Blindsided

I receieved a phone call yesterday that has already begun to alter the course of my month, if not my year.  Up until two days ago, I never imagined such a conversation would take place.  In fact, it is safe to say that I am still stunned by the turn of events.

Four weeks ago, I felt a lump in my breast.  I wouldn't have thought much more about it, and would have assumed it was nothing more than a cyst, but for the pain.  It wasn't much at first, and generally only when I touched the side and could actually feel the lump.  I realized I should probably get it checked out, but was in the throes of reunion travel and excitement.  I also thought it might (let me have my fantasy) resolve itself and I needn't worry myself.

I can't say that my first thought was not cancer, but I promptly researched "lump and breast pain" with Dr. Google and found (according to most sites) that pain was not always associated with cancerous lumps.  I am sure if I was not a worrier, this would have been sufficient for me.  However, I knew what I really needed to do and it was just a matter of finding an Ob/Gyn that was not completely booked for the next year.

I found one rather quickly, but then life got in the way and I kept forgetting to call for an appointment.  Finally, after 3 weeks I realized I was delaying in the hopes that everything would magically clear up on its own.  It hadn't and I knew it was time to face the music, no matter what was in store.  I made the appointment, went in, the nurse practitioner reviewed my fabulous medical history and all went swimmingly.

She knew why I was there, but was not concerned.  I was "young and healthy" according to her, had no known risk factors and certainly this was just a fluke.  I was feeling quite positive until the exam.  The minute she finished her demeanor changed ever so slightly.  She suddenly seemed to have less pep and offered that she could not make a diagnosis, and recommended that I have a mammogram and ultrasound to rule things out.

Great!  I would go, "rule things out" and that would be that.  It would be a cyst, some type of infection, I would get antibiotics and head home.  I  filled out the online form that night, a scheduler called me the next day and set me up with a 12:45 p.m. appointment.  I called Nicholas's Montessori and asked for extended care and figured I would easily have him home by 3 p.m.  I wrongly assumed that only a long wait due to many appointments would keep me there.  

Never in my wildest dreams did I think that by 2 p.m., after having one ultrasound and two mammograms, I would be curled up on an exam table, freezing despite the warm room, shaking like a leaf and being prepped for a biopsy that, in the doctor's words, "couldn't wait."  I had not even had a chance to call Peter, only the time to send him a quick note indicating that the tests were taking longer than originally thought.  In fact, I had been so nonplussed about the appointment,  that I hadn't even mentioned it until a quick phone call prior to leaving the house.

By 3 p.m., I was in the car, films in hand and bawling on the phone with Peter like no one's business. It wasn't even the testing, but the sudden urgency after the two mammograms and the ultrasound both revealed "suspicious calcifications."  I had watched an 80 year old woman bounce out of the testing area and declare, "Oh, that was easy, it didn't hurt a bit" and had just assumed at my age, I would have the same experience.

Instead, I left with an ice pack tucked away in my bra, and headed to the nearest CVS to load up on extra-strength Tylenol to dull the pain from the biopsy.  I was stunned by the turn of events, but Peter and the 3 other (extremely supportive) people I told were sure it was nothing and spent 48 hours sending me good vibes and hope.

I can't say I wasn't nervous, but tried not to focus on the negative.  I kept reminding myself that no one mentioned severity or anything of the nature during the testing, they simply said it needed to be done.  For all I knew, anyone with anything remotely suspicious went through the exact same process and ended up with a phone call that indicated all was well.  

I gave the doctor's office 48 plus hours and finally threw in the towel.  Between the never-ending bidding process (no, we still don't have a post) and this situation, I was started to unravel a bit.  I just wanted the news, no matter what, so we could move forward if something was wrong.  I called my doctor's office, but no one picked up, so I left a voicemail.  I then gave the actual diagnostic center a call, but all of the doctors had left for the day.   

Not five minutes later, my phone rang with an unknown number on the screen.  I figured it was likely a wrong number, but picked up anyway.  It was the OB/Gyn returning my call and letting me know that the test results were in.  The doctor did not waste time and while she was very thoughtful, she did not mince words and the next thing I knew I had a diagnosis of breast cancer* (DCIS), a list of doctors to call and a plan of action to start.

Thus far, I am not sure what to think.  I know that it has been caught very early, and that is extremely good news. I know many people have gone through much worse and I should be grateful it is what it is.  I know that there are so many treatment options and that in all likelihood this will be but a blip on my medical history radar.  

