Sunday, December 27, 2020

Remebering My Teal Sisters Gone in 2020

 At the end of every year the media always makes lists of the celebrities that have died throughout the year. All these "important" people we are not supposed to forget. Well, last year I decided that there are many every day people that are more important than celebrities who we shouldn't forget. 

These are special women: Teal Warriors. Women, girls who heard the same words I did - words that changed their lives forever - "You have Ovarian Cancer." 

These words changed every aspect of their life and the lives of their loved ones. They not only were dosed with poison that was supposed to kill the cancer, even though most treatments are over 30+ years old, most of them were told they were a Stage 3 or 4 because this cancer is so difficult to diagnose!! 

Ovarian Cancer has symptoms, symptoms that speak loudly. Symptoms that may be pushed off as other things - women's regular issues. If you or someone you love has these symptoms for more than 2 weeks consistently, push your doctor for a pelvic exam, pelvic ultrasound and a CA125 blood test!! 


The women and girls, young and old, had lives. They had families, jobs, children. They were mothers, daughters, sisters, aunts, best friends, wives. They ARE loved! 
They were nurses, teachers, students, business women, chefs, bankers, athletes. Advocates, Educators!

Each of these women still had much to do in their lives, some were just starting their first chapters; some were starting the later chapters. NO MATTER WHAT - they are real women, real people, real lives no longer on this earth!! 

We remember the following Teal Sisters: 

Desiree Baker - 1/2/20
Susan - 1/3/20
Leila - 1/6/20
Jean Maday - 48 - 1/11/20
Julia - 1/17/20
Terri Gerace - 64 - 1/20/20
Vicky Michelis - 1/27/20
Bernadette Zielinlinski - 50 - 1/29/20
Elena Lowry - 1/30/20
Sue Knabel - 2/1/20
Michele Entenman - 48- 2/5/20
Sam Ainuddin - 2/3/20
Andrea Smith Turley - 2/7/20
Shelia Mullins - 2/17/20
Helen Powell - 2/20
Sarah Ludinich - 24 - 2/20/20
Jeanne Evert - 62 - 2/20/20
Elizabeth Meier - 2/20
Elizabeth McConnell - 3/1/20
Marilyn Calingasan - 3/10/20
Lynne Sherren - 3/11/20
Aleida - 3/20
Kathleen "Kitty Ann" Baierl - 65 - 3/19/20
Janet Fogg - 57 - 3/22/20
Stacy Lewis Cardwell - 3/26/20
Michelle - 3/27/20
Brittany Jayne - 24 - 4/1/20
Anne Hendricks Bass - 78 - 4/1/20
LoriAnn Scoville - 46 - 4/6/20
Kathy Cusworth - 4/8/20
Heather Haefliger - 25 - 4/8/20
Petra Karr - 4/20
Constance Valentino - 4/16/20
Tammy Nicastro Savage - 5/4/20
Carolyn - 71 - 5/5/20
Jenny Freisen Pomerleau - 48 - 5/9/20
Jutta Fans - 5/13/20
Jenna Marie - 5/17/20
Jeanette Weber - 53 - 5/24/20
Sherril Hougui - 5/30/20
Jill Anne Lyman - 51 - 6/4/20
Noel Johnson - 47 - 6/9/20
Terry - 6/13/20
Wencke Helliesen Haug - 6/15/20
Tawsha Dawn Sparks - 6/23/20
Lisa Sanders - 7/10/20
Carol McClintock - 7/26/20
Jodi Sandoval - 8/1/20
Edna - 66 - 8/5/20
Col. Kim Ward - 8/6/20
Seana Roubinek - 52 - 8/26/20
Kimberly Brett - 55 - 8/28/20
Jenny White - 9/3/20
Gabriella - 26 - 9/5/20
Ilse VanMele-Verrassel - 9/10/20
Amy Rose VanWagner - 49 - 9/10/20
Katie Maxwell - 9/12/20
Delicia - 54 - 9/24/20
Julie Kershaw-Dellar - 9/29/20
Gloria "Glo" Roberts - 66 - 10/4/20
Amanda Lackie-O'Brien - 39 - 10/10/20
Natalie Jean Jugan - 10/11/20
Anne Marie O'Donnell - 10/11/20
Pat - 10/20
Kayleigh - 12 - 10/15/20
Widget Bennett Richards - 10/19/20
Terri Lynne Baeder - 58 - 10/26/20
Kathy Bounds - 10/30/20
Brenda Steelsmith - 11/1/20
Karen - 11/6/20
Jeni Barclay - 11/11/20
Susan Schaefer - 11/13/20
Liz Johnson - 34 - 11/13/20
Leighton Accardo - 9 - 11/24/20
Kathy Heck - 11/25/20
Terri Kassmer Giengreco - 12/11/20
Sharon Dantzler Kinsaul - 12/14/20
Faith Ann Tice - 12/14/20
Linda - 12/16/20
Cecilie Elizabeth Lovaas - 12/17/20


My Dearest Teal Sisters Rest In Heaven - We'll Take it from here . . . 




