Monday, September 18, 2017

Dr. Grant, you have forever changed my life

"River, where are your pants?"

My heart did a little flop as I heard my son's teacher's words to my bottomless two year old daughter.  Every mom knows the sitch: you're in a hurry, you can't find shoes, socks, pants, or whatev's for the toddler, and you are faced with two options.  You can be late, or you can just let your child free style
it like a boss.

Pant-less Hot Mess
So there you are, surrounded by moms and teachers, with a toddler that isn't wearing all their clothes.  Normally, you feel a little embarrassed.  You feel like you aren't as put together as the other moms.  You feel like you're the only one who can't seem to get it together.  You feel like the teacher is thinking "this mom is just a hot mess."  Your spouse gets home that night, and you tell them how embarrassed you were toting a half naked toddler to and from school.

But some of us moms have thoughts beyond those.  Some of us feel more than embarrassment.

My son LOVES his teacher, and therefore I LOVE his teacher, but as those words came out of her mouth, my stomach froze as I thought to myself, "is she going to call CPS on me?"

I know, I know.  You're sitting there, reading this, telling me that I'm paranoid  If a pant-less two year old is child neglect, then they need to lock up every mom that ever lived.  I mean, seriously, in the middle of a Texas summer, it's almost child neglect to put pants ON a child.  Just walking across the street to drop off my son is pretty much torture.  I would love nothing more than to laugh off the embarrassment of being caught with a partially dressed child, but I'm not embarrassed.

I'm scared.

Dr. Grant, I sometimes wonder if you even remember us.  Do you ever sit at your desk and think "I wonder what happened with that five week old infant with the broken leg?"  Or ask yourself if you did the right thing signing an affidavit that our children needed to be taken from our care.  I wonder if it was even hard for you to make the decision, since you did it so quickly.  I was still sitting in a hospital room crying, mere hours after arrival, when that affidavit was notarized.  You didn't even wait for the blood work to come back.

But I remember you.  I think about you everyday.  I remember that you had a baby yourself.  You told me about making your own baby food with a blender so you that you knew what your little one was eating.  I remember that you talked kindly to me as long as it wasn't about my son.  I thought that I could trust you to make his health your top priority.  Yet, as soon as I asked questions about my five week old's broken leg, you would clam up.  The moment I even mentioned that I thought there was something that had been passed down to him by his dad, you shut me down.

Do you know what that's like?  To be sitting in a hospital room with your infant and have every doctor and nurse that comes in refuse to tell you anything about your crying child's health?  The only thing anyone would tell me was that I wasn't allowed to feed him in case he needed surgery.  Surgery.... I kept being told my son might need SURGERY.... yet not a single person would tell me what this alleged surgery was even for.  It wasn't for his leg.  So then for what?

You let me sit and cry hysterically for hours without being allowed to hold or feed my son.  You let me sit in fear that someone was going to start cutting on my child without even telling me what the surgery was.

And then it only got worse.

I have a whole other blog post dedicated to the nightmare you caused me, Dr. Grant, so I won't go into it.  I will say that our lives are almost normal now.  It has been such a blissful feeling.  We are now slowly paying off the massive debt we accrued over those two years.  CPS is no longer in our lives, Charlie no longer has criminal charges looming over him that threaten jail time, and his ex wife had to drop her petition to remove his legal rights to their daughter.  Sometimes, I can almost forget that the nightmare ever happened.

But then someone makes a comment about my daughter not having pants, or the pediatrician mentions that my kid is a little behind on the vaccine schedule.  Or maybe I forgot to brush my daughter's hair and she looks like Mogly from The Jungle Book.  I'm even too scared to post some of the pictures I have of my children on Facebook.  Why?  Because the living room behind them is a mess.

You know that saying that mom's use to comfort each other?  Something like this:
If you have dirty dishes in your sink, it means your kids are being fed.
If you have piles of dirty laundry, it means your kids have clothes.
If there are toys all over the floor, it means your kids have things to play with.

But you know what I learned over those two years?  CPS doesn't agree.  I've read the hospital and CPS reports in my son's case.  The doctors, case workers, AND POLICE write down and take note of the cleanliness and state of your children, you, and your home.  When my home is messy, I don't think "ugh, how embarrassing.  I suck at parenting."  Rather, I think, "what if something happens and CPS makes a visit?"

Dr. Grant, I don't remember if your little one was a boy or girl, but right now, they are three, possibly four years old.  I'm sure you take them to the park and they play and laugh.  You watch them climb up the slide and go down the fireman's pole.  They might even be brave enough to try the monkey bars.  I'm sure you've on more than one occasion held your breath and hoped they didn't fall and break a bone.  But me?  I'm a helicopter parent.  When my four year old climbs on equipment, I have to fight panic attacks.  I try to take slow, even breaths as I wipe sweating palms on my pants.  Sometimes, I tell my wife that she gets to watch her so I can walk away.

I'm not scared of a broken arm, doctor.  Kids play and break bones.  It happens.  What I'm scared of is running into you again.  I'm scared of CPS re-entering our lives.  When I watch my daughter climb on park equipment, I'm scared that she's one fall away from being taken away from me.

Do you know how hard that is?  To live like that?  Do you know how much you kick yourself because you feel like your paranoia is holding back your children, but you'll be damned if you let CPS take your children from you?

I do get that you see some pretty awful stuff sometimes.  There really are parents out there who hurt their children.  I've seen pictures that made me cry.  I know being an ER doctor and seeing these hurt, abused children who can't help themselves must be heart-wrenching.  But that wasn't my son.  He was clean, he was well fed, he had an older sister that was also clean and who was snuggled against her daddy that showed no fear.  No bruises were found on anyone.  And if that wasn't enough, we had TWO experts diagnose my son with EDS, a genetic disorder both were willing to testify can cause bone fragility.  One expert is an endocrinologist who specializes in bone metabolism, and the other is a geneticist.  Know what the prosecution told us?  They said that you admitted you were not familiar with EDS, you acknowledged that we had experts on our side, but that you were still standing by your statement and would still testify against us.

Come on, Sophia, let's be straight.  That's not a doctor that cares about a little boy.  That's a doctor that doesn't want to be wrong.

