A Support Community for Moms

Category: FAS

An Exclusive Club

I ran across this introduction by an adoptive mom that has joined a Yahoo Post Adoption Support Group I’m in. Have you ever been tempted to judge an adoptive parent of a child who has FAS? Do you think they are somehow responsible for the behavior of a child who has been damaged by their birth parent’s drinking? Do you think you could have done better? Have you ever wondered why it is that even though you have taught your adopted child how to live right they totally ruin their lives with bad decisions once they are out on their own? Well, welcome to our club – the Adoptive Moms of FAS Kids Club. It’s exclusive club. You have to have loved someone else’s child and been ostracised because of it to join.  

Our questions may never have any answers, but God knows that the parents of these kids have been faithful and are not responsible for damage done way before they came on the scene. That’s really all we do know for sure – God understands and knows. Well, maybe there is something else we know for sure. Others who haven’t adopted and raised a child with FAS don’t understand and don’t know. Am I bitter? No. God has taught me way too much to dwell on the ignorance of others and to let it affect my view of myself or God. Am I disappointed? Yes. I am disappointed for this adoptive mom – that she’s not supported or helped by those who ought to care and have the resources to help. BTDT!

Here is Mrs. Smith’s introduction:

I am an infant mental health specialist, certified teacher ART k-12 and general ed K-8. I have a Master’s in Early Childhood Education, and specialist in FASD [A term used to identify damage to a child because the mom drank alcohol while pregnant] issues. I’m on the state’s FASD Task Force as a parent, but previously as a professional I was the coordinator for Wayne County’s FAS Awareness project. I live in the Ann Arbor area. I adopted 2 children from foster care…. long story but I am a single parent…. I became involved in foster care when I decided to participate in a grant to take in drug-affected infants. That must have been about 16 years ago, because my son is now 14.

Yes, my ds [dear son] was my first infant I took in on the grant, 3 days old from the hospital. As an infant mental health specialist I worked hard on the attachment piece. The attachment had a bigger impact on me that I expected, and when his birth mom’s rights were terminated at age 2, I decided I would adopt. About 4 years later I decided to adopt one more. That is my dd [dear daughter], who is now 9. Interestingly, my son looked good at birth, full term, full head size. Only “alleged” drug use. My daughter, on the other hand was premature, low birth weight, tested positive for crack and came out swimming in alcohol. Guess which one has the brain damage. My son! Go figure. This is one of the big mysteries that surrounds FAS. We know that of twins both exposed to alcohol, one can have the syndrome, the other not. We know that brain damage can be just as substantial with the facial features as without them! Kids with an average IQ, like my son, can have the same serious brain damage as a kid with low IQ, but people don’t recognize it as brain damage because of his IQ, and hold him culpable!

Ah well, enough preaching!

My son has been in residential for 2 years, supported by adoption subsidy. I have been facing threats of neglect charges for almost that long. I have come to understand that this is not uncommon in Michigan post adoption support services. It is sad for the parents who try so hard with the state’s most difficult kids. It is sad for the children who, through no fault of their own (i.e., alcohol and/or early neglect), must be abandoned by the state if they cannot be “fixed” within a time frame, or look like they will need a life time of support. I want to work with the state to find solutions to this problem. The solutions need not be expensive, but must be practical. “Punishing” parents won’t help. In fact, it will deter “good” potential foster/adoptive parents from considering the state’s children. It is a lose/lose situation. Let’s work to discover the “win/win.”

Adoption Drama – a Story of One Woman’s Difficult Journey

Here is a blog I just read this morning. I spent an hour reading it from back to front (blogs post the most recent first, and then you become so intrigued you keep hitting the back button to see what preceeded it). If any of you wish to read a story very similar to ours, please check this blog out. After you read it, spend some time praying for this woman. I could have written 99% of her story and put my name as author – it is so much the same as ours. Though I am so very sorry for what she’s going through, it was strangely validating. If you truly want to understand the plight of a family who has adopted emotionally impaired children, please read Adoption drama…. “The System.” I’ll start you from the beginning posting so you can read it in order of occurrence. 

The sad thing is, there is no answer. We are adrift in the sea of fear and regret. Only God knows…and those who have lived it.

