Tuesday, September 16, 2014

Learning to accept myself

A watermelon is 91% water and 6% sugar.    There's your random fact for the day, which was spurred by my 6 year old's question yesterday.   "Why is a watermelon called a watermelon?"


In this family, we are known for being random.    Questions such as the above on are asked every day, all day long.   I've often thought of keeping a tally of how many questions we are asked on a daily basis but I usually make it to around 30 in the first 5 minutes I'm awake and decide to try again another day.   Cycle repeats.    Toys bought for holidays are played with a few days then tossed into a pile of Rubbermaid tubs in the corner of the room.   Tablets have new apps downloaded every five minutes because the oldest child has more of an interest in working a computer than playing anything on it.   Middle child plays pretend ALL. DAY.     I mean it, all day.   We've had an imaginary pet, Wilbert, for over a year now and he has had 20 babies, some of which are named Mushroom, Muffin, Blaster, Tiki, and CeeCee.   Just today I've been the sidekick to "waitress", "news reporter", "beauty salon", "mailman", driving in a pillow car, been on a picnic in the hallway, and I'm sure I'm leaving a few out that I wasn't only partially conscious of because my brain started to shut her voice out while I dreamed of a hot bath and bedtime.   My youngest is 20 months and on a hitting streak, drew on my hardwood floor with a black marker and crumbled up pop tart throughout the entire house.  Let's be honest.   8 years ago I would have been horrified by the way a house like mine functions.   Now, here I am in this moment and in this moment I realize that I need to embrace who we are and not who I imagined we would be. 

Something has been happening to me over the past few months and I cant quite put my finger on the cause of it.   I'm almost 30 so is this maturity that comes with age?   Am I finally finding my place in the world and less concerned about the thoughts of others?   Am I so tired from being the mom of three amazingly smart, energetic, intense children that I don't have the energy to worry about what people think of me?   I'm guessing it's a little bit of all of those things wrapped up in a package that I feel like showed up as easy as a package on my doorstep does.    One morning I opened the door, felt the fresh air on my face and a peace come over me while an inner voice spoke to me.   "You are just fine the way you are.  Stop hiding your uniqueness just to blend into the crowd so people won't look at you.   The only person suffering from that is yourself.   How can you teach your children to accept and appreciate the differences in people if you can't accept your own?"    I suppose that's what they mean when they talk about finding yourself and I have to say it's been a long time coming and it feels pretty amazing.    The qualities and traits I absolutely love about my children are some of my very own yet I feel embarrassed about them coming from myself.  One of my biggest goals of parenting is to teach my kiddos how to love who they are from a very early age and here I am almost 30 and can't even do it myself.  

So, this year for my "teach myself something new for my birthday" idea, I'm going to work on loving myself.    I have a lot of work to do but this is a start.    So what if I am random and can't stay on a topic longer than five minutes?   Does it really matter that I like to paint every room in my house at least once a year, sometimes more than 5 times?   Who cares that I get so bored I can't really repeat a craft I've done more than a few times because it's not a challenge after that?   These are the things that make me, ME and I need to celebrate them rather than hide them because after this many years of friendships there is one thing that is for certain---you cannot change who you are.    You can hide it to fit in, but you sure can't change it.    You are blessed with the children you have and they probably won't be anything like the picture you used to see when you closed your eyes and dreamed of your family sitting around a table, eating dinner together, napkins on laps and everybody using the correct fork for their salad.   Life rarely goes as planned----thank goodness.  :)

Sunday, February 2, 2014

"Just" thyroid disease

Lately I have been feeling very determined.   I'm not sure if it's more from closing up the baby-making phase of my life or the fact that this year will bring age 30 upfront in my life.    It might be that I am sick and tired of being sick and tired.    Maybe it's all of the above.    It doesn't matter much which factors are driving me the most, but the fact that I have FINALLY arrived at this platform and hopefully publicly announcing my plan will keep me accountable for it. 

