Starting chemo Sept 05
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Hello girls, Just checking in on my September sisters.
Susan, I was so happy to read about your upcoming concert. What joy it must bring you to be able to play...I remember not so long ago the worries of the Taxol demon!
Leanne, Always thinking of you & keeping you in prayer. I hope that your port helps to make things easier and that you will be able to settle into to a new "normal".
Nicole, Yay that you are done with radiation...there's no place like home & the comfort of your own home for healing.
Sandra, good for you for not going back to work if it would cause you stress. I just returned to teaching after all the testing was done. We are very big on testing in the US and EVERYTHING is judged by how well the students perform on the tests. Money is allocated based on testing scores & that children are handicapped or do not speak the language makes no difference.I think the funniest thing I ever saw was a little boy who didn't speak English being given a test in English. He took the test booklet & placed it over his head & sat there. I might have stuck it elsewhere, but it just highlighted the ludicracy of these tests as the sole indicators of learning.
I'm actually on Spring break this week, so that was a nice way to ease back into work. I wish all my sisters a very Happy Passover & a blessed Easter. Enjoy your families as you gather for your celebrations! Love to all, Lynell -
Hi all - to cheer you all.......
http://www.jacquielawson.com/viewcard.asp?code=TS41842873
Sandra from the UK -
Beautiful card, Sandra!
Thank you so much! I hope you have a lovely weekend in York!
I had another busy week at work...again, more than 50 hours in 4 days. But I had a bit of a treat on Monday. I met Fitztwins (Janis) and her twins for lunch who was in NYC visiting another friend. It's terrible that we have to be here, but I must say, the nicest people are on these boards.
I'm afraid I still don't know the result of my biopsy. I missed the phone call from the doctor and then the office was closed for Passover. I'm not really worried.
I'll be going down to Maryland to visit my mother and sister for Easter.
I hope you all have a lovely weekend. Happy Passover! Happy Easter!
Love,
Peggy -
Sandra-- the card was lovely! Thank you!!!!
Peg-- you sound so full of life. Diving into work. Having met one person from this site, I bet that meeting Fitztwins was a wonderful time. Enjoy your trip to Maryland, but be careful, now that you have hair, keep an eye on that speedometer.
All is well enough here. Kid is home for the weekend. I think she just hit overload at school, and needed a home-cooked meal.
Hope that everyone is doing well,
*susan* -
Hello lovely ladies
I hope you are all enjoying your Easter and indulging in plenty of chocolate!!
I am not sure if I told you all that I didn't have chemo this week?? (I forget what I post- chemo brain returns!) Blood counts way too long so it has been delayed for a week and a bit. I have been suffering with a cold these past few days so I am so glad I wasn't treated. However I hate delaying the inevitable and just want to get this over and done with and find out if it is working. Approximately another 4 weeks to go now with this delay.....
I am very grouchy and bitter today. Lately I have been getting around with a bad attitude, saying and doing whatever the hell I like and not caring about anything or anyone else. Selfish? you bet! I hate now knowing that my "expiry date" is sooner than everyone elses. I feel robbed and cheated for both myself and my little boys. How do we ever make any sense of this?? I am sorry to be on such a downer but I know I can come here and speak truthfully and know that somone will understand my musings. I have been crying alot again these past couple of days and being so ANGRY I can't believe it. I am making everyones life miserable at the moment I know but I can't help it. I know I will be okay again soon but man, it is UNFAIR. Not just to me but to little kids, 3yrs and 10 months who will know nothing but what it is like to have a sick mum or be motherless.
I am very tired today so I am sure that is affecting my mood greatly.
Scott goes back to work tomorrow. I get used to him being around but I realise a sense of normality and routine is important however I always feel so lost when he goes back.
I just reread my post and it is awful!! Sorry ladies. I really needed to rant.
love you all
xoxoxo -
Rant away Leanne! I would too! (and I did)
WE all love you very much. I will call on the power that made us all to correct your body and bring full health back. You are doing all you can and sadly, that is all you can do. Slam thru the difficult thoughts as you have with courage and grace. Get antidepressants if you need them, I would. Actually I did, Prosac seems to be helping me.
Our thoughts are with you. And may you powerfully beat this thing. -
Leanne,
Vent away! Of course you have the right to be angry. Yell at the trees, yell at the bushes, yell at the ocean or yell at the mountains. Get the anger out....
