Brenda's Child

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

Saturday, January 9, 2016

Jumping the Gun: More Fipple problems

It's almost six o'clock on a Saturday and I've just been able to peel myself off the couch...kinda. I was so excited to finally see my new fipples, which look like they will be great once all these stitches dissolve. This was exactly one week after my surgery. My surgeon removed all of the bandages and instructed me to lubricate all of my wounds.
With bandages...don't they look perky? Relax they'll drop some later, but they are smaller

He used skin from underneath my foob to create the fipple

Here I am all oiled up. Can you imagine wearing a bra over this?



He forewarned me that it would be tricky finding the right bra for now, and for some reason, I didn't quite absorb that until I tried to actually wear one. On one hand I was told not to wear anything that could flatten out my new nipples, like the sports bras and  tanks with built- in bras I've grown to love. Then with my lovely  stitches in the uncomfortable spot underneath my breast, no underwires, or hell, any kind of bra. With my green light to go back to work I surely couldn't show up with my headlights beaming. So day one I wore a cupped Victoria's  Secret bra to allow room for my fipples. Unfortunately my day was filled with anguish. Firstly, I was back to driving and turns and backing out hurt all over. Secondly, that expensive ass bra sucked! It cut right into my sore spots, and it wasn't as supportive as my surgical tube top, so every time I bent down...ouch.
 After work I did what he had suggested in the first place, I got some nipples protector cups; the same ones for breast feeding mothers. i wore those with my go to sports bra and it was a better. However, by the end of the day, I was sore from the nipples protectors. Those things are not meant to be worn for 9 hours! So here I am exhausted from only 3 days of work, and uncomfortable unless I'm laying with pillows propped under my arms. It's surprising and disappointing to me
because week one went so well with the bandages and the tube top. No bra= no support, bra= support but flat nipples, or support but pain to my stitches. So I'm laying here for this reason and because  I'm tired. It I may even be slightly depressed; not at my fipples, because they are awesome, but because I'm not 100% and everyone that knows me, know I hate to slow down. I just have to remember that this is temporary, and by summer I'll be more back to normal. Damn Patience!

Sunday, January 3, 2016

Happy Foob Year!

5 days later, here I am wearing the most hideous surgical garment ever. I mean the last ones were ugly, but they were all white and  made no attempt to be cute. However uncomfortable and unattractive this contraption, it does what it’s supposed to, which is support my newly lifted foobs and sewn on fipples.





 I have to say this surgery was a breeze compared to the last two. Aside from the fact that we had our first snow/sleet/ice storm the night before, which caused my surgeon to arrive 15 minutes late, everything went as planned. At 7:45am the anesthesiologist injected my IV with the feel good stuff. At 11:10 I was awakened by a nurse placing pillows under each side of my arms. She told me I could keep sleeping, which I did for another hour. Then I was ready to get up and go. My fiancée came for me, and other than feeling light headed and dizzy, I felt relieved; no more surgeries, I did it. I was home in time to watch Judge Mathis, which I eventually fell asleep on.  With the help of some narcotics, I slept on and off the rest of the day.  The next day, I was still groggy and my only discomfort were the stitches were underneath the foobs. It felt tight, and itchy, but nothing unbearable.  Because I wanted to celebrate with champagne on New Year’s Eve, I was hell bent on not taking any pain meds at all. So I sucked it up. My reward was spending my holiday surrounded by family, and wearing scarves and sweaters to cover up the bulky surgical tube top. I tried to go the whole week with only sponge baths, but once 2016 came around, I gave in, being sure not to wet my bandages. In two more days I will get to see an updated version of my foobs and fipples. 

At this point I’m not even excited about it because I’ve just become more and more accepting of my body no matter what it looks like. Besides, it’s amazing, I mean look at all it’s been through and it continues to heal and allow me to do whatever I set out to!



