The title of this post may surprise you. Because it surprises me. Because...I forget. The two words that felt so heavy months ago, like iron chains that shackled me and pulled me beneath waters that choked and suffocated me until I almost drowned. They're gone, those shackles. I float happily now, light and free, aware of its presence in our lives but...well, just that. Aware.
This is what I wanted. As I was scraping away layers of who I was months ago, discovering our new meaning, rearranging things in our life and finding a place for the new term to live in our spaces, I hoped I'd end here. That life would take center stage and Down syndrome would move to the back like a stage assitant whose name appears in small print at the end of the credits. I searched the Internet for families that did it like I wanted to and put band-aids on my heart when I found them...familes that moved on and loved life--the ones that you'd never know "it" happened to them unless you dug a little deeper. Families that were not defined by it. And it happened on its own. We became that family, the one I wanted to be.
But every once and awhile, it appears. Last night as she was playing, grasping toys and waving them in front of her. And her movements were a little choppy, up and down, up and down, pounding her forearm to her chest like a hammer. And Brett looks up at me and says, "Is that normal? That choppy movement? Or is that Down syndrome?" And for one tiny little second, my mind starts spinning. Is it normal? Did Lainey do it? What if it's not? And I want to Google it, but I don't know what to search. And I don't want to see what it says. And I laugh it off and go to bed but it's 6:00 right now and I'd be lying if I didn't say I woke up early and have let the bus hit me again. It could have been a light and easy hit, but no. I asked the driver to hit me hard. "Smack me real good so my body flings up in the air like a dummy and I hit the pavement hard on the way down," I tell him. And he obeys.
See, I don't usually think this way. In fact, I was commenting to a friend the other day that my acceptance of Down syndrome is much like her acceptance of having two boys. Like sometimes it will hit her for a moment that she never had a girl. And for one second it might be sad...that "I'll never know what it's like to have a girl" feeling...but then instantly comes this love for her boys and she smiles and moves on. The same argument could be made about only having girls and never knowing what it's like to have a boy. And that's just what it's like for me. Mostly I don't think about it. But sometimes, for one second it will hit me..."My daughter has Down syndrome," and my throat will start to tighten and for one second--one tiny, tiny second--it hurts, but right before it closes to the point of robbing my oxygen, it opens back up--as quick as it closed--and I breathe. "Yeah? So what. She has Down sydrome."
My friend might never know what it's like to have a girl. I might never know what it's like to have a boy. And I'll never know what it's like to have a Down-syndrome-less Nella. But there's a lot of things we'll never know. Every choice we make eliminates another. Random as it is, I'll never know what it's like to be married to an Asian man, an Australian man, a British man with a sexy Hugh Grant accent. I'll never know what it's like to get wasted on my 21st birthday. I'll never know what it's like to have triplets or to travel around the world before I get married. I'll never know what's like to be a natural blonde. And I'm not going to cry about any of it because there's a million random things I'm never going to know, and everyone's life is custom-made for them. And when I hear about moms who kiss their babies before running to their chemo appointments or kindergarteners who draw pictures of their daddy-less families and nonchalantly tell their teachers that their daddy's in heaven...well, I'll take my custom-made situation just as it is, thank you. Because it's beautiful and I am grateful.
I am reminded that I had these same feelings with Lainey. That there were plenty of nights I woke up early like today, unable to sleep because my mind wandered over unexplained fevers or scabs that didn't heal. I've been hit by the bus in non-special needs land too, and I guess that's a comfort. And hell, maybe she grabbed toys and jerkily hammered them to her chest too. It's okay, it really is. I just had to put it out there. Peel off the painful layer, type it out and put it to rest where it belongs.
Parenthood is hard and beautiful. Scary and rewarding. Sad and Happy. All at once. Last week my friend traveled to Texas to be with her best friend when she welcomed her baby early...just three-and-some pounds. It was scary...and although my friend doesn't have babies yet, I had to sit back and smile at her account of it all after she kissed that baby goodbye and headed back home. Because she was smitten with the love of that little boy and what his family went through and being present to witness the transformation welcoming new life does to you. Especially when it's a little bit scary. It rocks you to the core. Picks you up, smacks you down hard and then rebuilds you with all new parts. Loving littles is one of the greatest, most wonderful things that will ever happen to you. And the minute you welcome one into your life, you inherit a thicker skin...because the bus will hit you plenty of times to the point you'll think you damn near died. But you don't. You pick yourself off the ground, dust off your knees...and move on. Because beauty awaits. The beauty that fills in all the holes and rough spots.
So, I guess I didn't feel that one coming. But it's out. And yes, I do have these days.
On a lighter note, we're off to Key West to engrave some sweet memories in our sweet littles' minds...and don't forget to check out how to pack The Perfect Picnic over at Babble.com
Tuesday, July 6, 2010
On Down syndrome
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503 comments:
«Oldest ‹Older 401 – 503 of 503My nephew was diagnosed with autism today.
I took a page out of your book and sucked the marrow out of life today.
http://robynnealane.blogspot.com/2010/07/yes-just-yes.html
You always brighten my day with your lovely, and truthful words, and your gorgeous photos. Those girls of yours are truly beautiful. You are so blessed and I love being able to read about your journey of being a mother!!
So well said. There will come a day, if it hasn't already, where you'll be thankful that Down syndrome has graced your life because of it's part in making Nella the unbelievably superb person she is.
Kelle, I wrote a post on your glasses today :)
http://mylittleheroine.blogspot.com/2010/07/i-want-rose-coloured-glasses.html
Yes, those bus moments will continue to come, often at the most unexpected times. As the years go by though, they hit less and less. You just keep on keepin' on! :)
Enjoy your vacation!
Laura & Ryan
http://nowimamom.blogspot.com/
Ok I was going to post and be all riled up on kelle's behalf but then I read this annonymous post from Carmen in Boston and I can't stop laughing -
"I wish the people passing their negativity farts would grab their haterade, go home, and stop stinkin it up for the rest of us!"
Negativity Farts = Bwahahaha!
"Negativity Stinks!" I feel like I should put that on a sign and start picketing it somewhere.
Isnt it awesome that you have so many friends that are willing to freshen the air with the febreeze of positive comments?!
xoxo
can't wait to see pics from key west!!
Team rose colored glasses!! Love you Kelle!!! My little has DS and your outlook has literally changed my whole perspective. I am a better mother because of you, your words, your example.
I have been following your blog for some time now and I absolutely love it. I am compelled to comment on this post ... I so needed to hear these words today. Thank you so much for sharing your life, your girls and your wisdom. You are amazing and inspiring and I am so very grateful to read this today.
Poppa LOL - you hit the nail on the head about boys that age and pictures and being on a family blog. I am taking a ton of pics of my 6 month old ( with my new camera thanks to Kelle). But my 13 year old is out playing with friends, etc. When I try to take an incognito shot of him he makes a goofy face or accuses me of trying to be dramatic :). He is a " step son" to my husband and the love that has grown between them Is so special because it has been earned and cultivated not automatically inherited.
Kelle - thank you for sharing the " bus moments" as they help all of us as much as the positive finding the beauty posts as we are all our human and go through easy to be happy times and sad so unfair events.
