November 17, 2014

Balance

Went to a funeral today. Haven't  been to one for a year, since my Mom's and that was way different cause I was sort of the boss of it.  My Mother left explicit instructions as to how her funeral would go down.  I knew all about the hand written instructions, reassured her many times that I had everything in a folder and would carry out all her wishes.  Wellllll.... When my Mom died, I went home and went to the folder and opened it up and guess what?? Everything was there in order to get her all buried up in the right spot and all paid for and everything was there EXCEPT her handwritten instructions. They had seriously vanished. I looked and looked and they, and I swear this were always there when I had opened that folder before. They were gone and stayed gone and I never did find them.  I think that she had a nice, lovely funeral even without her marching orders.  So I figured that gave us license to do as we pleased.  She was quite controlling in her life. It made it hard to deal with her when she had to have everything just so. I suppose that was her way of maintaining a secure feeling.  I am quite sure she has still not forgiven me for moving her out of her home of 45 years.  I was not very sympathetic at the time, what had to be done, had to be done. That was that. Looking at it now, a year later, I get it. I have not had much control over my life during 2014. I went through it all, cause that's what you do. You just do what has to be done.  That is no way to lead a life. I really wish I would have spent more time thinking about what we all experienced this past year, because eventually you have to think about it. You have to REALLY think about it, and it is not pleasant and it is damn scary. I fight and fight and fight with myself to stay positive which must be why people are so kind and say I am so strong and that I am inspirational (WHHAAT?) and all that kind of stuff when really they just see me dressed with my fohawk nicely parted and on my feet. They don't know how I have handled any of it, really.  They are just seeing me, looking and acting normal. There is no normal anymore.  Once you have cancer, every single day is a struggle not to worry. It was suggested to my by one of my life coaches (bahaha) one of my shrinks that is, that I not shoot for having a positive day, but maybe just a realistic day.  So, being the excellent client I am, I am taking his advice and shooting for real days. I wish I knew someone like me, someone that is just so much like me that they would just know what I was thinking and feeling. I know, I know, you are all saying that I do, and of course I know that "I am a daughter of a Heavenly Father who loves me, and I love him" I know he is always there. I know that, but sometimes I need a real person right next to me that "gets" me. But then again, maybe, like the funeral of an absolutely stellar individual, I need to think less and just live a little more.  The motto of this man was "Work hard, Play hard".  When I think of him, I think of three things. First I know this man has a testimony that is second to NONE! He has strengthened my testimony, at girls camp, several years in a row. The second thing I think of is a picture in my mind of him with a toilet plunger, cause trust me, at girls camp, if you sign up as a priesthood leader, you must  know your way around the biffy!  The third thing I think of when I think of this man is what a hard worker he is. I didn't see much down time for him. He worked hard at girls camp but apparently knew how to play hard also. All I can think of is that he must have been "Too good for this earth". So, as a little shout out to Randy Loveless, I will "work hard, and play hard". I hope to be able to have balance as he did. I hope to be a force for good as he was. Needless to say, I will not be writing out my own funeral plan, accompanist included! Peace out my friends.

August 6, 2014

Read at your own risk. I am writing this for me. Just me. As Holly mentioned in a facebook post, "Chemo leaves a trail". Yes it does. It is very, very common to experience major depression and anxiety when your treatments are over.  The doctors don't tell you this and it makes sense that they don't because then you would be anticipating it and setting yourself up for something that might not even affect you.  But when it happens, no one who knows anything about cancer treatment is surprised. NO ONE. I don't know why, but I have no warm fuzzy feelings when I hear that it is normal and they all promise it will go away and Hell's Bell's it is a rough row to hoe!
I am well versed in anxiety. I was born anxious and had parents that were really busy with my Hell raising siblings. I was quiet. I stood still, I held still and hoped desperately that someone would notice that I was scared. I think most of my childhood was spent in a suspended state of  "What or who is gonna GET  me today?" Therefore, I as I became an adult I thought I had the world by a string cause by golly I was going to do things differently.  So I had five kids, and shiz, guess what? some of them are pretty anxious at times also.  This is what I learned about how I raised my kids.  I learned that no matter how much I wanted to protect my children from fear, from hurt, from bad stuff in general, it was not my job to hover over them and wreck my own psyche worrying about them. They are supposed to learn how to deal with bad crap and it is my job to let them while hanging around the edges of their lives, to support them and cheer them on when they struggled with the bullies in this big ol' life.  I tried very valiantly and quite successfully to do just the opposite of much of what my parents did and guess what? It was not in my children's best interest because I was doing it for ME! Now, don't get me wrong, I have five extraordinary people as my children and they are all law abiding upstanding citizens and no one is socially retarded or anything like that They are kind, considerate, employed, hug their Mom regularly individuals, but I should have protected them a little less. I should have been late picking them up every once in a while so they would know they could be ok on their own and stuff like that. Having said all that, I don't really have a lot of regret, just a little.
Anyway, as I said before, I am well aquainted with the demon that is "Generalized anxiety" and if you know anything about it, you know that anxiety and depression are good buddies. They don't like to hang without each other, but this I do know, and have a hard, HARD time believing and that is that it always passes. This is my first legitimate go-round with depression and I think I prefer it to anxiety. but both of them together? well that is  just not fair!!!!   I am so sorry for any and all of you who struggle with either because it's just Hell. That's all, it is just so tough and oh..another thing that Chemo does is turn on your tears!  I am so dang stinkin' good at crying now! I seriously didn't even know how but now I do, you better believe me when I tell you that if you are all big and bad and never let your kids see you cry, then they will feel like a freak when THEY cry. They might think that they are baby-whimpy-whimps. They are not and neither are you. It takes courage to cry right out loud. It takes courage to let people know when you need help. It takes courage to get up every day and face whatever it is that seems to beat crap out of you. Other people want to cry more than they do, probably just like you do. You are not the only one.
My mother-in-law whom I adored in life and now, said that phrase that we all either get really pissed if someone says it to us, or, we take it into our hearts, and our brains. At first I was real immature and got irritated when she said it, but one day I realized this: SHE KNOWS MORE THAN ME!!!! And after that I knew she was right almost all the time. Wanna know what she said? She said "This too shall pass" This too. So....what....are you mad or do you believe my awesome Aussie Mama?

