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Saturday, January 29, 2011

Tiger Mothers


Amy Chua is on the cover of Time Magazine this week.  She recently published her memoir, entitled The Battle Hymn of the Tiger Mother.  After reading the article, I purchased her book on my Kindle.  The article talks about her method of parenting, which she describes as being the Chinese way of strictness and inflexible structure for her children.  Her kids were never allowed to go to a sleepover, watch television, or participate in a school play.  They studied – in elementary school – into the night, and practiced their instruments up to six hours per day.  She has received much derision and anger – with some even calling her methods child abuse.  However, the article alludes to her exaggeration, and she even confirms that she has eased up over the years and learned from her mistakes.  She asserts that her methods are the norm in China.  

As China becomes a world power – its economy is second only to that of America, and students in Shanghai wipe us out with their test scores - do we need to consider that maybe she’s onto something?  She says that her children developed self-esteem through having “mastery experiences,” and through their success in most of what they attempted.  She feels that Americans, with their Little Leagues that sometimes don’t keep score, and teachers that feel that everyone is a winner, regardless of their amount of effort, are coddling our students and teaching them that others owe them praise to improve their self esteem.  In this I agree with her.  We are developing a nation of students who expect that in life, rewards will be handed to them regardless of their abilities and work ethic. 

I plan to read The Battle Hymn of the Tiger Mother with an open mind – and look for areas where she might be correct.  I abhor her purported treatment of her girls, and I agree with most people that she did irreparable damage to their emotions.  But I also feel that maybe I can learn something from how she dedicated herself to ensuring her girls’ academic success, and how she taught them that hard work and dedication can make them successful.  

I don’t want my children to quit when something is difficult, or to learn that they can “get by” without doing their best.  I want them to develop a work ethic that allows them to keep on practicing, even when they aren’t seeing much progress.  I want them to experience the feeling of completing something difficult, and knowing that it was better than they thought they could do.  I want them, above all, to develop their self-esteem based on knowledge of their abilities, and faith in the fact that they can thrive in a world of competition.  

Friday, January 28, 2011

Running Out of Time


Following my post of yesterday, I researched a bit and found this list of almost-14 year olds waiting for a family on China’s “shared list,” which means that most agencies with Chinese adoption programs can place these children.

I think that it might be about a month out of date, so if you find a child you are interested in, please contact me (brennensmom@yahoo.com) if you are interested in him/her and I can give you a few names of adoption agencies that advocate for older children and who can check on the child to see if they are still available. 

Two great places to research medical needs common found in Chinese orphans:

Love Without Boundaries special needs site
No Hands But Ours

These children MUST be adopted by their 14th birthday or they will NEVER find a family!!!  For the ones “aging out” in the next 3-4 months, a family must already be in the process of adopting, with a completed homestudy and most – if not all – paperwork complete.   Children are added to the shared list all the time, so there may be more.  

 23 Girls
> > 1/9   IT IS ALREADY TOO LATE FOR HER
> > 1/17  IT IS ALREADY TOO LATE FOR HER
> > 1/24 IT IS ALREADY TOO LATE FOR HER
> > 1/28 Healthy  IT IS ALREADY TOO LATE FOR HER
> > 2/1 1 spina bifida; 2. enstrophe of both lower limbs; IT IS ALREADY TOO LATE FOR HER
> > 2/9 Dumb and  deaf, forearm obsolete scar IT IS ALREADY TOO LATE FOR HER
> > 3/20 Healthy
> > 5/15 height and  eight lower (middle), spine bent to the right side
> > 5/31 congenital right cornea leukasmus
> > 8/1 Epilepsy
> > 8/7 Post-operative cleft lip and palate
> > 8/22  congenital deaf and dumb
> > 8/24 congenital deaf and mute
> > 8/31 Skin Condition  (scar)
> > 9/30 Beta thalassemia
> > 9/30 CHD: good postoperative recovery of VSD  repair, minor incompetence of  TV 2 HB
> > 10/2 HBV carrier, pulmonary  tuberculosis to be excluded, IQ development is on borderline level
> > 10/4 HBV  carrier, arthritis deformans, CHD (ASD) repaired
> > 10/6 postoperative drainage of hydrocephalus
> > 10/9 Dwarfism
> > 10/10 Post-operative cleft palate; HBsAg:  Positive, HBeAg: Positive, HBcAb:
Positive; Limb deformity
> > 10/30 Hepatitis B  Positive
> > 11/18 postoperative spina bifida, incontinence