My thyroid disease was discovered in October of 2008, but looking back I believe it started when I was about 8 and I had 2-3 flares of it before it was discovered.   After I had Mason, I was EXHAUSTED.    He slept 12 hours a night from the time he was 5 weeks old, yet I was exhausted, had insomnia, sudden anxiety/adrenaline rushes, hair loss, extreme pain through my body, and a host of other random problems that scared me.    The first doctor I saw told me I was tired because I had just had a baby.   He was 3 months at the time and I told him I REALLY didn't believe that was the problem.   So, off to doctor #2 I went.   This doctor gave me anxiety meds and told me it was probably hormonal fluctuations so I felt okay with that and left with the meds.   They helped slightly, but then I noticed I was breaking out in hives after hot showers, and my clothing hurt to wear.  Every inch of my ribcage felt like a bruise and sleeping even hurt.   I scheduled an appt with another doctor and met my favorite doctor so far in my life.   He put in blood work to be done and I had 18 vials of blood taken.   Results showed I had low thyroid, sky high thyroid antibodies, vitamin d deficiency and vitamin b12 deficiency.    Diagnosis:  Hashimoto's Thyroiditis.  

I started generic synthroid at this point and scheduled follow ups to see how it was working.  I would see him once a month for blood work and each time I'd complain of new symptoms so he'd test me for more possibilities.    Rheumatoid arthiritis, lupus, celiac disease, lyme disease, antiphospholipid disease (blood clotting issues), diabetes, irritable bowel syndrome and I'm sure more I can't remember or pronounce.   My thyroid labwork was within normal limits (minus my antibodies because they never go away), and I still felt horrible.   At this point, I was referred out to an endocrinologist to better manage my thyroid disease.    I went in with a list a mile long of symptoms I was experiencing and was ready to meet this problem head on.    What I got was,  "take 4,000 Iu of vitamin daily, here are b12 shots you need to give yourself weekly, you could have Multiple Sclerosis but we will wait until you show more symptoms of it before we do a MRI.   You are a beautiful young woman, have many babies".   Um, what?!

Having babies is what revved up this disease at this point in my life, so while I wholeheartedly love my children this just didn't seem like great advice.   Plus, who tells a person suffering from anxiety and feeling lost in their own body that they might have MS?   Yes, please let me leave and NOT have panic attacks while I wonder if there are lesions on my brain causing my symptoms and no answers can be given.    Oy. 

I let my general doctor manage my thyroid labs from there on out and decided to seek out alternative treatments.  Well,  we decided to have another baby because like the endocrinologist said----I was young right?  Haha.   After Lydia was born, I felt great until she weaned.   The problems all came back after this point.   Desperate for relief, I had read about new research on selenium supplements and their effects on thyroid antibodies so I added that to my daily regimen and found a good chiropractor to fix my back.   I'd been bucked off a horse 5 years before and had been living with a severely misaligned back for years so I thought this could be a lot of the issue.    Adjustments and accupuncture were my main treatments at his office.   In the time I saw him, he suggested I had chronic fatigue syndrome, fibromyalgia, multiple chemical sensitivity syndrome, myofasical pain syndrome, arthiritis in my back, spondilytes "fixating" two vertebrae together and that living under powerlines was causing all of my issues.    After adjustments I'd break out in hives and shake for about 30 minutes.    He did wonders for my back alignment but I started having exertional headaches and visions problems so I went to see an optometrist.  

The optometrist said that I may have inflamed optic nerves.   I asked what that really meant and she said "a pressure change in your brain is causing it" but that finding that cause would be a needle in a haystack.   I went home in panic attack mode and with a referral to an opthamologist for an ASAP appointment the next day.    Once again, eyes dilated and he said my optic nerves were fine--that that was just my normal, and that he didn't know why I was having so many floaters in my left eye.   It looked like a hair in my eye but there wasn't one.    He told me if anything changes to go to the ER, so the next day when I got out of the shower and my right pupil was so dilated that it looked blown, off to the ER I went.   There, they did a CT scan (because I was not leaving without it lol) and said I was sensitive to the medication used to dilate eyes and for some reason my right eye was re-dilating with heat.    No signs of stroke or brain bleed "but it could be possible that you have blood flow restriction to the back of your head" and it was recommended that I have a vascular study done.   *sigh....*

My thyroid calmed down and I began to feel better about July of 2011.   I was having more side effects from the thyroid medication itself than my actual thyroid so I stopped my thyroid meds.  (big mistake).   One month later, I was "diagnosed" with endometriosis after a surprise pregnancy and another miscarriage, third one total.   That led to me being put on birth control to suppress my cycle and hopefully the endo pain as well.   During the miscarriage, my IBS was so bad I couldn't leave the house for three weeks and a colonscopy was ordered because my body was in total freak out mode.   The colonscopy ruled out anything more serious than IBS and two months later we were on our way back to Kansas.    Birth control made me mentally crazy, and pregnancy helps endometriosis (HA. lie.) so we decided to have our third baby.  

