On 6/23/10, at the age of 26, I was diagnosed with invasive ductal carcinoma...Stage 3 Breast Cancer. On 7/25/14, at the age of 30, I met Lolli, a 1 inch tumor in the left side of my brain; I have metastatic disease. On 2/3/17 Lolli became active again and as a result of treatment I have limited mobility in my right leg. I want to share my experiences so that loved ones, friends and others can follow along while my journey continues. Enjoy.
Saturday, July 7, 2012
cry me a river
I had a great blog that was almost complete about how wonderful and crazy things have been. How I went to my 10 year high school reunion and my sister Kristi got married. That post is going to have to wait..I am in the middle of a cry-fest that is so epic it needs to be documented. I am crying because Scott feels guilty, he can't seem to relax and his mind is always going. I am crying because he has caregiver guilt and I can't give him the support he needs. I am crying because I am mad that he feels guilty, I am mad that I am not healthy enough for him. I am mad that when he looks back on our relationship all he talks about is how I was sick, I am crying because I know he is right. I am crying because I think he should be with someone healthy. I am crying because there isn't enough positive thinking in the world to heal somebody and that just creates open-season for negativity. I am crying because I am sitting in my bathtub in my clothes with the door locked. I am crying because my entire body hurts and no one knows why....I am crying because stress makes the rash worse and I have small lesions in my mouth now and my husband thinks I worry too much.
I am crying because earlier today I was feeling great. I am crying because that feeling has been pulled out from underneath me. I was thinking of ways Scott and I could work together, give him something to do other than work and was thinking of putting a race together to raise money for breast cancer. Now I feel like I am not sure if I will be able to get out of bed tomorrow. I am crying because I feel behind in life. Because I got a fucking infection after surgery and life could use a good slap to the face. I am crying because my fingers hurt from blowing my nose so I have decided to just let the snot run down my face. I am crying because I feel alone, I am crying because I like the solitude. I am crying because I am in the bathtub and my clothes are wet from the bathmat. I am crying because I will now have to change my shirt and I am not sure if I have any more soft ones that are clean that won't hurt my rash. I am crying because it hurts to lift up my arms to change my shirt.
I am crying because Scott can't relax. I am crying because I am not the person he needs to talk to. I am crying because thinking of crying makes me angry, which in turn makes me cry. I am crying because I am sure that our versions of healthy are completely different. That we have expectations that don't have a common ground and I am afraid it will cause a drift we can't breach. I am crying because I need this feeling to go away. I am crying because I don't want to feel this way anymore. I am crying hoping that when I am done I will feel lighter, that something will have come out of it. I am crying because I know that won't happen.
I am crying because I miss my dad. I am crying because I know if he was here there wouldn't be fights about fixing bathrooms or garbage disposals. I am crying because I know my dad would be able to help Scott, that it wouldn't be a chore, they could bond. I am crying because my dad missed out on seeing me be so strong--I am crying because in times like this I feel like I am failing at being a survivor. I am crying because in the medical world after treatment is done they just let you go, but your body is then reeling from all the treatment and you need more support than you did during chemo. I am crying because our bathroom needs to be gutted because the sub-floor is soaked and we don't have the money. I am crying because being an adult is hard. Because being an adult means you probably shouldn't sit in your bathtub and cry hysterically with the door locked--but we do. I am crying because you should be able to, I am crying because it is the only way I know to cleanse myself of some of the weight on my shoulders. I am crying because I feel like I need to fix everything, and I can barely fix myself. I am crying because I am afraid to tell people what is going on because they will think "here she goes again" blah blah blah medical, cancer, blah blah, complaining, blah blah. I am crying because I worry the cancer is back. I worry that the reason I have all these problems now is because my body is busy fighting a cancer and can't focus on healing wounds or fighting off other infections. I cry because I am afraid my oncologist, husband, and others will roll their eyes if I tell them.
