Tuesday, October 27, 2009

the future looms



I have never really been very afraid of the future. I'm not now, either, but suddenly it feels a little...near. I have been thinking about Ciarra being 11, and what the future might be for her that is different than what I have expected it to be. I wish we had a crystal ball to know what to expect. But we don't. I wish we could just allow time to open up like a flower, exposing every day a little more of whats to come. But we have so much to DO, so much to plan. so many concerns, worries, so much OPENNESS in the future. Parenting a child with special needs has not been the hardest thing I have ever done. It certainly isn't the easiest, either. But it truly requires more thought, love, and emotion (and planning!) than anything I have ever done before.

I met with Ciarra's teachers yesterday, a sort of gut check for me, is this working? is this the best thing? What can I do better, what have I missed? As we walk this tightrope of Inclusion and Special education, sometimes it feels like I am just about to fall off into nothingness and fly naked into darkness. I feel exposed, not in control, and sometimes, frankly, afraid. There is in every step a sense that I just might be making the wrong decision, ruining her chances for a good future, destroying something precious and vital of her childhood. I am, by nature, a worrier. What happens to her if I get this wrong?

For anyone still reading, some background. Ciarra is currently in 5th grade. She is funny, witty, stubborn, determined, and incredibly incredibly special in ways that have absolutely nothing to do with having Down syndrome. She is world wise and innocently naive all in one. She is brilliant, and yet has gaps in her ability that still today astound me. She loves to read, she loves words, people, animals, her family, and a very few people outside of our family. She is easily motivated, usually. And then all at once she is stubborn and taciturn, demanding and...well...hormonal. She makes me laugh and she makes me cry, sometimes all in the space of a minute.

I fear for her future, not because of anything in her, but because every once in awhile some idiot will remind me that the world is not a gentle loving place for the most gentle, loving people. Sometimes, it even sucks. I watched an episode of My Super Sweet 16 yesterday, the rich girl was handing out birthday invitations, and other kids stood there, waiting to be deemed "good enough" or "not". And I knew, in this world, Ciarra would never be one of the lucky ones who got handed an invitation by the shallow rich girl throwing lavish parties. Of course, I know I wouldn't want that for her, but still...

Preteens with Down syndrome are a lot like typical kids. They want certain clothes, listen to the "cool" music (with a little bit of barney and doodlebops on the ipod for good measure) and they crave friendships. Ciarra is lucky to have a few very good friends. And one friend that we had had to distance her from a year ago has reached back out, with new rules and a new awareness and some maturity, it seems to be going well. But the girl who always made Ciarra a part of things at school moved away over the summer. Her absence has had an awful effect, without her there to encourage Ciarra to join in, be a part of things, without her friendship, Ciarra is choosing to sit away from that gang of girls. Without the buffer Jenna gave her, she seems a little bit lost. Besides, the other girls are talking about things she isn't into yet, that emotional maturity is just not there. She knows they talk about boys and makeup and parties. And she still wants to talk about puppies and kittens and Hannah Montana.

I feel like, in some weird way, I am letting people down by telling this story, like somehow because so many things have been relatively easy for Ciarra that this should be, too. But it isn't. Not always. She is SO blessed to have some really good friends at school and at home. But it is changing now, the kids are maybe leaving her behind a little bit. (I can almost hear "I told ya so" from the chorus of haters that almost will our kids to suffer, the people who want to see DS take the same toll on my kid it took on the ones they chose not to deliver at all.) And while Ciarra's life is changing, it certainly is not a bad life, or an unhappy one. But the realities of being a preteen with a significant disability in a world that only tolerates perfect are there.