July 25, 2014

What's up buttercup? What's the word, hummingbird? What's the jist Physicist? I love Big Bang Theory. I have been frowned on by others for watching this ever so hillbillyarious sit com. Last night I watched episode after episode cause that sort of thing is my comfort. I, like Sheldon,, have my own 'spot' on the couch, well actually it is the whole couch. After five or six or seven hours in Chemo getting fluids, magnesium and potassium I can only think of my spot on the couch under quilts made especially for me. Then I watch one show over and over, I also absolutely adore "The Middle". I did not know about this little gem of brain candy till recently. Sue Heck is my HERO! Holly made me a little poster with lot's of pic's of Sue with the title "Sue Heck never gives up!" and I look at it every day and it makes me happy. My family will do just anything to keep the Mama happy. I don't think I blogged about my last day of Chemo. Just as I was finishing up, my entire family except Carly who was working all trooped through the door with matching shirts on, which featured a montage of wacky pictures which Holly took one day of me. then they all were personalized with a message from each of them, even the babies! even the tiniest baby Weston. It was so dang awesome. I never feel worthy of the Love and concern and work they all go to for me.  Then I got to ring the "Done with Chemo bell" which is cool but embarrassing all aat the same time.  I have been here many times when other patients have rung that bell. It's a nice touch.
So how bout that texting law?  Myself, I have noticed a large decrease of idiot behavior behind the screen, (not the wheel). For me, I have never texted while driving as I cannot walk and chew gum. Plus, who? who? in their right mind would text while driving after seeing those anti-text commercials on tv, in particular the one where the teenage girl is trying to write an apology to the parents of the child she killed while texting. HOLY SHIZ that would make me stop gum chewing while driving (I can drive with gum, just cant walk across a room). When that ad comes on I just want to jump through the screen and hug that stupid girl! I am a rescuer by nature, and a lover of the underdog. Call me the stupid one but I always think of them and hope they have a good support system as well as and  MORE IMPORTANTLY the victims of the said mayhem. I am getting better about the rescuing thing, as I have to keep my mouth shut much more now that I am a MeeMaw. I am doing pretty well I think, but if you ask the parents of my G-Kids, they may express a wish that I try a little harder.
My parents always taught me not to complain about the weather. Ever. They believed that if you complain about the weather, you are complaining directly about, or to the Big Guy upstairs. So, it stuck and I really try not to complain. This becomes challenging in my most disliked season, Summer. I am not complaining. I am saying that I cant freaking, creaking, wreaking, WAIT for Autumn. I about go nutty nuts when the apples get red, and I can hear the football games commentated just like "Friday Night Lights" and the grass looks nice again, and you get that second wind that helps you be motivated to get back into the yard and make it look all beautiful after the ravages of summer have, well ravaged the yard and my get up and go.  Since I started the big "C" treatment something weird in me will not let me wear short sleeves, even if I am hot sometimes. It is odd. anyone have any ideas why I am wearing a hoody, and yoga pants, shoes and socks? let me know your thoughts.  Chances are, I am just being my own weirdy self! and that's ok. Cheerio Mates!