Yet…I'm still in shock.  Not only did my body betray me, but at an inconvenient time at best (I know, I know, there is never a good time).  I don't know what to think and at least for the next few days, there is not much I can do.  I have done my share of Googling this type of non-invasive cancer and think, for the moment, I am going to take a break.  On that note, though, if anyone has any experience with this type of breast cancer, please feel free to share on or off-line.  I'm just going to give Google a rest for a couple of days.

Instead I'm going to think that perhaps leaving the choir was a better call than I ever imagined, and enjoy the fall weather.  The kids don't know anything yet, so in certain respects, I can try and live in blissful ignorance.   We will hit a pumpkin patch or two, enjoy the long weekend and try to hold onto our little piece of normal for just a few more days…

 

*This was the preliminary diagnosis over the phone. I expect to have a more detailed pathology report on Monday to review.   

 

 

 

49 Responses to Blindsided

  1. Jill's avatar Jill says:

    From my long winded email earlier today, and your ever so sweet reply, you know that I am here for you… in mind, body, and if need/want be, a quick flight out to be there to hold your hand.
    You’re a strong soul and will get through this quickly, with the help from your family and friends.
    Take care of your kids and let us take care of you – however that may be! xx

  2. Melissa's avatar Melissa says:

    Oh – Jen!!! You and your family will be in our thoughts and prayers through this blip along the road of life. Please let me know if there is ANYTHING I can do for you!

  3. Berta's avatar Berta says:

    Sending you lots of love and warm thoughts, Jen.

  4. Rachel's avatar Rachel says:

    My thoughts are with you from Vancouver…

  5. Becky's avatar Becky says:

    Thinking of you Jen

  6. Eve's avatar Eve says:

    Jen- I am on Capitol hill. Just a metro ride away. Free babysitting whenever you need it. Are you at falls church oakwood? (no car on my end but i could rent a zip car) I would like to stop by with some food and a care package next week. (kombucha tea, of course!) please call me and tell me what you need. Don’t be shy. 313-585-4844 xoxo

  7. Sara Roy's avatar Sara Roy says:

    Jen – I’m so sorry to hear this. If there’s anything I can do let me know. If you have someone to watch the kids and you want to escape to Costa Rica for a few days, just say the word!

  8. Susanna's avatar Susanna says:

    Jen…whatever you need…just ask. You can get me on facebook, email (mctalzeme2003@yahoo.com) or 571-330-2168. I can pick up kids, watch kids, clean kitchens, pour wine…just please ask.

  9. Camille's avatar Camille says:

    Oh Jen – our thoughts and prayers are with you.

  10. Antoinette's avatar Antoinette says:

    Hi Dinoia Family,
    I’m an FSO and a habitual lurker on FSO blogs. Just wanted to let you know how much I enjoy reading your blog. Good Luck with everything and you will remain in my thoughts.
    Best Wishes,
    Antoinette

  11. Dear Jen-
    I’m so sorry for your diagnosis. I am praying for you. Please do your best to take care. You and your family are in my thoughts.
    -Emily

  12. Jennifer Pope's avatar Jennifer Pope says:

    Jen – You are in my prayers. I am sending out a big hug for you. Keep breathing. I’m just glad that they caught it in the earliest stage.

  13. Anne's avatar Anne says:

    I know we’ve only exchanged a few blog comments and I’m practically a stranger, but I’d like to throw my name in the hat with many of your friends above. I’ll be arriving in DC next weekend with literally nothing to do with my time until my few FSI classes start mid-November. If I can help you in any way please let me know.

  14. OHmommy's avatar OHmommy says:

    Jill sent me over. Please know that tonight a stranger in Ohio will be praying for you.
    All the love in the world,
    Pauline

  15. Kristina's avatar Kristina says:

    Jen and Family,
    I have enjoyed your blog for a long time and I am sending positive thoughts to you and your family during this time. My prayers are with you.
    With regards,
    Kristina

  16. I’m here via Jill too. Sending you much love and good thoughts from Israel.

  17. Donna's avatar Donna says:

    Oh no, Jen, what an awful thing to happen at the worst possible time.
    I have a dear friend in the SFFO who went through this same scary experience a few years ago, while posted to Egypt. If it would help, I’ll gladly put you in contact with her. At the time, I think what helped her the most were the friends who had been through it and could tell her what she would be facing in the months ahead. She’s also obviously done battle with the State bureaucracy. If talking to a fellow DS spouse who has been there would help, please let me know and I’ll send her your way.
    Prayers your way from Jordan.