I have to wonder, who really has the disability here? Ciarra doesn't judge, she doesn't hate, she is rarely angry. But what she is is different. Her world is so full, and she has so much. But as she grows, as she begins to make her way in a world less inclined to be accepting and tolerant, without me there to guide her, she gets hurt. ALL kids do, she is certainly not the only 5th grader to not get the coveted Birthday party invitation. Its just that she feels it so keenly, and I cant help but think it is because of the DS that she isn't being invited, I cant make that better, or promise she will outgrow it like I could if it was knobby knees or zits. Ds is a part of her, a part I treasure, but with all of its beauty comes a certain sadness, because the world is simply not as accepting of people who are different. And I have to wonder if this isn't the beginning of the end for this emotionally stable, healthy, confident little girl. Will she stay strong and continue to believe in herself? will she think Ds is no big deal, or will she wish with all of her heart to change it? Down syndrome is not something I would ever change for me. But for her, if she wanted to change it, would I ever have the right to stand in her way?

I have been asked many times since she was born, would you change it if you could? No, I wouldn't. But I will have to fight like hell to make her not wish she could, and make her comfortable with who she is, knowing that who she is is beautiful, funny, smart, gregarious...and sitting home on Saturday while most of her peers attend a Birthday party she wishes she too could attend. My other kids survived it, and I was sad for them, too. But with Ciarra, there is always the "might have beens" and sometimes those hurt even worse.



Sunday, October 18, 2009


To Select a Bauble For Your Blog
CLICK HERE


It is already nearly time for the 2009 Christmas Angel Tree Project! We have nearly (200) children with Down syndrome in need of sponsors and adoptive families in (25) countries around the world. (172) of them already have their own Christmas Warrior, folks who have signed up to provide focused efforts to raise $1000 or more for their Christmas child's adoption grant fund.

For those of you who are new to RR, when you donate $35 or more for one child's grant fund, you will receive a beautiful porcelain photo ornament of your sponsored child to hang on your Christmas tree! These also make very personal and meaningful GIFTS for people you know who are advocates of children with Down syndrome or adoption in general. Nobody wants more scented hand lotion! GIVE THE GIFT OF A FAMILY this Christmas instead.

The Sponsorship Page goes live on November 1. The project runs until December 31. But NOW is the time to prepare, sign up to be a Christmas Warrior, and help 2009 be our most successful Angel Tree EVER! All donations are tax deductible.

God bless each of you, we are so excited for this time of year and grateful for each of you sharing this ministry and this special project with everyone you know! Post about it on your blogs, your FB, your Twitter, your MySpace!

Andrea Faris Roberts
Executive Director, Reece's Rainbow



Saturday, October 03, 2009

We have a WINNER!

we have a winner!!! Mr. Grifyn Bedford and his brother Xander won the software package. Be watching for the next giveaway, which will be drawn from all entries. Congrats Grifyn!



imagine, reading sight words already? Not too long ago, this little guy was in an orphanage, and had never heard english in his life. Amazing.



An unannounced REBLOGGING giveaway for 31 for 21



I have not been blogging lately, Facebook has become so easy that I rarely blog anymore. Tonight, that changes. As a part of 31 for 21, I will begin REBLOGGING. And in order to make up for my missed first days, I will be doing a giveaway!

The above prizes will be given away over 3 days. Tonight, to start the giveaway, we will give away the 2 Laureate programs pictured above! Be watching for the other prizes, including a copy of Play To Talk by Dr. Jim McDonald.


To the FIRST person to respond, who links me back to a blog post about their child with Down syndrome and the ways they learn academics, will go a TERRIFIC prize package!

You will receive a brand spanking new copy of Laureate's Nouns and Sounds software Value $125



PLUS! a copy of PREPOSITIONS, also by Laureate. value $210




these 2 programs are values at $335 dollars, but they are PRICELESS! Laureate puts out some incredible programs. They have been kind enough to allow me to donate these 2 programs to a lucky winner.

Ready? Set? Let's see who is still reading?!