 


Wednesday, December 23, 2020

2020: Can Anything Good Come From A Pandemic?

 

2020 started out like any other year. January was cold, snowy, sometimes rainy - regular weather. We had our colds like normal. Saw our friends, went bowling, made plans for the bowling tournament, life was "normal." 

As the months went on I even did something I never did before - I attended the OCRA Advocacy Day in early March! We were just starting to hear about this new Novel Coronavirus that was found in Wuhan, China and was starting to make its way to other countries. I had a great time on Capital Hill with my Teal Sisters and friends. 




Sarah came with me too - we were able to meet with our representatives & Senators. We also attended Monday Night RAW - the last one with a live audience before EVERYTHING was cancelled.







In the beginning, I was angry. Angry at being forced to be at home when I wasn't sick. Not being able to go to work and see "my babies", being shut up in the house, not being able to do things with friends & family, only being able to go grocery shopping, having to argue and be on the phone with unemployment forever!! 

Then came the mask mandates!! Having to wear a mask EVERYWHERE, then ALL DAY AT WORK! This caused panic attacks and irritated my asthma. It also caused PTSD! Bringing back everything from when I needed to wear a mask during my cancer treatment, being stuck in my port, and even when we needed to after Britt had her bone marrow transplant. During those times it was the sick who were quarrentined and masked, took the the precautions. NOW I had to do it when I was healthy - it wasn't fair. It made depression, anxiety and PTSD much more difficult to deal with. 

But then  . . . .  a light, good things started happening. Little by little good things started happening. At first it was just being able to visit with mom & dad, and Angela & Andrew. Then we had a small, socially responsible bon fire with a few friends and there was laughter and s'mores! 

Then a Faceboook group where people were putting Hearts and Happy messages on their windows for everyone to see. I joined and even found people in Menomonee Falls & Germantown that I drove past everyday who were in the group! I painted our window, Monty suggested some Christmas lights to make it more festive. 




Other things started to happen, some bad - a friend ended up in the hospital for over a month. But good came of that too! People far and wide rallied in prayer for him and his family. People they didn't even know started doing porch drops of food, craft supplies and other things for the family to help them "survive" not only being forced to stay at home but also the not knowing if he was ever going to come home from the hospital. 

Not being able to go to church and be a church family in a building became THE CHURCH! We began to gather online weekly. The message not just from our pastor at Grace in Menomonee Falls, but almost every other church worldwide going onto the internet and being broadcast for anyone who could click on the link and watch. A revival close to that during the time of  Acts! Anyone and everyone could receive the Word of God from the church of their choice anytime day or night!! The pandemic couldn't stop the preaching of the gospel, it helped spread it!! 

We could have prayer groups and bible studies virtually, via zoom and facebook groups. We could pray via Facebook live! Social media was starting to be used for good - God was using what the devil had intended to bring the people of God down for HIS good! 

I was missing my babies, doing my lesson plans - teaching. I started a Facebook page and read stories on video, uploaded them and invited the parents from our center to join the page. I added activity ideas, homemade toy ideas and other books for parents who were now home with their infants, toddlers and preschoolers 24/7.  https://www.facebook.com/msdebandfriendsstorytime  

This pandemic was forcing me to move past my depression, move past the poor me and from the inside of our homes figure out how to reach out without touching. Porch drops - whether surprises or notifying the person became a thing. Calling your friends, family and neighbors became a thing again. Running errands for people who couldn't go out became a thing again. Looking past ourselves started to become a thing again. Families began having family dinner, family game night and doing puzzles again. Families began to get to know each other again, took time for each other again.

This pandemic forced me, forced us, to look out, look in and look up! This past week the entire world became focused on two planets crossing and making The Christmas Star (12/21/20). This sight hasn't been seen in hundreds of years. There are many speculations as to why this year? Why 2020? 

