Showing posts with label cancer. Show all posts
Showing posts with label cancer. Show all posts

Monday, April 01, 2019

Then Cancer Returned in 2019

I looked back at when and what I wrote in my last posts. Now here is the odd part...

The week after I wrote those posts in January of 2019 this year, I found out my Colon Cancer came back. Since then, just like last time, it has been a whirlwind. They found a tumor the size bigger than a grapefruit in my ovaries. We thought it was ovarian cancer so we were told to go to a Gynelogical oncologist. He removed the tumor and I had a hysterectomy removing everything. The tumor had leaked into my abdomen and inflated my belly. While in surgery they did a biopsy and found it was colon cancer. AGAIN. I healed from surgery and then had a PETSCAN. That revealed I still have cancer in my pelvis and abdomen. No surprise there if the cancer was leaking in those areas but not what I wanted to hear.

Image result for metastatic colon cancer recurrence

I started chemo right away.

This is all so different than last time.

This time I am taking Irinotecan, Avastin, 5Fu, Leucovorin. That's my new cocktail.
That's what the doctors and nurses call it. Either way, it sucks. This time I have a higher chance of losing my hair. This time I have different side effects, yet some are the same.  This time it is different but the same.

I have had two treatments now and I will tell you, this time the chemo is kicking my ass. I have been queasy all week. Even now. I hate that. Chemo really wreaks havoc on your body and sadly your mind as well.

I'm awake now because I am afraid to go to sleep.

Which is odd because when I think if I will die, I feel ok with it. I feel like I am a good human. I feel like I left a good legacy. But yet, still afraid. Maybe that is just being a human as well.

I am supposed to do chemo until August. There is a lot left unsaid, unknown.

Metastatic Colon Cancer is vengeful, aggressive, scary as hell and the chances of surviving are 14%!!

That is because this tumor was called a Krukenburg Tumor in my ovaries and the fact that it was a distant site is not good.

I am still being me.

I am brave.

I am courageous.

Sometimes I am very sad.

Sometimes I am happy.

Sometimes I am just here.

Sometimes I sit and my closet and cry late at night so I don't bother my spouse, who is still trying to work, provide for me, caregiver to me and be there for me.

Sometimes I cry in the shower while listening to inspirational music.

Sometimes I am numb.

Sometimes I am pissed and angry as hell at this cancer coming back.

No matter what, I am always me.

I do not know the future of my world.

I am focusing on my next book "Always Wear Peals: Living Life with Style and Grace"

I even started a FB group for it for me to place my thoughts and encourage others to do the same no matter what they are fighting.

I thought my next book would be directly about cancer, but something in me changed.

Perhaps cancer itself.

It can do that.

It really matters to me to "Inspire the World" and I felt this book could inspire more people. Especially women.

Life will pull the rug out from underneath you when you least expect it. Handling that with style and grace is something I work on doing daily. I aspire to be like Jackie O and Audrey Hepburn. Maybe one day someone will "aspire" to be like me. Maybe I can give them hope in the darkness. Maybe I can teach them how to be a positive influence in the world. Maybe I can be a role model for them. Maybe I already have been.

Maybe, this is just another struggle I need to Fall Into Fabulous for.

Maybe this is why my cancer returned. Maybe you need to live vicariously through me. Maybe you can't handle the trials but I can. maybe by me going through it, you are growing, learning, becoming. Maybe I am here to learn. maybe I am here to teach by example. Maybe I need to be there for you.

As I said on Facebook, if that is the case, I gladly will. Because I love you. Humans of the World. Yes, you. I love you and I would do anything for you.

xoxo ~Trixie

Wednesday, July 18, 2018

1st Year Remission-Teeth Extraction-I Can Do Hard Things



Today in Trixieland,

My mouth hurts like no tomorrow. Partially my face feels bruised from them grabbing at me I think to pull the teeth. I had 18 and 31 removed because they had a bad infection in the back teeth and we considered a root canal but because of my past history with illness and infection, we opted to just have them pulled. My teeth were all mashed in my head anyway and this allows my teeth to move a bit and maybe rid me of some of my headaches too! The two teeth were both in the back on both sides. I am wearing a wrap just like the guy in the pic because both sides of my mouth hurt.

I am only on soft foods so HunePants went to the store and bought, cooked and mashed with a blender, mashed potatoes with milk and cheese. He also bought jello, pudding, and a twice baked potato in case I run out. He has checked on me every day in addition to taking a half day on Monday so I could get my teeth pulled.

He told me today "Honey, I am so proud of you for all the hard things you do. You are so brave and so strong and so willing to go through things that no one would ever want to, but you do them anyway and I know you are better for them."


We only have three weeks left before we got to France. I really wanted to enjoy my food and drink and goodies while in France. I did not want to miss out on yumminess because of a tooth infection. while I hate having to go through this pain and suffering, I knew, in the long run, this would be better for me. I mean, I have heard my teeth were pretty bad and the infection could have been there for some time affecting my body in other ways as well. Now, there is no more infection or issues with my teeth to get in the way.

You see chemo deteriorates the calcium, enamel and made those teeth worse. What I am learning, however, is that there was most likely an infection already there, but the chemo made it worse. This has been my year of this knowledge. 

I am still waiting on biopsy tests but since I have heard, I feel no news must be good news. they already tested my kidneys, found I had a UTI, tested my cervix and did a biopsy there, nothing happened, now the endometrial biopsy. The first year of Cancer remission has been a lot of tests but a lot of ruling things out as well and so far everything is coming up roses, minus this tooth thing.

As far as the teeth, they are concerned about the two teeth near these two and think there could be cause for other issues, but I, like always, look to the positive.

We will deal with all that other crap when we get to it.

for now, heal the teeth and gums and mouth.

Get ready for France.

Momma is gonna be here soon to watch my furbabies.

Life is what it is.

Sometimes, we just need to to do hard things.