Monday, December 28, 2015

After the Storm:Foobs & Fipples

I’m beginning to feel like a pro. Wash all the clothes, clean the house, take out button up and zip up clothes (because I won’t be able to reach over my head), pick up my toddler all day (because I won’t be able to do that again for a few weeks) and prep him for mommy recovery again (he is not happy about it and threatened to punch the doctor’s for giving me boo-boos). Before I take my shower tonight I’ll take one last picture of my foobs before I get my fipples. The way my oncology gyno explained it is that he will pretty much do origami with my scar tissue and create semi erect fipples. In order for them to be even, my surgeon will do a freast lift, which means now I will be EXTRA perky.


I know it seems painful, But I have no sensation in my freasts




 Still it will be a couple of more months before Toya the Remix is complete and I finally get my areolas tattooed.  As prepared as I feel, because of course I’ve done the research, I still get nervous about going under. And while I know the pain will be minimal compared to last time, I hate pain and pain meds and being limited physically.  I know it’s temporary. I know it’s worth it, but I still get nervous. Who wouldn’t? And I’m still looking forward to spring when I will be healed much more internally so that I really get back in to my fitness. I mean what do I look like with a flat stomach, perky foobs, but jiggly arms and a flat ass??? And no, this is not me putting myself down. I  have loved my body through all its stages, but since I found out I need more stomach fat in order to have these nice breasts, I had to go through some major changes. Prior to all of this I was killing it at boot camp. I felt strong, powerful, I had some cut in my arms and my backside was getting good and round from thousands of squats. I tried it few weeks ago and I was filled with adrenaline as I pounded the medicine ball to the floor, and did jump squats and planks (I used to do 1 minute, now it’s like 15 seconds). But two days later I was almost incapacitated at work, abs were sore, the muscles underneath my boobs were sore, okay no sore, straight hurting. I had to quit. Okay, not quit, but postpone until 2016.

 I know I’m powerful, I’m still here. But I cannot wait to get back to being the weight lifting beast I was becoming last year around this time!

Storm- a friend gave me a little statue  of her to help me weather "The Storm"


 But wait is exactly what I have to do.  Tomorrow I check in at 6:00 am signing off. Later folks

Sunday, November 29, 2015

From FREASTS to FOOBS: Part III: Recovery



WARNING: THIS POST CONTAINS GRAPHIC MEDICAL IMAGES and  one sexy image!

As my aunt wheeled me down the hospital corridor, I was mixed with emotions. Happy to be out the hospital… away from the substandard food, the constant interruptions from folks trying to get vitals, and from the inconsistency of great nurses and awful nurses. I would get to be in my house,  around my children, and the fact that I was being discharged meant that I was well on my way to recovery. But I was apprehensive, what if something went wrong? I had learned how to navigate my way from my hospital bed to the bathroom,  but  once again all of the research I had done indicated that I would have a hard time at home. It was recommended I get a shower chair, a raised toilet seat, and that I sleep in a recliner since I couldn’t fully stretch out.  (The recliner was and still is my best friend).
 The trip home left me depleted. With the help of my fiancé I got myself adjusted on the recliner sofa in the living room. That night both he and my toddler slept on the couch next to me. Every four hours my fiancé woke me up to take my meds so I wouldn’t have to be completely exposed to the pain. The next day, turned into two weeks of the monotony. Sleeping and awake at odd hours of the day and night; visits from my aunt angels, cousins, and good friends; meals being cooked and delivered; drains being emptied.
Oh the dreaded drains. The absolute worst part of this whole experience. Two hanging from each side of my upper rib to collect fluid from my Freasts (fake breasts) or what I now call FOOBS(fake boobs) and two hanging from either side of my hip to collect fluid from my abs. They had to be emptied and the disgusting fluid from them measured and documented.  Because of this, I wouldn’t need a shower chair, because I only took sponge baths. And I got to wear cotton old lady button up robes. Thankfully I had my aunt, and a very good friend who stepped in when the visiting nurse couldn’t.
courtesy of breastcancer.org

With all that was going on, there were some amazing facets of my recovery. First of all, I didn’t need that raised toilet seat. Turns out all those years of Pilates helped me build an awesomely strong core underneath that once thick layer of belly fat. It was much easier than anticipated. Secondly, I wasn’t totally freaked out by what I saw when I looked in the mirror. I mean, my foobies had no nipples, but still it wasn’t nearly as traumatic as I thought it would be. I think other people were more uncomfortable than me.


