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

Sunday, January 29, 2012

Still Here

Still Here!



this post comes from my carepage, I edited it a little, got a little more personal and added some pics~

hello to friends and family,
I haven't posted in a while, mainly because there hasn't been that much to share. Since Thanksgiving, I have been getting stronger every day and have even had moments that feel normal. I have been teaching some of my regular fitness classes. I am not doing any weight training, but, I am happy to teach step and cycle.
coaching BootCamp
Love my bootcamp ladies!

I was visiting the Plastic Surgeon every week up until the week before Christmas. I would get a 'fill' each time. The doctor finds the port in the expander, injects it with a huge syringe and adds saline to the expanders. This is the most uncomfortable procedure, not during, because I don't feel a thing, but after. Muscle spasms, pain, tightness and shortness of breath are all side effects. The purpose is to expand the chest wall, stretch the skin and save a healthy pocket or space for the implants. I get very self conscious as my chest grows.
________________________________________________________________________________________

Implant Reconstruction Procedure 

from http://www.mdanderson.org/patient-and-cancer-information/cancer-information/cancer-topics/cancer-treatment/breast-reconstruction/implants.html

Following mastectomy, your reconstructive surgeon will insert a tissue expander (a silicone balloon filled with saline) in a pocket formed under the muscle and remaining skin on your chest wall. More saline solution is gradually added to the tissue expander during outpatient clinic visits, stretching the muscle and skin to the desired size. Often the skin is stretched slightly more than needed because it has a natural tendency to shrink when the tissue expander is removed. 
Implant ReconstructionThe amount of saline needed for each expansion may vary depending on the tightness of the skin. This process usually takes 2-3 months, but may take longer if you need other cancer treatments, such as chemotherapy. 
Once the "pocket" has reached the desired size, the expander is left in place, stretching your skin for approximately 1-3 months more. Surgery is then scheduled to remove the tissue expander and replace it with a permanent implant, which is an outpatient surgical procedure. The permanent implant will either be filled with saline or silicone and will be much softer than the tissue expander. Your reconstructive surgeon can discuss the various types of available breast implants.
___________________________________________________________________________________________________

There is still some scar tissue along the lower part which is why I had the last expansion to hopefully soften and stretch the tissue. About three weeks ago I started having severe chest pain, difficulty breathing and taking in a deep inhale. So, Dr. Fabulous took out 30 ccs on the left side to hopefully decrease the pressure. It hasn't really helped, and I am still feeling lots of pain. I have been told that the serratus and intercostal muscles were strained. It feels like I have a broken rib! I have been given a new muscle relaxer that doesn't make me sleepy and I take it to help with the pain.
expander1.jpg
tissue Expanders are hard and uncomfortable.
they must be one size fits all...because they poke me
all over!
source http://www.concannonplasticsurgery.com
I must say that this part of this whole ordeal has been the most difficult for me. I think that my family has all exhaled and feels really relieved that all the danger is gone, and I do too. I have always had the mentality that if I push harder, try harder, don't give up...I will get better, do better and survive stronger. But, with reconstruction, if I push too hard, I hurt myself and that has been frustrating. I am learning (not very willingly) patience. It is very difficult to sleep and I wake up a lot having huge spasms across the front. There's still a lot of numbness, especially down my right arm where the lymph nodes were removed. I also have had moments of being really sad, I miss the girl I was...maybe it is because these tissue expanders are so dang HARD that I feel hard and I miss feeling soft. (tmi?) I think that there is a total of 480 ccs on each side!! wow!
Next Thursday, February 2 we are scheduled for the exchange operation. This is when the doctor takes out the expanders and replaces them with permanent implants. This is an outpatient operation and should only be a few hours long. We are the first operation of the day, 8 am! It will be at Patewood Hospital. I am very anxious about it...not very excited to be back at the beginning of healing again.I am so happy that my dear love and friend JD will be working in the hospital that day...somehow, knowing when I am out and asleep in anesthesia world that there is a love watching me, I feel settled.  I have done some reading and it seems that some women recover quickly and others have a slower process. I am thinking about 10 days. This week and next week are full of pre-op appointments. I am visiting the allergist again to try to determine which medicine caused that horrible reaction on Halloween.
Today I had a dentist appointment to get a crown and nearly had a panic attack...the drill and and being so vulnerable was way more than I was ready for and I left the office nearly hysterical. I sobbed all day and had visions of being attacked and violated and hurt.  Bless my Dentist!
can't wait for my next Mud Run!
Chan and the kids and I are looking forward to a fun spring and lots of new beginnings! We are training for a 1/2 marathon and the children are training for a 5k. (well, Marshall runs and Sophie runs half way and then cries...)