Pregnancy. From. Hell.   I repeatedly asked to have my thyroid treated but because my labs "were within normal limits", nobody would treat me.   In the last 4 weeks of my pregnancy, my blood pressure was 150/105, heart palpitations were so bad I had to lay in bed to handle them, and the brain fog was UNREAL.  I still don't really remember how I ended up to the day before my due date at an induction but I knew she needed out.     A week after I had her I had major bleeding issues,  my blood pressure has been a mess since (it's been over a year now), and I've had skin issues, hair loss, depression/anxiety, joint pain and swelling, right upper quadrant pain,  nerve pain, muscle weakness/stiffness/twitching,  fatigue, migraines, ringing in my ears, pressure changes in my head, etc.    I went to a new endocrinologist and he told me that until I was consistently hyperthyroid/hypothyroid there was "nothing he could do for me" and we could treat my symptoms but not my thyroid.    Oh, okay....I'm sorry that I was under the impression I was paying to see a doctor and not an idiot who read the wrong website on google.    Clearly, I haven't been back to him.

Well, here we are up to date!   I've had NO luck with doctors understanding that Hashimoto's is an autoimmune disorder.   It comes with the same type of "side effects" as all other autoimmune disorders.   It cannot be treated exclusively by giving extra thyroid hormone.  That makes NO SENSE.   You wouldn't treat a patient with rheumatoid arthritis with only ibuprofen, would you?  You have to treat the source of the problem and not the symptoms or we will all end up feeling 80 when we are 40 and nothing will be left of our thyroid or the rest of our organs.   This past week I finally found some information that I feel could save so many people from suffering.   I don't have sites to give since I found them all mobile, but basically the problem in autoimmune disorders is an imbalance of the T-receptors in the body.    T-helper cells are what keep our immune system fighting invaders and there are two sides that need to be balanced--- Th-1 and Th2.     90% of Hashimoto's patients are Th-1 dominant so taking supplements and working towards stimulating the Th-2 side can help to balance the immune system and suppress the autoimmune attack.   This is true for several disorders, including chrons's, ulcerative colitis, lupus, rheumatoid arhritis, sjorgen's syndrome, etc.   There is blood work you can have done to break down the immune system and see which side is dominating your system specifically.   Once this is done, you can research what supplements and/or foods will boost your weaker side to help get you back to where you need to be.  

It's also been proven that upwards of 60% of Hashimoto's patients have a sensitivity to gluten.   The gluten molecule is so close to the shape of the thyroid molecule that it's even been suggested that the body starts to see thyroid molecules as an invader in the same way it does gluten, so that alone can trigger Hashimoto's and make it worse.   It is very necessary to cut gluten out of your diet to stop the extra stress on your gut/body and help stop the attack on your thyroid.    There are thyroid cells in every organ in the body.    If the attack continues, it's only a matter of time before the rest of your body starts to fail as well.    Slowly, and you may even contribute it to getting older and not being as active but it will happen.  

It won't be easy to cut gluten out and I am terrible at swallowing pills, but I am so tired of not having control over my body!   I know I cant cure my Hashimoto's, and there is a genetic predisposition to it so I was born to have it essentially, but I cannot sit back and let it do this to me anymore.   I want to be able to run a 5k.   I want to be able to participate in my kids sports activities.   I want to be able to play rec volleyball.    At this point, I'd really be grateful if I could carry laundry up and down the stairs without my knees hurting.     I'm ready to feel better, and I'm willing to do what it takes.     Please share these ideas with anyone you know suffering from thyroid disease, because I wish someone would have told me them years ago.   


"Take care of your body.  It's the only place you have to live"--Jim Rohn


*chriskessler.com gives a short description on the basics of balancing the immune system for Hashimoto's. 



Tuesday, October 29, 2013

For you ADHD mamas! A glimpse into my world.

Flash back to grade school:   You are in a classroom with a disruptive child.   He can't control his actions, frequently shouting out random words or asking irrelevant questions without raising his hand.   He can't keep his hands to himself, or he stares out the window all day. You can't understand why it's so hard for me to conform to the rules set by the teacher and you grow more annoyed as the year goes on because it's always something with him.   I remember those children well.    Now, I am married to one and raising another (possibly more than one). 