I always think it's such a joke when I see articles about suing for emotional distress.  How much emotional distress does a doctor or CPS have to cause before it's unethical and inhumane?  Why do I get to live with a specialized form of PTSD while you, Dr. Grant, the Cook's children's ER staff, and CPS get to sleep each night without ever having to think of my family or my little boy ever again?  Why is it up to me to learn how to forgive you when you probably don't even remember me?

I know you won't ever read this, Dr. Sophia Grant, but if you ever do, and you actually are interested in knowing how that little infant with a broken leg turned out, I'll tell you.  He is wonderful.  Thanks to early diagnosis, the EDS is not much of a problem as of now.  He is on the autism spectrum, but I called ECI and he was receiving speech therapy by 20 months.  He's now enrolled in PPCD and spends 3 hours a day in school.  He LOVES it and his teacher is absolutely awesome.  He is already
reading at a basic level and can count into the thousands.  He is obsessed with music and loves to "play" the piano and guitar.  And when that little guy smiles... oh man, I just have to squeeze him super tight and give him a giant kiss.  That grin is just heart-melting.

Life is good now.  We're busy and sometimes overwhelmed, but in the "normal American family" kind of way.  We laugh, make plans, order pizza, have play dates, you know, all the wonderfully normal things that people do everyday.  We do them and it's wonderful.

But don't worry, Dr. Grant.  I'll never forget you.  I'll think of you every time I take a child to the pediatrician, every time one of my children climbs rocks or park equipment, every time they fall face first off the couch.  I'll think of you every time I take my daughter out in public without pants on.

I remember you Every. Single. Day.  I remember you, Dr. Sophia Grant, because you have forever changed my life.

Friday, March 4, 2016

Two Years Later


This picture was taken just a couple hours ago.  I had just gotten home from class, and everyone wanted a piece of mama.  Things have been going rather smoothly the last few weeks.  All three little ones are healthy and doing great.  I'm in the middle of my second semester at UTA, working on a bachelor's in Psychology with an emphasis in neuroscience.  And Erryn's ex was finally forced to drop her case against her due to lack of any evidence to back her claims of abuse and neglect.

Today is still a hard day, though.  It's March 4th, the same day two years ago that we took Zeph to Cook Children's hospital.  It's the same day two years ago that Dr. Sophia Grant disregarded Erryn's medical history and signed an affidavit stating our son was abused and needed to be removed from our home.  The same day two years ago that we were told we were no longer allowed to be alone with our children.

It's been two years, and it's still a part of our lives.  In spite of an EDS diagnosis and two specialists willing to testify on Erryn's behalf, criminal charges are still pending.  Seriously.  Two years later.  I'm not sure how that's constitutional by any means.  She's still on the abuse registry.  Until the criminal charges are gone, we aren't allowed to appeal the CPS's decision of abuse.

Over the last two years, however, I have painfully discovered that we are so incredibly lucky.  Among those that have reached out to me who have also found the hard way that their little ones had EDS or OI, I haven't come across anyone who was allowed to keep custody of their children during their CPS case.  We had the fortune of being allowed to keep the children in our home under a supervisor.  While Erryn was asked by CPS to move out of the home, she was allowed to "visit" at anytime during the day.  Those who have stories like ours were often denied visitation all together, or were allowed one to two hour visits weekly.  Even if a family member is given temporary custody, it is still common for the parent to only be allowed specific visitation monitored by a social worker.

So many moms and dads, parents, lost their little ones and did not get to see them start to crawl, see their first steps, hear their first word.  Erryn and I got to see Zeph grow.  While the caseworker let us take our children home, she informed us that once the case was closed, they were going to take them from us and that we would have a chance to "work to try and get them back."  Thanks to a tip from a friend, we hired an attorney, and CPS immediately backed down, never again mentioning taking our children.  But the fear was still real.  Any time I had a moment alone, I cried.  What would I do if they took my babies away?  What if we were never allowed to have them back?  I still have nightmares about people coming away and ripping my children away at gun point, and it never even happened to me.  I'm a different person because of what we've gone through, and it turns out we were the lucky ones.  How much more scarred and damaged must those poor mothers and fathers be that actually lived it?

Two years ago, our family was nearly destroyed by a rare genetic condition called Ehlers-Danlos syndrome, and the pride and ignorance of a doctor.  Now we're waiting for the poorly named justice system to end things so we can finally finish healing.

Please protect your children.  Know your rights, and know what CPS is and isn't allowed to do.  Know what you do and don't have to say when a police officer speaks with you.  And most importantly, spread awareness that fractures in small children can be caused by Ehlers-Danlos syndrome, Osteogenesis Imperfecta, and rickets (vitamin D deficiency).  I actually read an article written and circulated by a doctor on the internet that said these things do not cause fractures and that doctors who aid parents with court testimonies are assisting abusers.  I can't speak for others, but I know that my son was not and is not abused.  He is fiercely loved.  I've had the pleasure of getting to know some of the other mothers who have also discovered their child had EDS through fractures and abuse allegations.

I feel I need to take a second to say something about these other mothers.  You and I will never cry as much as they have.  You and I will never know just the kind of agony a silent house can truly be.  I have experienced no pain or fear in my life that matched the mere thought that my children were going to be taken from me.  To those mothers, if you read this, know that many of us pray for you daily.  You're not alone, and I know that there are an arsenal of women who have tasted the same grief who are a simple email away.  Keep reaching out.  Keep being brave and telling your story.

As for everyone else; love your children, and know that you are so blessed to have them.

Sunday, January 25, 2015

Thank you!!

