I haven’t done one of those posts in several months and since I have a new book out (here are all my books on Amazon if you’re looking for them :-)), I thought maybe it was the right timing. I’m not good at asking for things. But this doesn’t only apply to me, it applies to all your favorite authors, to all the books you couldn’t put down, to all the stories that transported you into their worlds…
What you can do for those stories and those authors really doesn’t take a lot of time. You don’t have to buy the book. You can ask Overdrive or your library to borrow it.
Leaving a review doesn’t mean writing an ENG 101 essay, it just needs a few words.
And if you’re on other social media or readers’ group, then share that review there too. A couple of minutes. Super easy. If you have a book club, don’t hesitate to recommend that book to your book club. I was in one book club right around the time I was diagnosed and I actually almost went to that book club 🙂 And I just found out one of my readers’ from my cozy book recommended my book to her book club and I’m still smiling just thinking about it.
Did you love a book? Tell your friends. Tell your family. Tell your library. 🙂
Why does it matter? It does for many reasons. As an author, you’re not supposed to look at reviews but seeing your book not getting a lot of reviews can be tough. I’m not talking about the “oh my nobody loved it. No one cares. I’m going to go hide now” which happens from times to times, let’s face it. I’m mostly talking about the fact that there are secret and not-so-secret algorithms at play. If a book is bought and gets reviewed, it might be put in front of more readers…which means more reviews and more readers.
If you’ve read all of this 🙂 Don’t hesitate to tell me what are the latest books you’ve reviewed and where you reviewed it.
It’s my book birthday. TRUST ME, TRUST ME NOT is my 8th book. And this book has been with me in some pretty difficult times and yet helped me move forward. And what better way to celebrate this book birthday than to hopefully raise some awareness and share my own experience to maybe help someone else.
Yesterday I shared my book release campaign. I’m donating $1 per purchase to the Leukemia & Lymphoma Society for the entire month of September for #BloodCancerAwarenessMonth and my friend (and very talented author) Katy Upperman is matching those donations up to $100. And while I was writing I was thinking on how even though cancer doesn’t define me, it’s not like I can simply wish it away. I can enjoy the moments and be present and sometimes I wonder if I talk too much about it. But, you know what, even though it doesn’t define me, it’s part of my daily life. I see the scars. And I feel it in the neuropathy in my feet. I see it on the calendar as I start mobilization in about 10 days. I also do a lot of other things. And I can talk about a lot of other things. It’s a balance. And it’s important to me. It’s also important to me to share what I wrote in the author’s note of TRUST ME, TRUST ME NOT.
So, I thought that on my book birthday, I’ll share it with all of you.
So here we go….
All my books feel special
to me. But this one? Those characters who have become real in my imagination?
They feel extra special. Maybe because there is so much of me in them. Maybe
because they have helped me move forward. Maybe because I am so proud of this
belong to you now, but for a while they were only in my mind. I started writing
this book what feels like forever ago, even though it’s been maybe over a year or maybe two years. It’s kind of a blur.
I was diagnosed with Hodgkin lymphoma in October 2017. After months of feeling tired. After months of coughing. After months of backache.
started with shooting pain in my shoulder and arm after drinking a sip of
alcohol. It was so bad that I started taking Tylenol if I knew I was going to
have a glass. It was the holiday season. And I do enjoy a glass here and there
and really didn’t want to miss
drinking Champagne on New Year’s Eve.
I googled my symptoms as I do and I found that having pain while drinking
alcohol could be an early symptom of Hodgkin’s lymphoma. I thought I felt something underneath
my arm too, but it wasn’t always
there. My mind went on overdrive. And did I mention I have anxiety?