Here is a free coloring page for you with the saying "I can do hard things"

I love to color and thought maybe you do too.

Since I can't do much else today, maybe we'll all color.

And remember....you can do hard things too!

~XoXo Trisha Trixie

Rt click, save, enlarge, print, color

Tuesday, February 27, 2018

Insecure after Cancer Remission

Image result for Insecure after Cancer Remission

Ever since I have been "announced" Cancer free, I have been feeling less and less like me. Which as I am saying it makes me feel pretty silly. I knew things would be different. They, the doctors, the nurses, others who have had cancer, they all told me, "You're life ill never (emphasize NEVER) be the same. I thought, "Yeah but you don't know me" and then here I am.

Sad
Depressed
Feeling neglected
Feeling insecure
Feeling out of sorts

Just...feeling...not me.

Damn.

I don't want to just be another statistic.
I don't want to be like everyone else.
I want to be the overcomer
I want to be the one who rises above it all

THAT'S ME!! THATS WHO "I" AM!!

Damn it.

So frustrated right now I wanna scream!

I haven't shared on here for awhile and I came home tonight, from being with a group of girls all watching the Bachelor at one of the ladies home and the whole time I am sitting there, I am feeling completely insecure. I got in my car and cried all the way home.

 The rational me says to myself "What the heck are you feeling insecure about? You are here with friends. You love them, they love you. You are safe"

You see, I did not feel safe. I did not feel validated for my words. I felt like I was in the wrong tribe.

I learned something tonight. In that group of women are a CORE group of fabulous ladies that I get along with and I adore them and love them. The other ladies, not my cup of tea. The external people just kept getting weirder and weirder and the more the other ladies spoke, the less I wanted to. and I had an epiphany.

You don't have to like your friend's FRIENDS. Simple as that.

Being kind and respectful is still desired.

I realized after tonight, some groups of people just are not healthy. As much as I love my friends, I just can't be with those other women.

I also realized, Cancer remission sucks.

I am struggling to overcome the lack of support.
It really is a struggle after you have been dealing with this battle, fighting and fighting and you have fought for so long you forgot to stop fighting. Then there is the fact that all through the battle, everyone is in your corner, people constantly telling you how much they love you and care for you and you can pick up the phone at any time and then when you hit cancer remission...

crickets...

I feel lonely.
I feel anxious.
I feel insecure.

I found some articles that explain and I am linking them here in case you, whoever might be reading this, might want to go check them out like I did.

This one was the first one I read and it hit home so hard, I cried again.

"Everything you're feeling right now is normal for cancer survivors. Recovering from cancer treatment isn't just about your body — it's also about healing your mind." https://www.mayoclinic.org/diseases-conditions/cancer/in-depth/cancer-survivor/art-20047129 

Here are the other links if you want to check them out. They all say the same thing in different ways it seems to me, but all still worthy of reading.

http://www.dailymail.co.uk/health/article-2003214/Cancer-survivors-Depression-exhaustion-anger-downside-beating-disease.html

https://well.blogs.nytimes.com/2013/07/12/anxiety-lingers-long-after-cancer/

https://well.blogs.nytimes.com/2009/09/29/after-cancer-treatment-waiting-for-the-sadness-to-lift/

https://bmcpublichealth.biomedcentral.com/articles/10.1186/1471-2458-12-538

Know this...

you are not alone.

Others feel this way too.

You don't have to have cancer to feel this way. Illness, trials, adversity, life, can all make you feel this way. What you do with it is up to you.

Take care of yourself.

Get help if needed.

Love yourself.

We will all get through this one way or the other.

The silver linings are in the clouds.

You can choose to look at them as storms or fluffy unicorns.

I vote unicorns. :)


Image result for unicorns in clouds

Sunday, May 21, 2017

As Birthdays Go...



As birthday go...last night was one for the books.

This year, everything just seems that much sweeter. I did have a birthday party last year and though it was fun, this yer is just even that much more wonderful, memorable and sweet. This year, I have been battling Cancer. Though I hate that phrase, it is the truth. Everyday is a battle, though I wear it with a smile. I conquer this battle with positivity, encouragement and inspiration. To celebrate my life this year, was my birthday gift to myself. I'm here. I have survived. Cancer did not kill me. chemotherapy did not kill me. Hemorrhoids  did not kill me. Though out of all of them, that one has been th worst, I am still here and I am still going strong.

As birthdays go....this one will always be remembered.

This is the birthday I fought Cancer.

Now I would say, this is the year I fought Cancer and won. But until my net PETSCAN I "technically" can't say that. Though I was NED (No Evidence of Disease) at my last scan and I have no genetic predispositions to cancer from my family. Which is also good because that means the likelihood of it coming back it slim to none. Which, in turn, is good news for me all the way around.

I always love my birthdays. But this birthday is sweeter, grander, lovelier, wonderful, stupendous, marvelous and the most fabulous birthday I feel I have had in my adult life because  I AM STILL HERE. I AM STILL LIVING. I STILL HAVE BREATH. I STILL HAVE LIFE.

And that , folks, whether you celebrate birthdays or not, is definitely a reason to celebrate life!


I am so thankful to be alive!

XoXo Trisha Trixie



Tuesday, February 07, 2017

7 Steps to Caregiver Love

My mother recently reminded me, as a caregiver herself, that we on this side of the fence often forget our wonderful caregivers who are there to help us.

I am so ever grateful to my Hunepants for being my caregiver and honestly don't know what I would do without him. So to pay respects to all caregivers, here is a little post just for you. This is for US patients and those around us to remember the caregivers as well as the needy.

I recently was hospitalized and didn't even think about how much he needed a break from me as well. Times like these help those us who have caregivers hopefully realize that they do a lot for us and we need to not be so dern grouchy, irritable and insensitive. We need to be thoughtful of those who cNOTare for us and do so much. So here is a little post for the patients to remember the caregivers. This is NOt a post for caregivers on how. This is for YOU the one who NEEDS that caregiver to remember them and be thinking of them.