Possible Way to Diagnose FASD

Here is an article about an eye exam that that could possibly diagnose Fetal Alcohol Syndrome.

14 Year Old John’s Therapist

This is a sample of what “Mrs. Smith” encounters when she attends a family therapy session at the residential center that houses her son, John, who has FAS. If it weren’t so ridiculous, it would be amusing. This is why some of us whom have adopted FAS kids do not seek out help. 

I am updating you all, thinking that you will be in a position to appreciate, in a special way, this particular segment of my FASD odyssey.

I just got a copy of the treatment plan they (John’s residential program) “forgot” to give me in September.  These treatment plans are always a good read, if you have a sense of humor.  They have ratings and give scores for areas they consider important to the treatment of the child in the residential facility.  They rate the child and his progress.  They also rate the family.    Each facility seems to have some variation of this basic “treatment plan” which they are required to write and submit every 3 months to the adoptions subsidy dept. [who pays for his residential treatment and housing]. 

This time I was rated high in the “social support system” category (a +2).  I guess they figure I must have some support somewhere if I could pull off getting him funded for another 6 months, but my ratings went way down in the “parenting skills” category.  This time I got a -3 (improvement needed). In “communication/interpersonal skills” I got a -2  (limited or ineffective skills).

Why have my parenting and communication skills taken such a sudden drop?  The answer is: the therapist has uncovered the “real”  problem in this case – John, a relatively normal, impulsive child has a mom who does not “believe in him.” Their assessment rates me in various other ways, if you’re ready, here we go:

intellectual capacity: 0 (average or above average)
literacy: 0 (literate)
resource management: +1 (strong money management skills)
sexual abuse: -2 (failed to protect child from sexual abuse)

But here is where we see the real “new insight” the therapist has come to (as listed under the family strengths and needs assessment section:

“…It is clear that he (John) does have problems.  However, all behavior occurs within a context.  The context of the interactions between John and Ms Smith are becoming clear.  There are some significant communication problems.  In addition to this, there seems to be a problem in the relationship….” and on and on.

Under the “parenting skills” (-3) section we get to the crux of the matter:

” ….the parental relationship will be addressed in family therapy to address this issues so that the underlying skills “(my underlying basically appropriate parenting skills)”can again be used.  In addition, some new skills and specific interactions for John could be learned.  The issue related to John having FASD is one such problem.  It is clear that John has some brain damage and this is probably related to his in utero exposure.  However, this does not have to scar him for life and he can retrain his brain.  John has picked up on some of her negative views.  This has been addressed in family therapy and will continue to be addressed with Ms Smith individually as well as between her and John.”   

So if we can read between the lines here we see that John’s main problem is that his mom thinks he has a brain problem that will scar him for life.  She has subtly communicated this to him, and this has caused him a real problem that underlies all his other behavioral problems.  When this gets cleared up, his behaviors will improve.  His wounds from this parental mistreatment will be healed. When Ms Smith comes to her senses and recognizes that John has a mild form of FAS that can be overcome, stops sending him negative messages, and start “believing in him,” then all will be well.  Mr. Therapist will work therapeutically to enlighten Ms. Smith and, if successful, major family issues will be resolved, John’s behavior will be impacted in a positive way, and he will be ready to be reunited with his family.       

Mr. Therapist met with me privately before last Wednesday’s family therapy session and began is “therapeutic work” with me.  Finding it somewhat difficult to sit through this “therapy,” I took notes, just to be sure I was not misunderstanding his intentions.  Although Mr. Therapist became somewhat heated and loud at times when I asked my questions, I was able to maintain my composure most of the time, though my pen did slip once or twice.

I will only quote highlights:

Mr. Therapist:  “You are only just focused on FASD and its limitations” 

(I, who have advocated for FASD strengths possibilities publicly for some time, sat calmly, and kept smiling… using my listening skills learned as a therapist) 

Mr. Therapist:  “Yes, there is brain damage from FAS, from trauma, from abuse, it is all damage to the brain.  Other parts can compensate for the damaged area.  There is nature and nurture.  Down’s syndrome, autism, that is nature, that is genetic.  FAS is not genetic, it is environmental, in the womb.  You, Ms Smith, see it as all nature, and think it can’t change.  Other areas of his brain can compensate for the damage.  You need nurture.”