the pain wasn’t going away and my
upper back pain was actually intensifying, I went to my primary care physician
at the end of 2016. But he basically told me that he’d never heard of the pain with the alcohol symptom
for lymphoma, and that based on his physical evaluation he really didn’t think I should be too worried. He dismissed my
concerns and told me I should do physical therapy for my upper back because it
could very well be muscle weakness. And me having anxiety, I thought, Okay…my
heightened concerns stem from my over-imaginative mind, so I’ll do the physical
therapy and see. He also told me I could
do bloodwork but I figured if he was really worried and not just appeasing my
worries, he’d tell me otherwise. I
didn’t do my bloodwork (which could
have very well shown nothing at that stage because Hodgkin’s lymphoma is funny like that).
months of physical therapy. I changed physical therapists so that it was closer
to my work (I was teaching German at a wonderful community college then). None
of them asked me to undergo x-rays. I went back to my primary care physician
because of a lingering cough in August 2017. Unfortunately it was a different
one and she dismissed my concerns. She also didn’t notice I had lost weight. I hadn’t noticed either but it was summer and I was
wearing clothes that fit. I did have to buy new pairs of jeans but I figured it
was because I had been more active. After all, I was doing physical therapy.
cough continued. My back pain was keeping me up at night. I was feeling like
remember driving to work one day, coughing and yelling in my car that no matter
what was making me cough, I was going to be okay. I knew. Deep inside, I knew
there was more going on with this cough.
started jogging again which in retrospect and after finding out what was going
on in my body makes me wonder how I managed to run. Granted it wasn’t fast or long, but still…
decided to continue working out too. But one day, I felt dizzy while working
out. I blamed it on not drinking enough water.
teaching two classes and writing and doing a thousand things as always. But one
day, I felt dizzy teaching, which I blamed on maybe not eating enough. I
started eating more snacks despite the fact that I wasn’t hungry. I continued working and writing and
telling myself it was okay. Because I went to see my doctor.
I had an
itch and a rash during that time too, but I also have sensitive skin so what
are the chances?
found a lump above my chest in early fall of 2017. And then I went back to see
my primary care physician and everything went very fast after that.
time I got diagnosed I had a very large mass in my chest, which was now
basically poking out of my chest wall, hence the lump. It was such a large mass
that the thoracic surgeon who did my biopsy told me I shouldn’t sleep laying down because the mass could be a
risk to my trachea. That was scary. I remember sitting with my husband on our
bed and we were crossing our fingers that the surgeon would call me back to let
me know the biopsy showed Hodgkin’s
and not some other cancer which had way less of a good prognosis.
laughed and reassured my family when I got the diagnosis. Because we got the
news we wanted. But still it was hard. And it got even harder.
was a time we weren’t quite sure if I’d still be alive today. And I am. And I am
I’m still in treatment today. Hodgkin’s is a very treatable cancer but sometimes it takes
longer when you’re not in the majority
of patients who are cured with first-line treatment. I didn’t talk about cancer much online at first and I didn’t tell many people, because I thought I was going
to be part of the large percentage of patients that go into remission after
their first-line treatment.
I had experiences which plainly sucked. I could probably write a book about fighting
for your rights, fighting to be heard, fighting for your care as a cancer
remember telling one of my oncologists that I was worried about getting a PICC
line (peripherally inserted central catheter which is a form of intravenous
access) because the mass was narrowing my SVC (superior vena cava), and that
oncologist dismissed me. I asked him twice. I asked the nurse who told me, “Well, if they say it’s possible, we should try.” My husband wasn’t in the room with me and it was painful and I was
scared and the nurse kept on hitting a snag and then my heart galloped and she
said, “I’m never doing this to you
again. If they want you to go through it again, they need to send you to
met with that oncologist again (who wasn’t my primary oncologist but higher up), he smiled,
raised his hand, and walked back out of the room. Like it was nothing. Like
that wasn’t traumatizing. I mean,
granted it was nothing like a bone marrow biopsy, but still…(that’s
another story). That same oncologist told me once the first chemo didn’t work as well as it usually does, “Now you’ve
become interesting.” Oh and I could
tell you so much more. Like how he dismissed a treatment that was not coming
from his “group” as inefficient and
yet our third opinion from MSK saw it as possibility because “studies have shown it works.”