1. They probably won't do it YOUR way.

No, they probably won't put the dishes away where you want them to go, and no they probably won't do the laundry the way YOU like it done. Who cares? At least they are TRYING to help out and do their part.  Be happy and THANKFUL they are helping. they could just leave everything for you to do as well as trying to be the patient. Even if they only do ONE thing. Say thank you. Be thankful. show them thanks the way they like to be thanked. If you don't know how they like tobe thanked....find out. It matters.

2. Consider hiring help

Maybe you can't afford to hire help as in a home health aide or maybe insurance won't cover it. My insurance won't cover an Aide, like my sister is, to help people clean and do shopping, but they will allow me to have a Health Nurse. This week we are considering hiring one to help out so he doesn't have to be the doctor, the nurse and everything else too.

We also have started hiring someone to come in and do Prep Meals for us and clean every other week. I can't do most stuff, but getting down and scrubbing toilets and showers are not in my wheelhouse right now and he is the one working and paying the bills so I don't think he should have to either.

Plus, as a joke, now we always have someone to blame as in "Oh, where did M, put that this time?" or "Must be M's fault we can't find anything." I told her and she laughed so I know it doesn't even bother her and this takes the stress off us.

3. Do little things for them once in awhile

This morning, after being in the hospital 4 days and nights, I was so thankful to be home, that I got up early and made Hunepants tea the way he likes it. I also woke up early and told him to get in bed, because most nights he sleeps on the couch as not to disturb me and sometimes him to so he can get some rest. I would have made him breakfast too but I actually haven't been paying enough attention to know what he eats in the morning anymore.

Note to self: pay attention to the little things as well

By the way, he made an English egg muffin with turmeric and cheese. simple. DUH. Maybe tomorrow If I am feeling well I will make him tea AND breakfast.

4. Use your resources

I have a church family who offers me meals. Many churches offer this or other community members. Think about your friends and other family who may be able to give you rides, clean, do things for you so the caregiver doesn't have to. There is no reason on earth and no one said

"The caregiver has to do it all for you." So stop expecting them to. Use what your momma gave you, yourself and use your resources.

5. This may not be "short term"

You or your caregiver may have thought "Oh I'll just help out for a bit." Next thing you know it's 4 or more years down the road and they are still helping and you are still griping.

"Did you know, most caregivers have been helping out their loved ones for 5 years or more?"

That little bit of helping has maybe turned into a lot of helping. If they, like my spouse, are the breadwinner too (meaning they bring in the $$), that is a lot to take on. Be aware of your needs as things progress as not to over stress your caregiver. think about the other things I have mentioned, like hiring help, using your resources, etc as a way of helping out.

6. Caregivers have mood swings too

You don't get to be the only one who gets to fly off the handle one minute, cry the next and then be happy. Sorry folks, we are both humans here. Unless you found a way to have a robot as a caregiver and are rolling in the dough, most likely your caregiver is human and has emotions JUST LIKE YOU.

GO FIGURE.

Remember that. So give them a break like they give you a break too. Let it pass. Breathe. Let them have their mood swings too. Realizing that you both are gonna have these up and down days, moments and time really will make things a lot easier.

Now, that being said, I don't think it is wrong to point it out on either side of the scale. Sometimes, maybe you don't realize that you are being a raging B* and sometimes maybe they don't realize they are being a royal arse. Not rudely, but kindly maybe ask if things are ok and if they realize they are being that way. they can do the same do you. This is a rule in our house we allow. That doesn't mean either of us are going to stop being that way, because in reality, sometimes you just need to let those emotions out. We just go to our own corners (areas of the apartment) and let the emotions surface and then it tends to dissipate on it's own. That may or may not happen for you, but it works for us.

7. Make sure they have their ME TIME too

They need to take care of themselves. They need time to themselves. They need to do their own thing and release all that they are dealing with...YOU. They need to nourish their own souls too. Let them have that time. Make sure they have that time if they aren't already. Be patient when they want or need that time.

My Hunepants likes to play video games. he likes to code. He likes board games. He likes to read news online. these are none of the things I particularly like to do, except the Board Games part. So I give him his space. I let him have his morning to read Reddit (boring to me) or listen to CPR (Colorado Public Radio) in the car (again boring), but I know it makes him happy so I let him do these things.

Whatever your caregiver likes to do for their time, let them do it. don't make fun of it. Don't hassle them about it. It isn't YOUR TIME it's THEIRS, so ZIP IT and just ALLOW IT.

You both will be  happier.

My mother likes to help others, sew, craft, bead, quilt and write. Sadly, she doesn't always get to do these things and I am on her constantly about her having her own time. She can't just be the errand girl or the doctor girl or the nurse. She needs her time too. (Are you listening mommie dear?)


*********************************************************************************
All in all, obey the Golden Rule. Treat others as you want to be treated. 

Until next time,
Always Be Fabulous
Trisha Trixie













Saturday, January 14, 2017

Feisty, Fierce and Fabulous in 10 Easy Steps

This year I have been working on focusing my goals, desires and habits towards positive and uplifting things. a friend recently bought me a gift of Brave Girls Club courses and then today I got invested in Daily Om Courses.

Out of all the things that seem to resonate with me the words of my title are what keep popping out to me

 FEISTY FIERCE AND FABULOUS!!



I strongly feel that is what I need to power through this year.

I need courses and guides and planners and dreambooks that put me and keep me on this path.

So far January isn't over yet but I already feel like I have a great plan for my upcoming year to do just that! Stay on the path. I laugh inside because my mantra for my successful businesses in teh past few years have been "Stay True to the Brand". Of course, why wouldn't I do the same with my own personal life. Stay True to My Path. or Stay True to the Path.

To do this, here is what I have done so far.

