September 2013 Chemo Group
Comments
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Ugh, no fun Simplelife! A few weeks is long enough! I just noticed a couple areas of the hypersensitive skin on my chest. I put on a tight tank top that I had. I just can't stand a shirt rubbing against me.
I have some fluid buildup today. What is done about that, if anything, and how much does there have to be? It is pretty uncomfortable. I probably got my drains out too early but I couldn't stand those sons a beaches. Do you think it will affect my fill tomorrow? I hope not. I really want to get one one so it will hopefully do some unfolding and fix some other pain issues, and I am going to a good friend's birthday party this weekend. Never imagined that I would be feeling anywhere up to it when he invited me a month ago, but I think I will!
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just checking in. Nat is doing well, stopped the Percocets thus morning and just in Tylenol. Her parents have been a big help. I'll be working from home all week.
Nat says she just feels sore and achy, especially the left armpit.
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Art: good to hear she is doing so well! I am still taking Lortabs. I was down to a half a pill twice a day until today I had a bad day. Tell her not to be a superwoman though! If she needs them, she needs them. It helps the body to heal easier when you don't have the psychological trauma of pain.
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simplelife,
My Lymphedema PT doc said to use the regular compression shirts you could get at sporting goods stores like Big 5 and Sports Authority. She said to get one size smaller than I would normally get. I found a couple at the store and then ordered a few more. I tried three different brands, Russell, Underarmor, and Nike. By far, I liked the Nike's fit and feel best...http://www.sportsauthority.com/product/index.jsp?productId=13129145&view=grid
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Art, Glad to hear Nat is feeling a bit better.
KJ, Interesting about the compression shirts. I wouldn't have thought of that.
Mama, Hope you get your fill today! Glad you heard those 3 amazing words!
Simplelife, I hope you get some answers about the hypersensitive skin. My skin on my chest is not hypersensitive to touch, but it does seem to be hyperreactive now. Any adhesives and I break out immediately. They had to give me benedryl after my exchange because of one piece of tape. I do not get the same reaction on my arms, etc.....odd. I hope you can get some help with the cording too.
Betterday, I hope those hair sprouts take off and grow, grow, grow this week.
Running, hope the exercies help with the cording.
LHL, I hope the headache is gone.
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This is my brain
This is my brain on chemo
This is my brain with chemo residue at 5:30 in the morning ...... IMRT....Idiot Mother Returns Turkey...WTF..Why on earth would she return the turkey?? True story.. I think I need help. I guess this site affects me more than even I realized lol. Thanks KJ.
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I thought my fill was today but it is Wednesday. Soooooo sad
70s charger: O....M....G... is that yours?!!!!!!
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I am obsessing about my hair too and 7 weeks PFC, it is growing a little , but not fast enough! I am taking the biotin as well!
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Miss Mamma The first pic ( dark green) is ours. That was taken at one of the car shows last year.
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Charger
I used to have a 72 dark green Charger, white leather interior, bucket seats. Nice car but didn't like NH winters! LOL
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Hair watch girls - there is hope!!! This first pic was me the other day, 12 weeks PFC. The second pic was two weeks ago.
Still not enough to go topless (for me), but getting there.
Had to take Hubby to the oral surgeon this morning. This man needs sedation for a teeth cleaning, so you can imagine how he was today. So stressed out and now he's SACKED OUT. He'll probably sleep the rest of the day.
KJ - Hope the rads boost goes ok today!
mama - bummer about the fill!
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LightHouse
you have hair!!!! Looks great!
I am almost 4 weeks post Taxol & have funky wispy short strands of white popping up. WHITE! With a shiny head showing through!
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vintagegal - mine was pure white when it first started coming in too! I still have about half gray but some of it did darken up.
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Vintage Thumbs up on the Charger!
LHL Time to go topless. Lookin Good.
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70Charger,
I hope you aren't saying you caused the crumple with a chemo brain accident?!?!LightHouse,
Looking good! Looks like it is thickening nicely. I probably have about the same, but mine is finer and very light.The boost rad went ok today. I decided to blindfold myself. Put my knit hat over my eyes once I got on the table. :-)
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KJ The crumpled charger is not mine nor was I the driver. But I WAS the driver to put the 1st scratch on our charger. Nothing major, buffed it out nicely.
This is my Challenger with custom decal that I had made. No scratches yet!
This is my 70 Coronet. Some old guy hit the bumper at a car show. Still have to get that fixed. Oh well. A scratch does not affect the fun of driving them.
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70Charger,
Those look like a lot of fun! Stay safe and don't accept any challenges from Bieber. ;-) -
Lighthouse, just imagine what your husband would have been like going through major surgery like you had, if he needs sedation for a teeth cleaning. I often wonder how well my husband would be handling things if our roles were somehow reversed. I think he is a lot more stoic about feelings much has a much lower pain tolerance than I do. You have a lot of hair and give me hope.