My blog on our experience with the injury of our son, Zeph, hit two thousand views today.  I have to be honest, I really never thought it would get that far, and I have no idea what to do next.  For months, I’ve made vague plans on how to raise awareness, only to have my heart broken when I realized that thousands of others like me have already tried, only to not be heard.  There are so many websites and Facebook groups dedicated to attempting to show the corruption behind abuse accusations by hospitals and CPS, so many people who are trying to force doctors and social workers to be held to a standard, only to be told that they can’t discourage a doctor from making abuse accusations, because then abused children would go unhelped.  They argue it’s better to let an occasional family be ripped apart.
   I want everyone to know that in my research, I came across quite a few pictures of legitimate abuse.  It’s devastating to just look at.  The idea that someone could even do that to their child is monstrous.  I’ve seen pictures of children with mutilated genitals, bruises from head to toe, and eyes swollen shut with blood leaking out from under the lids.  I can’t imagine what seeing that in person would do to someone.  Can you imagine working in a field where you see parents come in saying little Timmy fell out of his high chair, only to find cigarette burns, broken bones that had healed, and bruises the shape of hands all over his little body?  I couldn’t see that everyday.  Heck, I wish I could unsee those pictures.
   That said, there is so much damage and hurt done when a child is taken away from good, loving parents.  Hospitals and CPS say that if they make rules to help keep innocent families from getting injured, then abused children will start falling through the cracks.  That’s just simply not true.  Did you know that most of the time, when an accused parent requests their child be tested for an illness or disorder that can mimic child abuse, that the hospitals and CPS will refuse?  There is a family in Oklahoma right now who are in the process of having their parental rights terminated.  They have three children, and the youngest, a baby, suffered several fractures.  OI, also known as brittle bone disease, runs in the father’s family.  They have begged CPS to test for OI, but they refuse, saying that the test is “invasive,” and not in the child’s best interest.
   So… we’re not going to do a genetic test because it’s stressful, but we’re going to relocate all your children.  Because that’s not stressful or invasive at all.  For a government institution or hospital to use those reasons to refuse to test is absurd and alarming.  In what way is being taken from your home and parents better than having a genetic test?  When I was at the hospital with Zeph, they had no problem with asking me to hold him down as he screamed while they did x-ray after x-ray.  And do you have any idea how much radiation is in a CAT scan?  Waaaaay too much.  But they didn’t seem concerned with bombarding my 5 week old infant with enough radiation to turn him into one of the X-Men.
   Children need to be protected.  Child abuse is an evil that needs to be watched for and stopped.  But there need to be rules.  There are too many casualties in this crusade to make it a righteous one.  When you don’t care about the civilians you hurt to get to the bad guys, there is something very wrong with you.
   Thank you all so much for reading and sharing.  I want so badly to protest on the grass of every children’s hospital, to bang on the office door of every politician, to stand on the street corner yelling for anyone who has been hurt by CPS to come stand with me.  But you have to start somewhere, and this blog is my start.  I wasn’t planning on writing anymore; but the number of views I’ve gotten has been humbling and exciting.  Maybe I can spread the word.  Maybe I can save other families.  As long as people keep reading, I will keep writing.  There are so many parents hurting right now, not being allowed to hold their babies, going to sleep in empty homes, waking up to a lonely silence.  This is the side that no one sees, the side that maybe I can bring to light.
   If you’re interested in knowing more about the family in Oklahoma, here’s the Facebook page they set up in order to try and go public.  https://www.facebook.com/PleaseGiveMeMyBabiesBack

   Change has to start somewhere.

Tuesday, January 20, 2015

Becoming Blunt Update

Ok, so people have expressed interest in the contact info of the hospital that I referred to in my blog.  The president and CEO of Cook Children's Hospital is Rick W. Merrill.  The address and number for the DFW hospital council that he is a member of is:

Dallas-Fort Worth Hospital Council
250 Decker Drive
Irving, TX 75062

(972)719-4900

I sent him a detailed letter, as well as the pictures that are in my blog.  Anyone who wants to reiterate to him the importance of proper medical practice as opposed to witch hunting is welcome to drop him a line.

You can also help try to enact change, even if by required a differential diagnosis before accusations, by writing and/or calling Senator Birdwell and Representative Tinderholt:



Texas State Senator

Texas State Senate District 22--Senator Brian Birdwell
Capitol Office: EXT E1.706
Capitol Phone: (512) 463-0122
Capitol Address: P.O. Box 12068, Capitol Station
Austin, TX 78711
District Address: 900 Austin Ave, Suite 500
Waco TX 76701
Phone: (254) 772-6225
State District Offices 

Texas State Representative

Texas State House District 94--Representative Tony Tinderholt
Capitol Office: EXT E1.216
Capitol Phone: (512) 463-0624
Capitol Address: P.O. Box 2910
Austin, TX 78768
District Address: P.O. Box 2910
Austin TX 78768 

Monday, January 19, 2015

Becoming Blunt

  A little while back, I shared a video of a news clip about a family that had been accused of abusing their infant daughter.  The husband was singled out, charged with abuse, and only allowed to see his daughter a couple hours a week with state supervision.  Some of you know that the reason I shared that video is because we have a similar story.  Over the last week, several of you who know a little of what has been happening with us have messaged me, encouraging me to complain to the state or go to the press.  I really appreciate your messages.  It makes me feel good to know that you are angry about the way we’ve been treated.  But it also made me decide to truly and completely come out with our story, so that you understand why complaining makes no difference.  If enough people know what is happening in good homes, maybe enough of us can stand up and change what is happening.
   I need to preface this with something; CPS knows that on occasion a good home gets falsely labeled by them.  Police know that sometimes an innocent parent goes to jail.  When you ask people how they can justify that, their response is “it’s better that one good parent suffer a tarnished reputation than a child be left in a home where they are abused.”  That makes sense.  Better safe than sorry, right? **Erryn is a trans woman and this has been edited to reflect correct name and pronouns, except for certain direct quotations. It is important to know that she is the father of our children, presented as male, and was perceived as male at the time period being discussed as men are far more likely to be the accused in these situations.**


