Tag: Cowden syndrome
“An Accumulation…”
I once read a story where a special needs mom described her daughter’s seemingly “over the top” fear of needles to a phlebotomist who had no frame of reference, compassion, or desire to understand. The phlebotomist had written the child off as poorly behaved, and the mom as one with no control. This mom said plainly to the phlebotomist, “It’s not you. It’s not even the needle any more, at least I don’t think so. You are AN ACCUMULATION of botched blood draws and rolled IV attempts. You are an ACCUMULATION of her being stripped of her control, and of all the pain that has come from those needles.”
That story stuck with me in the deepest way. And I have told doctors, nurses, and phlebotomists alike, whose egos are sometimes easily bruised by an incredibly anxious 12-year-old, not to take it personally. That is if course unless they get it wrong and add to the problem…
Tomorrow morning Meghan will head to the oral surgeon for general anesthesia and surgery 15.
The surgery itself this time is not that unusual. The wisdom teeth are impacted and the bottom two will come out tomorrow. Years of orthodontics are complete, not to be damaged by over-anxious wisdom teeth making an unwelcome early appearance.
I say it’s not unusual. Except that she’s 12.
If you think about when you had your own out, my guess is you were somewhere between 17 and 21. And, at the time you had them done you knew at least a few people your age who already did it. And you were in turn “there” for your friends that followed.
Except once again she’s braving unchartered territory alone.
For those that have challenged her on calling this “surgery,” I will remind you that is probably how you referred to yours. At the oral SURGEON, under anesthesia.
There have been countless well-meaning adults, telling her about their wisdom teeth, and how it’s no big deal.
And while their intentions are good, I bet there aren’t going to be too many people absent from her junior high this year to get their wisdom teeth pulled.
As “normal” as things are, they just aren’t.
By the time her friends get theirs done they will not remember, and I’ll likely have to vouch for her story that hers came out at 12.
The oral surgeon’s office called to remind me she shouldn’t eat or drink after midnight. They shouldn’t worry. I stopped any use of NSAIDs, and fish oil, and unneccessary multivitamins a few days ago.
We’ve got this.
She just shouldn’t have to.
It’s a recurring theme. But, we will endure. Because we have no other option.
Defrosting the chicken for tomorrow’s soup.
We are BEATINGCOWDENS!
The War Ain’t Over Yet…
Tonight wasn’t one of our better nights. And, as we drove home, and sorted through a few things, I offered Meghan this outlet. I told her writing helps me sort out my thoughts and get refocused. Here is Meghan, as our GUEST BLOGGER….
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Tonight I couldn’t finish practice. Yesterday I hurt my knee, my kneecap clicked back out at practice and I got shocking pain through my leg. A lot. So I pulled the rest of practice and iced my knee when we got home. I went again to practice today and hurt my knee so much that I couldn’t continue. I went home in tears feeling like I just failed. I gave in tonight. I lost this battle, but I will win the war. Tomorrow I will not play gym, for I will save my strength for swimming.
So, I will go back to Wagner on Saturday, and I will finish practice and do it well. I love swimming, and I love the pool. When I swim I feel like I’m actually at peace. I won’t lose my favorite thing in the world. I will keep fighting, and Cowden’s Syndrome will not win the war. I WILL.
I cannot be normal, and I cannot play as much as I’d like to with the kids. I always have to watch and be careful about what I do to my body. Well, I am not going to let that stop me. I’m going to succeed and I’m going to live my life to the fullest.
Cowden’s Syndrome may win quite a few battles, but I will win this war. I will keep fighting and I will stay strong. I will get some injuries along the way, but I will recover.
Hey Cowden’s, did ya hear me? The war’s NOT over yet, and you will not be the victor. Take your small victories, for today was one of the days when I did give in, but it won’t be happening again any time soon.
Do What You Love

It was almost 8:40 last night as I drove down Grymes Hill with Meghan. She hadn’t been home since we left for school at 7:20 that morning. She was facing a shower, dinner, homework, and a later than normal bedtime. She had spent the afternoon registering for her after school drama program, and had spent the last two and a quarter hours in some combination of intense exercise- on land and in the water. She was exhausted and it was evident in her face. But, not it her voice or her mannerisms.

