Tag Archives: inspirational

Late Bloomers!

I love my garden. The cooler days of fall have left me longing for fresh winter blooms as my summer selections faded.  However, last week I noticed fresh new blooms on one particular hydrangea plant.

My hydrangea have the potential to bloom through spring and into summer but usually give one large show in May and then swiftly fade away. Yet on one plant there are five fresh blooms in September!

I had not done anything in particular to this plant to facilitate such a thing and I wonder if that is why it bloomed. It may sound crazy to some but God talks to me in the strangest of ways and I believe my perfect powder blue blooms are there to ease my doubts and fears about those things so completely out of my control.

Sometimes parents try to manipulate and prod their children to perform based on outside expectations. In my own experiences with autism I am very guilty of this as well. However, God holds the perfect timing for everyone and everything right down to when flowers bloom.

Some flowers bloom early and are killed off by frost. Their timing isn’t just right and they fail to enjoy the full luster of their season. Others bloom later than expected and instead of becoming lost in the multitude of blossoms, they are showcased all by themselves, standing out that much more because they did not conform to an expected schedule.

My singular blooms wouldn’t have caught my attention if mixed in along dozens of others just months ago. Yet, in their solitude I can appreciate each and every one. I can appreciate them so much more because they were not expected.

I am now at peace that my many personal expectations will not be met on my time-table but on God’s instead. I have finally learned His timing is always perfect and it makes the miracle that much more. More amazing! More appreciated! More marvelous!

My new blooms remind me that timing is relative. I don’t have to get myself frantic and panicked when my kids (or other things for that matter) aren’t moving along when expected, especially on someone else’s schedule. Schedules can be arbitrary.  Growth charts, developmental analysis and mainstream medicine don’t have the Ultimate say in my eventual outcome.

Only God’s timing, which is always perfect timing, is all I really need.

Autism has taught me that, though I admit I can sometimes forget. God gave me my late bloomers to remind me that He is in control and that oftentimes the most pleasant surprises come when you aren’t expecting them at all.

I’ve seen my fair share of miracles and am yet hopeful for even more! At times when I’ve feared my kids were losing ground or were at a standstill, their eventual and accelerated growth was even more so celebrated!

We are all too some extent liken to plants in God’s great garden. Some people bloom quickly only to fade away just as fast. Some are slow to mature only to later bring sustained and dependable beauty. And now and again there are those few plants over to the side that don’t appear to have that much going on, but when you least expect it and out of their scheduled “season” will shine and stand out among the rest!

I have relinquished to God my expectations of time. Autism has tempered the “control freak” that once consumed me.  I cast my cares over to God and allow Him take them from there.

I can now pray, prepare and wait with expectation instead of frustration.

My faith has not failed me and God’s grace remains unending. I have a confidence and peace that I cling to as I travel this adventure in autism.

Just like my flowers, I am surprised at my miracles that “bloom” unexpectedly and out of season, yet their sweet reward makes me appreciate God’s grace that much more!

Autism in the Headlines: part two

My last post on this subject revolved around the attempted murder and suicide in one Michigan family. Weeks before that story hit the headlines another family attempted to do the same.  However, that child did not survive.

Again, there are elements to that story that I’m sure will come to light later. Regardless, a life was lost. What is most unnerving is the unanswered question; could this tragedy have been prevented?

Parade Magazine ran a story in April about one particular family and how the costs associated with treatment for their child was an enormous hardship on that family. As a parent I also investigated the costs of schools in my area that offer the kind of teaching and support beneficial to children on the spectrum. The costs for specialized schools in addition to therapist visits and other treatments are mind-boggling. They are way out of reach for the average middle class family, even those that do have health care coverage.

Some states do not require insurers to cover the services our kids need. I find that appalling since these same companies have no qualms collecting increasingly expensive premiums. Most health insurance companies in America are extremely profitable.  Insurance companies increase their profits by minimizing services. Most companies claim they can’t afford to cover crucial services for autism patients. I argue they can’t afford not to.

Pay now or pay much more later.

Preventable health care services and screenings have proven to save money when compared to the cost of not providing such preventive care. I suggest Autism is no different.