July 16, 2014

So hey there all you sugar bears. So first, I am down in the Chemo zone where all the good fun happens!! You see, even though I am done with the tough chemo, I am still privileged to spend many many hours down here in this bright cheerful white clean as a whistle room with my nurses, whom we all adore. You see, I have had three kinds of chemo, two super mean ones, (not mean to me, they love me, they don't love my cancer cells). And one kind of Chemo that is going to keep me visiting the zone till, ohh, about February.  It is called Herceptin. it is a fascinating drug. I have a type of breast cancer that is called HER2 positive. (not the BRCA gene Angelina had, which really sucks if you have that one)!! Sooo I just bop in every three weeks and get me some Herceptin which costs my insurance co about a million bucks and I am grateful. Chemotherapy is EXTREMELY TO THE EXTREME expensive. Just so you know.
Someone took my seat today. I usually sit in the same chair in the corner of windows then I can turn my head when I want to forget where I am and look out at the landscaping which is very green and see all the cars go by on 5th west.  I also see lots of really interesting sorts walking the sidewalk. It's fun! But since my seat is gone and this place is hopping I sit in the middle where I can spy on the nurses. They kill me, they are doing a job that would make the average person cry and run away fast and they do it so wel an they do it fast and they also can just look at you and say "Hey doc, we think this one has a Pulmonary Embolism" and the docs, who are every bit as delightful and smarter than Hell say "OK." and guess what, they are right and then they let me cry and then they hug me and sneak over to buy flowers at the gift shop for me and hug me some more. My bad days in this white clean place are rare. There is not much chitchat between patients and that's ok.  I mean, we recognize each other and say hi maybe but before I started chemo I read up on 'Chemotherapy etiquette"  Who knew there was such a thing? But it says to use your brain and read body language and if they have headphones on then they would rather you leave them alone. Or if they are in the middle of a double issue of People Mag then for sure don't bug! We all just sort of ride this out in a routine that feels good to us.  I bring my favorite "Fight like a Girl!" bag that my friend Tiffany gave me and in it I usually keep my kindle, a real book, my crocheting, and a bunch of other dumb stuff I don't need. I kind of go back and forth and do this, then that blah, blah, but I have a tough time reading which I love to do. It is common to loose all means of concentration cause its sort of like your brain is like swiss cheese. Not gonna lie. It's frustrating as crap. I am spending three or four hours down here every other day because chemo really screws up my electrolytes and so I slide in, they hook me up, give me lots of magnesium which takes sometimes 5 hours.  Oh well. I am grateful for my garden variety of cancer. Who wouldn't wanna be ME!!
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July 13, 2014

July 5, 2014

Hello all my Peeps!  just sittin here in the Utah heat doing nothing. Fourth of July is such a fabulous holiday and my good noodles! the aerials around our house were very very numerous and I figure if my neighbors can afford to host the  100 south of fire,,, then why do they live on 100 South? Just a little thought that blew through my Chemo riddled mind last night.  I don't mind, after the first year with the new law, not last year but the year before, I swear I thought it was the end of days. People surely do enjoy their big bangs and pretty lights.  I missed them for the first time in a long time last night.  Sometimes my brain does not process my thoughts and emotions appropriately. Don't you just hate when that happens? I mean, you know for sure what is what, and your brain wont let you remember it.  Then you get it back, and all is well, and you can almost feel normal and look around and ground yourself (that's a fancy therapeutic word), grounding helps you know who you are, where you are, and that you are safe and its ok to be peaceful and happy. You look around you and see WHAT IS. You know you are ok but still, that little devil on your shoulder nags and nags.  That, my dear people, is when you need that word called FAITH. That's all. Love you lovelies.

June 27, 2014

Babysittin' and Residents

Hello All!  Big night for me. It's Friday, and everyone had a previous engagement and I didn't even have to have a babysitter!!Whoo Hoo! Sad but true, that there are about ten days after Chemo where I am a danger to myself and others and it's not a good id a to leave me home alone. Tonight I said to those worried faces, I said "Hey, ya'all just go along cause Samson and I are going to watch us an entire evening of the AWESOME wedding shows! Yes we will watch them until they start over again yes and then when that happens we will watch guess what??? No, really guess what my favorite TV program is? OK, I'll give you multiple choice.
A-Anything on food network
B-CSI reruns
C-The Middle
OK, please text me what your guess is cause it will tell me a lot about what you think of my character.  
I have been thinking today about Residents. It is June and June will forever remind me of Resident graduation, which happens tomorrow.  My seven years at Merrill Gappmayer Family Medicine is so full of fantastic and fun and FUNNY memories.  I love Residents.  I can honestly say, after counting them all up, about 45 in all that I worked directly with, that I cant think of a single one that I didn't care for. Ok, well I did think of one but I am sure if I knew this person better I would like him too. The huge majority, after working with them from little first years, and I swear they grow in three years, anyway, I loved almost all of them and cried at all the graduations.  I thought about what makes these people different than what I see on Grey's, well besides the obvious differences, and way the thing is, these guys and gurl's come into the Clinic and they are NICE! and when they are all done and totally truncky to get the heck out of there, some of them are even nicer. It is amazing to see them grow up and turn into Physicians. They are trained and taught and mentored and helped by a Faculty who sometimes, I bet, drag them through and these Faculty docs apparently, have not forgotten what its like to be residents. I know this because the interns don't usually try to hide when one comes 'round. They have been some of  the funest,  smartest, kindest, most empathetic people that I know and I am grateful for all of them (except that one which I don't have an apreciation for yet:)
While I am bearing my testimony of Family Medicine, just a huge shout out to all the staff that taught me ssooooo veeeerrrrry patieentttttllllyyy!!!! for all seven years.  There was never a day I didn't learn something, and never a day I didn't make a mistake and it was with the Patience of...OH gosh I don't know that they just kept NOT FIRING ME! I worked with a lot of the most Stand-Up people I know and I miss laughing till it hurts with them. Sendin' the love to you darlin' new GRAD'S