“I know I’ve got you running all over the place Mom, and I know it’s a lot of hours. But, I have to tell you that I LOVE it.”

I couldn’t help but smile in spite of myself. We all want for our children to do what they love. And here she was; registered for drama, swimming 4 days a week, pushing the herself at school, enjoying church youth group, and planning a fundraiser for February.

She feels rotten. A lot. But she pushes. And I have to believe that is how we have to live this syndrome – this life. Maybe I’m a good influence after all.
She plays in pain. Constantly.
She is always recovering from or anticipating something. But instead of waiting for the storm to pass…
She’s clearly dancing in the rain.

We have our spats. We’re supposed to. But, we balance each other too.
We keep each other motivated. We keep each other grounded. Her diagnosis still makes me physically ill. But, it does not, can not, and will not define her. I’m convinced.
Do what you love I tell her. Do what makes you happy. And she does.
And I do too. Watching her for hours, on the bench, in the basement by the pool makes me happy. Watching her on stage makes me happy. Watching her persevere makes me proud.
We will do this- together. We are BEATINGCOWDENS.
Hyper-vigilance
Hyper-vigilance. Although Wikipedia is not my favorite source for all things – it defines this quite well.
Hyper-vigilance is an enhanced state of sensory sensitivity accompanied by an exaggerated intensity of behaviors whose purpose is to detect threats. Hyper-vigilance is also accompanied by a state of increased anxiety which can cause exhaustion.
When we were first diagnosed, and I had a long conversation with a Mom who had been where I was many years before, she told me we would be OK, but we would need to be forever vigilant. Understanding now, what I didn’t then, is that Cowden’s Syndrome requires more than vigilance, it necessitates hyper-vigilance.
The two are very different. One is a state you may be in sometimes, when it is necessary. The other is a place you never leave. Ever.
I don’t compare illnesses, in the sense of one being, “better, harder, easier, more difficult, more painful…” than another. That to me is silly. I know LOTS of people who suffer on a regular basis. I can’t say I would want to trade places with any of them. And, I can only speak from my lens.
My lens is that of a mother, who is watching her child battle through a chronic (FOREVER) illness with potentially life-threatening, and definitely life-altering ramifications – while battling that same illness myself.
I don’t view us as “sick” people. As a matter of fact we are regularly called,” The healthiest looking sick people…” But, we aren’t “well” either. It gets complicated. Quickly, and often.
Hyper-vigilance requires me to do everything I perceive is in my power to try to stave off the tumors and vascular anomalies looking to create havoc, chaos and confusion in our bodies.
Hyper-vigilance necessitates monitoring food intake. Avoiding food allergens/sensitivities because they cause vomiting and severe GI distress. That means NEVER leaving the house without food. JUST IN CASE. It also means spending weekends cooking so that “quick meals” come out of my freezer and not a drive through window. It means providing the most intense nutritional products I can find to fuel a body that would otherwise be running on empty. It means driving far and long to get the right food at the right stores. It means making sure the sweet treats that are allowed are not full of dyes and preservatives because they compromise further a documented severely compromised immune system.
Hyper-vigilance means watching the medication intake. To make sure we don’t forget an antiviral. Because when we do it sets off a tirade of events that are hard to bounce back from. It means typing the list, and checking it over. It means teaching her to know her medicine on sight. It means avoiding everything we don’t need and willingly taking things like probiotics to help that fragile stomach. It means knowing that when you have chronic viral infections they are ALWAYS waiting for an “in.” It means leaving NOTHING to chance, and having spare pill cases in every bag with extra of everything, especially digestive enzymes. It also means spending HOURS AND HOURS trying to make the mail order medication people get it right. Which I sometimes think is just not ever going to happen.