And thank you for leaving the "negative comments" as the comments that it reacts also shows the reality of life and how all of your followers are sticking up for you and how we can learn from bad and good.
Any way since you have everyone's attention. Could you please stop the name-calling, And Poppa, I know your trying to protect the ones you love, so don't feed into it! I don't think it's good for positivity. Maybe you could do a blog on it! For Pete's sake people. Everyone is here for the same reason. Some of your readers have become bully's just like in High School.
Live and Let Live.
Kelle, please know that I run activities with a group of parents with kids with DS. We all read your blog religiously and talk about it every week. It's like our therapy as parents. Please don't let a small group of scared parents effect how you are raising Nella. You are doing such a beautiful job, and you are such a beautiful soul. I have never seen so much beauty and love in a mama, and you inspire us to do better with our littles too. I hope you read this comment. xo
@ anon
“You should be happy that Kelle is changing people's minds about Down syndrome. You should be happy Kelle is creating so much positive awareness all over the world.”
I am happy about this. I think Kelle is having a very positive effect on the perceptions about Down syndrome to those outside the community (and even inside). I am glad Kelle sees the beauty and focuses on it, and has the talent to present it visually to the world.
It isn’t really possible for me to do justice to what I have been feeling reading this blog on and off since the birth post in just a simple comment. There is a fine line between rose colored glasses and denial/acceptance, and I, as all of us must, am walking it too. I wrote a post called Say It which was my first reaction to some of what has been all a whirl over here, and I suppose at some point I may get around to another post. Or not.
TUC, I think Kelle has shown tremendous acceptance. This post is all about NOT being in denial, but accepting her beautiful Nella while still feeling scared every once in a while. What I gain from Kelle's blog is a beautiful sense of acceptance--rosy, yes, and perfect.
Lordy...what is UP with some people? I think you are amazing Kelle...I know coming from a grown woman who is a mother of 2 and another due very soon, this is a little strange, but Dude, I have a wee crush on you!!
Listen, I know not everyone can be as loved up and positive as Kelle is...sure, these differences make the fabric of life the interesting kaleidoscope of colours it is. But seriously, why the hate? This woman is sharing with us a tiny scrap of her full and busy life with her amazing family, and some people feel the need to attack her for being TOO POSITIVE? COME ON!! If you think this, MOVE ON. Dont read. Simple.
For what it's worth Kelle, you inspire me. I am the mother of 2 AMAZING kids, and am one of 3 sisters. I didnt know boys, had no idea how to raise boys, couldn't even imagine myself ever having a son. But I do, and I ADORE him...of course I do. Because like you were saying in your post, thinking that you know what you want, what you percieve your ideal family to be,no matter what the reality turns out to be (boy instead of girl, daughter with Ds v's not) this is your reality, your family, and you accept and love it with all your soul. End of.
You rock Kelle, and don't ever stop. By the way, your Daddy seems to be only the bestest Daddy in the world. You, Poppa, also rock ;)
-x-
I absolutely love reading your writing. Have you considered writing a book or something?
A number of years ago my son had an eye appointment with a neuro-ophthalmologist. He was near UCSF so we drove up through Haight Asbury. Due to my son's brain injury he has some unique issues with his vision. In an attempt to cut down on glare ,which troubles my son, the doctor prescribed rose colored glasses.
I have always loved this rx and think we should all have it filled!!!! Here's to optimism.
Team half full. That's why I come here. Love you Ms. Kelle. xo
Team half full. That's why I come here. Love you Ms. Kelle. xo
I think the thing that struck me most about this post were Kelle's husbands words "Is this normal? Or is this Down Syndrome?" And then her words, "Is this normal?"
As the mother of a toddler with Down Syndrome, I can tell you that one of the first things my husband and I did was strike the word normal from our vocabulary. Most parents of kids with DS use the term "typical". It may be PC, but to use the word normal implies that what your daughter is doing is..well...abnormal. And it's not. It's just her, part of her and her personality.
Reading that makes me wonder how much this family has really accepted the diagnosis, and really understands what Down Syndrome is and what they are dealing with. Claiming that your acceptance of Down syndrome is much like an acceptance of having two boys makes no sense and quite frankly shows that there is still denial going on.
Kelle I love reading your blog. Such encouraging words to every mama in every season of life! Your decisions to love (not just like, or deal with) every aspect of your life is such a refreshing aspect to read. As a stay at home mama I love that you embrace and rejoice in the trials of life.
oh crap..double crap...triple crap! I was hoping to get on here and not see another annoying..oops i mean anonymous comment.
"typical"..."normal"...aren't you kind of splitting hairs on that one. so you chose a word that you think is more appropriate then the other..hmmm...it all comes back to personal choice as how to handle your personal situation. oh my goodness. please for the sake of all who do not read things into this post that were never there...stop with this foolishness.
what i see is not denial..it is acceptance of what is ahead of them..and wanting to do it with a good attitude. maybe it is not how other people do it but does it make it wrong??? from where i am looking i actually see them taking the postive road down this long journey they have ahead of them..is that wrong?
what prompted this whole negative tone was what i believe could be called..hmmm..misunderstanding, jealousy, envy and even fear.
peace people...seriously this family is a family will that will love, nuture and handle ANYTHING that nella bella has in store for her...and they will do it in true hampton style..i am so excited to share their journey. ♥
It's crazy how much reading these comments hurt my feelings and they weren't even directed to me. It outs me in instant defensive mood like when someone attacks my family. I have grown to love Kelly and her family and it bugs me that someone feels the need to tell her she is wrong for feeling the way she did. Her feelings are hers and its just ignorant that someone thinks she shouldn't feel that way.
With that said, Kelly you have an amazing following and I love reading about you joys and your struggles. Please don't stop just because someone cant handle your honesty.
Megan from Missouri (Mabrey12@yahoo.com)
Ugh...the judgment...it burns.
Love your blog Kelle. I wish I could live my life as open and with as much happiness as you.
God bless you and your girls.
Nella is so stunning.
I love that bit about never knowing what's it's like to... but that's okay because our lives are custom-made. Thanks for the reminder!
Ooh, I normally wouldn't comment on the blog of someone I've never met, except for that little line... "I'll never know what it's like to have triplets". I stay in my comfort zone so normally I wouldn't want people to stumble across my comment, or for you to end up reading it... or not reading it and skimming over it..
anyways, I'm a triplet. Triplets run in my moms family. I have two triplet brothers who are identical. I don't know what it was really like raising me and my brothers, but my mom did it. She's Super-mom, believe me. Once in a while she'll tell stories about when we were babies, and just trying to keep all three of us out of trouble, and I have so much respect for her!
Great out look and one that I need to apply right now. Thanks Kelle
You know what, anonymous commenter splitting hairs about the words "normal" and "typical"? Kelle is on a journey. She is growing and learning at her own pace. If she hadn't accepted Nella, do you think she would be blogging? Do you think she would be putting herself out there? Kelle's journey may be different from the one you're on, and that's okay. What really makes me angry is special needs parents (and yes, I am one too), who are sanctimonious like you. I come to Kelle's blog because she uplifts me. She makes me a better mother, a better human being. Sorry to be so blunt, but based on your attitude and your condescending judgments of this beautiful, loving family, I would not visit a blog run by you. We come to Kelle for inspiration and positivity. If you don't think she's sad enough, go somewhere else. Seriously. People like you just make me livid.
