Recovery and Rebuilding

Nature, nurture and toxic chemicals…

The latest news about the autism rates have brought us all to another collective sigh of horror, outrage and disbelief.  We all knew that the current figures were off, we all knew that in reality, just in our own communities, counting the blogs, the books and the articles, so many more children were affected by a spectrum disorder than the often touted 1/150.  When our son was diagnosed in 2008, I think the figures were closer to 1/250.  It seemed astronomical even then.  Now, 5 years on, that number has shot up considerably.  Better diagnosis is blamed, well, forgive me, but 5 years ago we were still pretty much the odd ones out.  We would go to the mall, to a fast food restaurant, to a party, and we, the parents of our son, would be the ones sweating, the ones calming, the ones holding onto our son so he didn’t run screaming a high-pitched scream through the throngs of people.  Of course, eventually, we learned to manage with the behaviors, just not go, to stay close to home, to only be in situations that were controllable, but I digress.  Luckily for us, he isn’t this kid anymore.   We seemed to figure out the triggers for our son, and now thankfully for life, liberty and happiness, he is a totally different kid.  Still a little out of control but not as sensory sparked, not as in your face, not as aggressive, not as uncontrollable; however,  still not a kid I am taking to a nice restaurant. Although, to be honest, I am pretty sure a lot of parents could say that about their ‘typical’ kids.

Anyway, yes, those numbers, sending chatter across the universe.  Did we do this to ourselves?  Did something happen? Are we just seeing it clearer, diagnosing better?  I see some autism professionals suggesting you still vaccinate, don’t change diet, live with it, learn to work with it, this is just better diagnosed, and I wonder, really? When I look around, I can see the phenomenon isn’t just limited to autism.  Other things are happening to our kids, other rapid changes, other things that just are not quite right. Did we suddenly start adapting faster to our environments than we ever have before or is something seriously wrong with either the way we are raising our kids, or the food chain, or both of those things and more (BPAs, Coal Ash etc.) – I just don’t know, and until someone gives me an answer that makes sense, I think I will choose to err on the side of caution thanks!

I have been looking from the inside out now for many years, and it really started when we began our journey to become parents.  A number of firsts suddenly meant, I went from a fairly normal living, smoking, going out, having fun, starving myself to be thin, kind of late 20’s girl to who I became today. Gradually as we tried to build our family, we became the odd-men out if you will.  Now, for whatever reason you decide to think, I have a foot in many ‘groups and statistics.’ Originally we fell into the rates of infertility rising group, then we became members of the ‘adopting on the rise’ group, then we joined the ‘parents of a child with special needs group’ and we are the proud but also card-carrying members of the ‘culturally diverse family or parent’s raising children of a different culture/color’ group.

Along with adoption, comes other challenges – see “puberty before age 10” or the statistics I have written about before in regards to the mental challenges associated with adoption from a child perspective.  I know that my children will always belong partly to another Mother.  I have now accepted that – or at least I think I have, it took a long time, and part of my heart had to die to get there, but accept it I have, simply because I love my children.  We now live the other classic adage, “if you love someone set them free, if they come back …” We are in the process of getting ready to do birth mother searches. Most families don’t have to question this, they have their children and spend the rest of their lives comparing them to Uncle Jack, or looking like Aunt Stephanie, or singing so well just like my dad, or my aunt, mother, brother…. but in our house that doesn’t happen.  Our son’s drawing talent is becoming very evident and we wonder, who that came from, is one of his birth parents, aunts, uncles, an artist? Do they have his amazing insight? Talent? Gifts?  Or my daughter, struggling to come into her own, having many things she does well, but trying to find the thing she does great!  One might say, and we do, that our kids are full of untapped, unknown potential which is pretty exciting, but to gain that perspective we have had many hurdles and challenges to find a positive spin on the unknown, the questions, the grief of losing what you can’t remember you had.  I know other ‘typical’ families can have this too, I don’t think it’s only adoptive families, but for us, the question is never answered, unless we are able to find the birth families, and then who knows what we are opening up too.  We may discover personalities that match, talents that are family owned, but at what cost, what other feelings, emotions are going to be brought out, will I be able to cope?  I have to, but will I?  I know my thoughts on the media view of adoption, it seems to be mocked, Angelina is touted as some kind of freak, not an amazing person who brought a family together.  She is ridiculed, and made jokes of, but so many families are built on adoption and this alone brings its own challenges.  I don’t say this to differentiate, to say we have it harder, or better, I say this only because we are different, we are once again part of a statistic. In general, ‘typical’ families can go along without wondering, pondering, thinking… what would that be like I wonder?