Study after study indicates that early intervention does wonders if not miracles. Even small increases in communication and cognitive skills can make a world of difference in the quality of life for not just the patient but the parent as well. Access to services and therapies may offer the support some families need wherein the absence of these same resources only ignites a smoldering environment that is quick to burn.

I certainly don’t have all the answers but I do have a few questions.  How is it that insurance companies can choose to exclude coverage for certain diagnosis, especially when it was not a pre-existing condition? Many families have paid thousands of dollars in premiums only to have their insurer close the doors they need opened the most.

One commenter on a blog suggested that parents of autistic children are screened periodically as well as their children. I don’t know if the comment was intended to be sarcastic or not but in the wake of recent events, if it can save some lives, it may not be a bad idea.

Autism can be financially devastating and psychologically grueling for both parent and child. We have children losing their lives and not being allowed the opportunity to live up to their potential. Society is failing them. I would think heightened awareness would push people in a positive direction. Unfortunately increased awareness cannot erase ignorance.

Again from the headlines, one Canadian family had to endure hate mail from a neighbor.  Is this family not dealing with enough? At this point authorities still have not found the perpetrator. The family is forced to live knowing an unseen threat lurks nearby. Thankfully, other neighbors rallied around the family. But can the damage of the offender really be undone?

There are also unscrupulous scoundrels in healthcare who would take advantage of the uptick in ASD diagnoses to sell their treatments to devastated and desperate parents. Many families have paid thousands of dollars to receive only broken promises. These are not disposable dollars. Some parents are losing their homes, sacrificing the needs of other family members and clinging desperately to sanity all while trying to do all they can with what they have.

Autism is crushing families and now people are taking sides. It pains me to see such decisiveness when it requires all of us working together if we are going to overcome the challenges posed by autism.

Our kids are not disposable. We must be their voice. Yet, others will not listen if we are turning on ourselves.

Some would say autism is not their problem. I argue, oh yes it is. The numbers are increasing, alarmingly so. The upcoming change in how autism is defined within the medical community will surely have an effect on just who qualifies for what available benefits.

Treated or not, these kids are not going anywhere and will become integrated members of society. Our society benefits most when our kids get the care they need early so they can become adults living to their highest potential.

These recent stories in the news have had me in tears and I don’t cry easily. I have prayed and cried and prayed some more. I am grateful I have not had to endure the circumstances of others but I don’t delude myself into thinking that I am in no way unaffected.

This financial, emotional and mental toil is not isolated to autism. I have read several articles about children with other developmental issues and even elder abuse due to Alzheimer’s and dementia having a similar impact on families.

Where does the madness stop? How can we make a difference? I don’t have all the answers but I am willing to listen. I am willing to try.

Are you?

Autism In The Headlines: part one (impact)

Last night as I was skimming news stories on the web, I came across the article about a mother who attempted to kill her autistic child and herself. Furthermore, the article stated the mom indicated her distress on her blog, prior to the suicide attempt.

Having at least two things in common with the woman, I found the blog and took a look. There are over 500 comments on the blog.  Many people took the opportunity to post opinions and comments, some of which were cruel and others just plain ignorant at best.

I don’t condone this woman’s actions by any means, but I’m confident there is a lot more to her story than the snippets distributed through the AP news services.

Autism has an ever increasing presence in the news within the last year. I feared Adam Lanza’s widespread devastation would vilify Asperger’s after the Newtown tragedy in December.  It did heighten the awareness of Asperger’s and its related disorders to many in the public who had no clue or awareness of the increasing prevalence of ASD.

Presently, a family in Michigan is going through its own devastation. Thankfully, the daughter is making miraculous progress.  My prayer is that the mother now receives the medical attention she needs.

Some commenters on her blog spouted off that the mother deserves to die. My question is was she not already  to some extent “dead?” What degree of pain, helplessness and hopelessness existed that the mother couldn’t live in the present, let alone even imagine facing the future?

Mentally fit people do not attempt to kill themselves, let alone their children. We ask how could she?  This mother must have been so terribly broken to the point she wondered, how could she not?