My theory? Because of OUR focus. We wanted Hope, we needed Hope, we were seeking OUR Savior!

As we head into 2021, my prayer for myself, my family, friends and this world is that we don't stop living the lessons learned this past year, the good & bad. AND THAT WE DON'T STOP seeking or needing Hope, that we don't stop SEEKING OUR Savior. 

Praying for you all to have the Merriest of Christmases this year. 

Never Stop Seeking the one the Wise Men Sought 2000 years ago - Follow that Star. 

Tuesday, November 24, 2020

4 Christmases

Grief is a strange and interesting thing. There is an eb and flow to how it affects you. It affects each person differently and at different times. 

For me, missing Brittany and feeling her loss hits me much more as the holidays get closer. She loved Thanksgiving and Christmas. 

From the first years Monty & I were together, Brittany & Angela always tried to be at Monty's the weekend after Thanksgiving, especially Brittany. It may not have been on Black Friday, but that weekend. Britt LOVED helping decorate the Christmas tree that weekend. We would have a blast looking at all the ornaments and figuring out where to put them, teasing Monty about the tiny tree. 


Her last holiday season was 2016. The Saturday after Thanksgiving she helped me decorate the Christmas tree via Facebook Messenger. I'd put some decorations on, take a picture & send it to her via messenger. She'd let me know if they should be moved or if they were good. She was excited that we had a bigger tree too! She vetoed th angels we had for tree toppers. I tried to tie a bow with teal wire ribbon - she really poo-pooed that!! She finally settled on a Santa hat! Christmas 2017 - 9 months after she stepped into heaven, the Santa hat was back on our tree top. 

Every December Britt also made a point of coming one weekend specifically to help me make Christmas cookies. She LOVED making the sugar cutout cookies. She enjoyed that I have so many cooie cutters and didn't mind that she used more than just the Christmas ones. The freedom to frost & decorate how she wanted. We had so much fun! 


This year it will be 4 Christmases since she last helped me with the tree, since she last giggled and laughed at our decorations, showed us her smiled and got excited for her gifts. 

4 Christmases that I've had to figure out how I am going to get the inspiration to get going and get the tree out, get it decorated. 4 Christmases trying to figure out who I can find to help me decorate the tree, who can understand how hard it is for me to decorate it, why there might be some tears. 

4 Christmases where I just can't bring myself to get out the recipe make the cookie dough and get out the cookie cutters. 4 Christmases where I've had to ask my mom to make my husband the sugar cutout cookies because in my grief I just can't. 

4 Christmases of getting out the stockings, filling Angela, Andrew & Monty's with fun stuff and just adding a letter & elephant token to Brittany's. 4 Christmases of finding a special ornament to add to our tree just so we can feel like Britt is still a special part of our Christmas and celebration. 

4 Christmases of seeing the perfect gifts for her in the stores and being hit with the realization that we don't have to buy anything for her anymore. 4 Christmases of wishing we didn't have to go shopping because I don't want to see those perfect gifts.

4 Christmases and she's still not here. 4 Christmases and there are still tears. 4 Christmases and there are still times of forced smiles and happiness. 4 Christmases and the knowledge that there will forever be more . . . 

Sunday, October 18, 2020

The Ribbon Color Battle - Pink vs All Other Colors

I have seen the battle and the "Not all cancer is pink" posts. Seen them for years, even before I was diagnosed with cancer, even before my mom was diagnosed with "the pink" cancer. 

Cancer is NOT a color. Cancer is pain fear, anger, tears, surgery, poison flowing into your veins to kill an unseen beast. Cancer means scars - physical & mental. Cancer means never being who you used to be, not feeling your "normal" self and having to get used to a forever new normal. 

Cancer is more doctor appointments than you ever thought you'd have in your life. It's hospitals and clinis, scans, endless pokes with needles. 

Cancer is finding out who your true friends, family and supporters are. Cancer is finding out how truly strong you are when push comes to shove. Cancer pulls some families and friends closer and pulls others apart forever. 

Cancer does not care if you are young, old, male, female, black, white, yellow or red. CANCER DOES NOT CARE!!! 

It is not a COLOR. ALL cancer is horrible! Cancer is not pretty t-shirts, bracelets, bras, soup, cupcakes and all those other PINK products you see in every store in October. 

Let me repeat: ALL CANCER IS HORRIBLE!! It is a destructive disease. It destroys cells, organs, and bodies. It KILLS!! 