If you can, leave the anger out there. If you can't, maybe it is time to talk with someone who is a professional. Anger will eat you up.
None of us know how long we have on this Earth. Just a short story, my Mother's father died unexpectedly when she was four years old. She has only one memory of this man. She remembers standing in the bathroom with a huge man who was screaming at her for not putting her toothbrush back to its proper place.
When the kid was young and I felt angry at her behavior, I would remember this story. Somehow it dissipated my anger so that I was able to regain my composure.
I am sorry to hear that scott is off again. Do you have others to help with the children on your off days?
We are all thinking of you.....
*susan* -
Leanne, we are all here to hear you whenever you need to be heard. However, remember anger uses up your energy and you need your energy to be concentrated on helping this round of treatment kick in. Hugs and everything else to you Leanne.
My moan for today I ache all over is this an effect of radiotherapy? My last one is on Friday. My friend starts this long journey on Monday!
This may be a stupid question, but I take it Herceptin is not in pill form anywhere else in the world?
We had a good few days in York, taking in the performance Stars of Broadway which was excellent. I am sooooo tired though off to bed now. Peg enjoy your travels but don't overdo it - although I agree, you seem to have got back into long days very well. by the way the daffodils along side your new hairdo are lovely.
Speak soon.
Sandra from the UK -
Hello ladies!
Leanne - I think of you often. As others stated - rant away! That's what we're here for. You are always in my prayers.
Susan - thank you for the reality check. On days that I feel tired and cranky - I would hate to think of that being how my kids see/remember me. That really hit home - I hope to use that piece of advice to its fullest.
Sandra - congrats on finishing Radiation! I know that I was very fatigued by the end - but I don't remember the aches. It could be just the cumulative effect of laying on those *&^# tables! Something to be aware of as you complete rads: A few weeks past the completion of mine - I noticed some strange 'twinges' and slight discomfort. I was concerned about it, but was told that is very normal. As one of the nurses explained it to me - things are still 'cooking' for awhile after radiation completes. Of course contact your doctor if you have ANY concerns - but I thought I'd pass this on.
I'm making my summer vacation plans!!! I pretty much lost last summer - I'm going to enjoy this one as much as possible.
Warm thoughts to all of you! -
Hi everybody!
I just had to log on quickly to see the birthday cake next to my name.
What a beautiful day we had in NY today.
I walked in Central Park at lunchtime to see the latest blooms. I sure do love this time of year.
I worked a short day today getting out at 3:30, so my husband and younger daughter picked me up and then we picked up my older daughter at her college to go out for dinner. I'm so glad she's not too far away.
I've recently joined a team to do the Avon Walk for Breast Cancer in October. Since I love to walk anyway I figure I'll accomplish something as well. I'm doing it in honor of all of you.
Hang in there Leanne. The chemotherapy is tough because it has a hard job to do. I think of you and pray for you often.
Nicole,
I hope your family is getting back to normal now that you're finished with rads. It must be great to be back home.
I hope you're feeling better soon, Sandra. You have a reason to celebrate now that your radiation is coming to an end. I'm glad you had a good time in York. I've visited that city and loved it.
I wish your friend well as she starts this journey. Will she be logging on?
Have fun making your vacation plans, Hopeful. Let us know what you decide. I enjoy taking virtual vacations.
Anybody else making special plans for the summer?
We're still working on this endless home renovaion, but I'm hoping to plan something fun when we get our tax refund.
Best wishes to all!
Peggy -
Happy Birthday Peggy!!!!!!!! And many, many, many, many more!
*susan* -
Hi lovely ladies!
Happy birthday Peggy!! Hope you had a lovely day.
Thanks everyone for your "ears" for my rant the other day! I am much better at the moment and thanks to those of you who PM';d me and left lovely supportive messages on these boards. It is so helpful and touching to have you all!
I finally had my chemo today. 3 out of 4 so nearly at rescan time. Yikes!! I am getting used to living in denial! Anyway, I am hoping to get through this round relatively unscathed. Scott is working all weekend away from home which is a pain but thanks to some babysitters have tonight child free to get an early night.
And I have some great news!!! A close friend of mine has come into a SERIOUS amout of money (many, MANY millions of dollars) and has organised for a nanny/housekeeper to come and help us out between 25-30 hours a week!! Can you believe it!! She organised it all yesterday and a lady will come this weekend while the agency is sourcing someone permanent. Such a relief. I am hopeful this will make a major difference to our life including my mood! At least there will be no stress about household chores, errands etc! Yay. I am very excited.