Step One: Buy Dreambook and Planner from Dragontree http://dreambook.vision/



Step Two: Work Dreambook consistently to focus on my one year, three year, ten year and lifetime goals. (not an easy task mind you when one is fighting colon cancer) As well as stay up to date on regular planning, note taking and journaling.








Step Three: Stay active in Dragontree Facebook group for inspiration and motivation for the plan
https://www.facebook.com/groups/dreamingandplanning/?ref=bookmarks&qsefr=1


Step Four: Get reactivated in Brave Girls Courses (These really helped me back in 2011 when I was really struggling with some interpersonal things and I just knew it would do the same for me now. I am very grateful to my friend who bought me a 3 month subscription to this as a gift)
http://my.bravegirlsclub.com/courses



Step Five: Join Bad Ass Habits from Daily Om (I have done the first two days and am already enthralled with this course)  The habit I have chosen to focus on is Daily Yoga practice. I have had some pretty severe muscle fatigue and neuropathy in my body and hands from my first round of Chemotherapy. Lock jaw, teeth sensitivity as well, and slight nausea, but those went away in a few days. The muscle fatigue and the pain in my hands has been more than I can bear. Luckily after doing two days of yoga, I can type and function with my hands again. Which, for a blogger, make a HUGE difference in my overall emotional well being. I jsut always feel like even I am just typing my words down and no one reads them, I am getting those emotions out and that alone makes me feel better. Then add to it the fact that someone MIGHT see my posts and I MIGHT make a difference in someone elses life, that means the world to me. http://dailyom.com/cgi-bin/courses/courses.cgi



Step Six: (This is SUCH a girl thing) Only use the Bad Ass Purse. The Bad Ass Purse is black leather, studded and looks like a motorcycle bag to me. Motorcycles are bad ass, so to me, this purse is also bad ass, kick ass. It makes me feel empowered to use it and make me feel like I can conquer anything.



Step Seven: The Bad Ass clothes (again such a girl thing) I have a black vest that I wear as often as possible. I have been using black eyeliner nearly every chance I get. I put hair chalk in my hair to bring out the fierce and feisty and fabulous in me. I wear what I want, when I want even if others think my style might be a little outrageous. The more outrageous the better! I wear my kick ass (but easy to get into) suede boots or my little gray ones with a silver buckle because both of them say FIERCE to me.



Step Eight: Use Asana to keep all my projects in line and to stay on top of my goals and habits for this upcoming year of 2017 www.asana.com



Step Nine: Update and follow my Pursuit of Excellence Goals for this year. Also place in Asana to stay up to date with it. https://trishatrixie.wordpress.com/2016/05/10/pursuit-of-excellence



Step Ten: Live life to those ideals I have laid out. Remember to be Feisty, Fierce, and Fabulous no matter what, all year long, every minute of every day!






XoXo~ Trisha Trixie

Wednesday, January 11, 2017

Long Distance Cancer Love: How to Support a Cancer Friend when You Live at a Distance



Many people do not know what to say or how to support their Cancer friends when they live close by but it is much harder when you long distance and really want to reach out or help or connect with someone you know who is going through a cancer battle.

Here are some tips I found from "When Your Life is Touched by Cancer" by Bob Riter


  • Send notes of support. Let them know you are sending positive thoughts
  • People with Cancer often get lots of cards in the beginning but after things go on, those cards of support trail off. Be there for them by constantly sending cards and letters of support throughout their WHOLE battle. Not just at the beginning. The cards and notes they receive weeks and months after are especially treasured
  • Don't be discouraged if you don't get a response or they don't answer their phones. People in treatment often need to conserve their energy.  Know that your contact and attempt at connection really does mean a lot.
  • Educate yourself about their cancer. (Mine is Colon Cancer) Colon cancer is much different than lung or breast cancer. Knowing things on your end makes it easier for them so they don't have to keep explaining which can and does gets very exhausting.
  • Call, even if it feels awkward at first. Though they may not always remember what you said, they will remember that you called and cared.
  • Small gifts, unrelated to illness, are always welcome
  • Reach out to the primary caregiver as well. They are facing a rough road as well having to be the strength and support for their loved one.
  • Take part in cancer walks and donations to help out. It means a lot.
  • If you cant call or write, let them know via social media or text "Thinking of you" or things of that nature to help keep them boosted and supported.
More than anything the person dealing with cancer will appreciate the support in whatever forms you can give.

Distant friends and family can help people with cancer maintain the sense of who they really are and were before cancer.

Don't make their cancer or diagnosis or treatment about you. This isn't a time to be concerned with you, or your feelings, or how their cancer life affects you. This is a time for them. To be there for them. To love them. To care for them. I know I have had a few people say to me how much it hurts them that I have cancer and they can't be around me. It hurts when I hear that because I really want to say to them "You know this isn't about you right now, right?" But I don't. However, I will and am saying so right now so you understand how hard that is for a cancer patient to deal with because it isn't fair for me to have to console YOU about MY cancer.

If you feel cancer is changing your friendship, hopefully it is for the better. Be there for them. They really need you right now. they need your love, care and concern.

If you live close, then by all means, help out when and where you can. But don't bring sickness, illness or sick children around them as that could hurt them more than you know. their systems are weakened by the chemo and illness is deadly to a cancer patient. As much as you want to help, being sick doesn't help in the slightest.

Overall, just being there matters.

Show you love and kindness for them in the best way you can, just show it, do it and be there, one way or the other.

It will mean more than you know, even if you never get a thank you. A cancer patient is overwhelmed and going through a lot more than they proably share or talk about it. Be respectful and help them through it by not making it harder.

Send your love and light and let them know how much you care.