Here is my head as of this morning...6.5 weeks PFC. A 5 o'clock shadow combined with downy white hair,
I think the spots that look more pink rather than "5 o'clock shadow" will come in more grey. I used to have a solid grey patch right in front about the size of a quarter.
Here's me this morning with my five o'clock shadow hair. The eyebrows are make-up powder...my real eyebrows are just starting to show signs of coming back.
KJ, thanks for the info on the compression shirts. I'm wearing my running jacket in the picture I just posted because the arm pits are extra thin for breathability and to prevent chafing while running. I was just thinking about my running clothes this morning while I was trying to find something to wear that wouldn't hurt so much. I ended up with a sports bra on that has a lot of compression and no seams, an extra soft sweater (inside out) and my running jacket to stay warm. May not be the greatest look, but it is bearable to wear. I went to a gentle stretch class this morning at my fitness center for the first time since surgery. I noticed this afternoon that the hypersensitivity wasn't nearly as bad as it has been. Maybe it's just healing, or maybe the class helped. No matter what....I am so relieved. It's not gone by any stretch of the imagination, but I'm not close to tears all the time now. I'll take it!
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70 - I miss those cars! I graduated in '74 and the parking lot at my high school was filled with cars like yours!
simple - after ALND I found relief from the weird hypersensitive skin feeling with fabric between the arm and the skin on my side - as long as I did not have skin to skin contact I was more comfortable. The good news is that this does subside over time. At this point I have full feeling on all of the arm, the only place that is numb is the actual underarm and I only notice that when I shave. It took a number of months of gradual improvement though, so be patient.
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Love the hair LHL.
Radiation also gives you sensitivity to the underarm, but I finished rads today.
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congratulations on finishing rads Alfranco
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Alfranco - YAY for finishing rads. It will take a few more weeks but things will really start to get better. I finished rads mid january and just this week said to myself wow I am feeling (close to) normal. Maybe a new normal but I am able to count on myself to do what I need to do and am starting to really enjoy moments again (as opposed to forcing myself in the vain hope it would translate!). But it is slow and there were still days that I thought I had slid all the way back to October. Just be patient - ha - not the easiest thing to be...
I missed a lot this weekend but hugs to everyone going through recovery. Art - glad you too have help and you can work from home. Wishing everyone strength - this has not been easy.
I flew to LA and the plane was so hot and stuffy I had to take my hat off - first time in public. Ack. But no one fainted or gave me weird looks (probably because they were giving me dirty looks after seeing I had a 2-yr old - who was fantastic on the plane by the way - wow - thank you!). But I think very soon I am going to stop wearing it. It is still cold though and if I didn't always wear it I would never remember a hat so we'll see.
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Josgirl, they probaby just thought you had a hip super-short haircut. I whipped off my hat the first time in public last week by accident. My brother had just called on my cell phone and I couldn't hear him so I took of my cap to hear. It was several minutes before I realized what I had done. I felt naked, but nobody fainted. I was standing in a line to check in at the breast center for a doctor's appointment. If I had to be bald anywhere by accident, it was probably one of the best places to do it.
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So I've been having back pain near my spine for a little over a month. I got distracted by surgery, but now that the surgery pain has settled down, I can definitely still feel the back pain. A dull, constant ache in the middle of my back between my shoulder blades. My MO told me to take advil three times a day for the next 5-7 days to see if that helps. If it doesn't, she wants to see me. I knew that after treatment ended I would be paranoid about every ache and pain, but I'm not ready for that to start yet. I just wanted a little break where I didn't need to worry for a while. I know this is probably nothing, as aches and pains are normal after chemo and surgery. But still . . . I hate this.
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{{hugs}} Betterday - I know what you mean. I've been extremely fatigued the last 3-4 days.... like going through chemo fatigue, and this is after weeks of feeling pretty darn good post-bmx. So all of the sudden I'm like, what in the world is wrong with me?!?!??!
Saw my MO today and he didn't see any reason (other than having $##%$@#$ cancer) for me to be so tired. My blood counts were good, my weight is steady, blood pressure was normal, I haven't changed meds.... so why do I feel like I can't even get off the couch???? I was feeling good up until last week.....then it's like I hit a brick wall. Migraine Saturday and extreme fatigue ever since. I feel chilled, too, but no fever or any other symptoms. Very weird. Oh well... I guess if something was going on like an infection it would have shown up on my white blood cell count. Maybe my body is just telling me to slow the heck down. He is going to run thyroid tests, but I've had those before and they always come back normal, even though I have most of the symptoms of hypothyroidism.
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LHL, so sorry you are feeling that way. I hope that it is a chemo or surgery leftover side effect and that it is short lived. Just think about how much your body has endured over these last seven months. I wish we all could just get a break for a while.