It was during this recovery I got to see who my real friends were. I was surprised by the number of people who reached out to me in some way, and disheartened by those who I expected would but didn’t. Still with so much love and support around me, I couldn’t dwell on it for more than moments at a time.
Each day I was more and more amazed at what my body could do, how it healed itself, regenerating cells and nerves and FOOBS!   

Perhaps the best part of recovery was 19 days after surgery when with the doctor’s clearance I was able to get dolled up and receive my 100 women of Color award for my work.  Not only did I receive an award alongside 99 other phenomenal women, I also  got my own holiday in my hometown! Sure I had to tiptoe around, sit while everyone else was socializing and I was exhausted after the 4 hour event, but  when they called my name, I strutted across that stage like my foobs weren’t still swollen, and my abs weren’t sore. Because that’s what you do once you dub yourself the Queen of Self-Esteem!
19 days post op... pretty sexy considering all that was going on underneath


The Journey doesn’t end here. Stay tuned as I continue on to the next stage of reconstruction on December 28th. I'll get my Fipples 
 (fake nipples)

Monday, October 19, 2015

FREASTS: The Right Choice...Part II

When the alarm clock went off at 5:15am, I had only napped about an hour.  Although I was exhausted I was in good spirits. I had made peace with my decision and the changes it would bring. But I did tear up when I kissed my toddler as he slept, praying I would see him again. I went in alone, which was what I needed. As I lay in pre op, I meditated and focused on coming out of surgery and healing like a rock star. I was so calm as I changed into a gown, emptied my bladder, got weighed one last time (Whoa) and let them begin to hook me up to all of the machinery. I answered the same questions over and over about allergies, last time I ate, etc. Then my handsome (in a quirky way) plastic surgeon came in and marked up my body. When I told him how much I’d miss my belly button, he told me I would still have the same belly button, it would just be moved. This gave me comfort.  
Then the anesthesiologist  came in, explaining that I would have an a an epidural that would numb my chest muscles so that I wouldn’t feel pain when I awoke.  I leaned over on a pillow; the nurse held my hand, and the needle in my lower back was the last thing I remembered. 
This is what was happening while I was completely unaware:

 My oncologist would cut and remove both of my breasts, removing the fat, the muscle, mammary glands and all. Her reputation is that she is thorough and would scrape away all of the breast tissue. Like all. Next, my brilliant plastic surgeon and his team would begin what is called DIEP flap reconstruction.According to BreastCancer.org, DIEP stands for the deep inferior epigastric perforator artery, which runs through the abdomen.  In other words, they would cut a large portion of skin and fat from my lower stomach, and then transplant them to my chest wall in the shape of breasts. Crazy, right?  But not simple. It involves microsurgery, reattaching the veins and arteries one at a time.
This is a diagram showing one breast. I had both breasts removed and reconstructed
For my surgical team, it took 15 hours total.
 This meant that while my family thought I’d be done by 8 or 9pm, I was not out of surgery until after 1am (Tuesday).