Ms Smith:  “So, did you get some special training on FASD that I am unaware of?  I haven’t heard of this FAS teaching.”

Mr. Therapist:  “Yes, I had developmental psych in college.  I know all about FASD.”  

Ms Smith:  “If you’d like some more up to date FASD information, I can get you connected with FREE training provided through the State.”

Mr Therapist: “We don’t need training.  It’s not going to help because we already know, and it won’t have any direct impact on our treatment for John. “

Ms Smith: I find it interesting that after 6 months John is on level 3 in talk therapy, and is just now getting to level 1.5 in his behavior on the unit.  Can you help me understand why this is the case?”

Mr. Therapist:  “Well, yes.  This is because he came in to us at such a low level of functioning.”

Ms. Smith:  “You mean, like he started of at a -3?  And this would be as a result of his home environment?”

Mr. Therapist:   “Yes, that, and at [his prior foster home].”

Ms Smith:  “So, just let me clarify if I am hearing what you are saying.  The problem is mostly environmental.  You can address that here, and get good resolution with my cooperation.  Any FASD issues are minimal, and can be overcome.  And you don’t want any free training from the State to bring you up to speed on FASD, because you don’t need it.

Mr. Therapist: “yes”

Hope you enjoyed reading this entertaining saga…to be continued.

We are all on a journey!

I fully intended on just publishing this and not commenting on it, but I just can’t! I have no formal training on FAS, only personal experience, but apparently that is much more than this “trained” therapist has! No, this boy doesn’t act out because of her mother’s negativity or her focus on his FAS. He has FAS – brain damage – and all the negativity or positivity in the world will not change that. He is who he is – HELLO!

I have never once discussed FAS with one of my sons who has behaviors just like John. Her emails about what her son’s actions are like could have been written by me about MY son. I have never one time set limitations on what my son could accomplish or discouraged him from setting realistic goals just like anyone else who doesn’t have FAS. We have never treated him like he has a disability, and if you didn’t know him well, you’d never know he has FAS.  Yet, his behavior is the same as John’s. So explain that! How about we fire all the therapists and hire all the moms who really know? I especially was appalled at this statement made by the therapist: “Other areas of his brain can compensate for the damage.  You need nurture.”  

Uh, no you can’t! While it is true that FAS kids can learn skills and new ways of doing things, it is NOT true that you can ignore or wish away the alcohol damage. Everyone in the world, except apparently this therapist, knows that alcohol damage is forever and all the nurturning in the world will not change that! This man needs to quit his job and take up gardening – he needs to nurture plants far away from our children who need real help.

 

 

A Little Background on 14 Year Old John

An email sent to me from Mrs. Smith…
I adopted John at birth, 3 days old through foster care. I attended an FAS training, for professional purposes, when he was 2, and began seeing the unmistakable “red flags” that said he might be alcohol affected.  I’m a teacher by my training and experience, so I knew “normal” and what was outside the normal.
He had trouble in school, so I began homeschooling him at age 7.  He was diagnosed officially at age 8.  He is FASD….. has a normal IQ, and looks and acts for all the world as normal,or “very bright” when you first meet him.  Therapists have a hard time thinking he’s not “normal.”  He talks very well, and his thinking problems do not appear until you see him in action over time. 
 
He became increasingly hard to manage as he grew up.  I placed him in as structured a school program as I could find for 4th grade when he was 10, he went into residential treatment after being twice suspended and removed from his charter school, at the age of 12….. in the middle of his 5th grade year.  He’s been in residential since then.  He is now 14.
 
He is a physically strong and healthy young man.  He can cook, follow directions well, and is great at chores.  He planted and cared for a garden 2 years in a row.  He is a great yard worker, and landscape worker.  He has potential he can use.  He is sorry for his bad behavior in the past, and wants to grow up and do good in society.  I am very interested in the new farm idea being proposed here for FASD young adults.   I am hoping he can be part of that as it develops.
 

Neurobiofeedback for Children with FAS

Click here to read an article on a possible treatment for FAS or ADHD. Ther is also an article about a personal family experience with the neurobiofeedback treatment by Carol Cole.

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