Hey Kelle!
I know it's not the whamming herself in the chest that this post is about, really, but I wanted to tell you that my Anna, 20 days older than Nella, has been doing the same thing!! She whacks her toys on her legs over and over. I thought it was sort of strange, and I'm sort of relieved to hear Nella is going through that stage, although it is kind of funny, because you're right, how do you google something like that?! And googling things never makes me feel any better!!
Love,
Kelsey
love you!!!!
Kelle you are the best mom ever. Nella is so lucky that you are not projecting all your own insecurities on her like other scared parents! You love her so much and you treat her like she is the most precious gift! Do not change one thing Kelle!
I don't know how I came across your blog but can I just say...I love it. And you are truly inspiring. Oh and your girls are truly beautiful! :)
Beautiful.
Please keep writing.
Hmm...I am not sure I "get" why so many people are outraged by some of these comments. Yes, some of the posters have expressed themselves less than tactfully, but they are making some valid points. Kelle's blog has gone very, very public. She's been in the news media and she is writing a book. Obviously the more attention she gets, feedback (both positive and negative) will follow. I suspect Kelle can handle criticism just fine and takes it with a grain of salt. If she can't, then she needs to honestly rethink putting herself out there so much.
I am the mom of a little girl with Down Syndrome. I "get" what she's doing. I think she's done a great job of raising awareness about Down Syndrome among the public. Certainly many of her readers are people who have otherwise not exposed to DS, and thus are learning a lot from her on her journey. That being said, I would be lying if I said I could relate to her. Her coping mechanism is vastly different from mine. I am not saying I am right and she is wrong (or vice versa) but I grieved very, very deeply my first year. It took a long time for me to heal, and I still have moments. Most of the moms I know with children with Down Syndrome have gone through a similiar process. Quite frankly, one of the most honest things I ever heard said was from a mom whom I respect immensely, who has an amazing love and devotion to her daughter. She told me that she still sometimes cries at night wondering what will happen to her daughter in the future. I often feel the same way. It doesn't mean we love our children any less, or that we are lesser mothers. It's just that we have a different perspective.
Kelle is lucky that she has had such a tremendous support network. I am sure that that has helped her immensely. I unfortunately did not, which is one reason why it probably also took longer for me to heal.
I worry a bit because there does seem to be sort of a "good mother"/"bad mother" dichotomy on this blog, where posters who disagree with Kelle are automatically dismissed as jealous, or unable to cope with being a parent to a child with special needs. Parenting styles differ so vastly, whether your child is typical or special needs (yes, actually, the word normal is often frowned upon by parents in the special needs community, it doesn't particularly bother me but I know it bothers others so I don't use it.) I am very different from Kelle Hampton in general and have a different parenting style regardless, so it doesn't surprise me that our approach to our child having Down Syndrome would differ. Again, it's not that one of us is right and one of us is wrong. We just all parent differently.
I do think it's important to have differing opinions on this blog, and for people to feel comfortable posting that, as long as they say it tactfully. I am sure Kelle values all feedback, as long as it is constructive.
As the mother of a handicapped child i will say that i see so much of what it happening on this particular post happen in real life.
My husband and I try to look at our situation with the "half full" attitude while some in our situation opt for the "half empty". That does not mean that we do not feel the same things that other parents do, we just process it differently. But I have found for some reason that the "half empty" parents tend to attack our approach while we are not so bold as to tell them how we feel or how we think they should feel. I am not sure why this is but it has been our own personal journey.
I have been following this particular post and have not made a comment up to this point but feel that this may be my opportunity to get some of this off of my chest. If you do not like the "half full" way of thinking, well to each his own, but please do not be surprised when you are called out on it. Just as you feel you have the right to point out our shortcomings please do not be surprised when you get a response, freedom of speech goes boths ways And up to this point I have not seen anyone call anyone else a bad parent, please don't put words out there that are not there.
I worry that for some reason the "half empty" feel the need to challenge the "half full" when they express their way of approaching similar situations. I often wonder if it is the fact that maybe you would like to take the "half full" approach but do not know how to get to that point.
So with that being said, Kelle I would like to tell you that I follow this blog because you mirror our approach and it is refreshing to know that their are parents who do so.
I think the reason why the comments are upsetting is that Kelle is sharing her heart and it seems rude to me that someone is trying to say that she was offensive in the way she chose to explain her heart! Obviously, Kelle, has a pure heart and she didn't purposely try to offend anyone! Why would you do that to someone? The questions are judgmental, in my opinion, and since Kelle expresses herself so well, I am dumbfounded that someone would even suggest because she doesn't have more pics of her stepsons that she does not love them? huh? Or that she is in denial because she chooses to wear rose colored glasses!!! So now she isn't politically correct because she used the word, "normal"? Unbelievable! See how rediculous it all starts to sound? Lighten up people!!!
Kelle, you keep doing what your doing! I love your website and I continue to come because I love your heart! I do get it! I too am raising a child with Down Syndrome and there are so many families I know that choose to wear the rose colored glasses too!!
Cheers, from a mom in
Sunny CA who is rocking out with her rose colored glasses! Woohoo!!
You nailed it with a golden hammer!! The bus hits us all. What we do with the pieces left behind is what defines our character.You seem to have learned that getting off the bus at YOUR stop offers opportunity that the other stops can't offer. There really is beauty and pain in every life. There is such a fine line between the two and we can't have one without the other.You describe life poignantly.Thank you. The bus hit me hard 30 years ago, and I still feel the bruises. My sons have proven to be the salve to ease the pain. It will never go away, but it is bearable and I am thankful! Now, stop blogging and f\go kiss those babies!!
There are 10 million children in the United States with "special needs" and due to increases in survival rates of low-birth weight babies, this number is increasing.
So this "community" of people, parents who have kids who are "different" - many of them celebrate the differences that their children have.
Let's all take a page from that book, and celebrate those differences...differences in parenting styles, grieving styles, differences in self-expression, differences in what color glasses we wear, differences in the perception of the level of liquid in the glass from which we imbibe.
Let's not get into the comparison of pain pitfall. Most comparison is a pitfall.
Your miscarriage at 6 weeks isn't as bad as Julie's miscarriage at 20 weeks which isn't as bad as Mary's stillborn at 38 weeks which isn't as bad as Susan's baby who died of SIDS at 7 months which isn't quite as bad as Monica's teenager killed in a car accident at 19.
We all cry. We all suffer.
And we are all waves in a sea. We have our moment to rise, to dance, but we will all return to the sea, sooner or later.
And not one of us are promised a tomorrow. But in the meantime, let us dance, let us be passionate, lit up by life, inspired, let us be generous, let us give more than we take, let us laugh much more than we cry, let us comfort the hurting. Let us bring wonder and possibility, where there is resignation, cynicism or despair.