Hyper-vigilance means scheduling the doctors. All of them. All the time. It means making sure all the screenings, for all the ridiculous number of cancers we are at an increased risk of developing, are done on schedule. It means often following up on those appointments, with imaging studies and more appointments. And then repeating those “unclear” imaging studies, again and again. It means getting blood work done, often. Usually at least once every 4 weeks. It means talking to the endocrinologist and problem solving with him when he admits “it doesn’t make sense” as you strive to help your girl at least feel better. It involves medication adjustments. Making sure it’s taken on an empty stomach, and every single day. It means there is always a list nearby of who needs to be scheduled next. It’s right alongside the pile of bills that have inevitably been messed up by someone, and now need receipts faxed and hours on the phone to be kept out of collection agencies.
Hyper-vigilance is hearing the symptoms every day and trying not to panic. When there is a headache, sharp and sudden, or a pain in the knee, or the back, or the shoulder, or the leg, and you know your kid is NOT a hypochondriac as some others would like to think, you have to listen, sort, and mentally file all of these. Hyper-vigilance is keeping track of which ones repeat and which ones go away on their own. Hyper-vigilance is being very aware, but never panicking. It’s a fine line.
Hyper-vigilance is Physical Therapy. As often as we can fit it in. Because something always hurts. When one foot is 2 sizes smaller than the other because the treatments for the AVM in the knee cut the blood flow to the foot, so the bone stopped growing, you end up “off sides”. The hip, the shoulder, the knee. They all hurt, and it won’t get better. It will only get managed. For as long as we can fit in the PT.
Hyper-vigilance is also finding balance. It’s also searching somewhere for “normal.” It’s making 4 swim practices a week, often on raw nerve. Because she wants to feel normal. She wants to compete. And let’s be truthful, she wants to win. It’s about me never really leaving the grounds of the college 12 extra hours a week because we are always one step away, and sometimes a half-step from “just in case,” and “what if.” It’s getting her to drama, because she’s skilled there. And she fits in. And the teacher is awesome, and the kids know her for who she is. It’s about balancing the schoolwork, and doing her best, while teaching her not to beat herself up. Too much stress is no good for anyone. Especially when you have this random tumor growing condition that preys on extra stress.
Hyper-vigilance is remembering I have this “Cowden’s Syndrome” too. It is making sure I am at my best so that she is at hers. It’s remembering that I sport fake silicone boobs as a constant reminder that I’m not invincible and cancer found me. It’s remembering they were worried enough to take the uterus and the ovaries too. It is working hard, at my job, and my life, and showing her it can be done. But it’s also about letting her know I get tired too. Because in those moments she sees that she is normal. And yesterday when I struggled to even walk up a flight of stairs, I saw the concern in her eyes. And she picked up the vacuum. And she helped. It’s teaching her to take care of herself by some days letting her take care of me.
Hyper-vigilance is walking. Me. Walking 4-5 miles a day almost every day. Because my bones are already crapping out. After 30 years on thyroid pills and 3 years after a hysterectomy, at 41 I’ve been placed on warning. It’s necessary for me to take good care of me. To fuel my body properly. To limit the junk in. To respect this body because it’s already got a lot going against it.
Hyper-vigilance is making decisions in the moment. It is having to say no, we can’t go. It’s not being able to tell people in advance. It takes away from advance planning, even the fun stuff. Because life with chronic illness is day by day. It makes me feel badly, often. So sometimes I avoid making plans. I don’t even like to volunteer for too much because I just don’t know whether things will be ok that morning.
Hyper-vigilance can be very isolating.