The last post on the blog indicates she was attempting to get her daughter the help she needed. This mother, obviously, was very much in need of help as well.

I read a few of the posts on her blog. The frustration is evident. Her road in parenting is far harder than mine. I can’t even imagine her daily routine.

I readily admit I can’t comprehend how she could have attempted such a tragedy and I’m grateful that I can’t!

Yet, I have no doubt that there are people reading her story with empathy for her and an understanding of how she felt.

Autism and its related disorders are affecting more and more people; there is no doubt about that. Just how much so is a question waiting for a definitive answer.

Some parents of ASD children are at a loss and shut down, often oblivious or indifferent to the consequences of leaving the child without resources that not only benefit the child but also minimize certain behaviors, especially those behaviors that can potentially harm others.

Some parents shut down because they can’t face the diagnosis, and especially so when they are forced to do so alone.  Many kids are cast aside (and I’m not just talking about ASD kids here) left to the tether of video games or solitary behaviors that isolate them from people who don’t want to be bothered and that can sometimes incubate destructive behaviors.

Some parents shut down in denial, not wanting to accept a less than perfect child as their own, let alone admit a problem to anyone else. They may gloss over issues or ignore the “quirks” in their child. Yet, failure to recognize or address the situation certainly minimizes the probability for proper medical and cognitive care unless there is outside intervention.

In contrast, other parents and guardians are so overwhelmed with trying to provide everything possible for their kids, they break down. Their kids may be violent and require extensive services the parents don’t have the resources to offer. These parents are often drained from their daily duties there is little energy to fight for the scarcity of resources available from social services. These same people are often struggling with several “crisis” situations all at once, trying to provide for other children and God only knows what else.

I noticed on the mother’s blog how many commenters were confident they had all the answers. I wondered how these people could be so knowledgeable when there are seemingly many unspoken questions.

It appears this mother spent the last fourteen years caring diligently for her child. In addition, there are other family members in this picture to consider. Only that family will ever know the toll ASD took on them and is still taking…

Many commenters blasted how they would never do such a horrendous thing. I certainly hope they would not!

However, I ask would these same accusers offer encouragement, kindness or even prayer to a parent going through a difficult situation? A situation that can be brutal, never-ending, and overwhelming for everyone involved.

I am certainly not casting stones or providing justification.

I am asking painful questions and suggesting conversations that may possibly prevent this type of tragedy from occurring again.

I work in the health care sector and have the opportunity to see many parents of special needs children going along, taking it day by day with God every step of the way. They will eagerly and enthusiastically tell you He is the only way they make it.

I have also witnessed abusive parents who are aggravated and bitter about the condition of a child, doing little more than necessary to minimize their own inconvenience.

People come to me for advice, that’s part of my job. I try and take the opportunity to encourage those parents who are at a loss or distraught and point them in the direction for the best resources. I also emphasize that parents take care of themselves so they can properly take care of the child. I am willing to share my own experiences. Sometimes it is enough for a parent to know they are not alone on their journey and someone else really does understand.

I remember many years ago feeling alone and helpless. Autism was not a “hot topic” as it is these days. But I have one friend whose grown child isn’t on the spectrum but suffered a great physical disability. Her testimony of how she endures a far greater “hardship” than mine and how she continues to make it through with God, her great attitude encouraged me when I had no one to talk to or lean on.

She didn’t have to say a thing. We often talked about everything else besides our kids. But I looked toward her example. If she could do it and make a very hard role look easy, I could at least try; give it my best, and not give up hope.

Now, I want to be that encouragement for someone else.

It is so easy to say what you wouldn’t do, but what would you do?

Would you offer a hand, your heart, a listening ear or even your prayers?

A blogger I follow shared a great story about how one family paid for the meal of another at a restaurant. There was a family with a special needs child and apparently they were not having a good dinner. The frustration was very evident from the parents.

I have seen parents out to dinner with their kids and trying to make the best of it as other patrons give them the evil eye. Sure people want to get out and have a nice dinner, but guess what, these parents do too!