58 Boys
> > 1/9 IT IS ALREADY TOO LATE FOR HER
> > 1/10 IT IS ALREADY TOO LATE FOR HER
> > 1/18 IT IS ALREADY TOO LATE FOR HER
> > 1/21 IT IS ALREADY TOO LATE FOR HER
> > 1/27  deformity of both feet and hands IT IS ALREADY TOO LATE FOR HER
> > 2/16 both ears complete deaf  IT IS ALREADY TOO LATE FOR HER
> > 2/20 congenital binocular eyeball dysplasia
> > 2/20 Basically normal (right ptosis)
> > 3/7  congenital cataract (postoperative); 2.nystagmus
> > 3/7 congenital  dumb-muteness
> > 3/11 Cleft Lip/ Palate
> > 3/15 Healthy
> > 4/3 postoperative  flexion contracture deformity of both wrist joints
> > 4/6 Cleft Lip/Palate 
> > 5/2 postoperative meningomyelocele
> > 5/2 postop left kidney resection,  hydronephrosis, right ureterectasis, HB carrier
> > 5/7 congenital muteness 
> > 5/8 Healthy
> > 5/16 Healthy
> > 5/19 cerebral palsy, exotropia of  left eye
> > 5/22 postop congenital cleft lip and palate, cleft right upper  alveolar bone, absent uvula
> > 5/25 Postoperative repair cleft lip and palate, appendicitis
> > 6/1 Deformity of right lower limb
> > 6/4 Healthy
> > 6/9  Not translated
> > 6/22 Cerebral palsy. ;Motions of right limbs are confined   TWIN BROTHERS
> > 6/25 strabismus, amblyopia of both eyes
> > 7/1 glaucoma (after  surgery)
> > 7/1 Postoperative VSD repair
> > 7/10 cerebral palsy sequelae,mental  retardation,motive disorders of both lower limbs(minor)
> > 7/10 Not  Translated
> > 7/10 deformity of both feet and both lower limbs
> > 7/12 Not  translated
> > 7/14 Operative cleft lip and palate
> > 7/16 CP
> > 7/22 HBV carrier  2.postoperative cleft lip and palate
> > 7/27 blind of both eyesï¼›post-operative  left eye
> > 8/3 postoperative cleft lip and palate, bendingness deformity of  bilateral tibias - this might be rickets?
> > 8/6 esotropia, low intelligence 
> > 8/29 Healthy
> > 9/1 Hepatitis B Positive
> > 9/1 Healthy
> > 9/5 CP
> > 9/6  Decreased muscular force of upper limbs
> > 10/1 hemiplegia, HBV carrier
> > 10/2  21-trisomic syndrome ? Downs Syndrome
> > 10/20 deaf-mutism, positive HBsAg,HBeAg  and HBcAb
> > 10/30 hypospadias repaired, HepB
> > 11/10 Epilepsy
> > 11/25  congenitally deaf
> > 12/1 post orthomorphia of varus of both feet - repaired bilateral club foot ?
> > 12/5 Healthy
> > 12/9 congenital  absence of forearm of left upper limb
> > 12/10 postoperative congenital heart  disease (Fallot's); postoperative hypospadias
> > 12/18 Healthy
> > 12/24  Cleft Lip/Palate postoperative
> > 12/29 left  cataract

Thursday, January 27, 2011

Can you read this without tears?



Amy Eldridge has written eloquently today on the Love Without Boundaries blog about older orphans and their desperate desire for a family.  I challenge all of you to read this without tears…and then pass it on via your blog, via Twitter, via Facebook.  As Amy says about these children, “If not us, then who?”

ON MY OWN, by Amy Eldridge


Under Chinese law, after the age of 14 children are no longer adoptable.  Can you imagine the anguish and despair these children feel when they have their 14th birthday without a family?  Options in China for orphans are few.  Family is everything.