It’s hard for some people to understand. And I get it. Because a few years ago it might have been hard for me to understand too. It makes people uncomfortable that this thing we have is never going to get better. People feel better when things can be fixed. But it can’t. We are not going to grow out of it. It’s here. It’s part of us. Like the ‘elephant in the room.’ But, we understand other people’s problems too. We get the myriad of health issues that surround us. And we empathize. And we don’t need to be sheltered from them. As a matter of fact, we might like it is sometimes people shared their worries with us too.
Hyper-vigilance is exhausting. And today I took a two-hour nap. Because my throat started to hurt. And my body was giving me all the warning signs that I had pushed a little too far. I shortened the walk. I stayed in mostly.
It’s like training. For real life. Because there is not an event at the end, that will finish with a medal and a sense of accomplishment, and a new goal. My forever goal will be to keep us healthy, and to keep the Cowden’s Syndrome at bay. The only path to this end is hypervigilance. And even then, just like in life, there are no guarantees.
We remain forever Beatingcowdens!
Summer List
I have been walking around all day with that nagging feeling in my stomach.
I have packed my bag, and Meghan’s too.
I have filed, organized, and made lots of lists.
There is a new schedule on the wall – color coded and everything.
The calendar says it’s time, but my heart, and my stomach beg to differ.
Summer was to be about beaches, and barbeques. It was to be about road trips and freedom. It was designed for friends, and fun, and get-togethers.
Except that most of that never came to be.
There was that knee surgery in May, that derailed any hope of walking long distances for a while, and thrust us into 2x a week PT. Which, even though we LOVE Dr. Jill, can be daunting in the schedule. And, it eliminated most day trips that could easily be taken for granted, if you don’t have to factor in that a walk more than about 3/4 mile is out of the question.
And while that was going on Daddy was rebuilding the deck. Alone. For three months. Every spare minute of April, May and June. It looks so beautiful. Maybe next year we will get some people over to relax and enjoy the deck, and the grass. The new grass, artificial, durable, and a drastic improvement over the old side yard. Yes, maybe next year.
We got the pool open the first week in July. And July had drama “camp,” and I use the term VERY loosely. And July had swim practice. And July had doctors, some regular, like PT, others on the 6 month schedule. And some blood tests, and some ultrasounds, and a bone density test for mom. I think I stopped counting at 30 appointments.
But, thankfully August had Disney. And there are few other things that can bring me such joy as a vacation with my family to the “Happiest Place on Earth.”
And August had it’s own set of appointments, including hand surgery to remove a vascular lesion from her palm. And setting up the whole wisdom teeth thing for September.
So it’s easy for me to be sad. And down on things. Because I want a do-over. But, I guess that’s normal. Because most people probably do.
I sat down tonight to get my head clear. To “flip it,” and get my head and my heart in the right place for tomorrow. I sat down to acknowledge the many things I have to be grateful for, and the things that went WELL this summer.
So, in no particular order…
- The new deck. No splinters. No maintenance. Pretty. And finished.
- The new grass.
- Walking barefoot in my backyard.
- Road trip to West Virginia, that I took alone, on a very rainy June weekend to meet some Marines. Healing help.
- Listening to my girl sing. In pain. In joy. In the shower. In the living room. In the car. Anywhere.
- Healing progress. From both recent surgeries. And the resilience to continue to endure.
- Laughter. Mine. His. Hers. Friends of hers. Strong laughter.
- Disney. I’d go back three times a year if I could.
- Graduation party, bridal shower, and a wedding. Mom being 18 years cancer free. Meghan turned 12, and Felix had a birthday too! We celebrated Pop’s 96th birthday. Celebrations.
- Board games.
- Green tea – together.
- Trips to Ralph’s.
- Watching my all time favorite movie, “Dead Poet’s Society” with my girl.
- Nutrition packed shakes, EVERY day. Even in Disney. Fueling my body.
- Reading a book my friend in Australia wrote about Cowden’s – for all the world to see.
- Antibiotics that heal recurrent infections.
- Walking. 5 miles a day, most days. and at least 10,000 steps every day since July 8th. Goal met.