Whenever I'm upset about some silly expectation that was thwarted, I recall some facts that a friend recently sent me, kinda puts all my meager problems into perspective:
"If you have food in your fridge, clothes on your back, a roof over your head and a place to sleep, you are richer than 75% of the world. If you have money in the bank, your wallet, and some spare change, you are among the top 8% of the world's wealthy. If you woke up this morning with more health than illness, you are more blessed than the million people who will not survive this week. If you have never experienced the danger of battle, the agony of imprisonment or torture, or the horrible pangs of starvation, you are luckier than 500 million people alive and suffering. If you can read this message, you are more fortunate than 3 billion people in the world who cannot read it at all."
I think most of us can relate only to the "fortunate" side of this equation. So let us count our blessings, own our "custom-made lives" and try to contribute to others, to ease the burden of those around us, in the world, and in the blogosphere.
-Promise
Kelle,
I happened to come across your blog a month or so ago. Everyday I find myself running to the computer to read your words. In saying that...I want to thank you for being REAL and HONEST. It takes courage to put your thoughts down let alone let THOUSANDS of people read them. You are incredible. Thank you for sharing your heart!
Erin Dedrick
Chandler, AZ
"Anonymous said...
I worry a bit because there does seem to be sort of a "good mother"/"bad mother" dichotomy on this blog, where posters who disagree with Kelle are automatically dismissed as jealous, or unable to cope.."
I say:
Hear Hear.
There are SOME (not all, thankfully) self-confessed 'glass-half-full' people out there judging and bandying about with smug comments which interestingly, usually follow a little sermon on how we should live our lives. I did not realize that to possess a positive attitude, one must accept everything everyone says?? A lively debate, of which this rates highly, is something most of our fore fathers fought dearly for. Jean Paul Sartre, the famous French existentionalist phhilospher said (sic) "I may not agree with your position but I defend to the death your right to say it". But if I may add to the Great Philosopher's advice by saying that everyone should present their ideas respectfully and without resorting to patronizing comments. This is the literary equivalent of giving a child a few pats on the head. Hear the music? I believe that everyone hears the music but perhaps interpret it in different ways.
Viva la difference!
Wooo Hooo to both Anonymous writers up there. Well said! Maybe the tide is turning. This is the sort of stuff that is good to read.
I was going to add my little bit but hey! this is the way we should be going. "Avoid comparing pain pit-falls." I for one am going to remember that one.
Don't worry. Be happy
"I did not realize that to possess a positive attitude, one must accept everything everyone says??"
That's right. Being positive means to accept everything everyone says and being happy for others.
"Hear the music? I believe that everyone hears the music but perhaps interpret it in different ways."
Disagreed. Not everybody hears the same music. Everyone hears the music of their own reality.
I just started reading your blog and I love it. Your post when Nella was born brought me to tears. You have a beautiful family and your photography is amazing!
i think the point that some of you anonymous are missing is that if you read this post the second time around, as i did, kelle is in no way comparing one pain against another. she was simply saying the pain that was first felt in HER situation no longer stings as much. she is being healed by all of the beauty of baby nella...the beauty outways the hardship. and most who experience pain or disappointment (whatever it may be) come to this point in the process of healing. not all can experience this, it truly takes a certain personality to be able to do this.
so why is it such an issue which way SHE chooses to handle this. keep in mind that this is HER blog, one where she has always shared HER view on the HER world. i applaud her for taking this route and in no way am condeming those who go the other route. her post was not in any way telling you which way you should look at things, which is why i am stunned that anyone would critize a person for intentionally finding the good in her life. and it does appear to me that jealousy motived this..calling her a yuppy, accusing her of not including her step children in her life enough..come on now, how much more personal can you get. you can't tell me those words would not get to any person reading this post. I can't imagine how kelle must feel right now. to me it appears as if one was intentionally looking for a reason to be critical.
hurting someone is not worth getting your point across..yet to some it seems to be all they care about. i don't know kelle but i care about kelle and i think it needs to end now.
thanks for sharing your opinions so openly and honestly! i had my 2nd son around the same time you had nella and was struggling with my disappointment of not having a girl. i totally get what you are saying, you always wonder "what if?" i LOVE that you look at life so positively no matter what happens, i try to do that too. your blog lifts me up and your photos are beautiful.
I agree with anony who said "hurting someone is not worth getting your point across..yet to some it seems to be all they care about."
This is a blog people, just a little space where a lovely young women shares her thoughts, pictures and her ups and downs. It is not a political arena where one crys "I may not agree with your position but I defend to the death your right to say it". seriously get a grip.
It seems like there are some who would rather sink the whole ship just so they can have the last word and feel that they are right in what they think. At this point if I were Kelle I would be thinking twice about sharing the things that some of us come here for. I hope that this does not in anyway change how she writes or what she writes about. I think that if you do not like her outlook on life you should perhaps check out a different type of blog..please don't ruin it for those of us who have been enjoying this lovely journey and would really hate to see it ended or changed in anyway.
I am finding myself sneaking away from the family to get "my hit" Which is losing myself and sipping off the joy that you elude through all of your blogs. You have a joy and a passion that most people don't have.
Thanks for being my drug!
I adore this blog and look so forward to new posts. Seeing a new post to read and savor....oh so happy. Did the gender disappointment comparison comment bother me? Yeah, it did. But Kelle, your blog and family are lovely. You have an amazing following and are inspiring hundreds. You inspire me. Us readers can sometimes disagree and still rock out with you. It's okay. Hope you are having a great trip in Key West.
There has only been one thing so far that has taken my breath away, and that was the realization that came to me one night while I was washing my nine-month-old son's squishy little body, that I won't know how his story ends. I won't be here to see it, to bear witness.
I won't know how his story ends.
God willing.
Kelle,
You have opened yourself up to the opinions of others which I'm sure you can handle or you wouldn't put yourself out there like you have.
Everyone handles life differently, and I have personally appreciated many of your posts and beautiful pictures. I am grateful.
I think your entire family is beautiful. Nella is a complete blessing.
However, Kelle, after sometime I stopped coming here b/c I only saw "pretty" pictures and a "pretty" life. I need to see the other side of Down syndrome too - the reality that an extra chromosome doesn't always play fair. You are walking the walk you must, and I applaude you. But I encourage you to take a walk on the other side sometime and visit the community of Down syndrome bloggers who are fantastic writers, mothers, and friends. We have pretty pictures and stories too, but then again we have sad pictures - pictures that tell a different story. Some are not ready for those pictures. Some do not want to see those pictures.
I appreciate your honesty.
Faith, hope and joy - gifts of the heart uncontaminated by circumstances is what you share with others. A very wise man once said "Faith is the substance of things hoped for, evidence of things not seen." Not crutches for the weak - but the substance of life coursing through the veins of the strong allowing them to smile at the challenges of the new day and walk seemingly unscathed through any adversities that are simply living the life that is unique to each of us. Aware? Yes, perhaps even momentarily saddened because we are human - but not destroyed or embittered by the “bus du jour”. Words are power, they are life; building or destroying. It’s a choice. I believe the majority your readers would agree with me that your positive, hopeful, bright outlook is central to what has drawn so many to your blog. We’d be proud to pack up our bushel of lemons and set-up our lemonade stands next to yours as we encourage and laugh with one another. As iron sharpens iron, so one sharpens the countenance of her friends. It is these wonderful gifts of your heart that you share with each of us who like you choose to view the world through what some may consider foreign eyes - Eyes of hope, love, faith of good things to come, and above all gratefulness - the plumbline by which we view life. Thank you for providing a lanai where parched spirits are refreshed, encouragements are shared, and hopefully your garden is watered a tad while we visit as well.