I cry because tears are the only outlet at my disposal. I am considering turning on the faucet and taking a shower in my clothes. I am wearing my velour pants (as I call them, my plastic surgery pants) and I am wondering if they will soak up enough water to act as a cold compress for my leg with is unbelievably painful. I am crying because I can't come up with the words to understand where Scott is right now. I am crying because I am frustrated that I can't be his outlet, I am the last person that wants to hear about how me being sick has affected him. I am crying because I know this will make others cry. I am crying because I feel like I lost the momentum I had before I was diagnosed. I am crying because I can't seem to get a foothold on anything in the future. I am crying because I am afraid to make plans, afraid to drive my car, afraid to be around too many people, afraid to be afraid. I am angry I am afraid. I was a ball-to-the-wall type of girl....I wasn't afraid of anything, now all I seem to be is afraid. Maybe afraid isn't the right word, maybe I am crying because my life isn't perfect. That my hard work amounted to something small, and then moved backwards. Maybe the tears are a result of my disorganized brain and piles of laundry. Maybe it is because I feel behind and am overwhelmed.
Maybe it is because it is the one thing I can control when it starts and stops. I am crying because I know Scott is out there crying. I am crying because people may read this and view it as weak. I am crying because they are wrong (but I am not sure how to prove it).
Now if you'll excuse me I am going to move the computer out of the tub and possibly take a clothed, cold shower. Then there is a very good possibility that my illness, rash, swollen face and tears could use a drink.
Tuesday, June 12, 2012
normal is just a setting on the washing machine.
my pre-op cheer squad! |
my post-op fan club! |
my swollen boob, you can't really see it, but it was about twice the size of my other boob and BRIGHT red hot |
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actual syringe used and it is HUGE (like a banana) and it sucked out 165 cc's of fluid |
the drain added yesterday, AFTER 165 cc's of fluid was already taken out....lovely |
Friday, June 1, 2012
move, get out the way!
Scott and I at the Northwest Hope and Healing Fashion Show |
Hi there, nice to see you again....it has been too long! My apologies for the lapse in time, I have been overwhelmed, underwhelmed, sick, tired, angry, frustrated, and too stressed to type. But typing is what I should have been doing all along.... Today I have surgery to remove my right implant, scrape and slit the scar tissue from radiation and have another implant placed--we are hoping that this will allow me to no longer have a boob on my collarbone.
Since my last post things have changed--some things have become clearer, and others seem like a dream that I will not be able to achieve. Since my diagnosis (and during treatment when I was really isolated) I have begun to have anxiety, panic attacks over having to go to the grocery store, social anxiety of big places, anxiety of things that won't even happen, I worry about worrying.... So I decided to take it head on, I walked in a fashion show in front of 400 people with other survivors--if that isn't a bitch-slap to cancer, I don't know what is. And it helped, I was empowered and I had a great time, afterwards I felt like I could do anything...........
That feeling didn't last forever, but it did give me the boost I needed to get out of a rut. I still have some wounds on my legs and arms that aren't healing, my shoulder hurts more than ever, and I have surgery scheduled this coming Friday at 3:30pm to have my right implant removed, more scar tissue scraped out and cut, and a new implant placed. We are hoping that the result will be less pain (having the implant off my lymph nodes and collar bone) and my gals will be more even. Honestly though I could care less about them being even, I just want the pain to go away--and then I will have better result from physical therapy (which I am still going to for the car accident).
Waking up daily and being in pain has become my own "cry me a river" story. I don't mention it much but I am on edge all the time. The pain makes everything else amplified, I get overwhelmed easy, I snap at my family, I have trouble sleeping or focusing on something for a long period of time. Sometimes I have a day where I feel "normal" and I do as much as I can that day, but the next day is like a bad hangover.
I am ready for a new start....I have started to get extremely nervous for my upcoming surgery. I have done it before and I know the routine, I love my surgeon, and I thought I wouldn't be getting the butterflies that are currently making me stay in the bathroom like it is my job. I think it is because this surgery could take away a lot of the pain and give me back the opportunity to heal physically. I have been working really hard on healing mentally (putting things together and making sure I surround myself with supportive people) but not being able to heal physically has made it feel disjointed--they aren't lining up with each other and as a result I feel like I haven't made as much progress as I should be.