It makes my heart ache to now understand what those children in class were going through when the rest of us sat and tried not to judge them.    In those years, ADHD was not something you talked openly about.  (This is the part that angers me....)  Parents were in denial that their children suffered from the disorder and refused to accept that something was "wrong" with their kids.   They frequently argued with teachers, social workers, psychologists, and general practitioners.   They came up with excuse after excuse why ADHD wasn't what their child had.   There was no way!  Not their child! 

I live with a husband diagnosed with ADHD.    Statistics show that marriage with 1 or 2 partners dealing with the disorder have a much higher rate of divorce.   If I remember correctly it's 70% higher than those not dealing with it.   Marriage is HARDER.  Everything in our house is HARDER.    Miscommunication, lack of short term memory, hyperfocus (which is never cleaning the house), fatigue and irritability from trying to focus, anxiety/depression due to low self esteem from not being able to focus and being upset with themselves that they can't.    He cannot be on time---it is not possible.  If there isn't an alarm set for an alarm, set for an alarm, then it isn't going to happen.   Some days it feels like all responsibility is left for me.   You can see where this can become exhausting.    We have gotten to a point in our relationship where we can laugh about it most days, but it took a looooong time to get there. 

When Mason was born, I knew something wasn't typical about him.   He was bored with toys early.   He was having tantrums due to overstimulation when he was very young.   His hands couldn't be dirty.   He could only use certain sippy cups.    He cried in the car no matter how long we were in it.   (Try a 14 hour trip to visit family with that going on....)  To this day, if you change his routine and don't tell him several times ahead of time he has a meltdown.    There were so many days in my life I worried:  Is he on the autism spectrum?  Does he have OCD?  WHAT IS GOING ON WITH MY BABY BOY???   After my husband was diagnosed and I saw a change in him on meds,  I could rationalize Mason's behaviors better.   He has sensory issues because he is overstimulated because his brain is going faster than his body can handle.    His brain is going 100 different directions and there are only a few outlets for that information and as a 5 year old he just doesn't know what to do about it.    On the plus side, he knew his colors at 10 months and he could write his alphabet at 18 months.  He would sing full songs in the car by 2.5 and he has always been one step ahead of most adults for the majority of his life.   To compensate for all of this I have no choice but to plan steps ahead.   Not 2-3 steps but more like 10.   I have learned in this house that I have to be prepared for any situation/reaction because I don't know what will happen and I want to help him get ahold of his reactions and learn how to deal.

Today was the first day we tried Ritalin with Mason.   Two weeks of being exhausted after school with massive, immature temper tantrums and I knew something was wrong.   He cried Saturday and told me that he can't focus at school because it's too loud.    He's always been his own worst critic.   If something might be wrong then he won't even try to answer it.   He came up to me yesterday and asked me what "1+1+1+10+5" was, but 2+4 at school overwhelms him.   It was today that all of this hit me.   5.5 years later and today was the day I finally accepted that he does, without a doubt, have ADHD.   I keep throwing around the question, "why is it so hard for me to accept?" because I knew that the chances of having a child with the disorder were higher.    I didn't want to admit it because I now have to face it head-on.   I don't get to hide under my covers and wish it away.   I don't get to send him to school and brush off the social issues that come with the disorder.   I don't get to do that because I WON'T do that.    I won't be the mom who refuses to help her son because of what others may think of it. 

There are days that I see the look on other parent's faces and I want to slap them into reality.   My son cannot control his impulses.   If we are at the park and he is excited, he will probably cut in line on the playground equipment and I will be there hovering like a hawk to remind him over and over and over and over and over and over and over not to do it, but he will do it anyway.   When he gets done cutting and finishes playing, he will be upset with himself.   He will know that he cut and he shouldn't have, and he will be so frustrated that he couldn't stop himself that he will have a meltdown over the way his zipper is sitting on his coat on the way home.    So, what do these parents want me to do?   I won't avoid public places because they lack such compassion and understanding of the disorder.  I won't yell at him and degrade him in public because they think I'm a bad mother so I need to make sure they know that I know how to discipline.   I will remind him, probably sometimes in a tone that is too harsh, that cutting in line isn't socially acceptable and he needs to learn how to handle him impulses no matter how hard----even though I know it really isn't possible.    I want to carry fliers to pass out everywhere I go to raise awareness.   ADHD isn't just hyperactivity.  It is a LOT  more.   It affects every person differently, which is why it can be hard to diagnose.  There are actually 6 different types of ADHD.    Each type responds differently to medications, therapy, etc. 