Please do your research on the organizations you give to - find out how much of the money you donate goes to research and the programs they profess to have. Does the organization help those it says it serves or does most of the money go to their staff? Does that can of soup you're buying just because it has a pink ribbon on it really send money to help those who are diagnosed with breast cancer or help provide mamograms or is it a marketing gimic to get you to buy more soup? 

Just because you or your family may not have been affected by cancer yet doesn't mean you never will. When you get a cancer diagnosis, you want something to help you connect and identify with others. That becomes a color - an important identity. Pink for breast cancer, Teal for Ovarian Cancer, Peach for Uterine Cancer, Yellow for Sarcomas, Grey for Brain Cancer, Gold for Childhood Cancer. But please, please remember, the COLOR IS NOT THE CANCER, the COLOR IS NOT THE BE ALL END ALL. 

What I'm asking is that when you reach for that pink spatula, sunglasses or box of cereal; ask yourself if it's because you've been conditioned to "think pink" or "save the ta tas" or if it's because it is really going to bring more awareness to breast cancer. 

Remember, we use the color for awareness, for people to ask us why we are wearing a particular color ribbon or what our shirt means, - but color is NOT cancer. Because ALL cancers suck! 



Monday, June 22, 2020

What to Say and Do

The first thing most people say when they find out you have cancer is "Just let me know what you need. I'm here for you." Here's a tip from someone who's been there - We really don't know what we need. Our brain is mush! We just heard the words "You have Cancer". We have no clue what we need, we can barely put one foot in front of the other, much less take in all that our oncologist is telling us and remember all the new appointments we now have. 

It is also difficult for so many people to actually ask for help. Sometimes it is pride, sometimes it is just being tired or not wanting to bother people with our problems. 

So . . . instead of "I'm here for you. Just let me know if you need anything." I'm going to give you a list (not comprehensive by any means) of things you can do and say that will really help. 

1) Make a specific offer. Specifics are much more helpful that something general. 
    One example of this was when one of the groups I was involved in at church contacted my husband and I asking if they could put meals together for the week after I would have chemo. This was a wonderful help. They woul bring 3 meals the week after I had chemo. I got to see 3 friends. We had food and my husband had leftovers for his lunches for work. 
    Some other examples of specifics can include: 
    - "I would like to bring you and your family dinner? What day would work best? Are there any allergies or anything your family doesn't like?" 
    - "I know chemo must be tiring. I have some free time this week/weekend. I would love to come help with a few loads of laundry or dishes so you can get some rest." 
    - "I'm going to the grocery store. What can I pick up for you and your family?" 

2) Everyone thinks they need to say something when they see you, but honestly, you don't. However, if you feel compelled to say something to someone in treatment and you are a close friend, you can try some of these: 
     - "You seem like you have beem getting some good rest lately." 
    - "How has treatment been going?" (If you ask this one, be prepared to listen and have a conversation) 
    - "I love your hat/scarf. It looks beautiful on you." 
After treatment when hair started coming in


3) If you are going to inquire about how they are feeling - BE SINCERE. We can tell when you are just being polite and all you will get is "Fine" or "Alive". 

4) Just be there. Find out if they have someone to go with them to go to appointment, chemo, shopping or to be with them at home as they recover. Make sure you are healthy yourself and be prepared for them to ask you to wash your hands, use hand sanitzer and possibly a mask. Individuals that have spouses who work, may be too weak or don't have someone living with them may appreciate having a friend go with them to appointments. Having a 2nd set of ears helps hear ALL the information that the doctor gives and answers to questions. It also helps pass time during treatment. Having someone at home after treatment helps make sure they are staying hydrated, eating and taking medication they need to take, as well as not falling. 

Brittany, my youngest bonus daughter, doing homework during treatment


5) Pray and let them know you are praying for them. Ask if there are specific areas or things they would like prayers for. During stressful times and treatment, prayers are greatly appreciated and can be felt. 

6) Keep anything and everything you are told in deep confidence. Don't tell anyone else what you are being told in any conversations with your friend/family member unless they specifically tell you that you can. You may be close to the situation and the patient and hear and see things that are confidential. Keep this to yourself. Remember, if you are this close to the person and situation, you are being trusted. Don't break that trust - Especially not at this time. 

7) Treat the person like a NORMAL person. Even though they are "sick", they are still a person. They can laugh, joke and have fun. They aren't always going to mope, cry and be down in the dumps. Invite them to parties, out to eat and to events. Help the make memories! However, ask before you take pictures, not everyone likes their picture taken when they don't have hair, even though I didn't mind it. 