I cleared my circle. I spoke with another survivor and she told me how she got rid of things and people that she didn't like after she was diagnosed. I did the same thing! I didn't realize it but I did, even in my chemo and post-chemo haze I was able to weed out people that focused more on themselves than healing and support. What a great coping mechanism that I didn't even realize I had created until I looked at it as a whole picture.
Scott painted the bedroom and we changed everything around (it is no longer my chemo coffin) it is a place where I can relax and sleep. Though my anxiety has limited my social interactions, I still have a circle of amazing support that are unbelievably selfless and loving. I am in a place where I am feeling held.....where if I fall there are many hands to catch me, and if I need a boost they are there. I am hoping that with physical healing my anxiety will lessen...it has been hard to focus on things when the pain is always in the back of my mind, a continuous circle that then causes me to react physically.
We are working on switching up things at the house, finally doing all the things that we talked about doing forever. We are slowly making it our place, our place AFTER cancer, our place for me to survive and where we can thrive together and take on the new hurdles that life will throw at us, but hopefully keeping cancer as something we have went through, rather than something that is on the horizon.
I am not the same person I was three years ago--I look at photos and remember how it felt to not have real things to worry about, to just get to go about life, no lessons learned. There are a few things in my past that have changed how I view the world, losing my father, getting married, having cancer--and the woman I am today is who I was meant to be. I am using the strength that I have gathered to get through all of this, to be able to look someone in the eye and tell them I am a Survivor and mean it with every fiber of my being. I have been through hell and back and there is nothing I can do to change that. I have never been a "glass half-full" type of gal and my cynicism has definitely grown through tragedy...but I am honored to wake up each day and fight.
Today begins another journey, welcome aboard. I am off to check-in at the hospital!!
Monday, March 26, 2012
you don't leave the people you love alone
It has been awhile, so I put together bits of blogs I wrote but didn't publish to catch you up on what the last month has been like:
"If it isn't one thing, it is another. Insomnia, shingles, bitchiness, itchy red spots on my legs, intense bruising, a collar high boob, lack of communication, overbearing stress, relationship concerns, tears, booze, migraines, lack of focus, no motivation, feeling overwhelmed, blah, blah, blah.....
I need to get my head straight (and a boob lowered). After a pretty intense breakdown (two days worth of it a few weeks ago) I have decided that I need therapy........though I planted my feet in the sand against it (yes, I know I have a masters in psych and counseling--and yes, I know it is ironic). But here is why I have waited...I wanted to do it myself. I wanted to be able to work through the mush my head has become and come out on the other side, "fuck cancer, I can take care of myself" type of mentality. Not to mention that traditional therapy isn't my favorite, so I am going to search out a therapist that has experience with breast cancer patients (hopefully under the age of 50) and see how things go.
I have gotten progressively more depressed since my car accident. A snowball affect that finally took over. I have been so stressed my body can't fight the slightest irritation. I continue to have shingles on my right breast (I am on my 3rd outbreak) and had a rash on my legs that was so itchy I couldn't walk, I remained in bed trying not to itch. I cut my nails short and wore socks to bed to help prevent me waking up with blood streaming down my legs. I have been on two rounds of antibiotics, one round of steroids and gave up internally. For being a smart lady, and professionally trained to support others, I have found out that I don't know how to support myself.