longer my oncologist for these reasons and many others. We trusted the Fellow
we had, but that same oncologist who had dismissed my concerns kept on pushing
for one treatment plan, making it seem like it was our one and only option. We
weren’t so sure about their treatment
plan forward, and when we asked questions, we didn’t get many answers. It was a very hard time. I
couldn’t talk without getting out of
breath. I couldn’t drive. I couldn’t walk without getting dizzy. And I was scared of
going through that treatment plan still feeling the way I did. Both the
oncologist we saw at MSK and the one we saw at the University of Maryland
Greenebaum Cancer Center gave us hope again.
is so important.
going to go into details because this is a note from me to you, not another
book ☺ Just like I’m not going to go into details on the ER visits,
and the neuropathy and dealing with health insurance and billing and all that.
treated at the Greenebaum Cancer Center and I’m very grateful to my team there. As I’m writing this, the plan is for me to go through an
autologous stem-cell transplant and yes, I’m very scared about the entire process, but I have
a wonderful team and I advocate for myself and I’m heard and I feel in control of the things I can
be in control of and I learn to deal with the things I can’t necessarily control.
As a cancer patient, I’m so grateful to the Greenebaum Cancer Center for truly being an comprehensive cancer center. My sessions with Vicky Wilson have helped me tremendously. I’m less anxious, less stressed. I know that it’s okay to not always be okay. And I owe it to her.
after switching chemo, I found a way to create different moments, like organize
a fundraiser for associations who help young adult facing cancer. And one of my
highlights? Jenna Fisher (who I loved in The Office but would watch in pretty much anything) not only
donated but she also tweeted at me ☺
get me wrong, there were a lot of hard moments, but there were also a lot, a
lot of good ones throughout treatment. And therapy helps!
grateful to my oncologist, Dr. Aaron Rapoport, for letting me be a part of the
team and especially for giving us hope—and for never making me feel like I didn’t matter. To the nurses (especially Liz and Meeghan
and the infusion nurses) and Meghan (from the Ulman Fund) and Nancy
(Survivorship Navigator) who always manage to put a smile on my face and who
also sometimes just let me cry when I need to cry.
I may be
tearing up writing this author’s note.
don’t know what to do for someone who’s close to you, who is going through treatment, is
in remission or might have relapsed, or got diagnosed recently, sometimes you
just need to be there. Organize a meal train (thank you to the Chemical
Engineer’s boss for starting one for
us and for his colleagues for keeping us fed during the months of chemo
treatment). Send a card. Mow their lawn. Text them. Call them. Connect with them.
Even if they’re far away. Don’t forget them. And it’s okay to talk about something else. And it’s okay to ask about it. Everyone reacts
differently. And not everyone has the same experience with chemo and treatment.
But I think not feeling like you’re left
behind is important. And when you’re
going through treatment, you may be too tired or too sick or too vulnerable to
be the one keeping that connection. So, reaching out without always expecting
an answer really helps.
Sometimes this cancer treatment thing takes a
long time, and it’s important to not
lose that connection.
you’re reading this author’s note, I urge you to advocate for yourself, to not
let your anxiety (if you’re prone to
it) be used as an excuse as to why you are feeling strange or sick. Sure, it
can be related to anxiety but you do need to be checked out.
to be listened to.
to have your medical team take your concerns seriously.
some days, I do wonder if maybe the first-line treatment would have worked if
we had caught it before the mass went through my chest wall. And I’ll never be sure so I don’t dwell on it. But still…it’s important that your worries do not get dismissed.
If you are
suffering from anxiety or depression, then my wish for you is to be able to
also find a professional who can help you get through the tough moments and who
can give you the tools you need.
know what else? Enjoy the little moments.
those little moments too, because sometimes you have to readjust. But those
moments, you can still find them. A ray of sunshine. A laugh. A good book. A
Those moments? They truly are the big ones ☺
I probably should add the “Buy links” here but you can find all those in my release campaign post here.
If you’ve read that far, you can also share that release month campaign by retweeting Katy 🙂
or retweeting Katy,
Or sharing this post…
But mainly, what you can really do is spread awareness and advocate for yourself and others if you can and enjoy the little moments.