So in the end, I have to admit our life hasn’t been the normal, leave home, career, wedding, family, retirement path that most of us envision when we are growing up.  You don’t imagine struggling through miscarriage, after miscarriage to be told it’s not going to ever go the way you want it too, those odds are too small, just move on. So we did, we chose adoption to build our family.  Interestingly, we chose to bypass some European countries knowing that baby homes and deprivation carried their own distinct risk, when the chance to adopt from a non-European country chose us, we went along happily for the ride.  This led us to where we are now.  Sitting in my little sun-room typing on my computer while my kids watch the Disney channel in our little living room.  Are we normal? I am not sure anymore what that even is, except for the famous line “normal in our house is just a setting on the drier!”  We are happy I know that, but we are isolated. We celebrate firsts in this house harder than most I imagine, we choose to celebrate little achievements and no longer push for the big! Both the kids are doing well in their new school, but to pay for it I work 40 hours a week, from home so I can be here with them, but still 40 hours on the clock.  So the compromises are many but the rewards are finally coming fast, that makes the trade-off worth it – right?  Do I sometimes wish that those 6 figures we have spent were still in our bank account, oh hell yes.  Do I wish I was in my bigger house, oblivious to the outside community angst and rising rates of autism, precocious puberty, infertility rates, and who the hell knows what else, well hell yes again. Who wouldn’t want to be oblivious? But that isn’t where we are at!

We are doing better than most.  We have been successful for the most part in dragging our son kicking and screaming to where we are now.  It took a lot of work on his part, and it isn’t done yet, but at least now, he is wiling to put in the work. For all those kids out there who will never recover from autism or their developmental challenges, I say to the parents, I know you love these children, I appreciate the hard work you put in caring for your child/children, the hours lost in sleep and the $$ lost in therapies.  I know you will die for these kids, I know you want answers, but where do we go from here?  Just how do we change these figures without anyone really in the position that matters, doing anything about it?  Will it only begin to change as it affects the budgets, then will people start thinking out loud?  or as the families who judge autism and developmental delays on bad parenting discover it in their own children?  or as the doctors who think parents who choose special diets are crazy, find it in more and more of their patients or their own children?  As the questions become louder and the answers more obviously incorrect?  Will it be as more special needs classes and teachers need to be hired, more adult carers, more community help, more medicare/medicaid?

I know for us, we are tired of being a statistic, we want to blend in, we want to be ‘normal,’ how do we make that happen? Oh wait, if the autism rates continue to rise, we will be the ‘new’ normal… time is on our side, time is truly on our side.

Not just autism, we should be worrying about. New York Times, Puberty Before 10.

Clean Air Carolina hosts Dr. Sandra Steingraber, March 20, 2012

Dr. Sandra Steingraber, biologist, author and cancer survivor, is an internationally recognized authority on the environmental links to disease. Her latest book, Raising Elijah: Protecting Our Children in an Age of Environmental Crisis, is a moving memoir combined with compelling research. Join us for a compelling lecture on protecting our children in a toxic environment and Dr. Steingraber’s call to action.

Tuesday, March 20, 2012
7:00 pm
Providence Day School
McMahon Fine Arts Theater

5800 Sardis Road, Charlotte 28270
Register here

About Dr. Steingraber

Called “a poet with a knife” by Sojourner magazine, Steingraber has received many honors for her work as a science writer. She was named a Ms. Magazine Woman of the Year and later received the Jenifer Altman Foundation’s first annual Altman Award for “the inspiring and poetic use of science to elucidate the causes of cancer.” The Sierra Club has heralded Steingraber as “the new Rachel Carson,” and Carson’s own alma mater, Chatham College, selected Steingraber to receive its biennial Rachel Carson Leadership Award. In 2006, Steingraber received a Hero Award from the Breast Cancer Fund and, in 2009, the Environmental Health Champion Award from Physicians for Social Responsibility, Los Angeles.