Maybe "gave up" is too harsh....how about so overwhelmed that it hurts to breathe. How about being blasted with great ideas and not having the energy to do them. How about being in constant pain and having a boob at my collar bone that refuses to play nice? How about being depressed and thinking I could keep it to myself and as a result, it just got worse. So I had a melt down, a BIG one....not a nervous breakdown or anything, but I sobbed uncontrollably for two days and was miserable. I have stopped wanting to go to the grocery store, social functions, or anything really..........the anxiety just builds and I find it easier to stay home. (luckily I love my job and can continue to do that no matter what state I am in, in fact...I find it keeps my mind of a lot of crap)
I have turned inward but with little return........I was thinking that I could just meditate and move past this, quick and easy. Wow, I was wrong. No one warns you what happens when treatment is over, when you don't get lab results weekly assuring you that your counts are good, that you feel crazy because every ache or pain is "cancer". I was so focused on "healing" I forgot to heal. I glazed over the pain and exposure I had and I stuffed it, I stuffed it so deep it made my ass bigger. There was no getting to it, I was going to move on and not look back. HA"
And my current update:
I am now making incredible progress...........I still have a rash on my legs and will probably need another round of something because it has begun to itch again, but I am not letting it put me back where I was. I am lucky enough to be benefiting from wonderful light therapy and a change in perspective. I am honoring myself on the days that are just too hard because of mental or physical pain, I am letting myself have those moments without letting it affect my perspective the following day. I am working on new routines to keep me focused on stuff other than the physical pain, eventually I hope it will include exercise, right now it is more like:
-wake up, try to not hate the fact that pain is already taking over my body
-move from bed to couch, drink diet coke (trying to quit............one thing at a time here people)
-check emails and work whatnots
-go from couch to office chair
-lay in bed for awhile to help avoid taking a pain killer
-smile at Scott so he knows I am trying
-watch some TV, read a book, talk to Lucy
-forget to eat lunch, eat a mid afternoon meal so I can take my supplements
-stomach ache from supplements
-lay in bed until stomach ache goes away
-decide bed feels nice, put Lucy on bed
-Call mom
-see Scott when he comes home from work
-fall asleep
....repeat
Progress, not perfection.
rash on legs...........not awesome. |
"If it isn't one thing, it is another. Insomnia, shingles, bitchiness, itchy red spots on my legs, intense bruising, a collar high boob, lack of communication, overbearing stress, relationship concerns, tears, booze, migraines, lack of focus, no motivation, feeling overwhelmed, blah, blah, blah.....
I need to get my head straight (and a boob lowered). After a pretty intense breakdown (two days worth of it a few weeks ago) I have decided that I need therapy........though I planted my feet in the sand against it (yes, I know I have a masters in psych and counseling--and yes, I know it is ironic). But here is why I have waited...I wanted to do it myself. I wanted to be able to work through the mush my head has become and come out on the other side, "fuck cancer, I can take care of myself" type of mentality. Not to mention that traditional therapy isn't my favorite, so I am going to search out a therapist that has experience with breast cancer patients (hopefully under the age of 50) and see how things go.
I have gotten progressively more depressed since my car accident. A snowball affect that finally took over. I have been so stressed my body can't fight the slightest irritation. I continue to have shingles on my right breast (I am on my 3rd outbreak) and had a rash on my legs that was so itchy I couldn't walk, I remained in bed trying not to itch. I cut my nails short and wore socks to bed to help prevent me waking up with blood streaming down my legs. I have been on two rounds of antibiotics, one round of steroids and gave up internally. For being a smart lady, and professionally trained to support others, I have found out that I don't know how to support myself.
Maybe "gave up" is too harsh....how about so overwhelmed that it hurts to breathe. How about being blasted with great ideas and not having the energy to do them. How about being in constant pain and having a boob at my collar bone that refuses to play nice? How about being depressed and thinking I could keep it to myself and as a result, it just got worse. So I had a melt down, a BIG one....not a nervous breakdown or anything, but I sobbed uncontrollably for two days and was miserable. I have stopped wanting to go to the grocery store, social functions, or anything really..........the anxiety just builds and I find it easier to stay home. (luckily I love my job and can continue to do that no matter what state I am in, in fact...I find it keeps my mind of a lot of crap)
I have turned inward but with little return........I was thinking that I could just meditate and move past this, quick and easy. Wow, I was wrong. No one warns you what happens when treatment is over, when you don't get lab results weekly assuring you that your counts are good, that you feel crazy because every ache or pain is "cancer". I was so focused on "healing" I forgot to heal. I glazed over the pain and exposure I had and I stuffed it, I stuffed it so deep it made my ass bigger. There was no getting to it, I was going to move on and not look back. HA"
And my current update:
I am now making incredible progress...........I still have a rash on my legs and will probably need another round of something because it has begun to itch again, but I am not letting it put me back where I was. I am lucky enough to be benefiting from wonderful light therapy and a change in perspective. I am honoring myself on the days that are just too hard because of mental or physical pain, I am letting myself have those moments without letting it affect my perspective the following day. I am working on new routines to keep me focused on stuff other than the physical pain, eventually I hope it will include exercise, right now it is more like:
-wake up, try to not hate the fact that pain is already taking over my body
-move from bed to couch, drink diet coke (trying to quit............one thing at a time here people)
-check emails and work whatnots
-go from couch to office chair
-lay in bed for awhile to help avoid taking a pain killer
-smile at Scott so he knows I am trying
-watch some TV, read a book, talk to Lucy
-forget to eat lunch, eat a mid afternoon meal so I can take my supplements
-stomach ache from supplements
-lay in bed until stomach ache goes away
-decide bed feels nice, put Lucy on bed
-Call mom
-see Scott when he comes home from work
-fall asleep
....repeat
Progress, not perfection.