In my wedding dress for our 1st Anniversary


8) Don't be offended if the person who is sick or their caregiver doesn't get back to you quickly or right away. There is so much going on, especially right at the beginning of everything. Appointments, surgeries, scans, new language, treatments, labs, and so many other things. 

9) Never, Ever, Ever make the sick person or their caregiver feel guilty!!! This is NOT about you! In no way at all, is this about you. It is about them - they are fighting for their life, their family. Every day they are fighting to not throw up, to not think about dying, to keep themself focused on life, living . . . They should NEVER have to focus on someone else's feelings. If you get offended easily or get your feelings hurt at this time - you're just gonna have to get over it. 

There are many other tips and things that other survivors could tell you. These are just a few that I found as I went through my own treatment and my bonus daughter's treatment. I was very blessed to have my husband, and that my family had gone through my mom's treatments 3 times. 

Praying these tips help you, whether you are newly diagnosed with cancer or another chronic disease; or you are someone who wants to help out. 
Thank you for visiting and reading the blog
Born With A Mother's Heart 


Sunday, May 24, 2020

The Things People Say


When you are diagnosed with cancer, you'll be surprised at all the things people will say to you. Some of those around you immediately become doctors and cancer specialist. Some who you thought were intelligent, will immediately show how insensitive and unintelligent they can be. While others will become totally oblivious. 

One of my first experiences with the oblivious and insensitive was when Monty and I made a stop at our local chapter of the American Cancer Society (ACS). My mom told me to check with them, since she had been able to go to a class called "Look Good, Feel Better" through their programs. She went and was shown make-up techniques and given make-up, a few caps and had a chance to receive a free wig. 

We entered the building and were greeted at the reception desk by a smiling volunteer. So far, so good. Right? The volunteer asked how she could help us. With Monty next to me, I explained I had recently (just the week before) been diagnosed with Ovarian Cancer. We were looking for information on the cancer and any groups,  as well as information on the "Look Good, Feel Better" class. 

The volunteer's response: "I don't know about that class. I know we used to have them, but I don't really think we do that anymore." She then moved some things on the desk and sat down, looked at us and said, "Oh, Ovarian Cancer? My mom had that when she was 80. She died from it you know." She handed me a pamphlet called Eating the Rainbow to Reduce Your Risk of Cancer. Yep! Sad but true. We haven't done much of anything with ACS since that day.

Obviously I didn't get to that class! 


Of course, I like everyone else diagnosed with cancer, had and still have my "experts without a MD": 
- A dear friend, who unfortnately a few years after my diagnosis was diagnosed with breast cancer and chose to fight her own way and is now in heaven - "After all those things we talked about, and I know God put on your heart about your family and having children, I just don't think the surgery and chemo is the way to go. There are so many natural cures for cancer." 
- A well-meaning Facebook Friend - "You know, I've heard using __________ and eating kale can help with killing cancer." 
- Several people giving their opinions to try keeping me healthy - "You know chemo is poison. It's worse than cancer!" (Thanks, didn't know that! Of course it's poison, it kills cells in your body! DUH!) 

Yep. I love all my friends dearly. Sometimes people just don't know what to say when confronted by those in their life who have a potentionally terminal illness. However, I personally feel if you don't know what to say or feel uncomfortable - not my problem. I'm having enough of my own issues dealing with this disease and fight, I don't have time to be nice and polite to your stupid!! 

Of course then there are those people who are totally oblivious to what's infront of them. I had several people at work who were just soooo completely oblivious it was painful!! 
- I had just gotten back to work for my 9 days after my second or third treatment, it was well known at work that I had cancer. (I worked in an office of 25 employees and was bald. It was too hot going through menopause and being summer to wear hats or my wig.) I was heating my lunch in the breakroom. One of our newer salespeople came in, looked at me then at the microwave. . . . 
    
    Salesperson: "Is that you're lunch in there?" 
    Me: "Yep." (just waiting for my food so I could go back to my desk, take off my mask and eat) 
   Salesperson, straightface, looking right at me, deadpan: "You know microwaving food in plastic can give you cancer. Right?" 
   Me, raised eyebrow, rubbing a hand on my BALD head: "Hum, REALLY?!?!?" (insert sarcasm) "Been there, done that, got the t-shirt and haircut." 
Before it all completely fell out, but you get the idea.