And yes, it’s somewhat related to my books. For some reason, I’ve been thinking about mental health and how therapy has helped me and I just posted my random thoughts on Twitter.
So I thought, I’d share them here too. Because…why not?
Deep breath, here we go.
I ‘m not sure who needs to hear this, but I’ve been thinking about mental health and that I should share my own experience. I was in therapy for 2 years in Germany. I have high-functioning anxiety and needed to deal with a few things on top of that anxiety and/or resulting from that anxiety. I was working full-time, and was gaining more and more responsibility at work. I loved my high-stress job (for the most part), and I was good at it (at least I want to believe so).
One of the reasons I was able to do that much was thanks to therapy. My therapist used Cognitive behavioral techniques.
She gave me the tools I needed. And it wasn’t immediate. And it was a lot of hours. I used to go once a week during my lunch break. Then once every 2 weeks, then once a month. I started because The Chemical Engineer very rightly told me that he couldn’t be my therapist.
I had tried it in the US too while finishing my first Master’s but it didn’t click. And I didn’t look for someone else. I probably should have tried to find a professional then, but I waited a few more years to really invest the time in myself.
Fast-forward four years and I’m back in therapy to deal with all those emotions and fears that come with cancer. I didn’t get therapy in my first cancer center and it’s a pity they didn’t offer it, because I was retreating and didn’t know how to deal with it.
When I started seeing my therapist in January 2018, I was a mess. And she has helped me so so so much. She listens to me and gives me the tools I need to deal with all of that.
The Chemical Engineer even went to a few sessions and it has made such a difference in the way we communicate through this. Therapy has made a big difference in my life. And yet, there still seems to be a stigma attached to it.
Maybe that’s why a lot of the characters in my books go through therapy. It’s not magic. It doesn’t happen overnight. And it can take time to find the right person. But I believe it does help. And if you need it, I really hope you’re able to receive it and seek that help ❤
And here’s a picture of Plato The Dog because that picture always manages to me smile.
Sometimes, you just need to enjoy a piece of cake (or whatever is your equivalent of a piece of cake).
Yesterday when I had that piece of cake it made me smile. Granted the company was also pretty good. Yesterday I cried (I didn’t take a picture of my crying face so cake picture it is not 😋). Yesterday, I was full of hope and my hope kind of got crushed a little. But hope is pretty resilient.
Yesterday I had a PET scan which was kind of mixed. On one side, it showed that the mediastinal lymph node I had before reduced in size & in SUV (activity level), which is wonderful news. On the other side, there are new areas of concern. I haven’t seen the full report yet but based on the discussion with my oncologist, it could actually be inflammation due to the immunotherapy.
I’m currently slated to have two more treatments & then undergo an autologous stem cell transplant (with my own stem cells). This has proven curative in Hodgkin’s. It’s better to have a so-called negative PET scan before undergoing said stem-cell, so I want to get another PET before the actual transplant. I might have to fight my insurance for it (again). I’m grateful cancer is no longer a pre-existing condition, because it would have the potential to make everything harder & honestly, I don’t need that.
Immunotherapy is pretty novel before transplant. It has shown to enhance chemo-sensitivity so crossing my fingers that this sequence helps me. I have to talk to my oncologist (again). I’m very thankful to feel like an integral part of the team. My oncologist listens & listens & listens.
I feel well. I’ve recorded several audiobooks. I work out. I got used to the neuropathy in my feet. I’m writing again and my goal is to ensure my next novel TRUST ME, TRUST ME NOT comes out as planned beginning of September (up for pre-order https://amzn.to/2SICKrf 😊)
Yesterday was a whirlwind of emotions. Today I feel better & calmer & happier.
Right now, I’m concentrating on this one step, making sure I’m in the best shape I can & in the best position possible. Right now, I’m thinking of the fun things ahead. Right now, I’m also enjoying the little things & the little moments.