I’m at a point in my life where I can tune out a screaming child. It’s not going to ruin my meal. Some parents don’t get an “outing” on a regular basis. Often, the needs of a child prevent that from occurring. Sometimes dinner goes well. Sometimes not.

Anyway, the gist of the post is that the waitress brought the paid check to the family struggling through dinner and the benefactor had written on it something to the effect of saying that it takes special people to care for special needs children.

I’m sure that generous gesture on one person’s part was the ray of light, hope or support the family needed right at that time. We have no idea of the struggles others are going through. How often do we gloss over opportunities to do good to others because we are so caught up in our own little world?

Many people glibly say they would take a bullet and die for their child and mean it. But would these same people be willing to take a proverbial bullet daily, one that did not offer a quick and sudden death, but instead rendered such emotional and mental agony than ever imaginable that physical demise looks like a blessing in comparison?

I challenge those commentors to instead of easily saying what they would have done to instead, get out of their own piece of paradise and actually do something that would encourage, uplift, offer hope or inspire someone else. A kind gesture is often all it takes to reaffirm to someone that they are not alone. We can become vehicles that provide God’s blessings when we open ourselves up to give instead of condemn.

My experience with autism has allowed me discernment to recognize some needs of parents of kids with disabilities. I offer encouragement when I can. A lot of prayers have gone up oblivious to the people I’ve prayed for. I don’t always know what God is doing in my life but I have learned to be more aware of what is going on around me and to look outward instead of always looking in my own tiny world.

I was told when pregnant with my oldest son there was a chance he would have Downs Syndrome. I got a very callous call at work with that information and quickly fell apart. Well, the tests were wrong, that bullet was dodged and my oldest is quite a brilliant young man, very well acclimated to his strenuous academic workload, his brainiac friends and the occasional video game.

Having dodged a bullet that with the first child, it really didn’t dawn on me anything would ever be “wrong” with the second. I was going through a strenuous time in my life moving cross country, twice, with one baby and pregnant with another. I prayed for a happy and healthy second child. I had my answered prayer and then something changed…

Lan is still happy, almost deliriously so at times. I have to rein him in so he can “focus” on the mundane tasks in life such as chores, school work, responsibilities and maturity. All of which are highly overrated in his eyes. But he is happy and thankfully a very peaceful child.

Maybe his ASD diagnosis wasn’t about him, but rather me. I have learned from it, grown from it and grown with it. I don’t have all the answers and I’m no longer looking for them. I lost interest in asking God “why” many years ago.

I will say that I am grateful for what God has given me, even with ASD and all its implications never that far off. God is allowing me to manage. Some days better than others but He is with me, I am sure. I pray that He is with all the others, like me, who need Him.

Maybe that’s what this is all about for me. My experiences have taught me to not just pray for my needs, but recognize the needs of complete strangers and intercede on their behalf.

Who knows? I am just trying to do the best I can with what I have like most people. I am turning not to my own abilities but leaning on His stability, a lesson I’m not honestly sure I would have learned at this point in my life if not for my youngest son.

Autism is here to stay for the moment. I am hopeful and prayerful for new therapies, remedies and medical innovation. I’ve seen a lot of things in my twenty-one years in healthcare. I know with God anything is possible. My prayers for a healthy child were not in vain, maybe just not quite answered… yet. Then again, “healthy” is increasingly becoming a relative term.

Autism is in the headlines more and more but I pray for more positive stories and more positive outcomes. Many stories focus on the child. There is an ever increasing need to recognize and inform others of the toil these disorders take on the parents, family members and the community as well.

I can’t provide a cure but can provide a smile. I’m not a psychiatrist. But I can pray. Prayer may not sound like much to some people, but I’ve witnessed God answer some “out there” prayers and amazingly so at that!

Instead, of asking “what can one person do,”   I challenge those who criticize and judge from afar to actually do something positive and find out!

Dont Lose Yourself!

I remember a conversation with my boys not that long ago where I was trying to convince them that I really used to be a fun and interesting person, recalling a long gone pre-kids era. I didn’t see what was so incredibly hard to believe. Instead, both boys looked at me dumbfounded as if horns had grown out of my head.

