journey into palpable words. Beautiful.

    Comment by mamoi — May 4, 2009 @ 11:49 am |Reply

  25. This is the first chapter of the book I dream of, the book of help and hope for parents joining the club. It is perfect. I wish I’d written it. Yes, what you said. Yes, parents in the club, new or old, we are here for you. You have our support. We are the other parents in the club, and we care, and you are going to make it!

    Comment by ghkcole — May 4, 2009 @ 1:20 pm |Reply

  26. I’m guessing I’m not the only parent of a child on the spectrum who read this while nodding my head in complete agreement as you nailed point after point.

    Isn’t it amazing how alone we all felt in those moments, and yet there is in entire community of people with a shared experience that can be almost identical?

    Comment by Russ — May 4, 2009 @ 1:42 pm |Reply

  27. This is so beautiful. Thank you for sharing such an inspiring letter…what an amazing feeling – to feel understood.

    We recieved our son’s Down syndrome diagnosis 10 months ago…and while I do wish that I had seen this then, I certainly am glad that I came across it now.

    xo

    Comment by Laurie — May 4, 2009 @ 1:47 pm |Reply

  28. Wow. That was so eloquent and written just for me. I am in the Mom of a Child with Down Syndrome Club, and it took me awhile to be able to breathe. Please send this to everyone you can who is dealing with a diagnosis that is difficult to bear. I know that I never, ever would have believed that looking back, one year after learning of Benjamin’s DS, that I would be as okay with it as I am. I never would have believed anyone, no matter how much they meant it. But it doesn’t mean we shouldn’t try. :)

    Comment by Angela — May 4, 2009 @ 2:19 pm |Reply

  29. Wishing I had this years ago. Glad I have it now.

    Comment by Osh — May 4, 2009 @ 6:40 pm |Reply

  30. Just beautiful. I am a fairly new member to this club, as my daughter Katelyn (almost 3) was diagnosed with autism in January. I also have an 11-month-old baby girl and there are many times that I feel like she is not getting the attention that she needs. But she is very resilient and independent already at her young age. I have high hopes for her that she will be an amazing little sister to Katelyn. She already has that way about her.

    Thank you for sharing this amazingly inspiring letter. It touched my heart and spoke volumes.

    Comment by Shannon — May 4, 2009 @ 8:29 pm |Reply

  31. So beautiful! I recognize that “cloak” my daughter has Down syndrome and I thought that “cloak was going to suffocate me at first but now it seems to be getting a little lighter to wear.Thank you for such beautiful words.

    Comment by Cheryl — May 5, 2009 @ 1:11 am |Reply

  32. As you know, even veterans like us somehow end up wearing that nasty old cloak again. I’ve been feeling a bit suffocated by it lately, and your words really helped me today. Through you, life is reminding me to ask for help.

    Comment by mama mara — May 5, 2009 @ 9:01 am |Reply

  33. Profoundly touching. “Singing our heart w/your words”

    Thank you-
    Cis

    Comment by ttfn (cis) — May 5, 2009 @ 11:09 am |Reply

  34. This is my first visit to your blog, I linked off of someones update on facebook. I want to thank you. You have no idea how much your words resonate with me.

    Comment by joy — May 5, 2009 @ 12:23 pm |Reply

  35. i am overwhelmed by the response to this. to those of you who are visting for the first time, welcome.

    i ‘m so pleased that you all have found value in these words and that you have, in many cases, chosen to share them.

    i am so very glad that each and every one of you is part of my village. i am incredibly blessed.

    Comment by jesswilson — May 5, 2009 @ 4:22 pm |Reply

  36. You are the most amazing woman I have (n)ever met!! Your posts make me laugh, cry, feel hope, and feel understood. I never quite know how to respond but I had to after I read this – this one is one of my all-time favorites! I plan on sharing it with the support group I belong to – I hope that is OK. I wish I had read this years ago but am blessed to have it now. Your journey is so familiar. Thank you for sharing!

    Comment by Marci — May 5, 2009 @ 11:50 pm |Reply

  37. [...] thought back to where she was when I was where my friend is now. I heard the words of her first teacher, as she shook her head sadly, “She has absolutely no [...]

    Pingback by playing games « diary of a mom — May 6, 2009 @ 5:34 am |Reply

  38. Someone just posted this on our Down syndrome pregnancy board to support a newly diagnosed expectant parent. It fits right in. It really expresses what all of us try to convey to our new moms. I know the diagnosis is different, but the feelings are still so accurate. Thank you.
    Nancy I.

    Comment by Nancy I. — May 6, 2009 @ 9:17 am |Reply

  39. [...] I am particularly honored to be a part of this club. [...]