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LHL: I have long suffered from all of the symptoms of hypothyroidism but the tests have always come back normal, too. I started looking into they hypothyroidism thing a bit shortly before I was diagnosed because I was REALLY run down and my PCP was trying to figure out what was up. I read that they only test a couple of the different hormones but the other hormones could still be low. I read this in reading about some natural hormone supplements that are derived from (I think) pigs (forgive the chemo brain). Then I read about iodine supplements after diagnosis. That is something that I think I am going to do. It is said to help with all the hypothyroidism type symptoms and that the American diet doesn't get enough iodine because there really is barely any in table salt. You would have to eat a lot of kelp to get it. Iodine deficiency is also said to be a possible cancer cause. I will get on it pretty soon and let you know what you find out (and if you look into it first, let me know!)
Went to my 2 week with my BS today. She was super excited about my surgical outcome and things I am going to have great results and that my PS should be able to fix anything that is cosmetically off. She okayed my appt with a Lymphodema PT to be proactive and also get me back up to par sooner. I don't have to go back to see her for a year! I teared up. That feels like a big milestone. One less doctor to visit.
70scharger: Thanks for the pics! I used to be really big into muscle cars and go to car shows all the time. Ooooooohhhh how I love them! Beautful stuff there!
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Thinking of Art/Nat, Cougar, and Mama as they keep recovering from surgery! Great news on the negative nodes. Healing and recovering is an up and down process but I'm glad you have friends and family helping you!
I love the HAIR reports too! Simplelife -- I can see it!! Audra and VintageGal - - it will come! LHL - - about time for you to show it off!!!! I GOT A HAIRCUT TODAY!!! 17 weeks PFC!!! Mostly my stylist just shaved the hair growing down my neck and the ones that are sticking out above my ears, but I felt like I was really making progress!!!! I have white tips on the end too! NO CHARGE - - just one more benefit of being a cancer survivor! :-)
70sCharger -- love the car photos! I drive a lame Honda Odyssesy mom-van, but a girl can dream!
Kbee - - enjoy the chocolate and the opportunity to grow a little fat! When I went for a consult with a PS, the funniest thing he said to me was, "You can pick your nipple color! It's fun!"!!! I don't know if fun is the right word, but I'm happy that you'll be finishing your reconstruction soon!!
Peacock and Alfranco - - Congratulations on being done with radiation!!! Love that pink hat, Peacock!!! Clickchick! Good luck with starting rads. I'm sorry to hear about the positive nodes, but those deadly rays of radiation will get rid of any pesky cancer cells!!!
I had my physical therapy assessment on Friday, and it was so wonderful to be finally getting help from someone with experience working with women who have experienced breast cancer, mx, and ALND. I will do PT 2x/week for a month. Yesterday, the therapist just spent a half hour massaging and stretching the muscles and nerves around my mx site, armpit, arm and shoulder. The tears poured from my eyes as she gently worked on my mx scar. I realized I had barely been touched in that area since surgery, and it brought up all the sadness about losing my breast. :-( But it also felt very nice to be touched in caring way in areas that have been very sore, and her work plus the exercises have already greatly improved the level of pain from cording. After the session, I cried and cried in the PT bathroom... like I haven't in a long time! We all have our moments of crying, that's for sure!
Have a good evening everyone. We are having the coldest winter in 139 years, but its a balmy 14 degrees right now!!!! My son has so much cabin fever, he is going ice-skating... and I'll relax in the tub with a tasty beer!!!
Love all your posts, but have a hard time keeping up!
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Alfranco,
Congrats on being done with rads!! You too, Peacock!!LHL,
Sorry you are still so tired. I think you are doing too much and expecting too much of yourself. ;-)Running,
I think we will all have that breakdown at some point in the next few months. I've been putting it off until after rads. There is just so much mental work for me to get through rads that I don't feel like I can break down right now.Had four appointments today. BS drew 70cc's from right chest (the infected side) and it is feeling better with the relief and the antibiotics. Doc didn't expect me to feel the needle. Well... I DID!!! Right before they started the procedure, I intentionally put my right hand below my bum so that I wouldn't grab anyone or anything if it was painful. They thought that was unnecessary until the needle must have hit the only remaining nerve in my right chest!! They wiggled around in there to make sure they could aspirate as much as possible. Felt that too. :-( Necessary evils.
Increasingly Maddening Right Ta-Ta.
Next was the appointment with the Lymphedema Doc. She took measurements and my arms haven't swollen since she first measured about 5 weeks ago. Then she measured my ranges of motion in both arms. Left arm actually was better than right. Then, she massaged the drain sites to help break up some of the scar tissue. It was painful, but will help in the long run with range of motion. After the PT visit, I headed to work for a few hours and then to radiation. After radiation I had my weekly visit with the radiation oncologist. My skin is holding up better than they expected (thanks to a little help from my friends here with the lotion plan!!).
All these doctor visits are deductible, right? The mileage? Start at home, drive 30 miles south to the BA appointment. Drive 30 miles back to my home town for the PT appointment. Later, 30 miles North for radiation. 120 miles. And I put in six hours of work today.
Needless to say, I am home now and exhausted. But, when I got home, my son had done the dishes AND made dinner!! Life is SO Good!! ;-)
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Running,
I almost forgot... CONGRATS ON THE HAIRCUT!!!
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