It took a minute or two bu then it dawned on me. My kids couldn’t believe it because they had rarely seen it! 

My kids are accustomed to seeing me perform my usual maternal responsibilities of keeping them on track and as organized as possible. Or they easily view me from the perspective of my “day job” as mom’s alter ego away from home. These things are easy for them. Fun? Interesting? Not exactly two adjectives readily identified with mom.

Before I was immersed in motherhood, I had a social life, hung out with friends, went to concerts, read lots of books and did fun things that normal people do. Even after my kids were born, I managed to maintain a garden, collect comic books and still pursue my many varied interests.

But somewhere along the line slowly and insidiously more and more of my interests gave way and faded away as their extra-curricular activities swallowed up time. My interests deferred to theirs.

My household was running along just fine. My kids were okay. I could check my husband off my list as present and accounted for. Work? Check. Everything was in reasonable order…but I wasn’t myself. In fact, I no longer recognized myself.

I could only remember the things that gave me joy as faint memories because I had deprived myself of them for so long. Everyone else in my household was moving along just fine, but I was lost. I lost myself somewhere along the way of trying to be everything to everyone.

I’m not quite sure what prompted my revelation but I guess another birthday may have had something to do with it. When I realized that I have probably lived half of my life already, I had a new found determination to actually enjoy my life!

I concluded I was doing myself a disservice by robbing myself of precious “me” time (locked in the bathroom away from the rest of my family would no longer count) and that I was robbing my kids as well.

If my world always revolved around theirs, I would be lying to them. The real world doesn’t operate that way and there was no valid reason to set them up for such an unrealistic expectation. I also realized that instead of smothering my personal interests I could not only enjoy them but also share them with my kids.

My kids now have a vast knowledge of the Marvel Universe. This may not be the most useful information ever, yet it is oh so entertaining as we can discuss super-heroes until infinity.

My oldest son is now a most excellent baker of cookies and cake from scratch. My youngest is a self-proclaimed pizza connoisseur, his home-made pizza is far better than any take-out.  Both kids have absorbed my love of cooking and nearly fight each other in  their attempts to conquer the kitchen.

My kids absorbed my passion for writing as well. They now write their own comic books and graphic novels creating characters and sketching them out. I am now “interesting enough” to consult about plot ideas, themes and costumes!

When we as parents allow parts ourselves to die, no matter how insignificant it seems at the time, we actually kill opportunities to share with our kids.

This decision to not just cast aside my own personal hobbies for my kid’s casual interests gave them a newfound respect for me as a person and not just their mother.

I can’t provide a balanced example for them to aspire to if I lead an unbalanced life. Lingering or latent resentment because I made a choice to diminish myself for the benefit of my kids actually benefits no one.

They don’t need a martyr. The do need a mentally and emotionally fit mother!

God created me not one-dimensional but with layers. I am daughter, wife, and mother each persona with varied facets. We are all gems that when turned toward the sun (or more accurately, the Son) reflect various degrees of light depending on how much we’ve been cut, honed or polished.

Sometimes we need a few cuts to better absorb the light. Sometimes we need to polish ourselves so that our best selves shine. Pursuing those interests that speak to us allow us opportunities to reflect God’s light on others and share His love with those we love.

It is in fact our responsibility to “use it or lose it,” in regards to those talents He has given us (Matthew 25:15-29). For what God has given us is not to be buried but multiplied instead! We multiply our talents when we share with others what we know and have. To bury our gifts is displeasing to God.

Learning that I don’t have to obliterate my own talents under the obligations of motherhood but that I can nourish them and share them with my children, provides them opportunities to learn new things, engage in new adventures and stimulate their curiosity in ways no video game or DVD ever could.

God loves me; of this I had no doubt. I had to re-learn to love me enough to nurture my talents and interests as God intended.

My kids and I now have more things to enjoy together. I have relinquished my role as just their “taxi driver” and relish my role as contributor and participant.

If you have lost a bit of yourself, I challenge you to find yourself and those things once held dear to you. Unearth those gifts, share them and allow them to make room for you!