Things I love right now:
training for the 1/2 marathon
Sunday Long runs have made me feel ALIVE
teaching cycle again, not just suffering through, but, KICKING ASS!
not taking ANY meds, not even advil
My son who is so tender, he whispers that I am his favorite
( I am sure I'm not, but, I love that he tells me that in his quiet serious voice)
my steadfast friends who won't let me be pitiful too long, who make me laugh and who comfort me
my friend Emily who does whatever I need no matter what
my friend Jennifer who runs with me and holds my hand
my friend Joy who whispers that I am a RockStar
my friend Darla who will knock anyone down if they say or do anything not sweet or kind, and loves me in all the best ways
my friend Susan who loves me SO and I feel it at all times
( I felt like shouting out to my girls today, there are more, but these are the ones I see and get love from every day.)

Joy and I and the 'girls' 
cleavage--seriously people!...nobody ever looked at my chest before...

Things I am struggling with right now:
prickly itchy skin under the arm where the lymph nodes were removed.
muscle spasms and pain all night and I can't sleep
fear of the transfer surgery...can't stand the thought of being vulnerable and in pain again
pulled muscles in the side, serratus and intercostal still can't breathe deeply
no weight training...boo...
skinny arms...Dr. Fabulous says, focus on toning, what is THAT???
cleavage----seriously, what am i supposed to do with all that!! I need new shirts, sports bras and I was mortified this week when I taught a class and my sports bra showed waaay too much skin...which I didn't figure out until I started teaching and just had to keep going and suck it up.
BootyBootCamp, I am coaching, can't
wait to DO the workout too...

my happy list is bigger than my sad list, I will take that any day. 
much love and thank you all for your prayers,
Surgery Date is February 2~~ new soft boobies coming my way!!!  We prayed at supper tonight, S. led the prayer, "Dear God, please let Mommy's surgery go well and that she comes home with soft boobies and that they aren't too big." M. said, "S! what are you talking about, she's perfect!"
love that's all

jumping fire with Big Daddy!


Sunday, November 27, 2011

Pink RockStar...Dear God...

Dear God I want to take a minute, not to ask for anything from you, 
but 
simply to say thank you for all I have.
hi friends and family,
Thanksgiving weekend was wonderful for many reasons. We feel that we have so much to be thankful for. Me personally....my health and my family and my close friends who have continued to step up and support us.
The big scare is over, but, what is left behind is still the scars of what we have been through in the last three months, and the pain of reconstruction. It is hard to describe this place...I know that the cancer is gone, I know that I am in the healing phase, I know that I should be exhaling and jumping for joy. I can't yet. I look in the mirror and I am reminded every day of what my body has been through. The scars and the places that still won't heal...I am frustrated at the not healing, but, I know it won't be forever. I do have my appetite back...great, just in time for Thanksgiving! I am going to have to really focus on my nutrition now...so, the chicken is on the counter waiting to be grilled. Going to the grocery store to stock up on green stuff. I did get a DELISH salad from a friend that had kale in it, I think I am going to chop up some tonight from the week. 
Those that still show up are the ones that have made the difference for me personally. I love you for it.
This weekend, I was able to be with family that I love dearly, got scolded by Aunt Fran for doing too much.
(it made me smile, because I love her so!)
I got my Christmas tree..we will decorate it today. It is a little early, but, I think it will be a fun distraction. I was able to see old friends, who brought an angel of a little girl to brighten my day! I was able to teach a step class...no risers, didn't use my arms, and it was FUN! I was able to welcome back to Greenville a family that we love very much...new twins and all.
I went to the Plastic Surgeon Tuesday for my weekly visit. The stitches appear to be healing well. I laugh and call my boobs those from the Bride of Frankenstein...stitches and zigzags. There are still some issues with healing, and I am worried about needing more cutting and stitching. I will find out on Tuesday. I did get an expansion on Tuesday, which is fun and makes me hurt all at the same time! I am not quite sure about these large 'boobies!' They really are tight, sore, get muscle spasms and are not very pretty. Sleeping is hard, Chan told me I wimper all night in my sleep. I think it hurts when I move or roll over.
my superhero...
some really happy things for me...
taught my first 1 hour spin class...oh joy! I was so happy to do it, really focused on using my legs, not arms, was able to pull it off without teaching off the bike much!
taught my first step class...it was JOYFUL to be able to move and it really didn't hurt at all...I did need a big nap that afternoon, but, it was worth it.
I get to take a nap everyday without having to be sorry or apologetic.
I am supposed to see our medical oncologist next week, we will talk about post surgery care and treatment.
I hope that your long weekend was wonderful and know that we love all of you...your love and support is so appreciated.
XXOO Lisl