            When I opened my eyes, my two aunts were there like angels…
Gloria(L) and Saundra(R) my mother's sisters
 because my vision was blurry. I was distracted by the breathing tube that was still in my throat. Panic set in, medical staff tried to calm me, but I kept trying to speak. I could hear myself saying, I can’t breathe, I was gagging telling them to please take it. When they didn't listen, I tried to remove it. I felt people grabbing my arms and I heard “Sedate Her” , which they must have because the next thing I remember  (12 hours later apparently)  I was waking up with straps on my wrists. But at least the breathing tube was gone. What I didn’t understand in my panic was that they had to keep it in because, just like with any transplant, there was the risk that my chest wall wouldn’t take its new FREASTS. If the tissue didn’t stay alive, they would have to take me back into the OR and remove those. Not to mention, they needed to make sure my throat wasn’t too swollen and that I could breathe on my own. Which was kinda important.This is why I was in the ICU, being checked in half hour intervals. I was under heavy IV pain meds (thank God) so the first 24 to 36 hours were a blur of nurses brushing my teeth, wiping my dry cracked lips and putting petroleum jelly on them, cold cloths on my forehead, I remember them being so great, and feeling comforted despite the fact that I could only open my eyes seconds at a time, and my voice was weak. Unfortunately, I also had a fever of 102 and they worked vigorously to drop it down with IV medication. What I also was unaware of was that they were trying to keep me awake and get my body’s systems going. One of the nurses had me verbally complete the health care proxy form and sign off on it.  I had no concept of time; I just remember when they told me it was safe to move me out of ICU and into a regular room because my FREASTS were still viable. As they wheeled me on a stretcher, I passed a blond haired, fairly young, handsome doc. He introduced himself (I can’t remember his name) and said that he was on the surgical team. He told me I was brave and bad ass for my decision and that I made the right choice.


          According to my family, I was out of ICU by mid-morning on Wednesday and into my room. It was there I remembered that I was going to be a rock star in terms of doing what I needed to heal quickly. I asked that the catheter be removed so I could go to the bathroom on my own. (Why not, I was on morphine?).  It was so weird. I didn’t feel pain, I just felt stiff and tight as I walked in  cave man like baby steps, escorted by a nurse. I still had a low grade fever, so they were constantly checking in on me; they still needed to check the FREASTS every 1 to 2 hours.  I remember it was hard for them to find that swooshing sound in my left breast, so that had to put it in a special spot.
They put on a surgical bra, which I would grow to hate over the next 3 weeks, which matched my waist binder, which I’d grow to love and hate. They wanted me to sit in a chair. I did, and I slept there. But I also walked the hall, ambulating like it was suggested. I was determined to be model patient.


 The next few days would include daily visits from my angel aunts, my fiancé, and my uncle, and special visits from cousins, my dad, my brother, my oldest son, and my sister.   It was my sister and one of my closest friends who took a lesson in how to change my drains (we’ll discuss those in part 3).  I had my friend take this picture of me:

I wanted to document this journey, which would be hard because apparently I had multiple conversations under the influence of drugs that I don’t remember. It was a blur of Law and Order SVU reruns in the TV, multiple sleep interruptions, wraps on my legs to prevent blood clots, breathing into devices to restore my lungs, picking out my meals, taking sponge baths. Great nurses and PCAs, and awful nurses. Looking at the clock, not sure if it was 4am or pm.
The day my fiancé finally brought my toddler to come see me, it all came full circle. He was soooo happy to see me. At one point I glanced up at my wall chart with all of the nurse’s names and the date. It was Friday, September 4th. The anniversary of my mother’s transition. I looked at my toddler, I was about his age when I would go see my mother at the hospital, and like I saved my dessert for him, she’d save her dessert for my sister and I. It was mind-blowing to me, and I was rushed with emotion.  I was sad for the little girl in me who had no idea that one of the times she left the hospital would be the last time she saw her mother. I felt sad as a mother, for my mother, who at 23 knew she wouldn’t be around to see her kids, and that one of those hospital visits would be that last time she’d hug her little girls.  But I felt grateful that because of modern medicine, I would be there. I would be there for my toddler, and despite missing me dearly, he’d see me again. That doctor was right; I’d made the right choice.
My oldest son
My 4 year old



Wednesday, July 29, 2015

Bittersweet Choices

   