- Another day at work when the air conditioning wasn't working right and my little desk fan was not doing its job either, I was talking to a friend/co-worker who was always cold. Another older female co-worker in the cubicle next to mine was listening in and just had to put in her two cents. 
   
   Cold co-worker: "I just can't believe you're always so hot!" 
   Me: "Well, that's what menopause will do for  you. Here," I stuck my arms out for her. "warm up on my arm, the perpetual heater." She put her icy hands on my arm and we laughed. 
   Nosey Co-worker: "What are you talking about? You're too young for menopause." 
  Both of us turn and look at her. 
  Me: "Um . . . remember those surgeries I had in April and May? When I was out for all those weeks? When they remove your ovaries they take out your thermostats and force you into menopause. So. . . . I guess I'm old enough!" 

However, the worst and toughest are those who have made it through college and are medical professionals, but as a cancer survivor, I still have to give them anatomy lessons. These are the most painful and unintenionally hurtful things I have ever had said to me. (And I grew up with 4 brothers!) Things not just myself, but many other of my Teal Survivor Sisters in the same poisiton feel we shouldn't have to tell or teach medical professionals such as: x-ray technicians, mammogram technicians, CNAs, nurses, doctors and anyone checking us in for medical appointments of any kind. Maybe if you're a survivor like me, you have guessed what's coming next, if not hang on and no judging the survivor!! 

At every physical with your primary care physician, if you are female, you get asked a standard list of questions every year. I personally think the medical professionals who have to ask these questions hundreds of times a week get stuck in a progression of asking and not take into consideration the patient's chart. 

One of the first questions is - when was your last period? This one makes me want to scream. My chart, which you have on the OPEN computer infront of you and I can even see what it says, states right at the top: Primay Diagnoses - #1 Ovarian Cancer. The next box down has a list of all my surgeries which include: Complete Hysterectomy, Salipingectomy, Oophorectomy and Omentectomy - 2013. When I point this out, I get a blank stare and "When was your last menstrual cycle?" Sometimes I'm sure when I dramatically roll my eyes they're gonna stay that way, especially when I sarcastically say "March 2013" After this information I am usually looked at like I am an alien and need to repeat the whole 15 minute rundown of what is on my chart RIGHT INFRONT OF THEM!! I have even gotten a response after that of "Is there any way you could be pregnant today?" I just shake my head in disbelief and usually give no answer! 

However, the most painful is every mammogram, x-ray, CT scan or PET scan when the question I most dread comes up. "Could you be pregnant today?" I usually get an eyeroll or strange look from the teck when I ask if they have even read my chart. I mean once again, it's right there on the top and I figure they had to have taken anatomy & physiology in college. 

I can honestly say, the worst day of my life was the day I had my first mammogram after I finished chemo. It was only 5 months after I had finished treatment and 10 months after my diagnosis. My emotions and grief were very new and raw. I was barely through my first year of dealing with being in menopause, was getting over a lot of the after effects of chemo and hadn't even started to face the depression and grief I had weighing on me. I was NOT prepared for this question at all. '

I was in my gown & robe, nake from the waist up. The tech & I were in the mammogram room. She shoved a clipboard at me with a stack of papers on it and said, "When was your last menstrual cycle? Could you be pregnant today?" 

I started to tear up and just looked at her dumbfounded. I tried to talk and was too choked up. I swallowed a few times and then the anger started. "NO! There is NO chance in hell I could be pregnant. I have Ovarian Cancer and just finished chemo! I had every part that it takes to make a baby taken out almost a year ago! You would know this if you took the time to read my chart you have pulled up infront of you!!! Even I can see from here under my name it says OVARIAN CANCER HYSTERECTOMY! THAT USUALLY INDICATES NO PARTS TO MAKE A BABY!!!!"  I sat there with hot, angry tears running down my cheeks. 

She just looked at m:e, handed me a pen and asked, "So is there a chance you could be pregnant? Just read and sign this form." 

"WHAT??" I looked at her in disbelief. "I demand a new tech to do my mammogram today! If you truly do not know your human anatomy enough to know that without reproductive parts I have NO CHANCE of being pregnant, I have ZERO trust in you to know where my boobs are much less know how to run this machine! Please go get me a new tech, NOW!!" 