Monday, February 27, 2012
oh balls
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the front of my Valentines Day card from Scott |
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the inside of my card...he did some editing |
I spent a few days at her house and then took my suitcase full of wiener paraphernalia to a suite on the strip to set up for my sister Kristi's bachelorette party. My sisters and accompanying bachelorette party arrived Friday. My body sure isn't what it was, but I surprisingly held my own. I walked more than I have since my car accident and despite having to go to bed before the rest of them I felt great. We then rented a van and drove (for 5 hours) to the Grand Canyon for one night and I was able to see the sunrise the next morning at the Grand Canyon. My sisters and I haven't always seen eye-to-eye (translation: I was a huge bitch and they tried to avoid my crazy wrath) but since we have been adults they are my best friends. The trip was an amazing opportunity to spend time with them. It was good to know that I could survive a trip, even if my feet were swollen and resembled balloons when I got home, I caught a cold, and my shingles are back with a vengeance.
Life doesn't get easier. I have been waiting for things to "get better", to feel better, to get easier........bullshit. I don't feel like that is how things go. Life is one obstacle after another, you are continuously changing and growing and sometimes it slaps you in the face, I have my feet firmly planted in the mindset that you just have to slap back, actually I would go with a swift kick to the balls. Prior to leaving for my trip I found out that a fellow doula and friend had been diagnosed with breast cancer. The "it's a small world" factor really isn't positive in this case. She is a fighter and I know will come out on the other side of the bullshit, but it still reminds me that life changes in a heartbeat.
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Good morning at the Grand Canyon |
I have gotten complacent. I stopped eating all the fresh veggies (not that my eating habits have gotten that bad) but I am not stuffing my face full of multicolored plates of fresh harvest anymore. I drink more than my fare share of wine, rather than avoiding alcohol as I did before AND I haven't been working out 30 minutes a day since my car accident. I then have nightmares that my cancer comes back. That because I ate chicken nuggets instead of a salad my lymph nodes are being attacked by cancer. That because I had a second, or third glass of wine my insides just give up and cancer takes over. I am rushed awake by these nightmares in a full body sweat and I just lay there looking at the ceiling. It takes me a few minutes to realize that I am okay and not a prisoner of my bed as I was during treatment.
I have done everything in my power to lessen the chance that my cancer will return. But a human being can only do so much, I can't stop my cells from turning on each other, wine or no wine. Life has a mysterious way of pushing you into a reality you weren't expecting, or prepared for....so you adapt. I am aware that my cancer may return, statistically it probably will at some point. But that doesn't stop me from kicking life swiftly in the balls.
A great picture of my VERY high right boob and normal left boob |
Wednesday, February 8, 2012
so I peed on it
I was looking for something in the bathroom of death (we have discovered that we have black mold, fuzzy mold that looks like it should be growing on fruit, and water damage in our tiny master bath.....which is a whole story in itself because the last thing I need is to be breathing in mold spores) but I ventured in looking for a mirror to pluck the ungodly hairs that Tamoxifen has brought to my face and I found a pregnancy test...........................ouch.
I remember the days when I would pee on them and cross my fingers (and promise everything holy that I would be the best girl in the world or whatever I needed to do) that they would be negative. Oh come on, we have all been there....ladies?
I remember the days when I would pee on them and cross my fingers that it would be positive, we were ready, apparently our world wasn't.
I remember the day I found out why, I had cancer and my estrogen was all over the place, my body is not the best host for a human, not then, not now, not ever.