Well that is it for me for now. I am off for a snack then any early night.
xoxo -
Leanne,
How wonderful! Just what you need; so _you_ time!!!! Whohoooo!!! I am all smiles here in Boston.
Hope this chemo round isn't too difficult.
*susan* -
Leanne - I am all smiles too! Does anyone remeber Susan's post from a few weeks back??
Quote:
There is hardly a day that goes by that I don't think of Leanne. How I wish that I was rich. I would send her cash to pay a mother's helper to come in the afternoons to help with the kids, house and to start a nutricious meal. ..... Such a utopian I am! Are you thinking that we would assign ourselves specific times for positive thought?
Made me once again a true beleiver in the power of prayer and postive thoughts! -
YES! Thank you for reminding us, Hopeful! I remember. This certainly has been an answer to prayer.
-
Hi all
Yes now you mention it I too remember the post! Well it is true, wishes come true!! Thanks for "putting it out there" susan!
Today has been a good day. Minimal nausea just extreme tiredness. I managed to sleep most of the day and will be heading off shortly for an early night. I am constantly eating though because of the steroids but it is better than a few weeks ago when I was too sick to eat I guess!
My helper, Mary (I like to refer to her as Mary Poppins!) is a fabulous help. I am only sad she isn't able to be our permanent lady! Riley is in love with her and Toben will be home tomorrow and will meet her then.
Keep well my lovely friends
xoxoxo -
Leanne,
I'm so happy that things are a liittle easier, now that you have Mary Poppins to help you. It's unfortunate that she isn't permanent, but I'm sure whoever else you get will be fine.
(Great thoughts, Susan!)
Michelle,
Is that hair I see? You look fabulous!
I have a story...
Do you remember how I got out of a ticket because of my bald head on my way down to visiting my family for Christmas?
I was on my way to Maryland again, the day before Easter. I stopped at a garden center just before I got to the thruway to buy plants for my mother and sister, and a pie for Easter dinner.
I exited the center, with just a mile to go to the entrance of the Thruway with no businesses or pedestrians. I was happy, Jimmy Buffett was playing on the radio, I accelerated and was coasting when I saw those flashing lights in the rear view mirror. $#*T! I looked down at my speedometer...50MPH. The speed limit is 45.
The officer who stopped me said he clocked me at 60.
The good news is I don't look like a cancer patient anymore.
The bad news is that he gave me a icket.
Back to good news, I was a mere 12 miles from home so I'm going to plead Not Guilty and go to court to fight it.
I hope you're all having a lovely restful weekend.
Love, Peggy -
Leanne, I was so happy to read your latest post. That's so amazing that you will have some help with your kids & house. Well, the way you are getting help is amazing, it's just so wonderful. I guess our collective prayers for you were answered. Now you rest as much as you can & focus on healing. I'm still keeping you in my prayers every night.
Peg, you better watch that speedometer. You look too cute & fashionable now, not at all like a cancer patient.(IE no breaks for you!) I was so excited to read about you doing the Avon Walk. I will gladly sponsor you.
Michelle, I love your new avatar. You look Fantastic!! I hope you are feeling as healthy as you look. Looks like you're a blond again.
Sandra, Congratulations on finishing up your radiation. Rest as much as you can. You'll regain your stregnth in time, so for now, take it easy & don't overdo anything.
As most of you know, I've gone back to work and I'm not being a good girl about going to the gym. I joined weight watcher's, so I'll stop at the grocery store on my way home & try to cook something healthy for dinner. After we eat & clean up, I'm often too tired to go for a work out. I also have been taking some medication for my rash and that seems to make me sleepy. Maybe if you girls collectively hope some pounds away I'll lose weight that way! Don't laugh, you ladies are a powerful force. It's been really cold & rainy here this weekend, so I don't feel like doing much. The warmer weather motivates me to do so much more. Enough excuses, I'm really going to go to the gym tomorrow.
Thinking of you all, Lynell -
Leanne:
Supercalifragilisticexpialidocious!! lol
Michelle -
Peggy
- great story (and not so great too!) For a moment there I thought you were going to say it was the same policeman! -
Lynnell and Peggy -
Thanks for your compliments re hair. It doesn't really look blonde to me (well not the blonde I'm used to!) The jury is still out on colour - will just have to wait for some length.