  On March 4th of last year, at 4 in the morning, Erryn woke me up.  “I think something happened when I was taking Zeph out of his swing.”  I rubbed at my eyes and sat up as she held our crying son out to me.  “I had a hold of his thigh and heard a pop.  I’m worried it dislocated.”
   As I took Zeph, he stopped crying.  “Seems ok,” I responded.  Just to be sure, I took hold of the leg Erryn had indicated and gently moved it.  Zeph let out a cry.  I looked it over.  No swelling, no bruising, just a normal looking leg.  His cries almost immediately subsided, so just to be sure, I slowly pushed his leg up.
   He cried out again.  We looked at each other and practically in unison said it was ER time.  Erryn brought me the car seat and we ever so carefully strapped him in, woke up Eliza, threw on some clothes, and climbed in the car.  The mother that got in the car that morning with her spouse and children never came back.
   I know that this will be long.  I’m sure not many people will even get halfway through it, but I think it needs to be said anyway. I want to give you all the reasons I’m writing this, justify taking so much of your time, but I think those of you who read this will understand those reasons without me spelling them out for you.
   Our first stop that morning was USMD.  The doctor palpated Zeph’s leg and told us it was broken.  X-rays were done.  We were never told how bad the fracture was.  He simply said not to worry, that these things happen, and that Zeph would heal just fine.  We were told that we needed to transfer to Cook Children’s hospital in Fort Worth for treatment.  What we didn’t know was that CPS had already been called.
   I was so proud of how calm and collected I was as I rode with my 5 week old son in the back of the ambulance.  I had cried when they had me hold him still for the x-rays, but other than that, I was doing good.  The doctor had said it wasn’t a big deal, just a simple break.  He’d be fine.  It was ok.
   Zeph and I got to the hospital before Erryn, who had taken Eliza home to grab baby supplies.  As soon as we were in the building, an ER doctor took my arm and directed me down the hall away from my baby.
   “How did this happen, exactly?” she asked.  I told her what Erryn had told me, that while getting an angry and squirming baby out of his swing, that she had heard a pop.  “Did they tell you anything about the fracture at the other hospital?”
   “They said it was broken but that it wasn’t bad or anything.”  The look on her face was dark.  My stomach sank.  “But I suddenly have the horrible feeling that they didn’t tell me everything.”
   “Your son has a spiral fracture of the femur,” she explained as we approached a room with an x-ray display.  On the display was a small baby’s leg.  The bone was snapped clean in two.
   My brain stopped and I couldn’t breathe.  “The halves aren’t even touching,” I whispered.
   “The only medical way that this could possibly have happened,” she answered, pointing to the gaping space between the two pieces, “was if your husband intended to break your son’s leg.  The only way this break could have occurred is if he grabbed your son’s leg like this and twisted.”  She held her hands up in fists, then twisted them roughly as if she was wringing out a dish rag.  “There’s no other way this could have happened.”
   I’m sure I said all the usual, like “my spouse would never do that,” and “she’s a good parent, there must be some explanation,” or whatever, but honestly, I don’t remember what I said.  I just remember knowing, in that moment, that they were going to try and take my children from me.  As I looked at that x-ray, I burst into tears.
   By the time I was escorted to Zeph’s room, Erryn was already there waiting, laden with bottles and snacks, and an Eliza who was now dressed with freshly combed hair.  She looked like a good, loving parent.
  She took one look at my face and froze.  “What’s wrong?” she asked.
   “His leg is broken clean in two,” I answered, fighting not to start crying again.  “They say you had to have done it on purpose, that there’s no other medical way it could happen.”  It didn’t occur to me in that moment to reassure her that I knew she didn’t do it, to tell her that I thought they were wrong.  She was my spouse.  If I thought her capable of that even for a second, well, then she wouldn’t be my spouse.
  I took the seat next to her.  She said nothing for some time.  I imagine now that she was probably wondering whether or not I believed them.  Zeph was on the bed in a harness that kept him from being able to kick his legs, blankets rolled up on either side of him.
   The next seven or so hours were spent being questioned by doctors, CPS, and law enforcement.  Dr. Sophia Grant was the child abuse specialist that questioned us.  I told her Erryn was a good parent, and didn’t even have a temper to lose.  I also told her that I was concerned there was a bone disorder in his family.  Throughout the course of her life, Erryn has suffered many fractures, none of which were done doing something that should have broken a bone.
   “I see.  So, Erryn, when you fractured these bones, were you doing something or was it spontaneous?”
  “Well,” she answered slowly, “I was doing something.  I broke my foot when I was going down stairs-”  That’s as far as she got.  She cut her off, then turned to me to continue her questioning.  Too scared to argue or insist, Erryn and I let it drop.
  I don’t remember when it was, but at some point during the day, a nurse came in to tell us the results of all the testing they had done on Zeph to check for “more abuse.”  They had done blood work and a urinalysis to check for internal bleeding and damage, a cat scan to check for shaken baby syndrome, and full body x-rays to check for other fractures.
   “Everything came back clean,” she retorted, looking disappointed at the results, “but your children can’t speak for themselves, so we need to be their voice.  This doesn’t mean they haven’t been abused.”  Then her face lit up with a sudden afterthought.  “They did find a cyst in his brain, but you’ll make an appointment with a neurosurgeon and he’ll discuss that with you.  It’s not an emergency.”
   As the hours went on, I kept trying to ask about Zeph’s leg.  Was he going to have a cast?  When were they going to treat it?  Every time I asked, the nurse would respond with “the doctors are still deciding.”
   Around five that evening, the CPS caseworker, Monica, informed us that she was putting a safety plan in place.  “Until we decide what happened to Zeph,” she said, “I want you both to be supervised at all times when you’re with your children.  Is there someone you could stay with or is there someone who could stay with you?”
   Erryn and I looked at each other.  For the hundredth time that day, I felt like I was going to cry.  That was such a burden to ask someone to undertake.  Who did we even know that was home all day?  Erryn pulled out her phone and, with furrowed brows, began skimming through her contacts.
   “What if we can’t find someone?” I asked, terrified that I already knew the answer.
   “Then I’m going to have to take your kids with me.”
   My wife is an angel.  While I sat there, holding Eliza and crying, she made phone calls.  An incredible, sweet, stay at home mom from our church was more than happy to let us stay with her and be our supervisor.  But there was one more condition put on the table.
   “You can sleep at their home” Monica said to me, but then she turned to Erryn, “but I would like you to find someplace else to reside.  You can visit your wife and children any time during the day, but once it’s bedtime, I want you elsewhere.”  She pulled out a paper for us to sign, saying we agreed to the conditions, and our amazing supervisor came to pick us up.  When she arrived, Monica started saying her goodbyes.
   “You are free to go now.  I’ll come by in the next day or two to inspect the home you’ll be staying in and to discuss the case with you more.”  She started to gather her things.
   “We still haven’t been talked to about Zeph’s leg yet,” I interrupted.  “I still haven’t been told if they’re going to cast it or how to care for him at home.”
   Monica looked surprised.  “Oh!  Well, let me find out what’s going on.”  She slipped out.
   A few minutes later, in came a man who looked to be maybe 30.  He inspected the harness that Zeph had been put in, then handed me a pamphlet.  “The harness is adjusted correctly,” he quipped, making minimal eye contact.  “I’ve made marks so you know where to put the straps back if you undo them.”
  