So I found this pregnancy test, and I peed on it. In case you are curious, it was negative.......considering I am on Tamoxifen and have an IUD I wasn't holding my breath. All the same, I peed on it.
My 2012 hasn't really been all that great. I went into this year with an internal gusto....a "I will kick its ass" attitude (and a bit of a hangover) and found myself somewhat of an emotional puddle of illness and internal frusteration. But I think that I am back on track now, thanks to some wonderful developments....that I will update you all on when I haven't been such a haphazard blogger--you can tell that I am not doing too well when I haven't blogged in over a month. I am working on it............I love doing it, but sometimes I just don't allow myself to do it as a punishment for not "being where I should be" or all I want to do is bitch so I feel like I shouldn't write ANOTHER blog about poor me bitching, but somtimes the bitching is funny, it is cathartic, so I will put it on my to-do list (maybe it will turn a switch on in my brain).
So we had a snow storm and an ice storm. Scott and I made our little snow family, lost some power, and found out that we have a mold problem in our master bathroom (see bathroom of death above).
The melting of the massive amount of snow and ice exaserbated the problem and it is now in quarantene until we are able to afford to fix it, or until I can even wrap my head around all of this. It seems like there is just one thing after another with this house--I loved it when we bought it, it was in a great neighborhood (come to find out we have not the best neighbors) but it isn't just the bedroom that reminds e of being sick, it is the whole house. I have memories that are tied to each piece of furniture, to particular dishes in the kitchen, to our patio (where I shaved my head). I can remember collapsing on the stairs, the numerous nights crying in the bathroom staring at the green walls that I once loved..........emotions are sucked into everything here. Scott and I have saged it, I have meditated about it, but when I am already feeling a bit down, it tends to overpower me.
Oh, and I had shingles on my right boob. This bitch of a boob is really not cooperating. It has actually gotten higher than it was after my surgery, it is now almost touching my collar bone. I saw my primary doc and was given prescription for antibiotics, we weren't sure it was shingles because I don't have feeling everywhere on that breast so I couldn't feel the pain. But then I went to my plastic doc and it was confirmed..........I had shingles like you wouldn't believe. I still have a little bit of the pain under my boob and some dried bumps, but haven't been contagious for some time and hope that it doesn't come back.
Alright 2012, let's work together on this. I am open to change....are you?
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My double mastectomy breast cancer awareness snow boobs!!! |
I was looking for something in the bathroom of death (we have discovered that we have black mold, fuzzy mold that looks like it should be growing on fruit, and water damage in our tiny master bath.....which is a whole story in itself because the last thing I need is to be breathing in mold spores) but I ventured in looking for a mirror to pluck the ungodly hairs that Tamoxifen has brought to my face and I found a pregnancy test...........................ouch.
I remember the days when I would pee on them and cross my fingers (and promise everything holy that I would be the best girl in the world or whatever I needed to do) that they would be negative. Oh come on, we have all been there....ladies?
I remember the days when I would pee on them and cross my fingers that it would be positive, we were ready, apparently our world wasn't.
I remember the day I found out why, I had cancer and my estrogen was all over the place, my body is not the best host for a human, not then, not now, not ever.
So I found this pregnancy test, and I peed on it. In case you are curious, it was negative.......considering I am on Tamoxifen and have an IUD I wasn't holding my breath. All the same, I peed on it.
My 2012 hasn't really been all that great. I went into this year with an internal gusto....a "I will kick its ass" attitude (and a bit of a hangover) and found myself somewhat of an emotional puddle of illness and internal frusteration. But I think that I am back on track now, thanks to some wonderful developments....that I will update you all on when I haven't been such a haphazard blogger--you can tell that I am not doing too well when I haven't blogged in over a month. I am working on it............I love doing it, but sometimes I just don't allow myself to do it as a punishment for not "being where I should be" or all I want to do is bitch so I feel like I shouldn't write ANOTHER blog about poor me bitching, but somtimes the bitching is funny, it is cathartic, so I will put it on my to-do list (maybe it will turn a switch on in my brain).