She stared at me a few more moments, then went to get her supervisor. I could hear them talking in the hall about "the patient from hell" and "what was all the yelling about". Worst mammogram and day of my life!! That day I decided I needed a shirt to wear to all future mammograms and scan appointments that said "Last Period - 3/2013 No Parts No Pregnant" (In all honesty I still need to get that shirt made.) 

Even though I have had to repeat the "I don't have the parts os I could NOT possibly be pregnant" speech to almost every tech since, I have come to realize, after 6 years, this is part of my educating others about Ovarian Cancer. I always have symptom cards in my purse or pocket to hand out to the techs, nurses and even doctors who don't understand what those big, long words on my chart mean for my treatment. And . . . this past October when I had the very first tech ever who knew what Ovarian Cancer was and what it meant to have had a hysterectomy, it was the BEST mammogram ever!!



I honestly hope people don't try to be mean or stupid. I really hope they are trying with the best of intentions, to hand their own discomfort with cancer and the possibility of looking death in the face. I also feel, that as the patient and survivor I don't always have to care about the other person's feelings or if they are going to be offended. Your issues are not my concern when I'm fighting for my life or dealing with issues you have no idea about. Yes we all have issues, but when you are a friend, co-worker or medical professional you need to sometimes put your issues down and focus on the person you are talking to, who is going through an obviously rough, trying time. Save your offense and "you're being rude to me" attitude for someone else. 

Close your mouth if you can't figure out what to say. Why? Because sometimes you run into someone like me.
T'MOC & AdvoKate





Sunday, April 12, 2020

"For I Know The Plans . . . " - Part 3

Wooden Blocks Hurt

After almost a year of living in the apartment, I had to give up and move back in with my parents. It seemed like failure. However, not quite a year later my mom was diagnosed with breast cancer for the first time. I was able to be there for her when my dad was working third shift.

I then moved with them to a 3-bedroom apartment a few years later. It worked for us. It was during this time in 2007 my stack of blocks began to go a bit higher. The tower was starting to come together and look more like I wanted it to. I found a church home I felt comfortable in, friends and a group I started to hang out with, a singles bible study with people just like me. Things were looking up.

In March of 2009 I started an account on Facebook. It became a fun way to find and connect with people I hadn't seen in a long time. At this time, they had an app called "Speed Date" that was free. Since all the other online dating sites sucked, I figured I'd try this one, just for fun. It was on this app where some more of my wooden blocks started to buld an even better tower. This is where I met Monty.

Monty & I started out chatting in the app, getting to know each other. We messaged each other and instant messaged. Our first phone call was when I was traveling from Appleton to Minnesota - yep, his fault I missed an exit and ended up in Minocqua. We started dating on April 9, 2009 and never really looked back. That June I met his 2 young teen daughters. Another bunch of those wooden blocks added to the ever grown tower.

Things were going well. We were happy, work was good - until May 2010 and I was let go from my job. A few blocks started tumbling. Monty was there to lift me up. We were both struggling financially, and that August made the decision to move two apartments into one. Both of us living in a 900 square foot apartment and occasionally adding his two girls when they came over. Cozy, and fun. I eventually got another job and life returned to normal.

Then, SURPRISE! On November 19, 2011 Monty asked me to marry him. I had planned his 40th birthday party, and we also celebrated Angela's 16th birthday at the same party. Before everyone started leaving he handed me 9 roses with a card that asked me to marry him. Of course, I said YES!  The girls and our family and friends were all so excited. More and more of those wooden blocks were being added to my tower. It was finally staring to look like a house. My beautiful dream house with my wonderful promised family.

We got married on July 28, 2012. The hottest summer I can ever remember, but the best day of my life. Surrounded by family and friends, I became Mrs. Monty Norris and gained two wonderful, beautiful bonus daughters. The day was everything we had planned. We were starting our life together, and now, the second part of what God had promised me could come too. I could now get my family, my babies. Our babies!!
 


February 2013 - wooden blocks began to fall, and they hurt. I began inital testing with a fertility doctor because I was having anovulatory cycles (not ovulating). During one test, a hysterosonogram, the doctor saw a large cyst on my left ovary. They referred me to a gynecologic oncologist (gyn/onc). This sent me spiraling to the fact that I had cancer!

Monty & I went to the first gyn/onc appointment on March 23, 2013. We met my doctor, Dr B. He didn't think it was much of anything since it was fluid filled. I was scheduled for surgery the following week - Monday April 1, 2013 - yes, April Fools Day!