    Pingback by Mother Stuff « Autism In a Word — May 7, 2009 @ 12:57 am |Reply

  40. My dearest Jessica,
    Your last paragraph says it all. You have always taught me far more than I have taught you. I have benefitted more from being your father than anything in my life. You are my hero as your babies (both of them), will be for you. What a great piece in time for Mother’s Day. It says it all about parenthood.
    I am so pleased for all of us that you have found your voice as it is a voice that echos everyone’s thoughts and feelings in the most eloquent manner possible.
    I am a very grateful daddy to have you as my child who has grown into a woman far beyond anything I could ever have dreamed.

    Comment by Dad — May 7, 2009 @ 3:13 am |Reply

  41. Jess, As I sit here crying (feeling very sorry for myself) I can’t find the words to thank you enough. I am the grandmother of a recently diagnosed granddaughter in OK. I live in CT. I was estranged from my son and Daughter in Law for almost a year because of my insensitivity and fear that they were not aware of what was going on with their daughter. I am not rich and neither are they but we are all richer because we have Emma. Emma is nearly 3 and I want to be with her and her parents to help in any way I can. Right now all I can do is educate myself and stop feeling sorry for myself. Reading the words that you wrote helps me to see what it is they are going through. Please don’t ever stop writing. I need to read your words. You have given me an insight and I know the more I read the more I will be able to help them, even if it is quietly praying for them to take care of themselves. They will take care of Emma and they will do a damn good job. I don’t have to fear that now. thank you. thank you and God Bless you.

    Comment by Sharon Deno — May 9, 2009 @ 7:48 am |Reply

  42. Sharon ~ I am so touched by your incredible comment. I know how hard it is to look back on things you wished you’d handled differently. I’ve spent far more time in that place than I’d care to remember.

    But as I said to my friend in the letter, ‘don’t let yourself live there for long.’

    Last summer, I wrote about a situation with my older daughter, Darby. The story went as follows ..

    “Out in the yard on Sunday, Darby had a typical 7 year old moment. She and Kendall were playing with a parachute and Darby had wrapped herself in it, shutting Kendall out. When Kenz tried to work her way in, albeit none too gracefully, Darby grabbed it away from her and shouted at her in a huff, ‘Well now you’ve gone and ruined it all, Kendall.’ I looked over and said, quite calmly, ‘We don’t speak that way to each other in this house. You’re done with the parachute.’

    She almost immediately began to cry. I called her over to tell her that I understood her frustration but I explained that the lack of respect that she had shown sister was unacceptable. I asked if she was crying because she was no longer allowed to play with the parachute. “No, Mama,” she said. “I’m crying cause I just feel really sorry. I didn’t do the right thing at all and I feel so sorry now and I don’t know what to do.”

    My smile confused her. I had to explain that I was smiling because feeling that way meant that she is a good person who made a regrettable choice. It also meant that she was learning something. I told her that feeling like she didn’t do the right thing meant she had the chance to a) apologize for it b) make it right and c) figure out what the right thing would have been so that she could make sure to do it next time. Thankfully, although she may not get a do-over, life will likely give her lots of other chances to do what she now knows is right.”

    The hurt can be good when we let it guide us toward what we know is right. It sounds like that’s exactly what you’ve done.

    We all wish we’d been more sensitive or had more compassion or been more tolerant before. Now is our chance. Guided by our love for these incredible kids, we can’t go wrong.

    Sharon, your love for your children and your grandchild shines off the page like a light.

    You are a wonderful grandma and both Emma and her parents are incredibly blessed to have you.

    Thanks so much for writing.

    And thanks to all who have shared these words. I am still in awe of the way that they have made their way through the ether, into neighboring ‘villages’ and across the world. I am overwhelmed by the power of people to find one another in the darkness and to help shine a light into a hopeful future.

    Comment by jesswilson — May 9, 2009 @ 9:24 am |Reply

  43. Dear Jess,

    I know the moment I found my voice. I am still looking for my village. I have not figured out how to find the time. I have taken the cloak off – but only for brief moments, not yet for a full day. I am sincerely grateful for the people who have restored my faith in humanity. But most of all I hope the quilt we build will always keep him warm and safe and wrapped inside of it I pray he will know how much he is loved.
    Thank you for this,
    Christine

    Comment by Christine — May 14, 2009 @ 8:23 am |Reply

  44. It has been eight months since my daughter’s diagnosis and I still feel like a new member of the club, experiencing all the grief, shock, fear, confusion, self-blame, and loneliness you so eloquently described. But time is a funny thing. It’s hard to believe that just eight months ago, I had never heard of ABA or sensory seeking behavior, and I lived under the misapprehension that autism does not affect girls.