- Last, and DEFINITELY not least, were my walks with Mom. My healing walks with Mom. There were so many mornings when she and I walked together, 2 miles, with 2 dogs. We talked this summer more consistently, and for longer, than we have in a long time. I think this was one of the best things that happened all summer. She is a strong lady. Lyme Disease took a stab at her this summer. Apparently for the second time. And she has told it where to go. So often she is a grounding force for me in this never-ending battle to remain BEATING COWDENS. I will miss those walks. They were not just for the FitBit, but so much for the heart and the mind.

My Mom. My first hero. My friend. We need an updated picture.
And that is just what my compulsive, reflective, organized self needed.
Because now, I feel a little better. It wasn’t what I had hoped. There was sadness, and worry. for my own girl, and for so many others. For adults I love, and for a former student fighting a formidable battle.
But, I woke up every day. And lots of days the sun shined. And fun doesn’t have to stop just because school starts.
So as I lay my head down tonight I will do my best to do it with gratitude. For new days. For new seasons. For a job with a kind boss, helpful colleagues, and wonderful children. For a job that begins new every year. For the knowledge that every day, every season, will hold blessings and challenges, for us and for everyone.
I wish you all a wonderful fall, but I’m not closing the pool just yet….
Losing Count…
In school I count children. Religiously. Especially in September. I count them in, and out.
I count pencils, to pacify my OCD. 12 to a table.
I count days until appointments, special occasions, and vacations. I love numbers.
I have a tendency to remember addresses, phone numbers, anniversaries and dates.
So it’s a really big deal in my mind when I realize I am losing count of Meghan’s surgical procedures.
I keep a list in my bag, that I update often. I have a 16 gig flash drive with a history spanning 12 years in that same ziploc bag in my purse. But, this year. Well, this year has been a little more wild than usual.
And every time I say it, I find the old saying, “You ain’t seen nothing yet..” coming true. But, every year I sit at an IEP meeting talking about discontinuing some services, and we always say, “When she goes a year with no surgery…”
Good thing I’m not holding my breath.
See I wrote, and I think I blogged, TWICE in the last week, that the hand surgery was Meghan’s 13th surgery. Except it wasn’t. It was the 14th.
And maybe, when I lose count, it’s time to stop counting. Because they are all starting to blur together.
2004- Epigastric hernia surgery
2007 – Gall Bladder Removed
2008 Tonsils and adenoids removed
2008 Back mass lipoma
2009 Oral “fibrous polyp”
2009 Embolization (internal) AVM right knee
2010 Embolization (internal) AVM right knee
2011 Direct Stick Embolization AVM right knee
2012 Direct Stick Embolization AVM right knee
2013 excision of mass from right palm
2014 complete thyroidectomy
Nov. 2014 emergency (direct stick) embolization AVM right knee
May 2015 Arthroscopic Surgery – Right knee
August 2015 Excision of vascular lesion from left palm
But, just as I think I should stop counting. Just as I think that this is “normal,” or that these procedures are somehow “minor,” I realize the ridiculous nature of that train of thought.
THIS IS NOT NORMAL. THIS IS COWDEN’S SYNDROME. And, BEATINGCOWDENS is what we do, but it is far from NORMAL!
This week, Meghan had a fever blister break out before her surgery. Maybe nerves, maybe coincidence, maybe a medication screw up. Whatever. It reminded me again, that her body is taxed. It is tired. I have been hunting through past blood work, another plan in place to try to deal with chronically low IgG levels.
She spent the 48 hours after the “minor” hand surgery with high fever and frightening headaches.
We had to postpone the follow-up to the “real” 13th surgery Thursday morning because she could not get into the car.
No surgery is minor. And we run the risk of confusing things we are used to with things that are not significant. And that is a dangerous road.
It is so important to keep validated, as an adolescent or as an adult. When we trivialize procedures, intentionally or not, we invalidate the patient. Cowden’s Syndrome patients will undergo insane numbers of procedures, surgeries, hospitalizations and testing in their lives. They all matter. Because we matter. And while we are forever grateful every time a surgery is smooth, benign, and uncomplicated, we are all a little more rattled than we were before.
So LOSING COUNT, is not acceptable. It somehow trivializes the nature of what goes on here.
We didn’t get to the beach this summer. We did get to Disney. Thank goodness. Because pretty much everything else we did involved traffic, a co-pay and a parking garage.
We are blessed. We are grateful. We are in tune to the tragedies and horrors around us. But, sometimes it gets lonely.
We miss barbeques and parties. We cancel at the last-minute. We rarely socialize. It’s not because we don’t want to. It’s because things change so quickly we can not keep up. And then it looks like we don’t want to. But, it’s just not true.
We are eternally grateful to the people who reach out. Just for a minute. Because it matters.
If you’re reading this because you know someone with Cowden’s or a similar syndrome, my advice to you is reach out. Text. Call. Email. It’s not about money, or grand gestures. It’s the 5 minutes you spend that will truly aid in the recovery process.
Because recovery is essential. Number 15 is just around the corner. And even though that’s a “regular” surgery, I bet not many of us have had our wisdom teeth extracted at the age of 12.
It’s physical.
It’s mental.
It’s emotional.
It does not stop.
BEATINGCOWDENS
Anticipation…
Funny how things creep into the mind. Then there was this Heinz commercial from the 70s.
Anticipation – is making me wait…
Tomorrow we do it again. Surgery 13. Vascular malformation, left palm.
Hopefully it has kept a safe distance from the artery.
Hopefully it is smooth and easy.
But, we worry. And it’s normal. Just because you’re USED to something, doesn’t make it OK.
Anticipation…
We will rest, although I don’t expect much sleep.
Pause…
Sometimes we need to pause. We pause only briefly, with hope of it lasting the whole week, and the reality that there will be interruptions along the way. We pause, knowing that pain is ever-present, acknowledging with gratitude any breaks we are granted. We pause knowing surgeries will always be forthcoming, but for right now they can wait. We pause because with the pace of this life it is easy to miss the little things, the important things. We pause to enjoy noise that is not NYC traffic, or the sound of a doctor’s office. We pause to quiet the phone calls that need answering. We pause so we are better prepared to battle this Cowden’s Syndrome. We pause to remind ourselves of the beauty, within our family, and around us in the world.