I've posted a before and after on the picture forum for a comparison. (like you did Peggy)
And do I feel well? Yes - but fat. The 10 kilos I've put on is "weighing me down" literally AND figuratively. All my clothes are too tight , but the budget is extremely limited while paying for this herceptin. (We are hoping by July to have the drug before the Australian Pharmaceutical Benefits Scheme. I am still lobbying, and speaking at a function in May) -
Hi Peg sorry I missed the fact that you were celebrating a birthday I have just sung a belated birthday song for you Im a terrible singer. Unfortunately my friend is not into computers so will not have the same support I have been lucky to have had. I have washed all my various head gear and will be passing them onto her. I have spoken to her today and she now just wants to get on with it.
Peg, can I sponsor you for the Avon walk? You certainly like a challenge, what with this and fighting your speeding ticket. Does being 12 miles from home make a difference Peg?
Leanne great news I am so pleased this friend has realised the real importance of having wealth. You will now be able to concentrate on the important things your health and your wonderful boys. Wow, thank you for reminding us of Susans post Hopeful 1 I have gone all goose-bumpy.
Michelle you look wonderful. My hair is coming on but oh sooooo slowly, or it seems that way to me. It is lovely to see the different photos now. When I have got my make-up on I will try and sort a photo out (promise).
Well ladies I have now finished radiotherapy and have no hospital appointments until 6 June. The Jury is still out on whether funding for Herceptin will be available to me. My Onc has assured me that it will not matter waiting for a month or two before receiving this drug??!!
Well I will not be emailing my work place this week as they have Inspection next week I have got to get my head round a timetable that will suit my current energy levels and start communicating with my line manager I am veeerrrry nervous about returning to work.
Hugs and best wishes to you all.
Sandra from the UK -
Leeanne, what a wonderfull friend you have! Enjoy Mary Poppins! You deserve it!!
Sorry to hear about the ticket Peg. I like the good news though!!
Sandra, well done for finishing rads! Hope Herceptin comes through for you! How did your skin react to the rads?
Well, I am 8 rads down, 20 to go! Will also go on to Herceptin every 3 weeks from this Friday!
Michelle, I have the same problem with the weight. I have also put on 10kg, FEEL HEAVY. Bigger now than I was at 9 months pregnant. I eventually relented this weekend and bought bigger pants. Had to go 2 sizes up!! How embarassing. What is worse is that all the weight is around my waist, so the new pants fit around my waist my bum, but are way too big around my legs. I look like a blimp!!
Good luck with Weight Watchers Lynne. I have joined Sure Slim. They work out an eating plan according to blood type, sugar and cholestrol levels to is supposed to increase your metabolism, and stimulate Growth Hormone release. They do a quick weight loss program, and then put you on a maintenance programme after that. Really hope it works. Exercise still a mission. My legs still very weak and tired.
Question, how do I post a pic? Tried before, but can't seem to get it right!!
Have a good week ladies. Lood after yourselves!
Liezel -
So great to hear how everyone is doing!
Peg, darn, I even mentioned the driving speed. From now on, only positive thoughts from me.
Lynell, finding the energy to work and workout seems like a lot from my vantage point. What does your doctor have to say about the rash? And, given the collective experience here, I bet a side effect of the drug is fatigue. Are any of us taking drugs that say "May cause extra boosts of energy?"
Michele, you look fabulous! I haven't been to the baldforum lately. Now I know that I must.
Thinking positive thoughts re: herceptin for both Sandra and Michelle. Good use of my brain's bandwidth. Seems so hard to believe that there is even a question about receiving this treatment.
Sandra, good luck figuring out how much work to add to your plate. How do we know how we might feel in three months time? Every day is a new adventure!
Liezel, good luck with the radiation. Do hope that your time is easier than the other treatments.
My daughter turned 20 yesterday, but was too busy for a visit from her parents. We settled for a nice phone call and an amazon gift certificate. Having a little anxiety here, my "badboobie" has been painful now for about 4 weeks. Can't feel any lumps, but it doesn't feel right either. I am sure that I am over reacting, but have an appointment to have it examined Thursday.
Performed several concerts over the past few weekends, and I am getting close to regaining my dexterity. Yea!!!!! Now if I could stay awake during the rehearsals. :-)
Also cut my hair. I was starting to look like Liberace, with tufts of hair turning into a pompadou. Don't like the new haircut much though. Daughter suggests using 'product' to get all spikey. I might just try that. I mean if I am going to have this silly hair, I might as well have some fun!