It’s my fifth publishing anniversary or The One With All The Thoughts…First: “The One…” is a reference to Friends’ episodes, I’m not trying to say I’m The One with all the thoughts. That would be a looooot of thoughts 😉 It was either going to be that or It’s my fifth publishing anniversary and I’ll write a blog post if I want to (imagine me singing…or not…you probably shouldn’t, I have a speaking voice :-))
It’s been five years since this picture was taken.
Wow. Five. Years. The Chemical Engineer and I were living in Mainz, in Germany with Peter The Cat. I was working at the European Central Bank as Press Officer. We now live in Maryland with Plato The Dog and Bobbie Voltaire the Cat, where after going back into teaching, I am now writing and narrating. A lot has happened in five years, both publishing and non-publishing wise.
But first, a little or rather big shout-out to my parents who are celebrating their 45th wedding anniversary today (June 26th,2019). Forty-five years! And let me just say, it makes my heart full of ❤
Now, when it comes to publishing. In those five years, there has been tears and laughter, total failures and resounding successes.
Some days, I feel like I still have no clue what I’m doing. Others, it feels like I have somewhat of an idea. Publishing has been a roller coaster of emotions. And let me make one thing clear, I am able to do it this way thanks to the Chemical Engineer. I definitely don’t make enough for us to live off my writing. And I’m very grateful he still believes in me after five years.
Five years ago, I published ONE, TWO, THREE…
When I published One, Two, Three, I thought it was going to be an instant bestseller.
You know the kind…even though I since realized that many (maybe most; I’m not sure since I don’t have any hard data) of the overnight successes had actually been in the making for decades.
Anyways, I believed I would wake up the morning of the launch and thousands of copies would have sold. I would be hitting all bestseller lists. Producers would be calling me, begging me to adapt the story for TV. Bookstores would ask me to stock it because people would be asking for it.
On the first day, it sold less than the number of my Facebook friends. Way less. Way way less. And nobody contacted me to adapt it for TV.
But I am still writing and I am still publishing and I am still selling copies of One, Two, Three today. And someone made fan art from the story!
Plus. the French translation got picked up as my option book with a French publisher.
It was retitled VIVRE, AIMER, DANSER… I love that cover!
And I still receive emails from readers who tell me how Natalya’s story has moved them, and how it has helped them somehow, and how much they loved getting to know her and Antonio, and Becca, and James.
Since I published One, Two, Three, I published one novelette (One Dream Only – Natalya’s story 0.5), one novella (A Summer Like No Other – Em & Nick #1) and four novels (Always Second Best, Em & Nick #2, Love in B Minor, Fear Me Fear Me Not and See Me See Me Not).
I went to writer’s retreats with talented writers and amazing human beings ❤
I participated in several authors’ events, and shared the stage with NYT bestseller authors and so many talented authors.
I signed a guitar!
I was featured in the Baltimore Sun.
Recently, I got my first BookBub promotion for FEAR ME, FEAR ME NOT. I’ve been trying for 5 years to get a BookBub 🙂 and I loved what they did for the promotion and how well it worked!
Some of my books are even available in audiobook! Like LOVE IN B MINOR which has been gathering wonderful reviews!
I started producing my own audiobooks, like LA PEUR DANS LE SANG (and soon UN SEUL REVE).
I started narrating other people’s books, like this Learning French audiobook.
As well as other audiobooks for which I use a pen name…;-)
During that time, I also got diagnosed with Hodgkin’s Lymphoma (in October 2017). After finding out that I needed to change treatments, I also organized an auction to benefit non-profits who help young adults with cancer. I was blown away by the amount of support I received from the publishing community for the Let’s Do Something Good auction! I mean I even got a signed book from Jenna Fischer! And she retweeted me and tweeted me directly!
I am back in treatment now and it’s not necessarily easy (for many reasons) yet easier (in other ways), but let me tell you: the book I currently have on pre-order, TRUST ME TRUST ME NOT, means a lot to me.