Wednesday, November 16, 2011

Pink RockStar...present and dealing

‎"There is only one you for all time. Fearlessly be yourself." -Anthon
y Rapp

My 9 year old drew this, I am Lisl the Cancer fighter....shooting bullets
at 'Evil Cancer'. He drew this when we were out to dinner one night
about a week before the Mastectomy.

My little girl who is 7 drew this. I am the angel floating up in the sky.


Someone said to me yesterday at the gym, "wow. you are back! you look so wonderful!"
I thought, to myself, "I am not back, I am just present."
I still feel really numb and a little shell shocked at what has happened. I am very emotional, sad, horrified even sometimes.
I had my weekly visit on Tuesday with Dr. Keller, my doctor in charge of reconstruction. He isn't happy with the way two of the surgery wounds are healing. So, on Friday I have to go in for an outpatient procedure where he will try to make those places heal better and hopefully look better. The skin is super thin and it has been stretched. It's not really cooperating, so, I am happy he is dong something about it. My heart skips every time I look down. The expanders are lumpy, misshapen, and hard. They are not very comfortable, and when people hug me, I know they feel hard. I am very self conscious about the way it looks and I get embarrassed when people say, "wow, look at your big old boobies". I really liked the ones I used to have, so, this isn't like an in improvement.


I have tried to go to the gym and workout. I can do the elliptical and I can ride the spin bike. I sweat alot, which is good and feels like I am working hard. Most importantly, I see the faces that are familiar to me and I speak to my friends and that is the best therapy of all. 

My HUGE array of medicine is down to nothing, thank goodness, no more pain meds for now, no more prednisone, no more antibiotics. They are all replaced with gauze, saline, triple antibiotic, bandages and big square bandaids. I have to change the dressings twice a day.
My little girls is funny, she likes to help. Every night she follows me upstairs, watches what I do, cuts the gauze to fit and gently puts on the bandaids. I see her being very motherly and it warms me and breaks my heart at the same time. Yesterday afternoon, I was especially tired and had an awful headache (most likely from coming off the prednisone) and she said in a very motherly tone, "Mommy, when I finish my homework, lets go upstairs and get in the big bed. I will hold you, we can cuddle, I will read you a story and I will stroke your cheek." It sounded just like something I would say to her.
Tomorrow I have a follow up with the Surgical Oncologist. I know they will be doing labwork.
Thank you all for the wonderful notes I still get, thank you my friend Julie for bringing me the yummiest salad yesterday, thank you to mom who is coming Friday to take care of me and thank you to all of you who continue to show up, even though it's inconvenient or you are busy or you really need to be cooking and cleaning and carrying on with your own stuff...this has meant the world to Big Daddy and I.
still have the 'deer in the
headlights' look....
oh, and to my sister in law, I broke down and fed the kids a dang Chicken Casserole from the freezer.

XXOO Lisl
This is about 2 weeks post surgery, tubes still in, and bandages covering the
'awfulness'.
Having an allergic reaction to some meds...
most likely the antibiotic. Spent three
days in the hospital.
It amuses me to play with the
implants in the Drs office!

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