It still takes a bit of diligence to maintain a good balance between me, them and us but it is well worth the effort.

“Amazing grace, how sweet the sound, that saved a wretch like me, I once was lost, but now am found, was blind but now I see,” 

John Newton

Kids can be…

This week as I skimmed my Facebook page, my attention fell to all the first day of school pictures posted.  Most of these were from my hometown where school starts later than here in Georgia. I quickly noticed the pictures had something in common.  All of the kids going to kindergarten or elementary school wore big smiles and their faces were aglow with anticipation.

In contrast, the kids heading off for their first day of middle school looked hesitant, wary and were marked with trepidation. I could relate to their lack of enthusiasm. I remembered exactly how they felt.

Three years ago now, I dreaded the first day of middle school for my youngest son, Lan. He was so eager to head off and join his brother in middle school. I, however, was a nervous wreck!

I didn’t share his enthusiasm of starting that next chapter of his life. Every other moment, it seemed, I found myself immersed in yet another news story depicting the callousness of kids today. Facebook nightmares. Bullying. Suicidal adolescents that fell through the cracks. My head throbbed with thoughts of everything that could go wrong. The overwhelming thought that hammered away in my mind was that kids can be so cruel.

My oldest son already attended the school and unbeknownst to me dealt with his own bullies the previous year. I just found this out months ago! This finally explained why he was hardly inclined to look after his brother. Cam was worried about himself! Sure enough, not even a week passed before a boy stepped in front of Lan and started questioning him.

A funny thing, or rather a blessed thing occurred then. One of the neighborhood kids stepped up to the perpetrator to defend Lan before the kid could get all of his words out. Kennedy’s defense of Lan set the tone that he was not to be harassed. With no prodding on my part, the other neighborhood kids also watched out for him throughout his three-year tenure in middle school.

Ramone in particular, would even let me know when major assignments such as science projects were due. Lan habitually would neglect to tell me of such pertinent information in a timely manner! In a day and age when most kids entering middle school were striving to get in the “in crowd” a good number of kids reached out to Lan and considered him their friend.

Lan’s confidence increased. He stayed after school to take part in art club and comic book club. He wanted to socialize. This was a major accomplishment!

Lan worked hard his second year of school to earn a place in the “A” band with all of his friends who were honor students. He wanted to go to Festival and compete just as they had done the year before. He set a goal, worked hard and achieved it.

I learned of many kind deeds well after the fact. The first day of middle school I fought back tears. Upon his eighth grade graduation, I let them flow.

In the last days of school, Lan’s principal saw me and asked if I would be attending the awards ceremony. I’d always done so for my oldest, a high achiever, and would do so for my youngest as well. Lan had just mentioned the day before that he did not think he would get any awards. He was rather sad about it. I told him it did not matter, not to worry and instead enjoy all the end of year activities with his friends.

Well, as my husband and I sat in the bleachers with the other parents, the principal began to explain a special plaque awarded each year. The Mandy Young Award is given annually to the eighth grader that overcomes some difficulty with a good attitude. When Lan’s name was called, he quickly made his way up front, especially so, for someone not expecting anything!

The gymnasium erupted in applause and kids stood chanting for him! Lan waved his hands to the crowd as they cheered, as if he were the president or some celebrity. It was quite the sight. I would have laughed if I hadn’t been crying.

Landon not only survived middle school, he thrived! Once again, a single thought hammered through my mind.

Kids can be so kind.

Letting go…

After dropping my youngest son off to high school this morning, I pondered, “at what point along this path did I gain peace in regards to letting go?”

I am not at all suggesting that I have given up on his development or have relegated myself to the status quo. Instead, I sit here in a rare moment of silence realizing somewhere along the way I finally let go of the frustration and worry that continually dogged me with every decision I made.

I still think about decisions I make, commitments I have and how they do revolve around the needs of my kids, yet the desperation I once felt is no longer there.

Somewhere within these last four years post Asperger’s diagnosis, I have miraculously (and it is very much a miracle) let go of the frustration and implications that haunted my every move.