I can’t tell if I love one of my books more than the other, but I can tell you that writing Lacey and Hunter has been cathartic in a lot of ways. Being able to write has been emotional and hard and easy at the same time. Writing always is, but having Lacey trying to move forward, not knowing if she really can has been hitting a spot.
During these past five years, I didn’t reach a point where both The Chemical Engineer and I and our four-legged friends (see pictures below because how cute are they :-)) could live from my income. I loss some (especially at the beginning), I gained some (I actually make profits from my writing now, whoop whoop!).
I still dream of getting contacted by a producer. So if you’re a producer reading this, don’t hesitate 😉
But most importantly, I am grateful I get to write those stories in my head. Writing helps keeping me balanced even when it’s hard and frustrating, I find that it helps me.
I am grateful to my family and friends and everyone who helps me and cheers me on along the way (my talented and generous writer friends, photographer, cover designers, translators, editors and more).
And I’m especially grateful to my wonderful husband (who did get a Best Husband Of The Year Award last year or was it two years ago? :-)). Sometimes I have the feeling that I should do more, try more ways to sell more books (and I do), but even when The Chemical Engineer asks me for Excel sheets for the business side (and full disclosure: we bicker ;-)), I know he believes in me. And that means the world.
And I’m grateful to YOU, dear reader, for taking a chance on my books…and for loving the characters as much as I do ❤
On Wednesday, the French translation of my novel A SUMMER LIKE NO OTHER comes out again in paperback. But this time, it is published by Dreamland (City Editions). They publish Jessica Sorensen too (I’m still pinching myself over this fact :))
That makes me a so-called hybrid author: self-published and traditionally published. I don’t regret my decision to self-publish one bit. However, I don’t deny that knowing two of my books are going to be available in bookstores is giving me a happy fluttery feeling.
Look –> it’s my book on the site of the Bibliothèque nationale de France 🙂
A bit less than a year ago, I received an email from City Editions asking me if I’d like to have the French versions of A SUMMER LIKE NO OTHER and ALWAYS SECOND BEST in bookstores in France.
I didn’t believe it was real at first. I thought it might be a service someone was offering but nope, they were a serious publishing house and they wanted my books. I signed a contract. I got an advance. Everything was real.
You have no idea what it did to me when I read in the contract a clause about possibly being picked up by France Loisirs in the future. France Loisirs is my youth. It’s a subscription service with so many amazing books and just a lot of memories of going to their stores too sometimes to choose the book I would get. Someone else might pick up my book one day after perusing the store or their catalog for hours. And that makes me happy.
But even if that doesn’t happen, my book, my words…are going to be available in bookstores. Fnac, Cultura, Decitre, local bookstores…even Leclerc. Who knows maybe I’ll also see it at Cora, the store I used to work at as cashier during part of my studies?
And I’m grateful.
To City Editions for reaching out to me. To the translator of A SUMMER LIKE NO OTHER & ALWAYS SECOND BEST, Edith Girval who is simply oh so talented. To everyone who’s read the books already which probably gave me the exposure needed to be seen. To my family and friends for their unwavering support. To my husband, who is every bit as excited about this as I am and who’s so proud of me.
Tomorrow is the day I become a hybrid author. And trust me, when we go to France in a few weeks, I’ll be walking into a bookstore and might shed a tear holding my book in my hands.
Tomorrow is also the day I’m going to reveal the cover of my next book, SEE ME, SEE ME NOT (with a bunch of fun things and giveaways planned). Stay tuned…
I cannot believe this! FEAR ME, FEAR ME NOT is out in the world.
I love love love Dimitri and Erin. I love their story. I cried and I laughed while writing it. And I hope you enjoy their story too. You can get it in e-book and paperback here.
Oh and there’s a book trailer 🙂 It’s the first time I use a book trailer 🙂
Let me know what you think!
Releasing a story in the world is still this incredible mix of exciting and anxiety. On Tuesday, I woke up at 2 a.m. to finalize a few things…and it seemed surreal knowing that Dimi and Erin would soon be in your hands. 🙂 Surreal and amazing.
Thank for your reading! I’m very grateful for all of you!