On April 9, 2013, I had my follow up from the surgery. It was that day, on the 4th anniversary of the day we started dating, we first heard the words "I'm sorry to have to tell you, but you have Ovarian Cancer." That "nothing cyst" was benign endometriosis coming from my left ovary, going behind my uterus and around my right ovary. In the surgery, Dr B took the endometrial cyst and my left ovary. Inside the ovary is where they found Clear Cell Ovarian Cancer. Wooden Blocks began to fall all over. I couldn't go anywhere to keep them from hitting me.

I had to have a second surgery for staging. This one was done on April 29. They took my uterus, right ovary and omentum. No other cancer was found. I was staged at Stage 1C Clear Cell. Because clear cell is an aggressive cell type of ovarian cancer, I had to have chemotherapy. I had an IP (interperitoneal) and IV port placed. Unfortunately the IP port didn't work, so I got 6 cycles of IV chemo. Wooden blocks falling and falling all over!!





No hair, bone pain, missing work, some nausea and in the end NO BABIES!!!
All those wooden blocks that had been so neatly and beautifully stacked were now crumbled at my feet, my body scarred, burised and broken by them hitting me as they fell. What could I do? There was no way to put these back together. None of it made sense anymore.




My husband didn't understand, no one in my life could understand.

Yes, I was alive. Yes, I had bonus daughters. Yes, there was always fostering and adopting. But I wanted to experience being pregnant, giving birth, holding MY OWN BABY!!!

Finally, a simple verse in a sermon at church one night began to bring a little comfort:

Jeremiah 29: 10-13 (NIV)
This is what the Lord says: "When seventy years are completed for Babylon, I will come to you and fulfill my good promise to bring you back to this place. For I know the plans I have for you," declares the Lord, "plans to prosper you and not to harm you, plans to give you hope and a future. Then you will call on me and come and pray to me, and I will listen to you. You will seek me and find me when you seek me with all your heart.

There were no more blocks. Only God. I just had to rely on Him. Seek Him, listen to Him. Stop playing with blocks and getting hurt. Go back and look at that promise, see what He had really said and what He had given me. What HIS plans for me were and are.







Saturday, January 11, 2020

"For I Know the Plans . . ." Part 2

Here I was, living in Minnesota almost 7 years after God promised me a husband and family. I had friends who believed the same thing as me, we had our own "Christian singles group" because we were tired of the singles groups we found at church. Most of the people who attended had been married once or twice before, had children . . . they needed different things spiritualy and we just didn't feel like we fit in; especially the night I went alone, and they were studying Ephesians 5. A chapter I hold near and dear to my heart.

Ephesians 5 talks about marriage, in some cases people know it as the "submission" chapter. After all the studying I had done, I had bought a Concordance & Bible Dictionary, so I was doing some serious studying. I knew what that Greek word "submission" meant. My "take" on it didn't go well with the group, even with Biblical backing. No more singles group for me at church!

Then the first BOMB hit! My pretty plastic block tower got bumped into by my brother! He's 15 months younger than me, had been dating a wonderful girl for many years and decided to get engaged to her!!! WAIT GOD!! I was supposed to be engaged first! I've been waiting, doing everything you asked me to! Doing it all right!!

Then bomb #2! More blocks fell as my next younger brother (3 1/2 years younger!) announced his engagement to the girl he had only been dating for a year and a half!! NO!!!! NO!! NO!

Then bomb #3 - 6 months after that first brother got married, they announced they were pregnant!
NOT FAIR GOD!!! NOT FAIR!!! More of those newly placed plastic blocks fell and I could put them back right.

In less than 2 years two of my brothers had taken my blocks away!

My first niece was born in 1999. She was beautiful, healthy and amazing. In 2002, her sister was born. She was also healthy, but born with the birth defect - Spina Bifida. I headed home to Wisconsin to visit the new addition. I wasn't working my office job anymore and was picking up hours at the Y to make close to full time, so it was pretty much an open-ended visit if I wanted (this was the beginning of November).

I came home again at Thanksgiving and found out they couldn't find a babysitter who would take both nieces and didn't want to split them up when my sister-in-law went back to work. Within 2 days my decision was made, I was moving back to Wisconsin to nanny my nieces.



My brother knew of a small apartment for me to rent, the upstairs of the new house they were going to be moving into and renting. This was great! I'd be back in Wisconsin, able to grow close to my nieces and have to be in my thirties living with mom & dad! What could be better?

It now seemed I had moved on to the more solid wooden blocks. A bit steadier when built with, or so I thought . . .