 I was still a little confused.  “What are the reasons I would undo them?” I asked.
   “I don’t know,” he blustered, looking agitated, “just if you do.”
   Remaining undaunted, I started asking questions about care.  The harness kept Zeph from kicking his leg, nothing more.  It was still very mobile and completely exposed to being bumped, moved, and the like.  I couldn’t even imagine how I was supposed to hold him without putting pressure on his thigh.  With each question, the wound tech would answer, “read the pamphlet,” instead of giving me an answer.  So I gave it a quick once over.  It was about hip dysplasia.  It gave me absolutely no instructions on how to keep from accidentally rebreaking his leg.  For crying out loud, it wasn’t even set or splinted.
   After continuous rejection from him, I tried one last question.  Apparently it was one question too many.  “I’m here to make sure the harness is on right and to hand you the pamphlet,” he snapped.  “I’m not here to answer your questions.”  With that, he got up and left.
   The first few days were a blur.  My mom and sister started making their way by car from Nebraska down to Texas to be our supervisors for a couple weeks, and we had our first meeting with Monica.  She sat us down, told us that she felt we weren’t capable of handling two children so young, and that when the case was over, their intention was to remove the children from our home.  She said we shouldn’t worry though, because they would give us a chance to try and get them back.
   My heart broke.  There are no words to describe what it’s like to have someone tell you that they are going to walk into your home and take your babies, and that you are going to have to let them, that you are going to have to watch them drive away, that you’ll get an hour of visitation each week.  And if you’re good and take all your parenting classes, you might get to have them back, but no promises.  Of all the things that have happened to me in my life, there is nothing that haunts me more than hearing her say those words.  I still have nightmares of police coming into my home and wrestling my children out of my arms.  That day, the state taking my children from me became my greatest fear.
   CPS was not our only concern.  You know good cop/bad cop from the Lego Movie?  He’s real, and his name is Officer Grant Gildon.  He was in charge of the criminal investigation.  He came to our home to do an inspection and to further question Erryn.  He looked around, took pictures, all the time being super pleasant and friendly.  As he headed toward the door to leave, he turned to Erryn.
   “Here’s the thing,” he said, sounding like he was about to tell Erryn some awesome life hack, “lot’s of times what happens is there’s an accident.  Maybe you’re holding the baby and trip, or you get clumsy and drop the baby, you know, something like that.  When that happens, people are too scared to say they messed up.”  He gave a shrug of his shoulders.  “But accidents happen.  We all know that.  So, look, if you just tell me what really happened, you’re not going to get in trouble.  We don’t go after people for accidents.”
   Erryn, in all his to the point glory, simply replied, “There was no accident.  What I told you happened is exactly what happened.”
   Officer Gildon’s face went red.  “I understand if you’re scared to tell me the truth,” he bit out, “but if you don’t tell me what really happened, someone’s going to jail.”  He turned and pointed a finger at me.  “And don’t you think that you’re off the hook.  You might have broke it, then realizing what you did, put your son back in his swing for your husband to find.”
   I think that’s the first time I started actually feeling pissed.  “I would love to tell you what you want to hear, Officer,” I said, putting my hands over my heart, “but we’re honest people and we don’t lie, as much as we’d love to right now.  I’d love to tell you that there was an accident, that Erryn tripped, or we didn’t strap Zeph in properly, but that’s not what happened.  I’m sorry.  We’ve told you what happened and we can’t and won’t tell you different.”
   The rest of that first month was a whirlwind.  It consisted of attorney visits, way too many doctor and surgeon appointments, an MRI, massive amounts of research on infants and fractures, and many lonely nights.  Maybe I’m needy, but not getting to cuddle up against my spouse at night is hard enough without the fear of losing my family hanging over me like a scythe.  We actually would webcam at night.  No, not the kinky kind; we would set up our phones so we could see and hear each other all night so we wouldn’t feel alone.  There were times I couldn’t fall asleep, my chest aching and my throat tight with tears.  Hearing Erryn’s soft snoring was the only thing that got me through each night.
  Monica, our attorney, and the family based services worker who would be taking over our case came around week 5 to discuss the closing of the CPS investigation.  Monica told us that they were planning on a finding of “reason to believe abuse” against Erryn.  As for me, she couldn’t promise because she had to ok it with her supervisor, but she said that right then the intent was that I would receive a letter stating abuse by me had been ruled out.  A couple weeks later, Erryn received her letter.  Sure enough, a finding of “reason to believe was marked.”  Even knowing that they were going to do it, looking at the letter made me angry.
   But my letter never came.
   I called our attorney to let her know of the oversight, and she in turn contacted Monica.  Turns out, Monica lied when she said both Erryn and I were being investigated for abuse.  Since Erryn had admitted it was on her watch, I was never a subject of investigation.  Our attorney was livid.  For more than a month, I couldn’t even get up at night to feed Zeph without waking up the supervisor so they could watch me, something that is not necessary for someone not being investigated for abuse, and actually was the reason I stopped being able to nurse.  I’m an extremely private person, and no matter how badly I wanted to give Zeph what was best for him, having someone sit and watch me literally killed my body’s ability to produce.  Our attorney told me to call the ombudsman for CPS, and to let them know that I had been mislead and coerced into signing safety plans that I should not have had to follow.  I did so.
   The phone call was aggravating.  As I explained our social workers transgressions, the person on the phone would just keep repeating, “I’m sure she had a good reason.”  The letter I received from them shortly thereafter to let me know what they found was enraging.  It read something along the lines of: “Thank you for your concern.  We talked to your social worker and she insisted she didn’t lie to you.  CPS knows what they’re doing, so please be cooperative and do what your case worker advises.”  When this is finally over, I have every intention of calling them again and giving them a speech that I have recited over and over.  Hopefully I can do it without the profanity.
   About three months after the event, I got a phone call.  The caller ID was Erryn.  I love getting calls from Erryn when she’s at work.  It’s never a long conversation, and it’s always whispered so as not to be heard by her deskmates, but it’s always good to hear her voice.
   But it wasn’t Erryn.
   “The police just showed up,” a voice said.  “I have her phone and things.”  It was one of Erryn’s coworkers.  My spouse had just been arrested.
   I waited by my cell phone for hours, waiting for that “one call” that everyone on TV gets when they’re picked up.  When it finally came, I was in for a surprise.  It’s not free.  It’s collect.  And not just collect.  You have to have a prepaid account with a specific service.  The phone told me I had a collect call from Erryn, but that I needed to set up an account.  Frantic, since I knew he was timed, I started setting up the account.  A minute in, Erryn tried calling again.  I felt time slipping away.  Just as I started approaching the end of the setup, it told me I had entered something incorrectly, and the call disconnected.  Hot tears rolled down my face as Erryn called yet again.  I had to start the set up from the very beginning.  By the time I finally had an account and had it prepaid, Erryn stopped calling.  I tried calling the number back, even though I knew it was useless.  I called over and over, crying like a little girl who just saw her puppy run over.