Sunday, August 16, 2009

summer is coming to an end

this has been an enjoyable weekend of ME time, no schedules, no huge plans. some groceries, some laundry, a small project to help me get organized.The kids had a mellow weekend too, I almost feel like we are in cocoon mode right now, plotting against the school days that will come a week from this wed. Ciarra starts 5th grade, Jesse starts High School, and kristin goes to college. Time rushes by, and for this moment, I just want to hold onto all of us and the easy days and keep them close.
alas, life needs me to make some decisions and get ready. I created a bulletin board project for our entryway, something useful and semi decent to look at. Im no artist, to be sure, but I wanted something nicer than your average cork board.



basically, this is a corkboard covered with fabric, divided into sections for Jesse and Ciarra (Kristin keeps track on her own) and for the family in general. It makes it that much easier to remember school papers, sports schedules, Dr appointments, etc. I need to get a communication folder going, and update Ciarra's notebook with most recent IEP, etc. and i really need to clean out my office bins for this years homework and stuff.

C's teacher has been in touch, she seems wonderful. she asked me about adapting some stuff, and has some great ideas of her own. We will meet this week to go over anything we can think of to make this year easier. One of Ciarras best friends moved this summer, and she was sort of the buttress that brought C into the group at lunchtime, I wonder how that will go now that jenna is gone. she was a true gift to Ciarra socially, including her in everything. I worry.

Jim and I are doing well, he has been very loving and sweet the last few months, we made a commitment to one another to be a couple and not just parents. We actually had a date night the other night, a movie, it was nice.


Saturday, August 15, 2009

what I would never change-and what I feared



how could I have ever feared a life with a child who would bring so much joy?


Monday, August 10, 2009

irreversibly prevented from being or becoming participating citizens

http://www.nypost.com/seven/07242009/postopinion/opedcolumnists/deadly_doctors_180941.htm?&page=1

this article talks about the elderly and disabled and health care, and quotes Dr. Ezekiel Emanuel, the brother of White House Chief of Staff Rahm Emanuel. He has two key positions: health-policy adviser at the Office of Management and Budget and a member of Federal Council on Comparative Effectiveness Research.

the article quotes him directly as follows:

Hastings Center Report, Nov.-Dec. '96

http://ncpa.org/pdfs/Where_Civic_Republicanism_and_Deliberative_Democracy_Meet.pdf



Ezekiel J. Emanuel

"This civic republican or deliberative democratic conception of the good provides both procedural and substantive insights for developing a just allocation of health care resources. Procedurally, it suggests the need for public forums to deliberate about which health services should be considered basic and should be socially guaranteed. Substantively, it suggests services that promote the continuation of the polity those that ensure healthy future generations, ensure development of practical reasoning skills, and ensure full and active participation by citi- zens in public deliberations-are to be socially guaranteed as basic. Conversely, services provided to individuals who are irreversibly prevented from being or becoming participating citizens are not basic and should not be guaranteed. An obvious example is not guaranteeing health services to patients with de-mentia."

The fundamental challenge to theories of distributive justice for health care is to develop a prin- cipled mechanism for defining what fragment of the vast universe of technically available, effective medi- cal care services is basic and will be guaranteed socially and what services are discretionary and will not be guaranteed socially. Such an approach accepts a two-tiered health system-some citizens will receive only basic services while others will receive both basic and some discretionary health services Within the discretionary tier, some citizens will re- ceive few discretionary services, other richer citizens will receive almost all available services, creating a multiple-tiered system

"The patient, or micro, level entails determining which individual patients will re- ceive specific medical services; that is, whether Mrs. White should receive this available liver for trans- plantation"


Obamacare scares the heck out of me, and it should ANY parent of a child with a disability, and especially those of us raising children with an extremely high rate of dementia as they age. This is not an email fwd, this is not someone elses words. This is me, fearing for our kids.