Aromasin continues to give me some nasty side effects, but so far, the bone and joint pain is all below the waist line which I can live with.
That is about it from rainy and cold Boston. Boy am I ready for Spring!
Hope everyone has a great week!
*susan* -
Hi everyone
Sorry i have been missing for so long.
This is my third week back at work now...started doing 9 - 12 for 2 weeks...this week im doing 9 - 2. It is going well. I had my catheter(port) out on friday, that went well.
I started arimidex three weeks ago...so far i get more hot flashes thru the day, plus the usual night ones...but they are not too bad. Only other side effect is legs ache when i get up...but it passes quickly.
Sandra
Good luck going back to work...i have found going back for a few hours at the start has really helped me "ease" back into working again.
Michelle
You look more beautiful with dark hair than with blonde.
I love the pics you have posted on the "bald" site.
Leanne
Im so pleased you will be getting the help you need.
Now you can focus on getting thru the chemo...im wishing you good luck when you get your scans.
Hugs ladies
Maxine -
Hello lovely ladies
Just a quick post tonight as I am feel very crappy both emotionally and physically at the moment.
I am feeling really down today. I have posted a few things on the mets boards (not sure if anyone looks there?) about how I am wondering now if continual treatment is now my "life" and the feeling of being tired, sick etc is just my new normal as well as how I swear even with this helper coming in all I do is yell and scream at my oldest son like I am some raving lunatic.
I know he is only 3.5- driving us insane is what they do at that age after all but boy oh boy does he push my buttons. Even the nanny today said he can be testing!!! At the same time he is loving and affectionate and my heart just breaks when i think about the things I say to him when I am sick, tired, bone pain ridden and have just had enough.
I have been told I need to just relax, not put so much pressure on myself to be this 'perfect' mother now I have bc and just be me but I just can't. The whole time I am thinking that all he will ever remember is an awful screaming mummy. Yet you know what? Even that thought isn't enough to stop me when I am OVER IT. I just cry harder when I am done.
I don't think I am depressed. I have a history of that and am very aware when I am 'slipping' into that mind frame. it is more being sick of it all. I am sick of being sick. I want to be better and move on. How do I move on when it comes back?? mets makes it IMPOSSIBLE to move on. You get stuck. That's it. Never will I hear the words that I am 'cured' after being NED for 5yrs. I mean for G*ds sake I couldn't even managed 5 WEEKS. I will never again live my life making plans for when I retire, or at my childrens wedding. Or even my childrens first day of school??
I am sorry ladies. Today is a tough day. I am upset and I am angry and more than anything I am scared. Terrified actually. I don't want to die. Not when my babies are so young. I don't even want to be sick while they are this young. It is so unfair for them to have to grow up with a sick mummy who just yells.
Sorry again. I said this would be short but I ended up ranting about a whole lot of stuff i didn't know I had on board.
love you all
xoxo -
Leanne,
{{{{{}}}}}}}. What an impossible situation. I have seen your postings on other threads, and the lovely responses that you have received. Your scared, your son is scared, you are exhausted, and there is a downward spiral.
I have no idea how you change this while you are still in active treatment. You are going to feel like crap until at least two weeks post-chemo if your past reactions to this protocol are an accurate indication.
Do I have a clue what you can do? No, but here are a few thoughts:
1. playgroup- a place for him to use his energy while having fun with other kids
2. favorite 'aunt'- is there someone who can do special activities with him once or twice a week? or, conversely, someone who takes the baby so you can do a planned activity with the older one?
3. hate to say it, but videos. When I hit my LSP [lauren saturation point], we allowed her to watch her kirov ballet tapes.
But mostly, I think you can't be too darn hard on yourself. You are a good mother.... who has some bad days; the same way he is a good son who has some bad days. Forgive yourself. Forgive him. And wake each morning optimistic that you will have a good day together.
Ask for help. Use your new helper to find any way possible to find glimmers of hope.
Okay, this is way too long. What I really wish I could do is give you a huge hug, and we would sit on a couch giving each other strength. But you are so darn far away.... so instead you will have to accept my virtual hug.
Hang in there!