   Erryn was in jail for five days while I tried to arrange bail and attorney fees.  In the end, it was because of her selfless and incredibly kind grandparents that she was let out.  Her grandfather handed me his credit card and let me put an outlandish amount of debt on it with nothing more than my word that we would make payments.  Don and Billie, I’m sure you’ll never read this, but you didn’t simply bail Erryn out of jail.  You brought a father home.  During those days, Eliza would often wander the house, looking for Erryn, calling out “Daddy!”  Every time the front door would open, she would come running, thinking that her daddy was home, only to be disappointed.
   As we met with now a criminal attorney, we were told it was our homework to find a doctor that could and would say that abuse was not the only explanation.  I didn’t think that would be too big of a problem.  When I had met with Zeph’s orthopedic surgeon, Dr. Jason Kennedy, I had asked him about the abuse accusations.
   “The doctors at the ER told me that the only way this could have happened was if my spouse did it on purpose,” I had explained to him.  “Is that correct?”
   He didn’t look very comfortable with the conversation, but he obliged me with an answer.  “Really, it’s nearly impossible to look at a single break and say it had to be abuse,” he drawled.  “There isn’t actually a way to ‘see’ abuse on a radiograph.  Of course, the more fractures, the more suspicious we are, but a single fracture really doesn’t necessarily say ‘abuse.’”
   Afraid that he was just saying what I wanted to hear so I wouldn’t cause a scene, I reworded my question and asked one last time.  “So, let me ask you this way:  If you were there, if you actually saw my spouse remove Zeph from the swing, heard the pop, and knew that what my spouse says is true, would you be worried that there’s a bone disorder of some sort?”
   “Absolutely not,” he said, with a dismissive wave of his hand.  “Yes, it’s a fluke, and yes, it’s not everyday that babies break bones during normal handling, but if he was fighting against your husband and the right pressure was put on his thigh, it could very easily have happened the way your husband said it did.”
   “So you wouldn’t worry about a bone disorder?”
   “No.  We don’t test for or worry about bone health unless the child keeps breaking things.”
   My stomach sank.  “If my son breaks another bone,” I responded slowly, “CPS is going to take my children away from me.”
   He suddenly looked uncomfortable again.  “Yeah…” he murmured, then changed the subject.
   Months after that conversation took place, I called his office.  After I explained that I was hoping Dr. Kennedy would write up something saying the fracture was not by itself indicative of abuse, I was handed over to a nurse.
   “We don’t really do that kind of thing,” she informed me, “but if what you say is true and there were no other fractures or signs of abuse, then typically the doctor will not rule abuse and CPS should be happy and close their case against you.”
   “My spouse just spent five days in jail,”  I retorted, getting tired of everyone being surprised that CPS still had their teeth in us.  “There was nothing to show the fracture was abuse, everything came back clean.  The ER doctor still says it’s abuse and my spouse is being charged.”
   There was a long silence on the other end, then “Oh my gosh… Hold on, I’ll go talk to him.”
   I waited maybe about five minutes, praying that this would get me what I needed to keep my husband out of jail.  When she came back, I could tell by the first word out of her mouth what the answer was.  Her voice was dripping with regret and sympathy.
   “I discussed it with Dr. Kennedy, and he’s very sorry, but our office just doesn’t get involved in child abuse allegations.”  The words were a horrible betrayal.  “I’m sorry.”
   “Not even just a generic letter?”  I choked.  “Something that just says single fractures by themselves are not evidence of abuse?  Even though it’s what he told me?”
   “I’m sorry,” she reiterated, sounding so much like she wished she could give me a different answer.  “We just can’t get involved.”
   It was not the last phone call I made to a specialist, asking the same question.  Over the course of several months, I called office after office.  I would tell them our story, and they would be shocked that the doctor had accused my spouse of abuse so lightly.  After they expressed their horror at our situation, I would then ask them the magic question:  Would they be willing to go over his chart, and if they did not think abuse was definite, would they make that statement before a court.
   I always got the same response.
   “Your situation is horrible,” they would say, “and we agree that a single fracture isn’t enough to diagnose abuse, but unfortunately, our office doesn’t get involved in child abuse allegations.   I’m so sorry.  We wish you luck.”
  I finally called our pediatrician.  I had been hoping for someone who specialized in bone health, but I had called every pediatric orthopedic and endocrinology office in a rather large radius, and a family practice doctor was better than none.  After a week of supplementing with formula, Zeph’s vitamin D was 23.  Our pediatrician, Dr. Cahan, had said that if it was only 23 with supplementing, it would have been much lower prior, when I was just nursing, making for weak bones.  So I gave her a call to officially ask her to testify to that when Erryn’s court date came.
   Dr. Cahan was out of the office, apparently having surgery, so I left a message for the nurses to pass along my question.  I then waited anxiously for her reply.  When I got the call back, I had butterflies.  This was it.  She was my last hope.
   I’ve never felt so out of control and angry as when the nurse told me that “Dr. Cahan doesn’t do that kind of thing.”  I hung up the phone, calmly set Eliza in her room and closed the door, then turned and unleashed hellish fury on my bedroom door.
  “F--k!”  I screamed, punching the door much harder than I had intended.  I heard wood splinter and it burst open.  In that moment, I knew my spouse was going to go to jail.  Every doctor sympathized with me, every doctor told me this was unfair and wrong, but not a single doctor would stand up for my family.
    I cried, and I cried hard.  Slumping defeatedly in the chair at my computer, I opened up google hangouts and proceeded to message Erryn.  I wanted to call her, but I didn’t want her to hear my hysteria.  She had spent the last nine months being there for me, comforting me when she was the one who faced losing her entire family.  As I typed I prayed, prayed for anything and everything.  This was so wrong.  My spouse is a good, kind person, and an amazing parent, and her life was about to be ruined.  And me?  I was going to be spending the next 5 or more years of my life trying to raise my children alone, counting down the years, days, and minutes until I could take my best friend home with me again.  My children would get to see their father at scheduled times.  She wouldn’t be the person who made pancakes on Saturday and took them camping.  She would be the person who they saw during visiting hours, wearing orange and watched by guards.  There wouldn’t be bedtime stories and family road trips with her. There would be a person in prison, accused of hurting her little baby on purpose.