To learn more about Chinese older child adoption, also written by Amy Eldridge, click through to Annie’s Wonderful Waiting Children blog.  It will enlighten and sadden you.

Then, visit Love Without Boundaries and choose a child to sponsor for an education, into foster care or for a surgery that will increase their chances of being adopted.  Spread the word about adoption.  Talk to people at your church, your office, your school.  But above all, pray for China’s orphans.

Wednesday, January 26, 2011

School Struggles


Have you ever had writer’s block?  Or been confused and anxious about converting measurements when cooking?  Or been so totally lost in a new city that you didn’t know which way to turn?  That feeling of helplessness is frustrating to adults – imagine what it does to a child. 


My oldest son struggles with these feelings daily at school.  He is extremely bright – is eligible for the gifted program – but he has a learning disability that is so pervasive that he is now so far behind in school that he needs assistance from me with completing every assignment. 
 
He learns well when he is given linear, step-by-step verbal instructions in math.  Unfortunately, his school shows a few examples on the board and then expects the kids to work through word problems that apply what they have just been shown – often in a group.  Math is taught in a “figure it out” sort of way, which seems to work well for many kids, but sets my son up for frustration and failure.

Writing is torture for him.  If I read the material and then ask him questions about it, he very clearly can state his opinions and knowledge on the subject, but you put him in front of a piece of paper or a computer and nothing comes out but anger and tears.

Knowing the material is never a problem – except for math – because what he hears he remembers.  He needs a lecture format, and then an oral test.  He would shine with those accommodations, as well as with direct math instruction.  

He has an IEP, but it doesn’t state clearly enough what he needs.  Nor do I think that the school can change its entire methodology to teach one student.  He could get help from special education outside of class, or during work time, but it’s not enough. 


So what we end up doing is that I read everything he is assigned, and I assist him with structuring every paper, every summary, every project.  He tells me what he knows and we get it down on paper…and then we structure it, and then we write it.  Do you see how many times I said we in that sentence?  I’ve become his teacher, his coach, and am frankly doing way too much work.  I also am using the Saxon math home school program to attempt to teach him the math that he has missed.  I think he is at least three years behind.

Another aspect of his problems is his lack of organizational skills.  He has learned to compensate for it – sort of – by carrying all his materials in a backpack to every class.  Otherwise he would never make it to class with the correct books and folders.  He uses a planner, but needs assistance looking at assignment sheets from his teachers and getting the due dates written onto the right days.  Every night we go over his work and write in his planner a few things that he needs to accomplish the next day, such as asking for clarification on an assignment, turning in the work we did the night before, getting a new math worksheet, etc.  

He struggles socially.  He is a sweet, gentle boy, and kids like him.  But he can’t seem to engage sufficiently with most kids in order to develop true friendships.  He has a hard time knowing how to have a back and forth conversation, or how to start one with someone he wants to talk to.  That being said, he does have a few friends that have reached out to him and accept his quirkiness and include him as often as possible.  He does better with girls than with boys.  He is so sensitive, and has little understanding of the difference between someone teasing and joking with him and someone being mean.  Because in the 7th grade kids are trying to figure out who they are, and are somewhat volatile and not always kind and gentle with each other (is that even possible??), my son feels like he’s being left out and picked on.

In school, he can’t remember where anything in his classroom is.  He wanders around looking for the folders where you turn in work, can’t remember where to put his science materials back when he’s done with it and gets confused when trying to remember the steps of how to do an experiment.

Now he’s gotten to a point that he begs every night not to go to school.  He says that he is humiliated when he doesn’t get his science lab done, or can’t write a summary that he can’t bring home…and doesn’t like to ask for help because the teachers show him something quickly and he still doesn’t get it.

So what do you do with a kid who tests to be exceptionally bright but can’t “do school” by himself?  We’re having him tested next week by a psychologist who specializes in learning disabilities.  After interviewing me for about half an hour, he asked if anyone had ever mentioned that he might have a non-verbal learning disability (NVLD).  I’d never heard of it – we’d had an Asperger’s diagnosis when he was younger, but as it didn’t seem to fit as he got older, we dropped it.  His IEP is written for someone who has high-functioning autism, but he doesn’t really fit that profile either.