Until next time,

Trisha Trixie 



Monday, January 09, 2017

Cancer Life: Timing is Everything


When the stars line up
And you catch a break
People think you're lucky
But you know its grace
It can happen so fast
Or a little bit late
Timing is everything
You know I've had close calls
When it could've been me
I was young when I learned just how fragile life can be
I lost friends of mine
I guess it wasn't my time
Timing is everything
And I could've been the child that God took home,
And I would've been one more unfinished song
And when it seems a rhyme is hard to find
That's when one comes along
Just in time
You can call it fate
Or destiny
Sometimes it really seems like its a mystery
**************************************************************************************************************************

I know that some people find it every hard to watch me go through this trial of mine. It isn't easy actually going through it either. When I hear this song, I think how lucky I was for the stars to line up at this time. I am sure many who know me might think what a whacked statement that is, since the doctors did NOT listen to me for the past few years when I kept telling them something was wrong. But you see, I can't stay mad about that. I had my moment and now I am passed it. Time to move on. Timing is everything, in all ways and in all places. The timing for me to meet Dr. K, was perfect. The timing for him to find out what was wrong with me, perfect. I got the right doctors, at the right time to get the best treatment possible. I feel like I caught a break. I got lucky. If we didn't find it now, it would have progressed further and I could have died. Now, I have a fighting chance.

I've had a few close calls in my life. Not just with this, but with other things and it wasn't my time. I was young, ten years old, when my father passed. I learned very young, just how fragile life can be. I've moment since then, that by the grace of God I am still alive.

I could have been the child God took home.

But he said "Nope, not done yet!"

I still have lessons to learn and life to live.

I still have starfish to make a difference to. I might be the only one throwing them back in the ocean, stepping into their lives and making the change in their life, that puts them on a better path or on the straight and narrow, or even that ONE someone who changed their whole life. I will never know, but I Do know that I am called to save those Starfish. If you are one of them, thank you for allowing me to make a difference in your life. Thank you for allowing me in. If I don't know you, and you are reading this, perhaps my journey will the difference you need to see. Believe in love. Believe in faith. Believe..
Together we stand. 

You and me babe! We've got this!
Until Next time,
Xoxo Trisha Trixie


Living with Cancer: Know When to Hold em



You've got to know when to hold 'em
Know when to fold 'em
Know when to walk away
And know when to run
You never count your money
When you're sittin' at the table
There'll be time enough for countin'
When the dealin's done
Every gambler knows
That the secret to survivin'
Is knowin' what to throw away
And knowin' what to keep
'Cause every hand's a winner
And every hand's a loser
And the best that you can hope for is to die
in your sleep


Life gives us all different hands. We are dealt those hands and can fold and walk away or we can be strong. Right now, I'm holding em! I am holding my own and fighting the best I can. I am keeping my poker face up and trying not to show my hand. If you look at me, I want you to wonder what I have in my hand. I don't want to show that my aces are gone. I am not going to think too much about this all because "There'll be time enough for countin'
When the dealin's done"

Every gambler knows
That the secret to survivin'
Is knowin' what to throw away
And knowin' what to keep
'Cause every hand's a winner
And every hand's a loser

I always see my hand as a winner, even if it were my time to go because this is the hand I was dealt.

I wear my pain with a smile on my face and encourage you to do the same. No matter WHAT you are going through. You can do it1 If I can do it, you can too!

Fight.

Go to the mattresses.

POW POW

Now, let's kick some cancer butt, shall we?

Until next time,
XoXo Trisha Trixie


Friday, January 06, 2017

Shooting Out the Walls of Cancer



Shooting out the walls of CANCER BANG BANG  I AM THE WARRIOR!
Today is Friday January 6th and I keep thinking about Monday January 9th, my Chemo day. Day one. How do I approach this? For me, there is only one way...to be a WARRIOR. Fight this with everything I've got! Put up my dukes, bounce around on the stage, and fight. POW POW!

What other way is there? To lie down and let it take me? Hell no. I've gotten this far through everything in my life, I am not about to let Cancer win this battle! I am a fighter, I will fight Cancer, I will beat chemo and I will succeed and survive! 

Bang Bang, I am the Warrior!

Watch out Cancer, I'm coming for you!

Monday, December 26, 2016

The Hardest Year

It's 2:40am and I have been up since Hunepants came to bed at 1 am. No matter which way I turn, my chemo port hurts, is uncomfortable and bothersome. I finally decided to get up about a half hour or so ago because I couldnt' take it anymore and I started getting very hungry. As I finished a show I had been binge watching (FRIENDS) I started balling and crying my eyes out. The only thought that came...THIS WAS THE HARDEST YEAR...

I looked back and remembered this time last Christmas. We were newlyweds, enjoy our first Christmas. First Christmas as a married couple. First Christmas in Colorado. First Christmas away from family.

We sent small gifts and I made treats for everyone. We sent my mother in law holiday cups from Williams Sonoma...this year we drank from those cups and as I set the table, it took all my might not to burst into tears.

In January, sadly right before her birthday, my mother in law passed away. She had Bechets and her immune system was often down. She had a minor cold, that turned crucial. We had just spoken with her the Sunday before. It was all so surreal. A week later she was gone. I was married for five months. Five months and no more mother in law. She was so kind and sweet and loving. Most of all, she loved me for me. I have been married before and I have never felt truly accepted by any of my past in laws, but I did by her.

Looking back, I remember the beginning of 2016. I had such high hopes for this year. I was going to make 200 aprons and donate them to the DSM Womens Club. I as going to be a Mindfulness Practitioner and help those to overcome their trials and adversities in life. I was going to do so many things and accomplish so many goals. I even did the Pursuit of Excellence this year and created a plan in Asana. I thought I was going to conquer the world this year....

Then, death happened. She passed away.

The grief overcame me. We lost her in May but they didn't set the memorial until June to go to Pickeral Lake, where all their family summered each year. Holding onto that pain until June was very hard for me.

It was a culmination of things. Remembering the loss of my father when I was young, losing a mother in law so early into our marriage, being there for Hunepants to be the strength and support for him through this trial and then the hurt from on of his family members who lashed out at me,  constantly telling me to stop being in pain because it wasn't about me. Which to this say bothers me because though I know that mentally, I felt like she was trying to stifle my feelings, and I felt I should have been allowed to feel what I felt.