I guess the hardest part of blogging is pleasing everyone that visits your blog. I am thankful that my blog has very few followers and none so critical as the ones I have seen commenting recently on this one. What one puts on ones blog should be what the author of the blog wants to share. I for one come here to view all that Kelle wants to share. I have read comments condeming her for sharing too much and some for not sharing enough. Again she can not please everyone out there because this blog is her blog and for some reason those who read it forget that. If you do not like her style or what she shares it is easily fixed, follow one that you do like and makes you 100% happy.
@ Jasmine
I have seen Kelle's comments on others blogs of parents with children with Ds. Of course, she doesn't have the time to visit them all.
Because this is her blog, she chooses to share the beauty of her life here. I'm sure she shares her sad times with her family and friends.
Blessings to you
Tuck this little tidbit away for times such as these.
"I don't know the key to success, but the key to failure is trying to please everybody."..Bill Cosby
Kelle just keep doing what you are doing in your own way. It is enchanting.
Kelle,
I was so blown away by this post. As a mother of a child with DS I totally understand what you are saying. It is like DS at first seems like this big glaring neon sign that is blinding and distorting your outlook on the future, then it changes into those tiny candle lights that you see in window of some homes..still there and throwing off a small soft light but not blinding anymore. It is part of our life but not the biggest part.
I thank you for putting into words how I felt when DS became a part of my reality, the future now has a very warm soft glow to it.
@anonymous
"Faith, hope and joy - gifts of the heart uncontaminated by circumstances is what you share with others."...."Eyes of hope, love, faith of good things to come, and above all gratefulness."
Well said and I am eating up every word of your comment, so uplifting and positive. So when you set-up your lemonade stand next to Kelle's I will be right beside you.
I came back today hoping for a new post and can't believe that the drama is still going. Kelle, I imagine you must be laughing at all the silliness or hopefully not even reading it at all. What strikes me as the most hysterical part of all of this bru-ha-ha is that it is all based on judgements that others feel that they can place on you and others because of our differences. Isn't that the one thing that we are all in agreement about when it comes to our own children: that we want them to be accepted for who they are and not for how they are different?? How can we expect that of others when we don't give it ourselves?? There is no manual that comes with out children that explains how we can perfectly parent them, whether they have "varying exceptionalities" or not. Nor is there an emotional manual that tells us how to perfectly cope with the mix of feelings that go along with being surprised by such a "special" child. What is beautiful about Kelle's blog, regardless of how closely we relate to anything she shares is that she shares. She shares what HER truth is. It doesn't have to match anyone else's. It is her own. But to those who can relate to her, it is a huge blessing. To those who feel uplifted in anyway, it is a huge gift. To those who how find it full of positivity with a small sprinkling of raw emotion every now and then, it encouraging. And what is even more wonderful...if anything about this blog bothers you in anyway you can think to yourself "I don't have to read this if I don't like it" and you can move on. There is nothing wrong with anything that Kelle shared because she was sharing herself. She did not impose any judgements or moral righteousness on anyone else. If you posted a judgemental response, sharing your moral righteousness to this post can you claim the same? Allow her to share her journey, because it is a journey. Add your two cents only if your intention is the same as Kelle's: to process life "out loud" in hopes that someone else will either be blessed or return blessing to her. Kelle, I appreciate that you put yourself out there. You and I are not exactly alike and I love that. What I love more than anything is that you have shared Nella with the world and that the people who read your blog love her and they think that she is beautiful and some are so familiar with her now that they don't even see the Down syndrome first anymore. They see how much she is growing and that she wears the most adorable clothes and that she has an awesome big sister and big brothers. They see that she is loved so completely by her parents. And the best part...the next time that the people who read this blog notice another child or adult out and about in their own communities who lives life with a Down syndrome diagnosis they are going to smile knowingly, because they are going to know that Down syndrome is nothing more than a diagnosis based on one's chromosomal makeup and that it does not affect that person's value or loveability. The more awareness that is brought to our children, who are way more "typical" not, the better for ALL of us. Thank you, Kelle. Mylie and I love you and your family for sharing yourselves with us. :)
I was the child whose mother kissed her before heading off to chemo treatments. My mom was 36 when she got Stage III breast cancer. After 2 years of operations, chemo, praying and a fierce determination that her children would not grow up without their mother, my mom emerged on the other side. And during those 2 years, she "got it." All of it. What really matters. What life is all about. One day at a time... for that was how she HAD to live. It is now how she CHOOSES to live. And the funny thing is, during those 2 years (I was 8 when she was diagnosed, my brother 5), I never remember anything of the cancer except that she would be in bed when we came home from school (she was really tired after her chemo treatments). So we would bound up the stairs and crawl on her big king-sized bed where someone had helped her to prop herself up and she was ready and waiting for us. And we would lay on her bed and talk about our day, talk about anything and everything. Funny thing, I still do that (and I am almost 35)... I lay on her bed and we talk. A sweet bond from a bittersweet time.
And then, 2 years ago, along comes the news that she had uterine and cervical cancer. And my mom handled that with the same grace and "one day at a time" approach as she had decades earlier. She would leave early in the morning, drive to her radiation treatments, drive in the other direction to her school and be ready to teach by the end of homeroom. She did this for 6 weeks. And she had plenty of leave, she could have taken off. But life is each day, this day. So she lived.
I always envied her perspective and longed to be like her. Then on April 12, 2009, my sweet Ian was born and rocked my world. After getting through the rawness of it all, I "got it." After all these years of worrying about everything that did not matter, this beautiful gift of a baby saved me. My mom and I bonded in a new way. We both knew what it was like to have unexpected things happen and emerge on the other side with this sweet appreciation for what really is important.
After watching my baby go through open heart surgery at 3 mos, I have an even deeper appreciation of life and all that makes it beautiful. Therapists in our house (besides their visits helping me to keep my house from becoming a total disaster!) are times I look forward to. They love my baby and celebrate everything he does. And doctor's appointments (an extra every now and again) are no big deal, really. I am grateful to those who saved my son's life and love him.
I've already done things I did not think I could do, survived things I did not think I could survive. And you emerge stronger and with an even deeper appreciation for the beauty of this life. You just do it. And find love and happiness along the way. And sometimes you find it in the most unexpected places, along the most unexpected journeys.
Having already raised my first sweet son to age 5, I know that parenting well is not easy... each of my boys is an individual, they are who they are. Ian is Ian and the Ds is a small part of him. He is much more this sweet baby who delights at clapping with everyone else, smiles so hard you can see a dimple when we cheer for him when he says "up", and don't even get me started on what it feels like to get a big, tight hug or a huge, open-mouthed baby kiss. Hugs, kisses, crawling, pulling to a stand, a word or two, toys all over the place, sippy cups thrown, food on the tray, floor, hair, face, you name it... he is a baby and he is my son. My son who saved me and I did not know I needed to be saved.