  18. hannah's avatar hannah says:

    Oh honey, I am so sorry – this is absolutely the worst time to go through this, although there’s never a good time for it. The positive – you caught it early, you’re in a place where you have access to good medical care, and there are lots of people there and around the world who care for you. I’m keeping you in my thoughts, dear. Be strong.

  19. Kate's avatar Kate says:

    Jen,
    We haven’t met, but I’ve been following your blog since my husband joined the FS. We recently moved to NoVA and will be here for the next year. I’m not working, have a car, and my kids are in school all day, so if you need childcare, meals, wine runs, whatever, I would love to lend a hand.

  20. Scary Mommy's avatar Scary Mommy says:

    Another one of Jill’s friends thinking of you today and sending the warmest thoughts…

  21. Hi, I’m here from Jill’s also. I just wanted to say I’m so sorry. I’ll be praying for you. I hope you get lots of support and help.

  22. Tara R.'s avatar Tara R. says:

    I’m here from Jill’s blog too. I will be keeping you and your family in my thoughts and prayers.

  23. theflemings1@mac.com's avatar theflemings1@mac.com says:

    My prayers are with you. You sound so positive! Hang onto it, hang in there, Sister.
    Christine, a friend of Jill’s, and member of the “home-with-three-while-daddy’s- overseas club”

  24. bfiles's avatar bfiles says:

    oh Jen, I’m so sorry. I read Jill’s blog post with a sinking heart, knowing it had to be you. If it makes you feel better, my mom had DCIS and is fully recovered. How I wish there was something I could do to help. will be thinking of you non-stop.

  25. Naomi's avatar Naomi says:

    Oh baby girl. Nothing I can say will make it go away unfortunately … So just know that I am here for you (though about the best I can offer is an email thread of support and venting if you need it).
    My heart sinks that you don’t really have time for this … But if anyone can kick this cancer in the ass, it’s you. Rock it sister!!

  26. Hi Jen,
    I am so sorry to hear this! It is such a hard thing to have to go through and it is such a difficult moment for you to have to worry about this on top of being a “single” parent while Peter is in Iraq. My heart goes out to you! I don’t know anyone with that same diagnosis but we have cancer in the family (my dad, my aunt, my mother-in-law, my brother-in-law) and what I’have learned from being around them while they were fighting their battles is that early detection, access to good care, the support of your friends and family and your attitude/outlook are the most important factors in beating this vicious disease. You have all of those on your side. Stay strong and don’t hesitate to ask for help, when you need it.
    I am in Falls Church and will do whatever you need. Just say the word. Don’t try to fight this battle alone. Looking at just your comment section, there are lots of friends (personal and virtual) who are more than willing and able to lend a helping hand. Don’t forget that. Don’t be shy or uncomfortable. My number is 727-776-9976 – I am here for you.
    Big hugs!

  27. Heather Rhodes's avatar Heather Rhodes says:

    HI Jenn, although I dont know you, Jill sent out her blog with the latest news and I had to write. My husband is also deployed overseas and I just cant imagine what you are going through. You will continue be in our thoughts and prayers. Wishing you positive energy and lots of love.
    Love, Heather Rhodes

  28. christy's avatar christy says:

    Hi, I’m Christy. I’m so sorry…I’m here from Jill’s blog too. I am from NoVa, and my family is all still there. Lots of drs in our family, and a history of C too, unfortunately. So, if you need dr recommendations, or anything, feel free to email me or leave a comment on my food blog (my personal blog is now private) and I’d be happy to help out in any way too. Seriously…I am not just saying this.

  29. Michelle's avatar Michelle says:

    Hi Jen, not sure if you remember me, Michelle (Kayla’s mom). Just read this news today and wanted to add my prayers with everyone else as you begin this fight…this fight to beat cancer. Sending you many prayers.

  30. Erica's avatar Erica says:

    My heart really goes out to you. This hits very close to home for me and I was so sorry to hear your news. I am glad that the cancer was caught early. I wish the best for you as you journey through your fight. May you always have the kindest nurses and the best treatment.

  31. becky skillin's avatar becky skillin says:

    http://wholelifecancercoach.com/
    I’m Jill Perlman’s friend, read your blog entry, and wanted to to know about a cancer coach who has survived two aggressive cancers.
    I have found this blog helpful.
    I will be thinking of you.