So we had a snow storm and an ice storm. Scott and I made our little snow family, lost some power, and found out that we have a mold problem in our master bathroom (see bathroom of death above).
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my snow "Dori" |
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Our snow family |
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snow "Lucy" |
The melting of the massive amount of snow and ice exaserbated the problem and it is now in quarantene until we are able to afford to fix it, or until I can even wrap my head around all of this. It seems like there is just one thing after another with this house--I loved it when we bought it, it was in a great neighborhood (come to find out we have not the best neighbors) but it isn't just the bedroom that reminds e of being sick, it is the whole house. I have memories that are tied to each piece of furniture, to particular dishes in the kitchen, to our patio (where I shaved my head). I can remember collapsing on the stairs, the numerous nights crying in the bathroom staring at the green walls that I once loved..........emotions are sucked into everything here. Scott and I have saged it, I have meditated about it, but when I am already feeling a bit down, it tends to overpower me.
Oh, and I had shingles on my right boob. This bitch of a boob is really not cooperating. It has actually gotten higher than it was after my surgery, it is now almost touching my collar bone. I saw my primary doc and was given prescription for antibiotics, we weren't sure it was shingles because I don't have feeling everywhere on that breast so I couldn't feel the pain. But then I went to my plastic doc and it was confirmed..........I had shingles like you wouldn't believe. I still have a little bit of the pain under my boob and some dried bumps, but haven't been contagious for some time and hope that it doesn't come back.
Shingles............not awesome. |
Alright 2012, let's work together on this. I am open to change....are you?
Wednesday, January 4, 2012
I waved my arms and flapped about
I am doing more than struggling lately, I am drowning. I have slowly slipped back into the mentality of being an "ill" person. The car accident immobilized me and as a result I was back in the bed (granted there is a new set of bedding) but the helplessness feeling is the same. Not being able to do laundry, prepare meals, keep the house in order, work at a normal capacity is a bit much. But I was working on it, I knew that I had to let my body heal, damn those "soft tissue" injuries.
Oh, and if you are curious, my right boob is still holding strong at my fucking collar bone, awesome.
So there I was, through both holiday's sitting with my 3 heating pads, smelling like menthol, but I could more or less be somewhat of a person. Then a few days ago a door slammed me in the face, hard (not literally). I have never been one to suffer from headaches, I mean nothing that would require anything other than a few Advil. One of my sisters has struggled with headaches a majority of her life, horrible headaches, and she powers through life like a trooper--trying alternative therapies and medications, but continues her life. I am currently in awe of how she does it, it has been three days and I am ready to throw in the towel.
At first I thought it was my newly placed IUD (yep, lady part reference--UTERUS (I bet I just lost a few readers....). I thought maybe it was because I was taking a different medication for pain so it was making me dizzy and I had to keep my head on a pillow--I have been there before. But then I stopped that medication over the weekend and starting on Monday I had blurry vision that would come and go, I felt like I wasn't able to make the connection between what I was thinking and what I was writing (or being slow in reactions), I didn't feel comfortable driving, I was sick to my stomach, they only thing that helped was being asleep, because I couldn't feel the pain. It was like a cloth was draped over my forehead and face and it wouldn't let go.
And here I am...........three days later feeling the same way, numerous medications, home remedies and a massage and I sit typing this in the dark on my keyboard that sits on my lap, facing away from the computer) luckily I am a pretty good typist so there is no concern to the knowing of the keys.....but I could really use a break here. My massage therapist said that it was a result of the pain from my back and neck moving up into my head, she did her best, but I left feeling just a tiny bit better than when I went in, now I am back to not feeling able to drive and am almost ready to hide under my covers....going to sleep at 3:00pm is warranted and I feel doctor approved, but ridiculous.
I have a life to live, I have stuff I need to do, but I can't seem to power through. I know that part of it is because when I sink into being that "ill" person things very easily compound on each other and I fall apart, literally my body just begins failing me and mentally I am not strong enough to keep the composure. I am at a loss here, and I am more overwhelmed than I have been in a long time. There is literally nothing I can think of to do to change the situation and the more I stress over it the worse I feel.