Thank you, Kelle, for sharing in our perspective and shouting it to the world! LIVE!
how touching it is that people from other countries write to you in a foreign language (for them) to tell you how wonderful, inspiring, beautiful you are!!! You are so loved, Kelle Hampton, and for good reason. You have a gift that makes you happy and it isn't any "thing"or certain socio-economic status like the negative commenter implied...it is this sweet, sweet spirit who loves and creates happiness for yourself, your family, your friends and for your readers with the ways you inspire!
I pump breastmilk in the middle of the night and read your posts (and comments) for entertainment. I recently read your 30th birthday post where you said you enjoyed being loved, and now you are one of the most well-loved women! Also, you wrote with such depth of what the 30s had in store for you, almost like your soul just knew. It is that soul that just knows... who knows the best path and I love being inspired by that path of loving life and our families and friends.
Cheers to you!
kelle, Amen , I get it! I get everything you said!
But, when my little guy smiles, I think , I am so lucky to grt that smile, b/c there is something totally heart warming and heart melting about the way my baby with DS interacts with me, that (shhh...., don't tell my other 4 kids) my other kids didn't have, so there ya go. I "forget" too, until someone holds him and his head still flops back or down, and I have to remind them to hold his head. I get it, Kelle, but I am in a happy place in my heart - and enjoying every minute of mothering Leo.
Pecore sono senza personalita.E mettere un altere un perfecta Dona.Eso solo os macanti.
Kelle e espone un solo che la tua privacy e la tua famiglia, egocentrico per poter credere che sia perfetto.e felice nel tuo blog e previsioni tutto non e reale..qualcuno ha bisogno di dimostrare la sua felicita pubblica,solo che no e felice, il tuo blog e sentimentale pornografia.Un upmo che dice di amare la tua famiglia e le mostre in questo modo!!!Qualcuno che si impregna 750 in fotografias a una riunione di famiglia, questo e normale?Just pensare che making situazioni felice di dimostrare cio che e ,e tu il culto? vite sietecosi vouta, che avete bisogno di os Kelle ovbias ricordate che le cose che como conto.
LAPIDEIS PRONTA PER ME.
Anonymous,Peter,Willie, Pam, Clinton.......
I do believe Kelle is feverishily writing and selecting photos of our recent hiatus in Key West. It will be good to turn a page. It will be nice to take a breather from the banter. We are all about the same thing, folks...celebrating one human family--all with special needs. We are in different places in the book...enjoy the page we have open. We really need each other. No one knows it all. We wound with words, when, rearraging them a bit, we might share some strength, understanding and healing. It has come here from other languages and other worlds. People who have never known anything about Down syndrome are reading...watching...listening. What do our words tell them. I put her to sleep in my arms the other day with made up songs sung into her cut little ears. We really love her and she will lead us on the journey.
awhhh poppa..how is it you know exactly what to say. your words are like breathing the fresh open air after being confined to a air of house that has been closed up for some time. breathe and enjoy..so i take it you are the original rockstar that has trained up the next generation of rockstars
that being said i can't wait for the next page in this lovely book...it is like reading a series book..you wait anxiously for the next release. i am so honored to be able to peek into this lovely nella bella's journey...makes my heart happy when i see her fabulous almonds eyes and her betty boop smile.
peace to all and can't wait for the next post...and i will let you in on something..we really love your nella as well. ♥
Yes, Gracee's Momma, she is our velcro...she fastens us firmly. Thank you for loving her.
THANK-YOU Poppa, that you are able to turn the page. You had me worried with some of your earlier comments when your claws came out and you loved theS___ word and your colors came true, not as shiny!. You were feeding into comments. People have respected and hung onto every word you have said. So please continue to be the positive force in Kelles world, This blog should not be used as a way to vent, throwing around the he said, she said. And EVERYONE has a right to their OWN opinion, especially when you are putting yourself out there, for which not all may or may not agree! It was like a school playground. She likes me better than you!! And makes you wonder if this blog is so popular because of portraying a fairybook story. What if a writer wasn't as pretty or couldn't afford some of the luxeries that you have talked about. Would there be as many followers. I think not!
So life will go on. Kelle will write her book. I just hope and pray everyone will live happily ever after.
THANK-YOU Poppa, that you are able to turn the page. You had me worried with some of your earlier comments when your claws came out and you loved theS___ word and your colors came true, not as shiny!. You were feeding into comments. People have respected and hung onto every word you have said. So please continue to be the positive force in Kelles world, This blog should not be used as a way to vent, throwing around the he said, she said. And EVERYONE has a right to their OWN opinion, especially when you are putting yourself out there, for which not all may or may not agree! It was like a school playground. She likes me better than you!! And makes you wonder if this blog is so popular because of portraying a fairybook story. What if a writer wasn't as pretty or couldn't afford some of the luxeries that you have talked about. Would there be as many followers. I think not!
So life will go on. Kelle will write her book. I just hope and pray everyone will live happily ever after.
THANK-YOU Poppa, that you are able to turn the page. You had me worried with some of your earlier comments when your claws came out and you loved theS___ word and your colors came true, not as shiny!. You were feeding into comments. People have respected and hung onto every word you have said. So please continue to be the positive force in Kelles world, This blog should not be used as a way to vent, throwing around the he said, she said. And EVERYONE has a right to their OWN opinion, especially when you are putting yourself out there, for which not all may or may not agree! It was like a school playground. She likes me better than you!! And makes you wonder if this blog is so popular because of portraying a fairybook story. What if a writer wasn't as pretty or couldn't afford some of the luxeries that you have talked about. Would there be as many followers. I think not!
So life will go on. Kelle will write her book. I just hope and pray everyone will live happily ever after.
Poppa, it is so true what you said about people who do not have experience with ds reading and learning from this blog. I'd never really thought of that- but after I read your comment, I tried to think of how much exposure to ds I've had in my life. Everything I could recall stemmed from my teaching experience. We watched Educating Peter in my exceptional child class. Then when I was a teacher, there were two boys... two of the sweetest first grade boys who had ds... they would often come have lunch with me and my teammates- their teacher asked if it could be a "reward" for them and we said of course. We just adored them and looked so forward to the days they'd sit with us in the teacher lounge. Though my experience was small, if I wouldn't have been a teacher I think I literally would have had zero experience with ds in my twenty nine years of life. So while I read this blog not even thinking of ds, I relate to it being about a mom with two girls just like me, it is very true that I and many others will learn a lot from all I read as I follow you guys on this journey.
Hugs!!!
Can't wait to hear about your time in Key West. I have family who lives there and I have spent many vacations away from Michigan visiting that beautiful island. We stayed at the Travelers Palm while there last time and LOVED it. Can't wait to go back!!!
I can't remember my google account info, but my name is Mindy and I live in VA Beach...
Great post! I love the part about accepting what life gives us. It's true that happiness is a choice.
The 2 boys thing can be a touchy subject. The ONLY time I get sad about it is when someone says "Oh, I bet you wanted a girl" or "Are you going to try again for a girl?" As if my life is somehow less meaningful or fulfilling. Just like moms whose babies have DS don't want us to feel sorry for them, I don't want to be pitied because I can't shop for girl clothes.