Re-posted from the CleanAirCarolina website.  Please consider attending to learn more about how clean air quality and environment does not just affect you, but so many future generations.  The time is NOW!

When self interest gets in the way, everyone suffers, no?

“… Culture writes on illness. That’s evident in the battle around a French documentary about autism entitled “Le Mur” or “The Wall.” Today, a court in the northern city Lille will decide whether the film, released online last year, should be censored at the request of psychoanalysts in the country, since it essentially charges that their approach to the disorder ignores decades of scientific progress….”

Unfortunately, until we know why so many kids have autism and how, I am not sure there is one person can say that what will work for one will not work for another.  Mostly, success is measured in families not in large scientific studies.  To those who go against the “scientific”, there is much mud-slinging, yelling and berating, but what else to do when there is not much offered by the scientific community in the way of cause, effect and cure!

Sadly, in our experience anyway, it led to much more in the way of fruitlessness, there was no help, no options, no answers.  It was basically figure it out yourselves, induce ridicule, often contempt, certainly a healthy dose of scorn and mirth, but still you endure, all in the hope that you will help your child out of the fog.

Which in the end, I suppose we did.  Although, in my house the last few weeks ~ sometimes I wonder, so when I read this:

FOX & FRIENDS: Dr. Bob Sears answers, “Can children outgrow autism?”

Jan 26

So…what does this mean? More confusion among experts? The top people still know nothing about autism: cause, cure, treatment, prevention, etc.

I have a hard time seeing what’s out there to smile about. Sears has treated over 500 kids with autism. WHY? Where did they come from? How did he treat them?

A.

Jan 26, 2012 HERE

On autism: “A new study claims that children can actually out grow it. Do you believe it?”

Dr. Sears: “I actually do believe it. The important message for autism is that autism is treatable. What made me mad about that study is that they found that about one third of kids with autism will outgrow or improve so much that they lose their diagnosis, which is wonderful. But they claim that those kids didn’t have autism in the first place. I don’t believe that. I think that’s wrong. As a pediatrician, I’ve treated over 500 kids for autism and I do see them lose their diagnosis. They have autism at the beginning but they don’t just … It’s not because they didn’t have autism in the first place. They’re clearly autistic and then we treat them. The parents spend hundreds of thousands of dollars. Weeks, years and years of therapy. Behavior therapy, developmental therapy, medical therapies. The kids improve and they lose their diagnosis and the researchers are trying to take that away from parents saying they didn’t have autism in the first place.”

I realize it’s maybe not just me that thinks this stuff… 😀

I took a full-time job…

I never thought in a million years I would be able to work while my son was young.  An obvious need to replenish was held against a desire to not allow him to slip into feeling un-loved or not wanted – again, but here we are just one short year working alongside him to heal his deep-seated trauma and I am back to work.  Now, I work from home so that obviously makes things a little easier for both of them and me! Still, they are respectful of my hours and for the most part understand that I can do this and still love and take care of them, which I do. I was worried, I was expecting a return to the behavior we had seen in the past when an event occurred that he was anxious about, but to his credit, he has handled it like a trooper.  It just goes to show how important it is to talk about healing, rather than medicating, his behavior.

Last week I sat down to watch ABCs expose regarding children in foster care and medications. “… Foster children are medicated with psychotropic drugs up to 13 times more than other kids. Michael Piraino, the chief executive of the National CASA Association, a foster children’s advocacy group, said that, as a population, foster children tend to be more troubled than their peers. …”

This makes me so crazy and so very sad, of course these kids are troubled, who wouldn’t be?  It seems to me that if we are going to take these kids away from trouble at home, we should have a better place for them to live. They certainly should be treated to mental care, because everything we know now tells us that physical care is just not enough.  Just for one minute imagine how it would be to be living in a troubled home with abusive or negligent parents and then someone swoops in to save you, to take you away and give you a better life.  It seems great on the surface but in “rescuing” this kid, what really happened is that the child was taken away from everything they know, and everyone they love, regardless of how bad that life may have been.  If that’s what and who you know, that is your normal.  They are confused, angry, stressed about what is happening, and worse, what comes next.  To me, as an adult, I get nervous and anxious in new situation, but I have coping skills, I have learnt through experience to handle my overwhelming desire to turn and run by looking at each situation rationally. Our kids don’t have that wealth of experience on their side to pull from. Their childhood is supposed to be safe enough for them to learn how to handle things like this, if we interrupt that development, that learning phase, how are they supposed to learn how to handle it?