I found a therapist and learned EFT and talked through the issues. I moved past things. I overcame, once again.

Then I tore my rotator cuff doing my New Year's Intentions to get more fit when I was lifting weights. I found a local doctor and started seeing him for the issue. He was an Ortho doctor and family so I chose him. (later I regretted that) He helped me get the right physical therapy, dry needling for my back issues, and got me back on track physically.

Mid year, we moved apartments to the other side of the building. The week of the move, I got terribly sick. I just kept vomiting over and over. We just assumed it was a stomach flu or something I ate. It didn't let up and I wasn't much help in the move. After speaking with my Chinese doctor, I was given some herbs to help out. My regular doctor was no help at all really. I told him of my issues and complained about bowel problems. He, like all the other doctors, said it was just IBS and not worry.

June we went back to Wisconsin and I felt like I walked around with baited breath. I was afraid I would be overcome again and the family member I had issue with would once again come at me, telling me to stop being so upset, that it wasn't my family and that it isn't about me. I did my EFT training and pretty much stayed to myself. Then another family barked at me for something completely unrelated and I lost it. I didn't even want to spend time with the family out to eat because I was so upset. They never apologized and the matter got swept under the table, like most family issues often are (especially in my family and now I guess this is how his family is too).  The once built relationship I had with those family members now is always tainted in my mind. though I forgive and move on, the apprehension of that issue is still there. The rest of the time, I kept to myself and didn't want to really be around one. I never feel accepted by his family, only his mother in law and his father and Step mom. With the mother in law passed, all I had was the other set of parents and was grateful when they let me hang out with them at  a flea market like I was one of their own.

August rolled around and I remember writing in my journal how much pain I was starting to be in again. I felt he pain was getting worse but I didn't want to talk to Hunepants about it because we had already been through so much that year, and I hate being a complainer. My family is a long line of bitchers, whiners and complainers and I didn't want to be like that.

A few more months went by and the pain in my belly was getting worse. I had problems constantly when I was going to the bathroom and my back was killing me. I kept calling my doctor and never got a response. When I was able to talk to him, like always, he discredited my issues for e mere nothingness.

Come Early October I tried countless times to reach him for my issues. to no avail, no answer, no return calls, even his nurse failed to get back to me. I couldn't take it anymore. I was fed up. I called the Clinic and talked to the head admin. I informed him of my concerns and that I had enough of trying to talk to that doctor. I had seen that there was another doctor int he clinic and I wanted him as my doctor now. I realized I just probably sounded like a bitchy patient, but I knew something was not right in my body, and no one was listening. The admin told me the other doctor was not accepting patients. After beginning a pleading and basically stating that since they are a business they mgiht want to keep me as a "client", that I could either take my business elsewhere, or see if this doctor would take me since the other one at their clinic had no desire to get back to me. LAter that week I had an appointment.

My first visit with Dr. K I am sure to him was an interesting one. I told him of my ailments and issues and to say our first few visits were "rough" might be an understatement. Yet I persisted. My spouse didn't want me on certain meds like Lyrica, I didn't want to be just given meds for everything and continued to complain of lower back pain and abdominal pain.

My friend A comes out to visit and during her stay I see Dr.K again. As I go in she says to me something to the effect of "Stick to your guns" and I smile.

I asked for colonoscopy and we talked about it. We talked family history and I found here and there some issues but mostly uterine and cervical. Dr. K wanted to rule out any issues in that area since that is where the majority of the family history was. I still thought it was something with my colon as it still was taking me two hours to have a bowel and that was with much pain.


In the ultrasound the tech is casually taking pictures of my uterus and calmly says "Honey, do you have problems with your colon ever?" There ya go. I mean, we aren't anywhere near my colon and SHE is even asking about my colon. She take a few more picture near that area and sends me on my way.

A few days later Dr. K brings me in and says there were some spots near the colon and he is concerned and wants to rule out issues and not to scare me, but this may be colon cancer. (How does it feel to be THAT doctor that has to tell you that? I have always wondered. Ar eyou nervous to tell your patient that? He seemed "genuinely" concerned.

I go back to the Touchstone Imaging Center and do a CT. I get a disk at the and as Dr. K told me to and when Hunepants came home we took a look at it. We are not health pros but we do have the ability to look things up online. One our two monitors we have the scan on one monitor and info on CT results on the other...We look left, my scan, look right, info. We look at each other. We both have a sneaky idea this is cancer but though we say it, neither  wants to admit it just yet.

Dr. K calls me the next day..."Don't be scared..." he says. I already know...he is going to say he thinks it is cancer..."I want you to get the colonoscopy asap because we think it may be cancer." I reply that I am fine and that is what I thought. I wonder if he believed me or thinks my BiPolar is making me be in denial. I am sitting on the edge of the bed as we speak. (talk about the edge of your seat) and he tells me he request Dr. N at South Denver GI to do the screening. Now they have something to look for.  This isn't a free screening anymore. Now we are concerned. Things just got serious. I hang up and stare at the floor. My kitties Mr. Dude and Mr. Booties both come nuzzle up to me (which is rare) and I start crying. I know if both my cats are near me, I should be worried.

Keep in mind, I have barely know Dr. K a week or two when all of this is going on. I am a brand new patient and this is what he has to start with. I feel sorry for him having to deal with this and me through this. I try to reach my current therapist. He informs me he doesn't have time for me. I decided I no longer have time for him if during this crisis my own damn therapist can't be there for me. i will deal with that one later.

Less than a week later I am drinking SuPrep and cleaning out my bowels to ready myself fro a Colonoscopy. I get through the prep (which I am told is worse than the procedure and I tend to agree). Hunepants can't take me to the appointment so I ask a brand new friend if he can take me. I have already called 7 people and no one else can. I remember calling my friend A and saying, "After all I have done for others, why is it when I am in need, there is no one to be found?" She agrees. Wished she could be with me for everything.