    Your essay spoke to me and comforted me, and I know that when I re-read it in the next few months and years, it will take on a new meaning and serve as a reminder of how far I have come. There will always be a part of me that longs to tear up my virtual membership card to this club and race back to the life I knew and had expected to lead. But since I can’t, I dream instead of all the changes and progress I will see in my daughter as my family and I travel down this road, supported by friends, a team of experts, and the village you have welcomed me into. Thank you.

    Comment by Beth — May 21, 2009 @ 12:05 pm |Reply

  45. Thank you.

    My son was diagnosed about a month ago, and he just came home (2 weeks ago) from 10 days in an inpatient psychiatric unit – he’s 7. I still feel very alone, and I can’t open the books yet – I know the time will come, but right now I can’t.

    Comment by sixgreenzebras — June 9, 2009 @ 8:00 pm |Reply

  46. sixgreenzebras ~

    take your time. breathe. you’ll get there.

    wishing you and your dear son all the best.

    and please, please know that you are NOT alone.

    Comment by jesswilson — June 10, 2009 @ 11:01 am |Reply

  47. Hi.

    Thank you for sharing that beautiful, truthful letter! My little one is 5 years old and some days it seems like yesterday that I heard those words that he has a rare-life-threatening disorder. He is doing great and he has taught my whole family sooo much.

    Comment by Joyce Opp — June 12, 2009 @ 9:19 am |Reply

  48. I stumbled in here by accident. But it wasn’t an accident. Your words above are exactly what I needed to hear at exactly the right time. Thank you for reminding me that I am my child’s mother because no one else could be, and he is mine because he wanted no one else. Just reading that somewhere out there is another set of parents, other moms who KNOW, is enough for now. Thank you.

    Comment by carlajordan — June 15, 2009 @ 11:39 am |Reply

  49. Beautiful letter!This is a great lesson for all moms and children alike. Thanks for sharing this.

    Comment by Potty training infants — July 9, 2009 @ 4:02 pm |Reply

  50. beautiful, profound words. Thank you.

    Comment by Trish — July 21, 2009 @ 5:08 pm |Reply

  51. What an amazing letter! It made me cry when I read it, because the words are everything that I have thought over the last 3 years since my daughter was diagnosed with autism. She was diagnosed at age 2, six weeks after my son was born. She is now 5 and considered high functioning, but it is still very challenging. Thank you for sharing.

    Comment by Helen — July 21, 2009 @ 10:06 pm |Reply

  52. HI JESS! It was really nice to get an opportunity to speak with you last friday at the kickoff event!
    Your blog info was shared with me last August – I just found the original email!
    I can’t believe I neglected it! This is the most beautiful, ,profound, heart wrenching, hope filled letter a parent could ever read for the newly initiated into the ASD world! I also checked out your Austism Speaks page – loved your touching words on Autism Speaks Kendall can fly, but she can’t do it alone…… Tears in eyes…. On my page I posted the letter to my son inspired by you. Here it is… Hope to hear from you soon!

    Kris

    Comment by Kris Naumann — August 11, 2009 @ 10:55 am |Reply

  53. Wow! What an amazing letter. Blurry eyed. At a loss for words. Every bit true. I wish I would have read this two years ago when my son was diagnosed. Thank you for sharing it.

    Comment by therocchronicles — September 12, 2009 @ 10:48 am |Reply

  54. Jess – This is my story! It is amazing that we feel so all alone but yet we are walking this path together!
    Thank you for sharing.

    Sharmel

    Comment by Sharmel — September 17, 2009 @ 2:00 am |Reply

  55. [...] would beg her to read what she will write to a friend three years [...]

    Pingback by middle ground « diary of a mom — September 25, 2009 @ 6:17 am |Reply

  56. I alone have been coping with my daughters Austism for 20 years now and this poem you wrote touched me. I am on the verge of giving up . I am so tired and it seems like just when you get the school system navigated and the child settled and the staff on board it is time for them to leave. I am so afraid of the next step and I am not sure what to do, your poem and words help some. TY

    Comment by A — October 14, 2009 @ 10:56 am |Reply

  57. Thank you for this beautifully written post. Your words are profound and candid and heartbreaking. You capture what many of us are struggling with — trying to make sense (if possible) of a heavy diagnosis and trying our best to move forward. I look forward to reading more of your blog. So very touched. Best, Katie

    Comment by Katie Donohue Bevins — October 19, 2009 @ 11:33 pm |Reply


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