  32. becky skillin's avatar becky skillin says:

    I forgot to mention that the http://www.wholelifecancercoach.com is from a Foreign Service mom who has also done tours with her kids while husband was in Afghanistan.
    If e-hugs can help I send them your way!!

  33. Sunny's avatar Sunny says:

    This post brought tears to my eyes. I cannot imagine how hard this must be for you. You have been in my heart and thoughts all day. You will be in my prayers.

  34. Digger's avatar Digger says:

    I am keeping you and your family in my prayers.

  35. Kelly's avatar Kelly says:

    Another person here via Jill….prayers and positive energy being sent your way from Florida. Praying for a swift, easy and COMPLETE recovery for you!

  36. Hi Jen – you don’t know me – Jill sent me to your blog – pls know that I am praying for strength and good health for you. I am praying for it to be simple and dealt with speedily. Wishing you a happy day today. Sejal

  37. Lisa's avatar Lisa says:

    Jen,
    I am here from Jill’s blog as well, you are in my thoughts and prayers. The good news is that they have caught it early. You have friends and it seems many new friends who will see you through this if you let them. Just remember Cancer can be beaten. I am sending you positive thoughts and energy from Canada.
    Lisa

  38. I’m so sorry you’re going through this. Remember to think pink, stay strong and that many women have, unfortunately, traveled the road before you and came out the other side triumphant. hugs to you and yours. I’ll be checking in… and thinking of you often.

  39. Katherine's avatar Katherine says:

    sending love and prayers to you Jen….hugs

  40. Becky's avatar Becky says:

    Anther blog follower. Also thinking of you and hoping for a speedy and good resolution to all this. You’re in my prayers today.

  41. Emily's avatar Emily says:

    I have no words. Just thoughts and support. You truly are amazing, your attitude and strength are qualities that make you quite remarkable.
    (Don’t worry about getting back to me. Just know I am thinking about you and your family.)

  42. Michelle J.'s avatar Michelle J. says:

    Oh Jen, I am so sorry to hear about this awful news but you are a strong woman and I know you can handle anything that comes your way. My thoughts and prayers are with you and the family. Hang in there!

  43. Wendy's avatar Wendy says:

    Jen, please know that in Mozambique you have State Dept family praying for your complete recovery. It looks like you have some great offers of help above, don’t be too proud to take them up. Use your strength to fight this for you and your family, and let us all share the yoke of this burden with you to lighten your load. God bless.

  44. Becca's avatar Becca says:

    You don’t know me but I am thinking of you.

  45. I just saw this post and feel sick. If you need help with the kids to make appointments, let me know and I can cover for you. If you need help with anything at all let me know.
    This is the same type of cancer my mom was diagnosed with five years ago. She’s been cancer free after a lumpectomy and radiation. There is hope and lots of love coming your way.

  46. Melissa V's avatar Melissa V says:

    Jen, you won’t be the first breast cancer survivor I’ve known – hang in there. I’m in Alexandria so if I can help, let me know.

  47. Unknown's avatar Mitchell-st says:

    Jen – not sure whether or not my comment made it through. Anyway, to recap, I was dx with DCIS in 2006 when I was 37. Had a partial mastectomy (was supposed to be a lumpectomy but the cancer was bigger than thought), 33 radiation treatments, no taxiform. Four years out and am still cancer-free. All I have to do is get a mammogram every year. My breasts look fine (bar a couple of scars), and I have two tiny blue tattooed dots for radiation guidance – that’s all. The biopsy was worse than the partial mastectomy, IMO.
    If you want to e-mail me privately it’s mitchell-st@hotmail.com. I knew Jill in Chennai, and still follow her blog, which is how I found out about your dx.
    Take care,
    Teresa

  48. I thought I commented on this days ago, but just just found the unposted comment sitting in one of the million windows still open on my computer screen…
    I’m a friend of Jill’s and I live in Northern VA too. Send me an e-mail – I’d love to help in any way possible. Watching the kids during appointments, or even just watching them to give you a break. It’s hard to be far away from family (even though I grew up in DC, my parents moved to Key West years ago). But friends are a great alternative!
    -Kate

  49. Fi's avatar Fi says:

    I’m so sorry Jen.
    I don’t know you but I will be praying for you ≈
    X

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