     Even though I’m consumed with
 my dissertation, I am also
 preparing for the biggest, most complex surgery of my life; my mind and spirit are all over the place.  First off, I am beyond grateful that because of technology I am able to take steps to prevent the breast cancer that took my mother away at such a young age. But when I look at my toddler, I’m sad because my sister and I were so close to his age when she passed away. My baby is 3 ½ and he comes looking for me in the middle of the night. I couldn’t imagine not being there for him, and knowing that I was dying and wouldn’t get to see him grow up. My oldest son just graduated high school, and last week I took him to get his college ID. My mom missed that. My grandmother missed that. And so many other things in between. So lately I’m extra attached to both of them (even though the teen is totally not feeling mom). 

    Then I feel blessed again because it was my choice to wear 
my fabulous wigs, and to chop all my hair off, and it wasn’t the case for my grandmother. I remember coming home from school one day and she was sitting on the couch with a pile of hair in her lap. She explained to me that it was an effect of her chemo. Looking back, her wigs were in no way as beautiful as her once long dark hair.  And when it grew back, it looked a lot like mine does now, just gray. I have options, and it’s amazing, and it’s still scary and bittersweet.

      Then there's my mortality, something I struggled with so
much as a young person, so much that I refused to wear bandanna scarves because I remember my mother wearing them while she was in treatment. 



Now that older, and I’ve outlived my mother, it’s coming into a play again.  I’m going under the knife for 10 to 12 hours. YIKES!!! I’ll be in ICU;  in the hospital away from my baby for 5 days. I’ll have to look at my breasts without nipples or areolas for about 6 months. I will have a huge horizontal scar across my abdomen; I’ll try best to look at that with gratitude because I have a choice. That choice doesn’t involve radiation, chemo, or not being here to see my sons grow and evolve. I have a choice, but it doesn't mean I'm still not apprehensive.


Thursday, July 24, 2014

BAD ASS!

This photo represents one BADASS woman who is feeling fearless, optimistic, confident, and blessed! 10 years ago, I was riddled with apprehension about my future, consumed with thoughts of what if I am next?  Next to have breast cancer. And in my vanity, I thought about losing my cleavage, my hair, my eyes brows…my life. I reasoned with myself, girl you can get new boobs, and you wear weaves and wigs anyway. They are just body parts. But still, no matter how hard I tried to convince myself, I was still afraid.
                Now that I’m over 30, with my cancer-filled family history, it’s time to face facts and be preventative. I’ve been doing Breast Self-Exams since I was 12 because if you know my story, you are aware that my mother succumbed to breast cancer at only 23. Her mother and one of her sisters also battled ovarian cancer and died in their 50’s. Science has found that there is a link between the two. So in addition to the mammograms that began at 30, last month I sought genetic testing. Apparently, this BRCA testing can identify two genes that will predict my chances for developing either or both. What this means for me is that if the test results are positive, I have an 87% of developing breast cancer. Whoa! Right?  (A lot higher than the 8% chance the rest of the female population has) I will also have about a 50% chance of developing ovarian cancer throughout my lifetime.  As scary as it sounds, thanks once again to science, there are options for how to deal with it, which includes having all of the above mentioned removed and a bit of reconstructive surgery.  But before I jump to conclusions, I will have to wait to get the results in a few weeks.

                Facing my own mortality has somehow put a little more oomph in my already vibrant spirit.  My thinking has changed so much over the years, from thoughts of doom to assurance; mostly because I’m living in my purpose EVERY SINGLE DAY. So while many people are searching aimlessly for theirs, I discovered mine around the same age my mother was when she passed away. I am living for all of those who did not.  I have legacy on my shoulders to carry, one that I don’t find burdensome, but more like honorable. So this is why I will hold nothing back and continue to be the BADASS I was destined! Shine on!