Last week we were in Walt Disney World, in Florida. It is our favorite, actually the ONLY vacation spot we have ever had as a family. We are fortunate to have celebrated Meghan’s birthday there for the last 8 years. Disney is crowded, and hot, and pricey, and all the things the haters of the big Mouse want to say. But, to the rest of us, there is a magic – a magic that endures regardless of age. It’s hard to describe it, unless you feel it, but we do. There is magic in avoiding doctors. There is magic in eating safe food from restaurants, and having a bakery that even makes cookies, and cupcakes for your gluten, dairy, soy free girl. So much of what we can’t do during the year is because of scheduling, and food. It seems silly, but with those obstacles gone, it is a recipe for success.
Even the negativity that tries to get at us, ultimately fails – https://beatingcowdens.com/2015/08/09/theres-nothing-wrong-with-that-girl/
The trip was one of the smoothest we have ever had. (Aside from me unpacking late the first night to realize I forgot the enzymes Meghan needs to eat! Fortunately I ALWAYS have extra, and Mom got them overnighted so they arrived in the nick of time Saturday. Tragedy averted. Magical.)
And I was only on the phone with one doctor. Once. The WHOLE WEEK!
I sometimes look at others vacation photos and think it would be nice, and perhaps a lot less costly, to change things up. It might be interesting to see a few new things. I would love to travel the country one day. But, there will be time for all of that – later. For now it’s about magic, and the treasure of having a preteen who still feels the magic in her heart.
Plus, we have some favorite rides…


Some Magical birthday wishes…

https://www.erinmckennasbakery.com/orlando/

And a birthday tradition…
A great view…
Spectacular nighttime shows…



There was plenty of time for me to walk. And think about whatever I wanted, or nothing at all. And we three started each day with our Isagenix… (fool me once – but never twice… for those of you who remember last year’s debacle!)
There were days I felt like I could go on forever…
And days to just be a little silly…
And as is the case every year when we pull away from our “home” for the week, I find my heart beating a bit faster. My mind begins to race back on track. And I don’t really like it.
This has been a wild summer. One too many doctor’s appointments, too few days of simple relaxation. And even as I am ALWAYS so conscious it could be much worse, I feel a bit of longing to do it all again, or maybe tack a few weeks on the back-end…
But, time does as it pleases, and eight days from now my girl will be recovering from another hand surgery.
We’ve begun to prepare for fall activities, and we are looking to sure up a date for our PTEN Foundation/ Global Genes Project fundraiser in February.
BEATING COWDENS takes stamina. Fortunately, we’ve got that.
And even more – we’ve got each other. And if we pause for no other reason, it is so we NEVER FORGET…

And then THIS happened…
And in the middle of the summer that wasn’t, Meghan’s drama teacher was out doing her thing, inspiring my daughter to step out of her comfort zone and reach new heights. I LOVE the drama teacher. And I LOVE that my girl has no fear.
Summer play. Broadway scenes.
She is SO NOT defined by Cowden’s Syndrome… Not today, not ever.
Kudos to my Mary Poppins, and the whole cast. (Even on their crackly public school microphones!)
I LOVE that she has an outlet that she enjoys so much. I LOVE that she smiles on the stage. I really LOVE everything about the peace it brings to her.
This passion, this will help her as she works at BEATINGCOWDENS!








