I bought a couple of books about NVLD on my Kindle, and after reading most of the first one feel that we might – finally – be on the right track.  It’s a pervasive disability that affects organization, writing, math, social skills and often spatial relations.  It fits better than anything I’ve seen so far.  

Getting a diagnosis is just the beginning though…what do you DO with it after you get a label?  Especially in a school that just isn’t set up to teach in the way that your child needs?  We will meet with them to see what they can do, but I’m not hopeful.

Which grieves me deeply, because I love, love, love this school – a charter school.  I love the teachers – ratio is 15:1, the kids, the method of education and the environment.  It is a protective space that has very, very few problems with behavior.  It’s the only charter Montessori school in the US that goes from pre-k to high school.  The junior high – which my son attends – runs a farm.

Public school is scary to me because of the fact that we live in a district with a lot of problems.  The schools are rough, the academic achievement scores are low, the teacher to student ratios are high.  The schools are huge, and the kids are numbers in a system that lets them fall through the cracks.  He wouldn’t last a week.

There are a couple of private schools that are for kids with learning disabilities, and that may be where we are headed.  They are expensive - $18,000 - $24,000 a year.  Also, they are both about 45 minutes away, so with taking my littles to school, I would be driving over 3 hours a day.  Of course I’m willing to do it if that’s what will help him the most.  

I hate watching him on feel like he’s about to fall over the edge into failure every single day.  I hate that he feels dumb and incompetent, and that he is on the verge of quitting.  And I hate how lonely he is at school, and how he feels so self-conscious all the time.

There has to be a solution to this – and I’m going to find it.

Tuesday, January 25, 2011

Responses and THANK YOU!

First, I want to thank everyone who took the time to write comments, respond on a Yahoo group or send me an email.  I received over 50 responses, and have read every one of them.  The opinions have been overwhelmingly supportive of changing his age, and there have been many suggestions ranging from contacting his foster mother to changing his age by just one year instead of two.

The responses that were not in favor of changing his age all made some excellent points, and I appreciate them greatly.  Definitely things to think about!  One person said that changing the immigration paperwork is next to impossible, another was concerned about the special education services he might lose if he suddenly starts doing better in school because we changed his age, and several people were concerned that he might enter puberty earlier than his peers.

Based on the questions and suggestions I’ve received, I’m going to work on the following:

1. Talk with my social worker and ask if she has experienced this before, and what her opinion on it is.
2. Contact Declan’s foster mother in China and ask her opinion on how old he was when he came to her
3. Research how to change the age, and if changing the immigration paperwork is necessary or if we can just do the birth certificate
4. Speak to the special education staff at his school about services.  He is partially hearing impaired, so his IEP won’t go away even if he starts doing better academically, but I want to know the possible ramifications if we do this
5. Call the pediatrician and discuss puberty question, as well as his opinion on changing Declan’s age
6. Contact the county court to find out the steps for applying for the birth certificate with a new age
7. Continue weighing the pros and the cons and make a decision within the next few months.

This is a huge decision, that will have possibly unforeseen consequences.  We need to be able to justify our choice to Declan in the future, but we also need to find a way to describe it to him now.  My gut feeling is that he will accept it fairly easily.  He’s just that kind of kid – he deals well with change, marches into his surgeries with courage and a smile, and will try something new with very little coaxing.  I hope that his natural resilience will allow him to move on confidently with a new age that makes him younger than Eva.

On another note, I started this blog about 6 weeks ago to keep friends and family posted about Eva's "surprise" heart surgery, and have already had almost 4,000 visits.  Thank you to everyone for being interested in my family and especially to those who have commented and sent me email!  

Today Eva took her yearly ELL (ESL) test - I took her in for an hour to get it done.  She still receives services, even though she's reading above her grade level and has a great vocabulary.  That test must be HARD.





Last night Christopher taught Eva and Declan how to cut french bread.  




Tomorrow’s post is about my oldest son, Brennen, and his experiences lately in school.