   As always, Erryn responded to my message about Dr. Cahan’s refusal with words of comfort, telling me it was ok, to not give up.  And how was I not to give up? I asked.  There was no one.  I had spent months making phone calls.  There was no one left to call.  She brought up a website that I had mentioned to her in my research of fractures, and told me to try and get in touch with them to see if they knew anyone.
   Nervous and refusing to let myself get my hopes up, I pulled up the website for The Vitamin D Council.  I felt bad for the person who answered the phone.  I was already crying as I gave him the sloppy short version of our story, ending in a tearful plea for any leads or information he could give me.
   “It’s going to be fine,” he told me.  “It’s ok.  We get calls from people like you all the time.  I’ll have one of our doctors give you a call, but in the mean time, I can give you some other people to get in contact with.”
   He gave me a couple names.  The last one was Dr. Michael Holick.  “If you want to call him, I would recommend it.  Dr. Holick is known as the father of vitamin D.  There is literally no one in the world who knows more about it than him.”
   First thing on a Monday morning, I called the Boston Medical Center, where Dr. Holick is a practicing endocrinologist and biochemist.  They gave me his personal email, telling me he was always more than happy to help “people like me.”  I emailed him the details of what my spouse said happened, of what the hospital labs said, and what the hospital’s doctors said.  He told me he would be happy to discuss my son with me via phone conference.  A time and day was arranged.
   As we waited for his call, Erryn and I waited nervously, huddled together around our kitchen counter.  I had done some research on Dr. Holick during the days leading up to that phone call.  The best way to word that man’s accomplishments and knowledge would be to say that he’s the equivalent of a geek celebrity, a leading expert worldwide in bone metabolism.  If anyone could help us, it would be him.
   When the phone rang, I thought we would be going over the entire story again, the one we’d told a hundred times over.  To my surprise, however, Dr. Holick was not particularly interested in the actual event of Zeph breaking his leg.
   “Are either of you double jointed?” he asked.  Erryn and I gave each other baffled looks.
   “No,” we answered in unison.
   I held my arm out, locking my elbow, even though Dr. Holick couldn’t see it.  “I’m definitely not,” I reaffirmed.
   “Yeah, I’m not either,” Erryn chimed in, mimicking my outstretched arm.
   “Erryn!” I exclaimed, shocked at what I saw, pointing at her arm.
   Confused, Erryn gave her arm a look.  “What?”
   I still can’t believe I had never noticed.  Reaching over and pulling her sleeve up so she could see her elbow better, I said, “Erryn, you are definitely double jointed.”  Her arm made a neatly unnatural v shape at the joint.  We started checking her other places; knees, fingers, etc…  Erryn was very “double jointed.”
   From there, the conversation turned to Erryn’s health history.  After a few minutes, I brought up the fractures that Dr. Grant had dismissed.  “She’s broken several bones,” I offered, “and they all broke pretty easy.  She also developed osteoarthritis at twenty.”
   “Oh, really?”  If possible, the doctor suddenly sounded more interested.  “Here’s the thing,” he said.  “What you’re saying sounds like all the classic signs of something called Ehlers-Danlos syndrome.  I really want to see all of you in my office.”
   But I had to, of course, ask the question any mother would be thinking at that moment.  “If you examine him and decide our son does have this disorder, is he going to be ok?  I mean, is this something that has a treatment?”
  “No, unfortunately, there is treatment for many of the symptoms, but he will have this and struggle with it his whole life.  It will however, explain things about him that you might have noticed as odd.”
   “Forgive me if this is random and unrelated,” I interjected timidly, “but one big thing I’ve noticed that’s ‘odd’ is that his toenails are constantly cracking, but they don’t break normally.  They crack vertically.”
  “Yes!” Dr. Holick practically shouted.  “Yes, yes, yes!  That is a classic symptom of Ehlers-Danlos.”
   That day, as I hung up the phone, we had hope.
   Two weeks later, leaving Eliza in the care of an AMAZING member of our church, we packaged up our infant son and flew to Boston for an appointment with Dr. Holick.  I was so nervous.  What if he looked at Zeph and decided he didn’t have Ehlers-Danlos syndrome?  What if we had spent money we didn’t have for nothing?  What if after all our heartache, my husband still went to jail?
   I wish so much I could remember her name, but I just can’t.  A very sweet, soft spoken doctor spent a massive amount of time with us before we saw Dr. Holick.  The reason?  He was teaching her how to diagnose EDS.  Histories, physical complaints, the works.  Then, when we were pretty sure there was nothing about Erryn or Zeph she didn’t know, in walked Dr. Holick.
   He shook my spouse’s hand, then mine.  Then, without wasting a second, he said, “Did she tell you why his legs are red?”
  I looked down at Zeph’s legs.  Yes, they were red.  They were always red.  “Well,” I stammered, “I hope this doesn’t sound racist or ignorant, but he’s got a good dose of Native American in him.”  I know I was definitely blushing.  “We always thought he was just a little ‘Redskin.’”
Those knees ain't normal
   He walked over and pressed his thumb against Zeph’s thigh.  When he pulled away, it left a burning white spot that was swallowed up by the red a few seconds later.  “That’s inflammation caused by mast cell hypersensitivity.  Mast cells don’t work properly in many people with EDS, causing allergy symptoms.”  He explained what EDS was, a genetic disorder of the body’s connective tissue that causes hypermobility in joints and wreaks havoc on body systems.  “You’re actually very lucky,” he told us.  “EDS can cause babies to fracture with routine handling.  You’re lucky your son only had one fracture.  I’ve seen many babies that have broken up to 22 bones.  Before infants start fully calcifying, their bones are made up of mostly connective tissue, leaving those with this Ehlers-Danlos fragile.”
I try to bend my thumb like that
every time I look at this picture.
   As we talked, he casually pointed out all the diagnostic criteria of EDS that both Erryn and Zeph exhibited.  Blue sclera of the eyes, hypermobile joints, a mass of food, skin, and outdoor allergies, and for Zeph, the classic “square head and protruding forehead.”  I couldn’t decide if it was good or bad.  We now could show a court that there was a good explanation for the fracture, but I was being told that my son would grow up to struggle with bone and joint health, constant allergies, and a plethora of other random health issues, some of which can be debilitating.
   We flew home exhausted and feeling a deep sense of relief that was practically physical.  The first thing I did when back at my computer was look up ehlers-danlos syndrome and infant fractures.  What I found was both hopeful and disheartening.
The "protruding" forehead
and square head.
   The good news was that there were many articles about parents who had been criminally charged with abuse, only to have the infant diagnosed with EDS.  With the diagnosis, the charges were almost always dropped without going to trial.  The odds of Erryn going to prison had just drastically gone down.
   The bad news was that there were so many articles about parents being accused of abuse, being arrested, not being allowed to see their children except for short supervised visits, only for the children to later be diagnosed with EDS.
   I thought back to our experience in the hospital.  I had brought up bone disorders.  Twice.  Erryn had tried to explain her poor bone health and was stopped.  We were treated cruelly and our concerns that something might be seriously wrong with our son were blatantly ignored.  Why?  It took Dr. Holick five minutes to diagnose both my spouse and son.  Why couldn’t Dr. Grant, who is supposedly trained to distinguish between what is abuse 