So, here I am.   Today went okay.  Mason did well on his med and I can only hope it wasn't a fluke.  I want nothing more than to see his self esteem flourish and see him reach his potential in all areas of life without having to be so frustrated.   I want to see him outgrow his anxiety when he learns how to better handle the stress of not being able to focus.   I want him to graduate high school, go to college,  have a marriage with a woman who researchs and understands the ins and outs of committing to a person with ADHD, and be there to guide his children if they end up inheriting it from him.   But above all, I want him to know and recognize that the anxiety and worry I went through while he was growing up was because I wanted nothing more than for him to be the best that he could be and I did whatever it took to be his main supporter.   Children with ADHD need support.  They don't need to be degraded and given dirty looks by adults.   They aren't stupid.  They know 100% that they are "different" and they dont need an adult to make them feel worthless about it.    Think twice before you judge a child who you think has parents who "obviously don't discipline or care about their child's behavior" because you never, NEVER know what goes on behind closed doors. 

Saturday, September 28, 2013

A Fresh Start

It's that time of the year again.   In just a few weeks October 16th will be here and I will be another year older.   In the past few years I have been focusing on either teaching myself something new or refreshing my life in one way or another.   Let's be honest--birthday #25 is about the last birthday you have marked by some type of milestone before you hit senior citizen status.   Lower car insurance may not be impressive, but it was at least a milestone!   Three years ago I went back to school to finish my Bachelors in Nutrition Science, two years ago I taught myself to crochet, and last year I honestly can't remember what I worked on.   My best guess would be focusing on making it through the day without my head in a toilet while my two children pretended to lose their lunch as I was.  (Pregnancy #3 was ROUGH, to say the least).   This year my family is complete, we have transitioned out of the Navy and it's been 2 years since my husband's last active duty day, he is finishing his degree and the kids are flourishing.   It's time to set some time aside to focus on myself.


I have been writing this post in my head for the last few weeks, and I will be the first to admit it was much more witty and focused when I didn't have to "say it out loud".   I still can't decide where to start so I will preface by explaining a little about the way my mind works.   For as far back as my memory goes,  I have been extremely empathetic.   Yeah yeah, I know what you're thinking.  "Well, so am I".    No.  This goes beyond normal empathy and makes my life extremely challenging some days.   If I see a boy on the playground get his feelings hurt, I CAN'T quit thinking about him.  I worry about him, worry about what he thinks people think of him, about how he is handling these new emotions that are hard to deal with as a child,  worry about whether he will stop trying to make friends because he now has a slash in his self esteem, etc, etc.   The list goes on.    Every memory I have is tied to an emotion and when I replay the memory I feel the emotion all over again.    Along with this extreme empathy, I also have some unmistakable intuition.  (this is the important part!)  I can tell when a person has a front up and why they do.   Sometimes I know how they truly feel before THEY even do.   It's impossible to lie to me.    I mean, you can lie to me and I most likely won't tell you that I know you are lying, but I know.   Every. Single. Time.    Most of the time I try to ignore these things because 1) I sound like I missed my ticket to the crazy house to most of you, 2) Almost nobody can really relate to me past the surface, and 3) I don't like being this way.    I want to be able to stand up for myself instead of worrying about hurting someone's feelings because before I have even hurt their feelings,  I am feeling how sad they will be when I do!   You can see by this mess that it's very conflicting and I essentially keep my thoughts to myself 90% of the time and avoid a lot of situations because of it.    So, since I don't like to hurt people's feelings and I feel empathy for people even when they have done wrong, this has made a key point in my childhood extremely hard to process and accept.   I have been dealing with anxiety since I became a mom, and I believe it's because the following situation took on a completely different light once I was a mama myself.