*susan* -
Oh lovely Leanne,
How I wish I could share with you some words of encouragement to strengthen you, or wisdom to inspire you. The replies you have been receiving on the various threads express my thoughts far more eloquently than I. (Susan, you are a wise woman.)
All I could say to you would be this.
I read your post, and it is distressing to see/hear you beating yourself over your reactions to your son caused by this disease and treatment, and to hear your fears and worries (understandable) for the future.
But what has been said and done 'yesterday' - the past - has passed. You cannot change it by worrying and fretting and beating yourself up over it. That will waste the emotional and physical energy you need today.
And what is coming 'tomorrow' - the future - has not yet come. Try not to worry about something that isn't here yet. It will only rob you of today's time and the energy you need for today. Worry about it when it is here.
There is a wise saying, which I have found to be true (although sometimes it is hard to put into practice, but I try to. It is from the Bible)
"Therefore do not worry about tomorrow, for tomorrow will worry about itself. Each day has enough trouble of its own. "
I know if today, I had to heap on all the concerns of the future, how could I bear it? It would be too much for one person to handle. I just have to get through today.
And this is my prayer for you TODAY. That you will have strength for TODAY. That you will have calm and fun with your son TODAY. That you will feel well TODAY. That you will have rest TODAY.
(When tomorrow comes, we'll start again - but just one TODAY at a time.
With my love and prayers
Michelle -
Leanne, My heart goes out to you. When I was first dx I went spiraling down. All I could think about was my two little girls being without a mommy and how unfair it was. I would watch a commercial of a wedding and lose my mind or I would see a pregnant young women with her mother and freak. I would torture myself and wonder if I would ever get to be there for my girls for those moments. How can little girls be left without their mommy. Girls need their mommies!!!!!!! I finally had to stop. Those thoughts were just too much for me. I turned it around by thinking how things could be worse. (Now this is really crazy thinking but it helped me). I would think about one of my girls having cancer and then I would be okay that it was me and not them. I would take cancer 5 times over before I could bear watch them go through it. I would think of sudden death. How if I died in a car crash I would not have any time to say goodbye. In the middle of my treatment I had a friend Adriana 30yrs old went to the hospital to have her baby this past Christmas. She had to have a an emergency C section and had complications. She died and so did the baby. She left behind 2 little ones. Ever since that day I am grateful everyday that I wasn't her. That at least cancer gave me time. How much time? God only who knew but it was something more time than Adraina had. These thoughts as horrible as they were actually helped me keep it in perspective and I was grateful for having just one more day. I still feel that way. Anytime I start feeling depressed about my situation I think of Adriana. Pray for peace. I did everyday for months and finally it came one magical day. I finally surrendered to God and accepted my dx and only then did I feel peace. I agree with Michelle, Just one today at a time. I continue to include you in my prayers Leanne and think of you often. I am glad you have great friends that look out for you. I hope you have better days ahead.
Michelle -- love the new pic. I am glad your posting, missed you. Thanks for the PM.
Maxine, I will have my oopherectomy on 5/9 and then will start Arimedex 2 weeks after that. Looking forward to hot flahes, vaginal dryness, fatigue, mood swings and osteoporsis.
Lynee, I started Weight Watchers too. So far 8.4 lbs. I decided that I have been given a second chance at life and I will be damned if I don't do everything in my power to help myself. I am about 50 lbs overwieght. I also started working out, will start weight bearing exercises this week to help with that bone loss I am expected to get after my ovaries are out.
Nicole -- congrats on you last radiation.
Peg -- Happy Belated BDay Lead foot!!!!!!
Susan -- WOW a real concert in June. You must be thrilled.
I started work 3 weeks ago. Love the new position. No stress, I create eduational workshops for the nurses and go out with them to visit patients to ensure that they do proper wound care, good infection control etc... M-F 8-5.
It is good to wear my scrubs again.
I have my Lap Ooph on 5/9. I will have my MUGA scan, bone density test and vaginal ultrasound on 5/5. Lucky me.
I will be out of work for 3-4 weeks. Remember I am a Her 2 girl and still fly to Houston every 3rd Monday for my Herceptin -- 11 more months to go!!!! Thank God I have a understanding boss. Life is good here in the South. Loving life everyday. Grateful for every minute.
Marg -
OH yeah, my hair is growing fast. I even got a mustache and little whiskers on my chin. What the heck is that all about? I am happy to report that I "Naired" them off 2 days ago and look much better. I will upload a new photo soon. Marg
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- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team