Erythema.  Now that he takes
Zyrtec everyday, his legs are no longer red.
and what isn’t, take a few extra minutes to discuss the possibility of a bone health issue?  It would have cost them nothing, and could have saved us so much heartache and hurt, not to mention the obscene amount of debt we racked up trying to keep our family together.  This has literally consumed our lives.  For seven months Erryn had to sleep at a friend’s home, wasn’t allowed to be alone with her children.  For seven months we had to arrange to have someone living with us whose sole purpose was to be there whenever Erryn was home.  I spent five days trying to figure out how to pay bail before my spouse lost her job for nonattendance.  And for the record, calls from the city jail are OUTLANDISHLY expensive.  Each short conversation cost about 25 dollars.  I spent 300 dollars in 5 days on our few phone calls.
Notice the bluish hue to the
whites of his eyes?
   Furious that all this could have been avoided if Dr. Sophia Grant had cared whether or not we were actually abusive, I started looking at ways to complain.  I found a forum that discussed writing your state representative.  It was full of individuals who had done so after being falsely accused by CPS.  They had all gotten the same letter, saying that they were grateful for their input, and they would pass along the complaint to CPS.  Translation: We don’t get involved in CPS cases.
   I called attorneys.  Surely, something the hospital did was malpractice.  Hell, they WANTED us to be guilty, refusing to consider disorders and family history, and most importantly, refusing to allow me to ask questions about how to care for my son at home.  Each attorney said the same thing.  What they did was atrocious, vindictive, and malpractice.  But they couldn’t do anything about it.  It’s pretty much impossible to sue a hospital when an abuse case is involved.  The state doesn’t want to “punish” them for reporting abuse.  One attorney told me that it was a horrible, broken system.  “All you can do,” he said, “is pick up the pieces of your life and try to move on.  You got caught in something terrible that isn’t your problem, and now you’re paying their price.  Be grateful you still have your kids and let it go.”
   Let it go?  My spouse is still facing criminal charges.  As of now, they have not been dropped.  I get multiple calls a day from Cook Children’s Hospital, wanting me to pay off the 8,000 dollars they racked up doing tests on Zeph to look for abuse.  We’ll be paying back Erryn’s grandparents for a very long time, and the criminal charges sparked a custody battle with Erryn’s ex that has financially only begun.  Really?  Let it go?
   I wrote the president of the hospital a very “firm” letter about our treatment, and I’m in the process of filing complaints with various agencies, but I expect I will get the same response from them as I have from everyone else:  Nobody gets involved in CPS cases.
   I wrote several news stations.  Only one got in contact with me.  The reason she didn’t take the story?  It’s happened so often that it’s not a new story anymore.
   I read an article not that long ago where someone said that cracking down on possible abuse cases was a must for protecting children.  When asked about the innocent parents that get falsely accused of abuse, she said that it was worth occasionally hurting an innocent person’s reputation for the sake of protecting more children.  I want you to understand something very, very important.
   When a person is falsely accused of abuse, the last thing they are worried about is their sullied reputation.  When you have someone look at you and tell you that you’re going to lose your children, the last thing on God’s earth that you are worried about is your reputation.  Sure, it sucks to have people think you beat your kid, but if you think that’s what a person is worried about when CPS and police make accusations against you, you obviously don’t know the love of a parent.
  Yes, I want to do something about what happened to us.  Yes, I want to complain, scream, make so much noise that no one could possibly ignore me.  I want the hospital to be held responsible for everything we went through, for trying to destroy my family, for giving my spouse a criminal record.  The problem is that the people who matter aren’t listening.  There are no diagnostic requirements for hospitals before they “diagnose” an injury as abuse.  There is no law saying they need to check for poor bone health or genetic disorders.  And CPS?  For them to rule “reason to believe abuse” against you, all they have to be able to say is that there is a reasonable chance it could have been abuse.
   Yes, I’m lucky I still have my children.  Not lucky in the won-the-lottery kind of way, more of in the I-was-hit-by-a-drunk-driver-and-lost-the-use-of-my-legs-but-I’m-still-alive kind of way.

   If you read this far, thank you, really.  I’m a private person, and this kind of thing is personal, though the part I hate the most is admitting how much I’ve cried in the last ten months.  This is a system that needs to change, but those of us who go through something like this are often too ashamed or afraid to say anything.  Erryn and I were not shy, and as we told people what was happening to us; I was amazed at the people who had stories similar to ours.  We came across them everywhere, from our church congregation to the manager of a music store we once browsed.  If you are one of those people, be brave.  I want to say something like “Let us gather and storm the castle!!” but for now, I’m going to simply say "don’t be ashamed."  Tell people.  No one can help change things if they don’t know it needs changing.