I feel like I have become a burden to my loved ones, these tremendous and amazing people, many of whom put their life on hold when I was diagnosed to meet my every need. I am worried that there is a breaking point, where you can only love someone through so much, then you need to begin to heal yourself. Being a caretaker is unbelievably hard, and as I continue to struggle with health issues I am worried I will lose parts of this support tapestry. I know there are times that Scott must think of how easy it would be to be with someone who could run a marathon with him, someone who doesn't end up in the ER monthly, someone who isn't broken. I just want to be that person so bad. I sometimes suffer in silence rather than speak up because I think it is unfair to those around me.
Yesterday I got off the bed and my left leg was numb and I fell on the floor, I have been having some serious cramping and with ovarian cysts before similar things have happened, but when I start to add everything together I begin to worry that there is more to the picture. But I know I worry more than the average person, especially medically after my diagnosis. I don't want to be the girl that goes into the ER and they talk about after I leave, but when nothing works I begin to think the worst. Where the hell did they hide the "Easy" button for this shit?
![]() |
me, the person I was years ago....I had nipples then (they were awesome) |
Oh, and if you are curious, my right boob is still holding strong at my fucking collar bone, awesome.
So there I was, through both holiday's sitting with my 3 heating pads, smelling like menthol, but I could more or less be somewhat of a person. Then a few days ago a door slammed me in the face, hard (not literally). I have never been one to suffer from headaches, I mean nothing that would require anything other than a few Advil. One of my sisters has struggled with headaches a majority of her life, horrible headaches, and she powers through life like a trooper--trying alternative therapies and medications, but continues her life. I am currently in awe of how she does it, it has been three days and I am ready to throw in the towel.
At first I thought it was my newly placed IUD (yep, lady part reference--UTERUS (I bet I just lost a few readers....). I thought maybe it was because I was taking a different medication for pain so it was making me dizzy and I had to keep my head on a pillow--I have been there before. But then I stopped that medication over the weekend and starting on Monday I had blurry vision that would come and go, I felt like I wasn't able to make the connection between what I was thinking and what I was writing (or being slow in reactions), I didn't feel comfortable driving, I was sick to my stomach, they only thing that helped was being asleep, because I couldn't feel the pain. It was like a cloth was draped over my forehead and face and it wouldn't let go.
And here I am...........three days later feeling the same way, numerous medications, home remedies and a massage and I sit typing this in the dark on my keyboard that sits on my lap, facing away from the computer) luckily I am a pretty good typist so there is no concern to the knowing of the keys.....but I could really use a break here. My massage therapist said that it was a result of the pain from my back and neck moving up into my head, she did her best, but I left feeling just a tiny bit better than when I went in, now I am back to not feeling able to drive and am almost ready to hide under my covers....going to sleep at 3:00pm is warranted and I feel doctor approved, but ridiculous.
I have a life to live, I have stuff I need to do, but I can't seem to power through. I know that part of it is because when I sink into being that "ill" person things very easily compound on each other and I fall apart, literally my body just begins failing me and mentally I am not strong enough to keep the composure. I am at a loss here, and I am more overwhelmed than I have been in a long time. There is literally nothing I can think of to do to change the situation and the more I stress over it the worse I feel.
I feel like I have become a burden to my loved ones, these tremendous and amazing people, many of whom put their life on hold when I was diagnosed to meet my every need. I am worried that there is a breaking point, where you can only love someone through so much, then you need to begin to heal yourself. Being a caretaker is unbelievably hard, and as I continue to struggle with health issues I am worried I will lose parts of this support tapestry. I know there are times that Scott must think of how easy it would be to be with someone who could run a marathon with him, someone who doesn't end up in the ER monthly, someone who isn't broken. I just want to be that person so bad. I sometimes suffer in silence rather than speak up because I think it is unfair to those around me.
Yesterday I got off the bed and my left leg was numb and I fell on the floor, I have been having some serious cramping and with ovarian cysts before similar things have happened, but when I start to add everything together I begin to worry that there is more to the picture. But I know I worry more than the average person, especially medically after my diagnosis. I don't want to be the girl that goes into the ER and they talk about after I leave, but when nothing works I begin to think the worst. Where the hell did they hide the "Easy" button for this shit?
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