Part of it, I believe, is the realization that my stressed out state was overflowing onto the other members of my family. They can’t function well if I am running around like a warden and cracking a whip like some crazed dictator. Lan has enough to deal with and doesn’t need the frustration of a “crazy mother” on top of that.

I always worried about making everything the best it could be, nagged my kids to meet set goals, badgered my husband to adhere to the list of commands I deemed crucial, all in my failed attempts to better control my situation.

Autism is such an uncontrollable condition, not always the same on any given day.  Often, you don’t know what you’re going to deal with before the day is done. A broken leg is simply a broken leg. You suffer through it, work around it and eventually it heals. Unfortunately for us, autism just isn’t that simple. Its intangible characteristics don’t have clear boundaries, often transforming, evolving and changing us as well….if we allow it.

Somewhere along the line I decided to stop allowing Lan’s diagnosis run all over me. He was doing fine. I was the one socially and mentally imprisoned. I’m not sure when it happened, but I am extremely grateful for the transformation. I finally managed to accept the peace from God that I’d been praying for. It had been there for the taking; I just wasn’t smart enough or mature enough to take it!

We will never see how much God will do until we admit to ourselves just how little we can do within our own power. I’ve witnessed miracles both great and small. Sometimes it is the smallest ones, like a good grade on a quiz or an awesome picture he draws that bring the greatest joy.

In the past, I was always looking ahead to meet some goal, get him through the school year, develop a certain skill, or make him responsible that I often lost sight of the present. Lan has a certain catch phrase, “what’s wrong with that?” which is his usual response when I scold him about doing something I think he shouldn’t be doing.

Well, the mad tyrant that possessed me for so long subsides as I decide more and more often that there is nothing actually “wrong,” with the behavior I berated. Lan’s behavior for my over-correction was never anything crucial or disrespectful. I would often chide him for things I would find silly like dancing in the middle of the floor to his own internal music or devising some crazed concoction he deemed to be lunch, usually the very sight of which made my stomach churn.

I have realized Lan is often correct and sometimes there is “nothing wrong.” He may not do things the way I would them but that’s okay too. Letting go and allowing my child to express himself (within suitable boundaries, I’m not that far removed from my old self!) allows me the freedom to stop trying to control his every move. The release of my iron grip allows me to breathe a little and actually relax.

There was one point in my life where I don’t think I relaxed for years. I was in survival mode and it is very easy to stay there if you aren’t careful.  The challenges of parenting, in addition to all the other stuff life threw my way, kept me very much on the defensive. The problem with my survival mode was that it became permanent and not temporary.  I was always trying to anticipate and manipulate the future. This frantic and desperate state left me hopeless to enjoy my present.

In my quest to make everything “right” I got overzealous and failed to appreciate some of the strides made, large and small. But I’ve gotten better for not only my sanity but his as well. I was actually able to let go enough for Lan and his brother to fly up to Maryland and spend a week with their grandfather this summer. It was only a two hour flight but it may as well have been a world away.

I received an email from my father-in-law this morning describing how he enjoyed the kids’ visit and how they did just fine. My world didn’t break in two while they were gone. Lan had a wonderful experience with relatives he rarely gets to see. Letting my kids go it alone, without me, wasn’t easy.  However, it was certainly good for them. Some things cannot but taught. They must instead be experienced.

My child is now very proudly in public high school among his peers. He practically runs from the car to get inside. I will admit I can waver from proud to terrified in any given day. But, I am learning to let go of my fears as well. Cautious? Yes. Fearful?  Not so much.

The previous school years are becoming a blur, having passed so fast.  I don’t want to “endure” his high school years, I want to enjoy them. They too will be gone so soon. Every football game he so energetically cheers for, his fascination with school mascots, his enthusiasm at being part of the crowd, I want to celebrate. I can vividly remember years ago when he would hold his head down and shy away from people. He’s growing up. I’m growing…wiser.

Letting go the vise grip I once held gives Lan and I both permission to try new things and even fail. I don’t have to hold Lan’s hand upon every venture, milestone and accomplishment he seeks to achieve. It is more important that he knows my hand is available; always near, should he ever need to grab hold.