Tuesday, July 14, 2009

mini minister girl



2 Corinthians 12:9-10
But he said to me, "My grace is sufficient for you, for my power is made perfect in weakness." Therefore I will boast all the more gladly about my weaknesses, so that Christ's power may rest on me. That is why, for Christ's sake, I delight in weaknesses, in insults, in hardships, in persecutions, in difficulties. For when I am weak, then I am strong.


Had 2 funerals this past weekend, my Uncle Russell's and my aunt Dot's. It was amazing to see cosuins and aunts I hadnt seen in many years. My aunt's son Michael is a big, strapping man now. I havent seen him since he was a teen. He had made a box to hold his moms ashes, and it was resting at the gravesite after the ceremony. He was standing there, lost in thought, just quietly saying goodbye I guess. Suddenly, Ciarra tugged her hand out of mine, and I turned to see her standing beside Michael. she looked up at him, very quietly said "are you sad?" and then put her teeny little hand in his huge one and started to pray. It was otherwordly.

She said a very few words, and I dont know exactly what she said because she whispered, but it was "Dear God and Jesus" something. Then she turned to this 6 foot plus many man and said as clear as a bell "I can give you a hug to make you feel better. Dont be sad, your Mom is with God and Jesus now." She hugged him very close, and then turned and left him there, he looked at me in sort of shcok, like "what the HECK?!" with a huge smile on his face and tears in his eyes. It was a very strange, powerful encounter.

What's most odd about it is that I wasnt shocked by it. She has done things like this a few times, she has this odd THING about her that just seems so self confidant and strong in cases of death. She is POWERFUL, like this little mini minister person. I am in awe of her ability to comfort people.

To me, it is a very overpowering feeling of kindness, love, goodness. I feel honored to have it near me, but it is so clearly NOT mine, not guided or taught by me, it just IS.

Matthew 11:25-30
Come to me, all you who are weary and burdened, and I will give you rest. Take my yoke upon you and learn from me, for I am gentle and humble in heart, and you will find rest for your souls. For my yoke is easy and my burden is light
.

Wednesday, July 08, 2009

July is here

I heard on the news this morning that we have not had 2 days of sunshine back to back since APRIL 15th!!! At the end of June, they said we had had rain for 28 of 30 days. It is now July 8th, and we have had ONE day without rain since then. Sigh. Todays high is 54. No pool, no AC needed yet. Just blah. But...life goes on.

My Mom and stepdad are here from Florida for my Uncle Russell's funeral. We leave to drive up North for that tomorrow. It will be hard to say godbye to him, I loved him so much. My aunt Dot died 6 days after he did, we will bury them beside one another in the family plot. I will be seeing relatives I havent seen in 30 years. Kinda exciting, kinda scary.

Things that have happened in the last month.

-we went out to eat at weathervane and Vern tried to pay the bill. he and Jim chased one another around the restaurant (really) for 15 minutes. Jim won.
-Jesse seems to have a girl. she is gorgeous. I found myself having the "talk" with him as we drove him to her house last week. Yikes. He doesnt completely admit shes his girl, but she texts him constantly, shes been here and he at her house. I am old, but it hasnt been THAT long.
-Kristin has decided to go back to college. Financial Aid, anyone?
-Ciarra turned 11. we had her party at her summer camp. she had a great time, and so did we.
-Ciarra learned to kayak, and is pretty darn good at it.
-My darling Sarah got married, and I took her wedding pics. Beautiful bride, the apple of my eye too.
-Rob and Wendy and Hunter came for a visit! It was wonderful seeing them, but heartbreaking taking them to the airport afterwards. Home is here, in maine. I hope they can get home soon.
-Someone very special to us did something very unlike him last fall. He was defending his child, but he made a terrible decision. he went to prison recently. we miss him more every single day. He will not be out until 2012.
-We finally sold my Grandparents old house. The closing is tomorrow. yay. Finally done payingfor that thing!
=we went camping in the Rangeley mountains. I finished a long hike to a waterfall, but it was TOUGH.
-I am working on this extra weight of mine, God give me the strength to make the right choices.