Wednesday, May 4, 2011

"Happy" Mother's Day



Mother's Day wasn't always a struggle for me. When I was younger I absolutely loved making gifts in school for my ga-ga (my maternal grandmother). Let's see, it was the plants in a Styrofoam cups, homemade candy (which she couldn't eat because she was diabetic), and plenty of specially written and decorated cards. Mother's Day became harder after she died because it wasn't until I'd lost her that I began to feel like a motherless child. All of the love in the world couldn't stop me from feeling this emptiness when Mother's Day arrived.


When I became a mother, it got easier; I saw my son come home with the cards and plants, and I'd smile. But then I found myself missing Brenda, my real mother. As an adult, I wanted that special relationship I saw all of my friends have with their mothers, so I still felt empty. To cope, everyone knows I deemed myself Brenda's Child, and I became that parental figure to other kids who were missing a mom for whatever reason.


Three weeks before Mother's Day also marks the anniversary of the death of my mother's sister ( she died unexpectedly at 36 from a seizure, which was a reaction from her medication. She had been on dialysis for years due to kidney disease.) Two cent was my homegirl. I use the old school term because growing up in the '80s, she was who you wanted to be: creative, stylish, sexy, and cool. What made her most important to me was that had if not been for her babysitting my son free of charge, I would not have been able to finish college and work full time. It's because of her that my son developed early on a love of reading and learning. That was 2002, and again I learn to cope. She was the 3rd person whose name would be tattooed on me, and I honored her memory by publishing some of her poetry in a chapter dedicated to her at the end of my first book, A Piece of My Mind.

In 2009, my friend Gail died the week of Mother's day from Leukemia. She was a mother of four, and like my mother, my grandmother, and my aunt, she liked working with kids. I used my words once more to honor her in my memoir, The Right Amount of Sunshine.

This is the only way I know how to deal, I keep their memory alive through the work I am still able to do while I'm here on this earth.

I'll light a candle for each of them this Sunday, knowing they are present in spirit always. And although I may shed some tears of remembrance, I will have "Happy" Mother's Day just for them!

:


Ga-Ga ovarian cancer 1991

Brenda Breast cancer 1982

Gwen a.ka. Two Cent 2002

Gail Leukemia 2009

Sunday, November 22, 2009

Knocked Off Focus


Anyone that knows me, understands that I am driven. However, there is one thing that knocks me right off focus...DEATH. It instantaneously reminds me that I am not in control of anything while putting me back in a state of missing, yearning for my loved ones. This year, I lost a good friend to Leukemia, and not a day goes by that I don't think about Gail. And when I think about her cancer, I think about my mother's and my Ga-Ga's (my maternal grandmother) battle with the disease, and the suffering they went through. And while I try to console myself with the idea that they have moved on to a better place, I am still haunted by visions of them weak, in pain, so thin they are barely there, and it saddens me.


My great uncle just died from cancer on Thursday November 19, pancreatic I believe. I have constant thoughts of him, and my friend having to plan their own funeral services, and it hurts like hell. Any loss is tough but to watch someone suffer is torturous for my spirit; traumatizing. I think about my friend Gail, who was just getting ready to find herself as a woman. She finally knew what she wanted to do with her life, found the job she loved and went back to school to further her career. Around the time of my birthday in 2008, she was diagnosed. Around the time of my birthday, 2009, she called to tell me that the doctors could do no more.



Not a day goes by that I don't want to call her or laugh with her about something that I know only she would find funny. And when things happen, like my paternal grandmother being in the ICU for her heart, (which has been going on for a month) I just want my mommy or my Ga-Ga to be there to hug me and to help me through it. Instead, I just shut down. I lose focus, I make it through the day just to get in the bed. I don't want to be around others, even my family who are still alive and well. I just want to be in my dark place until I'm ready to see the sunshine again. And right now I'm just not ready. With the holidays coming around, ( I lost Ga-Ga on Christmas Day when I was 13) it only gets harder.



And I have prayed, I have meditated, and now I am writing, but the reality is, nothing ever helps until I'm ready to come back, re-focus, and live for today, though I'm not promised tomorrow.