This little rant isn't directed at Kelle. I get what she's saying and think it's a wonderful sentiment about acceptance. Just wanted to give my thoughts on the matter :)
There are no claws here...just arms to hug. I laugh that you thought so...it must be like the thunderous voice of the wizard of Oz behind the curtain...the voice parents use with the bullies in the neighborhood...ha! It was a comment to me from one of the hundreds of friends I have encouraged to follow this blog. Friends who know nothing about Down syndrome...they know no one with it or with somone living with it. They have been telling me how they feel different now about "these children they have seen in restaurants and pass with their families at the mall." They are gradually, gently being enlightened. They love our Nella. They have opened their embrace to her and others like her. They stand with us as we look down a path and will walk with us...and sometimes skip with us...and sometimes stand strong so we can lean on them. It was one of these wonderful people who follows the blog and also enjoyed the comments as they heard from others and met other little "Nellas" through the comments. She heard something different in these comments and I could tell, it seemed like she might let our angels slip back into "these children I see in restaurants and pass with their families at the mall." I want more of our Nella...and I want more for my friends. So...no claws here...just hands holding small things and finding them beautiful.
Hey, noticed that you have a new tab on "Special Needs" and thought what you had to say was great.
I am one of your readers that came here with the Nella birth story and I don't have children with Down syndrome. But through this blog, I know that I have more appreciation for the people with Down syndrome, and those who love them. For me, you strike a great balance where Down syndrome is in the mix, but not the main event.
I think you are a great mother and am inspired daily by everything you do, so keep rockin' Kelle!
Marianne H. in Kansas City, first time commenter (I emailed you last week about the swim floaties, if you remember, thanks, I did find them on Amazon!)
Poppa knows best:
"Some have been pretty tough on a tiny little selection of commenters...but they, I believe, meant no injury...they are simply at a different place...and things look different from "there." We are here...and happy here."
There are people in all stages of life. That is what is so wonderful about this blog is it shows how to find happiness whether you are here or there. Learning to LOVE and appreciate the small things! The cup can be half full all the time if you allow yourself to see the beauty in the tiny things even on the bad days. Don’t read between the lines or mix the words. In the end it’s not about disagreements, it’s about getting past the negative and getting back to happy.
I now take my camera everywhere, blog more, love more, play in mud puddles with my littles, let my daughter wear her apron while making cupcakes and realize it really is OK if she makes a huge mess. Life is messy. It’s what makes it fun! A lot of great stuff gets forgotten in my life as I let the ‘busy’ take over. By Kelle letting us glimpse into her life it helps me to remember to take the time to appreciate little things and not take them for granted.
I hope everyone on here, whether you are in a bad place, have a differing opinion, are just starting to enjoy the little things like me, or those who have already found their rose colored glasses can all look to this blog and be reminded to find happiness in SOMETHING every single day.
Thank you Kelle for your beautiful blog and sharing your beautiful (imperfections and all) life.
You are a mother and woman above all, so it is no surprise that you feel this way some days. My daughter has CP, develpmental delays and scars from being burned by her birthmother....I too have my days. These children are so beautifully unique, I wouldn't change a thing other than for it to make life easier for her:(
Great post, you are a supurb writer and I enjoy reading your posts.
I love how you are learning and growing and loving thru this process. You always make me think and be thankful : )
Thank you. Hope your vacation is sensational!
love that perspective. so true!
One handed typing wgile my girl nurses, but I wanted to offer some reassurance, small as it might be--my little one is about a month and a half younger than your Nella and her hand and arm movements are also incredibly choppy. Like I was telling my husband last night, she was getting very offended by a rattle that kept punching her in the chin and trying to wedge itself up her nose. ;)
Anonymous--Rosemary--make no mistake. I focus on all the things my son can do. Doesn't change the fact that because of Down syndrome, my son will miss out on some things. That's just a fact. That's reality. I deal with it. I accept it. Doesn't mean it doesn't make me sad some days. Some days it is easier than others. I can and do see the glass full, but let us not forget that even though we may not choose to focus on it, the glass is still half empty, and at times, that emptiness hits you, and it is ok when it does. I try to embrace the whole glass! And, don't take that to mean that i think Kelle doesn't do the same!
that was a great post. good, good read, my friend.
that was a great post. good, good read, my friend.
heh. I have been criticized roundly in the past for being "too Pollyana" about my life with my daughter, who also has DS. she is 12 now, and guess what? I still think DS is a beautiful thing. She still has friends, and playdates, and a social life. She is still cute, and funny, and charming. And yep, she still has DS. I was told once that I wouldnt think DS was so great when she was older and lonely and shunned...lol. Sure, she gets lonely sometimes, but so do I.
You know, Kelle, I was born to a 16 yr old mother, my father was in prison and would be most of my life. He would get out, beat her up, abuse us, do something stupid, and go back to jail. I was adopted at 6, then abused by that stepdad to some extent. I survived some pretty signifigant emotional abuse, and I kept standing back up and dusting myself off. I got pregnant at 19, unmarried and dirt poor. Had another child 7 yrs later, then took in a nephew that was murdered 3 yrs after that. somewhere in the mix, I had my little one with DS. Im still standing, and life is beautiful. because i CHOOSE to see it as beautiful. I could bitch and moan and whine and cry why me. I could wish I had another life, a better life, that I didnt live in a mobile home and drive a car that is getting ready to die any day. I could wish for fewer bills and the ability to just not worry about money. I could wish for my daughter to not have DS. and my son to not have an attitude...and my 21 yr old not to too, lol. But this is MY life. I love that it isnt perfect, that it is a challenge, that I still get to see beautiful sunrises and laugh and experience the kindness of strangers. DS has made me a better person. I am going to enjoy my life, and PTTH to the idiots who would judge me for it, or who would have the absolute audacity to tell me that it is "obvious" that I am masking my "pain". Life is what you get, and Im gonna suck all the joy I can from it and recognize the good for what it is. One of the good things is you, kelle. Screw em if they cant find their own happiness ;)
Wonderful post. So vulnerable, so real, so true. Being a mom is by far the hardest and most rewarding job there is. Everyday we worry whether we are doing the right things for our children. And while there are days you may worry about something specific to DS, there are those days you worry about things completely not related to that, because that's what we moms do - is worry about the well being of children. That's par for the course. Yesterday was a horrible day for us, Lucas just wouldn't stop screaming from pain the docs simply pass off as colic - I actually told God "I hate you right now", immediately apologizing because I really don't, but I was that frustrated and upset. There is nothing worse than seeing your baby in pain! Ok, so I'm rambling. Love your post as always. Here's one of my most recent posts:
http://itrocks2bmom.blogspot.com/2010/07/i-woulda-breastfed-if-i-could-so-get.html
I've enjoyed reading your blog posts about little Nella. I first found your blog through your sweet baby's birth story and your first introduction to Down Syndrome.
And you made me really start thinking... I've often thought what my response to a downs baby would be if I were to ever have one. I can't imagine the responsibility that a parent of a downs must feel that moment they find out. And the tears that are sure to come. Your story helped me think about it in a more practical sense.