D picks me up and as we are driving to the test he casually asks "I don't mean to pry but what are we going to the hospital for?" I say, after taking a large gulp, "They are concerned I might have Colon Cancer." I hold back tears. He apologizes and wishes me well. I thank him offer him money for gas, he denies. He mentions to let him know how things go. I say I will.

I walk into the GI alone and start shaking.

I get through all of the paperwork and fill out the slip that says who will be picking me up. the nurse asks me if he is here and I softly reply no. I try not to let this bother me, though it does. I look around and everyone else has someone with them. I am a mix of mad and hurt that Hunepants isn't here with me, but I know he will be when I wake so I try to be ok with it.

The nurses are all great, everyone kind and sweet and sincere. They talk me through everything and get me ready. We go into a small room after I am changed and I meet the anesthesiologist. I feel ok but still nervous. They give me something to put me to sleep and I try to get comfortable, The one nurse tells me to get on my side and be comfortable the best I can because I will be asleep soon. I barely remember raising my arm up then down and I was out.

I woke in recovery and as I barely woke, there was a nurse handing me a glass of cranberry juice, someone pulling back the curtain to let Hunepants in and the doctor is telling me I have cancer. They are doing biopsies but he knows I have a tumor and I need surgery STAT!  He asks Hunepants is he can take me right away to meet the surgeon to get this scheduled. I don't even have my clothes or shoes on yet. DAMN. Now I am pissed. Not at him but at every Mercy Medical Clinic doctor in Iowa for not listening to me. For the back doctors not listening to me. for everyone discrediting me for years. I tried to tell them. Now I am wondering what stage I am. I try not to think about it. I get dressed and we meet the surgeon. Nice man, seems to know his shit. Dr. H. Eveyone in his office is very nice. As we talk I am stoic and he keeps telling me it is ok to cry, it is ok to have emotions about this. I feel like a tank just got dropped on me. The more he talks the more it is sinking in....I start crying now...he hands me a tissue and it appears he is relieved I am crying. Perhaps the not crying make doctors more concerned.

Mind you this is Wednesday and the surgery is scheduled for Nov 1 the following Tuesday. He tells me to stay on soft foods and I shouldn't' have to drink so much glug if I do. It is called GoLighlty and he makes fun of the name saying the makers of that need to change the name because it is nowhere near LIGHT. He tells me I might not have to drink the whole gallon. I hope not, that doesn't sound fun. We stop by CVS, hand over scrips and leave for them to let me know when they are filled. I let them know I had surgery so I needed them right away, but they have to order them because they don't have them. Talk about nervous. Ali, the Pharmacy tech tells me it will be ok and assures me they will have it in time.

We go home and I being to write cards. I pour myself into emotions of letting others know how much tye mean to me. The tech, Ali, the bankers at Wells Fargo, Sprouts manager, my vision place and so on. I think I wrote over 25 cards to hand out and another 25 to send. This is how I cope. letting others know their worth and value.

As the surgery gets closer I panic more. I cry and cry constantly. I have called or emailed every family member I can and put out the Facebook blast about my condition. The outpouring of love and concern is amazing. Here is that support I was wondering about a few weeks ago. It showed up. HARD. I wonder if my mother cried is worry about me. She seemed so strong on the phone but, hello, this is her baby we are talking about. My older son was stoic about it. That was to be expected. My younger son got completely silent and informs me his last girlfriend before his fiance dies of Colon Cancer. I don't know what to say. He offers me love and support. This too, was to be expected. Not that my older son doesn't love me, I know deep down he does, but he never says it. I mean it, I just told him I have Cancer and he still can't say it. I consign that this is just how he is and accept what he can offer me. Math jokes.

The weekend approaches and I am up all Saturday Night. Tuesday is surgery and the day and time are drawing near. I feel like I am having a panic attack. I get out of bed and start reading scriptures and praying. HARD.

Sunday morning. Early. 5 am. I pray for more knowledge and answers and peace and comfort. not knowing what do and feeling as if I will die. The spirit came over... "Call for a blessing". This prompting continues in my head...I decide to go to www.mormon.org and find out who my missionaries are.

At 7 am, I called in tears asking for a blessing. I left a message and they called me back. We schedule for them to come later than night and I tell them my story. I ask Elder Mork to give me the blessing and Elder Bjerga assists.

After tears and emotion being revealed and a wonderful blessing, I finally feel at peace.

Tuesday comes. My friend D accepted my request to go with Hunepants and I to the surgery. The staff was very nice, the doctors make me laugh before I go in and I am happy. I feel ok. They joke about not being professionals and I remembering commenting that if they were stuffy, then I would worry.

Surgery is great and I was in recovery two hours.

I remember waking and thinking "I made it! I didn't' die! I am alive!"

I have a whole new lease on life and think, geesh, if people thought I lived life out loud before, just wait!

I do great in the hospital, I sat up right away, I walked all the time, the nurses loved me, I loved them. By Friday I am eating solids and on Saturday Nov 5th I am home. The next week I walk for 3-5 miles each day around Fiddler's Green and think I am doing very well. he following weekend, I have diarrhea for three days straight. Uh oh. Somethings wrong. I call the surgeon, he isn't concerned. I still am. Though, thinking it is just food, I go with the church ladies to CFA and hang out. LM brings me home and I lie down for about 20 minutes. My stomach hurts and again I am worried. I call to see if I can see Dr. K and the admin gets me an appointment. I text Hunepants and tell him he needs to go with me. He comes home ealry and takes me.

I have CDIFF.

I end up on these monstrous anitbiotics. Which to me is dumb because too many Antibitiocs is what caused this in the first place. But I hear it helps. I text my Dr. friend Dr. I. he concurs so I decided this must be what I have to do.

The following week I am no better. followup with Dr. K. More Metrondiazonale. Yay. Not and he suggests a probiotic to get my gut flora back.