From the time I was a young girl I knew I was adopted.   My parents lost a baby born prematurely and were not able to have children so their doctor knew they were looking at adoption.    On October 16th, at 1:29 pm,  I was born at Asbury Hospital in Salina, KS.   20 minutes after my first breath,  my parents were called and told there was a baby available for adoption and they were first on the list.   Sometimes I laugh thinking about the shock on my dad's face at that moment. :)   They accepted, brought me home when I was released from the hospital, and my mom cloth diapered for a week before they both gave up smoking to be able to afford disposables.   You're welcome,  mom and dad.  Haha!   I don't remember asking many questions about my biological parents when I was growing up.   You see adoptive children searching endlessly and tirelessly for their birth parents, but I just didn't have that calling.   I knew my birth mother's name, that she was 16 when she had me, and that she couldn't take care of me so she gave me up for adoption.    I always believed everything happens for a reason and remember thinking that if I needed to go then God would find a way to tell me. 

God knows I am indecisive and read into everything from 6 different angles.   He has never failed to give me a very clear, unmistakable answer to my prayers or situations I have worry over.   That's what I love about Him.   He has always known exactly how I need to be shown something.   People asked me normal questions about being adopted my entire life, but shortly after I started 5th grade people began to ask me if I wanted to know who my birth mother was.   My response was the same every time: " If I need to know, God will find a way to tell me."   Some friends even went as far as telling me that their mom knew "my mom" and she worked somewhere in town.   I still denied this and asked them to please not tell me any more.   Middle school and most of High school was your typical time for a girl.    Volleyball, choir, church, softball, student council, summer classes for college credit.     In High School, in the matter of one year, 7 people I knew died the end of my Junior year to the beginning of my Senior year and most died of cancer.   One was a young boy I had worked with at vacation bible school, one was one of my great friends living in another town over, and one was my seminar teacher.   I'd been on a missions trip with my church when he started having the leg pain that eventually led to his diagnosis.   All of these people inspired me to take on the roll of Chairman of the Youth Relay For Life in my hometown and use it as my Senior Project.   The mother of the young boy from VBS was the city member on the committee and she also happened to be the neighbor of my best friend.    Life was going relatively smooth, until shortly after my 18th birthday......

I'd dug a book out of my back pack and sat down in Seminar for the required 20 minutes of reading time.    At this point in my life I was still early the majority of the time so my desk partner hadn't walked in.  He was 2 or 3 years younger than me and we were very different people.  We were assigned seats by the long-term sub we had, being as how a new teacher hadn't been hired to fill the spot of our recently passed teacher.     As the bell is about to ring, my desk partner walks briskly into class, looks at me and loudly expresses his shock that he knows who my birth mom is.   For the next 5 minutes I am in shock.   He tells me her name, that I'm so-and-so's sister, that he overheard this kid telling his best friend at the basketball game the night before.    I can hear my heart beating in my chest, but the rest of the class is a solid deafening sound of the air conditioner and pens tapping on people's teeth.   Slow motion but fast at the same time.   Stomach rolling, sweat beading on my eyelids, and no breath in my chest.       After 18 years, there it was.    

The next 18 minutes were the slowest of my life.   As the bell rang to signal the end of reading time, I hastily filled out my planner and signed out to go see my best friend.   She was still in seminar so I motioned for her to come out into the hallway NOW.   She knew something was wrong, but when I asked her bluntly if she'd known she spoke quietly.    She had known, but she didn't tell me because I always said I didn't want to know.     I remember signing into the seminars of other friends and meeting them in classrooms for the next hour, asking the same question to all of them, "did you know?" and almost all of them had.    Words can't explain what it's like to be in this type of position.   All my life I had been happy being adopted, and all of my life I knew in my heart my birth mom had done what she thought was best for me.    Now, at the age of 18, the fury inside my heart for someone who chose to expose my life when it wasn't her right was building.    You see, my birth mom is the woman who lived across the street from my best friend.   The woman who lost her son to cancer.  The woman who joined the committee of my senior project.   That same woman who showed up at softball games, volleyball games, and told most of the people she knew who she was in relation to my existence.   The woman who told her son this life-changing secret so he would bring his brother over to my best friends because she wanted me to know him before he passed away.    I often think about the weight that he carried on his shoulders when he was given this secret to hold.    There is always a way to forgive a young girl and understand her decisions regarding giving her baby up for adoption, but it's far more difficult to understand how an adult who "only wants what is best for you" can blow your life apart in a matter of minutes. 

It's been 11 years this year and I am farther from understanding today than I was then.   I thank God often that I am adopted but I cannot wrap my brain around the mother of a child exposing such a secret and leaving said child reeling with uncertainty, making her so vulnerable.   It's what I imagine being thrown to the wolves is like. 

(more on this part of my life and what followed this day next blog.)