But I really think that deep down inside, I would feel a special link to heaven if I were to ever have a downs baby. Because after growing up and living with my Downs brother, Zack, I truly believe that he has a connection to the eternal, to God, to That Place that none of us "normal" people have. Whether we admit it or not, we talk about heaven as the place you can go as long as you've been good enough to go there. But Zack doesn't think of it in the realm of good people vrs. bad people; he sees it as The Place that's more real than this place here. The Place where those he loves actually LIVE. Earth is a box of endless limitations to Zack. But Heaven is real life. Because people with downs are not crippled by earthly weights. For us to visualize heaven, we have to take our eyes off of the temporal and make a distinct effort to imagine a God so holy, loving and pure that has prepared a place for us to live. To Zack, he's already in that frame of mind. For him to think of this life and how to cope in a world so full of hurt, strife and competition takes the same amount of effort as it does for us to try and grasp That Life we all long for in the sky.
I treasure every memory I have of growing up with my brother and enjoy watching him turn into a man now. His dreams and aspirations that he'll never see fulfilled (wife, kids, driving, etc) do not deter his desire for a full and happy life. He's always hopeful and simply DREAMING about his future brings him fulfillment and happiness. He's so thoughtful and kind and even calls me on my birthday to sing an off-key "Happy Birthday to you" song. :)
I love the way you express your thoughts and experiences in going through this special journey. You have a sweet treasure in your possession. And it will only get sweeter as the years go by.
I know: because I lived with Zack. <3
I wanted to thank you, like so many others have, for sharing your story, your family’s story. We too had a daughter with down syndrome, born very close to Nella’s birthday. She was our first child and it was a surprise when she was born and we had the most difficult time accepting it and moving forward with life. I found your blog and it was as if someone shook me and said “what’s the matter with you, she is a gift!” You and your little girl were an inspiration to us. You showed us how wonderful life can be, even with a few bumps in the road. Our gift was taken from us only 2 short months ago. Unlike Nella she was born with many health complications because of the down syndrome, one of them being a severe heart condition. She passed away at home as we sat there helpless which is perhaps the most difficult part of it all. I read your blog religiously, watching as Nella grows and blossoms. She is a beautiful little girl. I read your stories and think about all the things we’ll miss doing with our Anne. But I want to thank you for sharing them with all of us. I hope that you will continue sharing for a very long time. Nella is such a lucky little girl to have such a loving family. Thank you.
wedge, just wanted you to know your story touched me. Such a loss...unimagineable. My best to you and yours.
Wedge - same here. Just read your comment and I am so sorry. Thinking about you even though I don't know you. xoxoxoxo
you deserve this more than anyone:
I am passing on The Sunshine Award to you! Thats right, you're awesome. “The Sunshine Award is awarded to bloggers whose positivity and creativity inspire others in the blogging world.” http://welcometocaliland.blogspot.com/2010/07/im-like-ray-of-freakin-sunshine.html
OK...Kelle so you're like a friend in my head. I've been secretly following your blog, admire how you love on those babies and capture the moments with your incredible photography. This post was so candid and so real. I feel your pain for the things we can not change. It took me a long time to learn there is more change in acceptance. Still we reflect, we feel sad and then we just gotta get up and dance through the rain.
Nella picked you for a reason...you inspire.
just wanted to say thanks for this amazing post. Just discovered your blog - what a gorgeous family you are! I have an 8 year old girl with autism and she has just been diagnosed with coeliac disease too - some days are hard but then something happens to lift you and on you go again. Wouldn't be without my 2 gorgeous girls. Love your pics - amazing
I oh so understand this post!
I oh so understand this post!
I was linked to your blog by a post in DesignMom. I was soo touched reading about the arrival of Nella and your response. You have a special spirit about you and I think it's special how much you obviously cherish your role as a mother.
I just wanted to share something with you. The church of which I am a member believes that your special Nella is exactly that, so precious. The core of our religion is families and their eternal nature. If you have any curiosities I encourage you to go mormon.org.
Thank you for sharing your special isights into life.
You have a wonderful and amazing way of putting things in such clear perspective.
I really enjoy reading about your adventures and how you approach your life.
You are such an inspiring breath of fresh air.
Thank you!
:)
This is her blog. She can write whatever she wants. If you don't like it, go write your own. I don't have to agree with everything she writes here, but it is her blog and she has every right to say what she wants.
Oh and thanks for the shout out to the Physical Therapists, Kelle :)
I thought you looked framiliar! Usually it's the kids that tip me off, but this time it was you. And when you were holding your youngest daughter, I really remembered :)
I followed your blog for a while when you gave birth to Nella. I cried reading your post, and I just cried again. You are such a wonderful, amazing person. Your girls are so lucky to have a mommy like you!
Thanks so much for sharing your story. I too have a daughter with Down syndrome--she is now 9 months old--and you are so right about the rollercoaster of emotions that you feel. Some days you can almost totally forget about the Down syndrome, or be totally comfortable with it as the new "normal" in your life. And other days, the reality of it hits you like the bus. Hang in there and keep sharing your amazing story.
PS-Can I post a link to your blog on mine? www.awellbalancedmom.blogspot.com
I think I'll save this post to come back to on the days and moments my breath escapes me as I "see" the DS everywhere- because your words are the cheerleaders to my journey.
So late to the party on this one, but...thank you. I never dreamed I would write a blog post titled "More than you ever wanted to know about ALS", but I have. It's my bus. Thanks for speaking my heart in this post and helping me remember that normal looks different at first...then it's normal again. To NOT know about ALS would mean to NOT have known these brilliant years with my amazing husband, so I will take this new normal and love our life. So many blessings to you and your beauties.
Hi, I've just found your blog...so beautiful.
Best regards from Buenos Aires, Argentina, Maricel
Thank You. I too, had a second daughter less than 2 months ago, 7 years after my first. And she too, has an extra chromosome. Many different people have directed me to your blog, and I must say, I am grateful for your words. Maite (pronounce my-tay) is healthy! And as far as I can see, Nella is too! I would love to have them meet one of these days! Perhaps, we'll see you at next years NDSS luncheon, as my mother in law in is NYC, so if it's there, so will we be. Keep it up, you inspire....
I love to read and look at your beautiful photos, not because I have a child with any needs at all, mine are now well grown. I love to read your blog because I think you have a wonderful way with words and a great attitude to life in general.
When I am feeling 'down' I come here and look around at all your links and go away feeling at one with my world again :) Thank you !
I have to post on this.. what a WONDERFUL post! I'm 3 months pregnant and realizing that I desperately want a girl (this is only the first of the hopeful two babies we will have) and I fear that they will both be boys. Ironic as thats what I always thought I'd have - I now long for a girl. And you know what? Just like an extra chromosome - if my babies are boys and not girls - I'll love them - I'll treasure them - and I won't care in the end. Your blog has been a GIFT to me and I will reward myself with your book - but for now - I'm finding joy in simply learning from your journey. Thank you, thank you - such beautiful words you have.. (and pictures!!)
I read about this post in your book, I remember reading it when you first posted and I always thought you were comparing DS with having boys but now after re-reaing I realize you are just compating the disappointment and that it is minor...I know I always wanted a girl...I am expecting now so we will see if we get lucky but having a boy would be good too just not what I really want.
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