Two days later I am better, but he says keeps taking it until it is gone.

Now we are here.

I have seen the oncologist and he alerts me that even if the scan is clean we still need to do chemo to kill any microscopic cells that might linger that have cancer that we can't see. This is th best we can do. I am in denial. Hunepants says do it for him. I don't want to. I want to wait and see what the scan is and then keep doing the herbs and juicing we are doing now. He keeps trying to get me to understand. I give up talking to him about it. We won't see eye to eye. I dont' get why I shoud put poison in my body if the scan is good.

This week was the crazy week.

Monday PETSCAN.
Tuesday. Scan was clean.
Thursday Chemo class to learn everything I can about my upcoming chemo treatment.
Friday. port put in.

Now it's December 25th. Merry Christmas.

I am still in denial. I am doing the chemo though I don't want to. They wanted to start right away and I halted saying "No, I need to go see my mother and family in New Mexico first" They schedule my first chemo for Jan 9th.

The year is winding down and all I can think of is how HARD this year has been. WTF.

I go through bouts of tears and happiness. Not really sure which to feel.

Today I made a dancing video and posted it online. I am determined to remain fabulous though all of this. Not an easy take mind you. But yet, I smile, and then I cry. My emotions are still close ot the surface and I am just trying to cope.

I will be glad when this year ends, though, for once, I am NOT looking forward to the new year. Six months of upcoming chemo.

Which of these years will be the Hardest Year?

This one...or the next?

We shall see....


Do you miss you hair? And other things I think of...

As I was sitting in the Rocky Mountain Cancer Center today I looked over and saw this lovely woman with a beautiful black and white scarf. I really wanted to say something encouraging but all I could think of what to say so I said "I love your scarf" She said thank you and went back to reading her magazine. Her spouse was next to her looking at his phone.

Though he wasn't paying grand attention to her, I kept thinking "That's nice someone was with her"

The more I sat there I though  Do people who have lost their hair from Chemo look at new cancer patients and start thinking things...

for instance...

That poor girl, I hope she doesn't lose her hair too

or

Just wait, you will see

or

Gee, I wish I still had my hair...

I know these are dumb things to think, but nevertheless, I think them.

As I was sitting there, all I could think of was ....

I am so glad I am strong and tough. I don't know many people who could do this, who could handle this. Here I am alone, trying to absorb ALL this information, and most often I am alone and that is okay. Sometimes, one must endure things and battles and fights in life alone to become the amazing person I am meant to be...

My thoughts run away with me more often than not and I swear I think the dumbest things while going through all this...but then I think about my thoughts, perhaps this is what others think. Perhaps it is just me. But jus tin case. That is why I am posting this

Thursday, December 15, 2016

How I Plan to Beat Cancer : Supplements

One of the things that HUNEPANTS got right onto was research what will help kill cancer and one of the main things he found was supplements. Right after I was home from surgery that removed my tumor, was he bought me and asked me to take herbal supplements he found that he found beats or kills cancer. So I responded. Ok.

If you wonder why I am writing all this on my blog is for two reasons.

One: I want to have someplace I talk about all this so if other are going through this too, they have someone to look at that has been through it.

Two: I want to have a place to track this like as if I am in a study. I am willing to try these and other things and want to record all of it, so there is a backing of proof or falsity of doing the things that I am researching and trying, that I keep hearing is more beneficial than Chemo.

Here are the supplements I am taking and have been taking since right after my surgery:


  • Ashwaganda: Kills any cancer in me now
  • Astragulus: Kills any NEw cancers that might try to form
  • Probitic (one with 30 micro living organisms in each pill): Keeps my gut flora healthy
  • Eluthero: For healing my surgery internal and external
  • Vitamin A: Helps my cracked hands and cracked ips
  • Vitamin B12: Energy booster and cancer fighter
  • Multivitamin: Because my appetite is low and I may not be getting everything I need
  • Tumeric Extract: #1 in cancer fighting
  • Two various Chinese herbs from my Chinese Medicine Doctor
    • Xio Yow Wan
    • Gu Pi
These are just the ones I am starting to do now. I may end up doing more. But this is just a start.

I am gonna fight this with everything I've got!

Xo Trisha Trixie

Wednesday, December 14, 2016

Happy New Year Chemo!

Oncology Update: Chemo starts Jan 9th, 2017...Happy New Year.

Oh yeah I get to do 12 rounds for 6 months every other week. One Chemo week, One "normal week" then ...a Chemo Week again and so on and so forth yada yada beetlejuice

December 19th I have my PET-CT scan to establish a baseline.
December 22nd I get to go to Chemotherapy Class!!
December 23 my port gets put in
and Then...January 9th, I get to start a long day 4-6 hours of Chemo! Woo hoo! How exciting! Doesn't that all just sound fabulous?

< in case you were unaware that is the my version of sarcasm>

So, with all that, I am running away to see my mother. I leave for New Mexico on December 28th until January 4th. That will give Hunepants a break before i really will need to rely on him. He agrees.

so, you are wondering...how am I?

Welllllllll...I'm sad.

I talked to my exspouse Scott and he said "That is not a term I remember ever seeing in you the ten years we were married? What does SAD mean to you. Explain."

I chuckled and explained...

Not that anyone really WANTS chemo, that of course wasn't what I was rooting or hoping for. I had all this research and basically was told those are great, but you still need to do chemo to make sure the microcells we can't see that MIGHT have cancer in them, are killed so they don't grow up and become bigger badder meaner cancer.

I now have all these appointments from now to then, and the start of my 2017 is starting with having to be on Chemotherapy. :(

I DON'T want to scream or shout or yell at the world and I have no desire or inkling to yell at God, My higher Power, or The Universe because well, it's not their fault or anyone else's really (with the exception of the idiot doctors in Iowa who could have caught this sooner had they listened to me and just done the damn colonoscopy years ago when I asked), I just am...I don't know, I feel sad.

That;s it.

Just sad.