To remove a child and be egotistical enough to think that you have saved them is ignorant or at least requires more forethought than I think we realize.

These kids are hurting, they are scared, they are angry and worried. How is that NOT going to give them some kind of behavioral problem.  Add to that, foster care is not permanent care, in effect they no longer belong anywhere, they feel different, alienated and alone, how is that better?

These kids are lashing out in pain, anger, anxiety, hurt and depression not because of defiance and probably not because of chemical imbalances – we poke them with a stick and then wonder why they scream.  It’s a problem certainly, so, to take away that natural response, to diminish that rage and angst, someone somewhere has decided to medicate them, to drug them so in effect, they don’t react to their situations.

In our case, we honestly thought that when we adopted our son, we were doing a good thing.  We truly thought it was beneficial to both of us.  Guess what?  Regardless of whether it was right or not, in his mind, he didn’t get a say, he never got a chance to decide, it was all decided for him. He was fearful, anxious, stressed out by all the changes, by his lack of voice and choices.  He had no idea what was going on, he was confused and scared and his brain remembers that. It has scared him, now he doesn’t feel like he belongs anywhere, he doesn’t feel normal or like he fits in. He feels thrown away and unwanted, he tells us he is a bad kid.

I could certainly medicate that anxiety out of him, I could medicate the depression, I could medicate the anger, life would probably be easier for both of us for a while. What I can’t do is force him, when he turns a certain age, to take his medication. Then what? Then how does he recover? How does he face all those bottled up, drugged down feelings in his teenage years? How does that work?

I don’t need to write about that part of the story because in our hearts we all know how that looks.  We have all seen the crimes committed, the suicides, and the behavior associated with many of these kids. We look around and shake our heads and wonder what happened.  Well, honestly, when it really comes down to it, we don’t need to look too hard do we?

Give these kids a voice, let them heal, let them talk, give them a chance to excel and achieve – then maybe we can say we did the right thing, but not yet, certainly not yet.

 

Trauma Center looking for participants in Developmental Trauma study!

PARTICIPATE IN THE DEVELOPMENTAL TRAUMA DISORDER FIELD TRIAL STUDY

The Developmental Diagnosis Study is a critically important study that is being conducted to improve and expand trauma-related diagnoses for children. There are seven Field Trial sites across the country including our site in the Greater Boston area of Massachusetts. Each site will interview at least 100 children and guardians. Eligible children are ages 8 – 17. Interviews take two- to three- hours to complete, and can be conducted at the Trauma Center in Brookline, our affiliate clinic in Acton, or at another office or program as available. Participants will be compensated $50 for each child participating in the study. Participation in this study is an opportunity to transform the field and to develop appropriate diagnoses and treatment models for children who have experienced trauma. Children do not need to have mental health problems or histories of traumatic events to sign up. All children ages 8-17 are welcome. To participate or make a referral, please contact the clinical research coordinator Regina Musicaro: (617) 232-1303, x 310 or rmusicaro@jri.org.

CONTACT INFORMATION FOR OTHER SITES:

Western Michigan University, Kalamazoo MI
Connie Black-Pond, MA, LMSW, LPC
(269) 387-7065
black-pond@uchc.edu

University of Pennsylvania and Drexel University, Philadelphia PA
Elizabeth Nicholls, Study Coordinator
(215) 571-4256
elizabethgnicholls@gmail.com

Beth Israel Medical Center, New York, NY
Emily Upshur, Ph.D.
(212) 420-2474
eumupshur@chpnet.org

Anchorage Mental Health Center, Anchorage, AK
Joshua Arvidson, MSS, LCSW
(907) 762-2817
jarvidson@acmhs.com

DePelchin Children’s Center, Houston, TX
Adrienne Tinder, Ph.D.
(713) 558-3912
ATinder@depelchin.org

University of Connecticut Health Center, Hartford, CT
Rocio Chang, Ph.D.
(860) 679-1728
CHANG@uchc.edu

University of Connecticut Health Center, Hartford, CT
Ms. Joan Levine, M.P.H.
(860) 679-2132
LevineJ@uchc.edu

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