My daughter and BC
My daughter, 29 years old, received her biopsy results on 10/1. She, too, is diagnosed with BC -- we are all in a state of shock, think we literally ran out of tears. No BC in our immediate family. She has her MRI this week but they say right now she is looking at a lumpectomy and radiation. Just bought their first home, moved in yesterday, with my 3-y.o. grandson -- very near by. I see from these posts I have a lot to learn about this terrible, terrible illness. My daughter's faith is so strong but it is hard to see her so scared and I can't do anything to take away her fears -- it is such a helpless feeling!
I'm sure this on and off again flow of tears will eventually let up -- she is going to need so much courage. Lisa works for the Alzheimer's Association for some years now, training caregivers. She sees illness on a daily basis but never thought she'd have to deal with her own terrible illness, one such as this. I want to just take it from her or have the doctor say, we made a mistake, or something to get it away from her! It is just terribly sickening - I thought I would put my hand through a wall.
I know I'm not the only mother out there having to watch her daughter go through this and knowing that your baby has this illness and you can't take it from her. God bless you all and God bless my lovely daughter!
Comments
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Hello fellow mother/supporter/chief worrier/courage giver...and all the other things that we do to try and make the rough path a little easier for our daughters.
My daughter was 29 in 2003 when she was diagnosed....shock and horror and disbelief. Five good years and then sadly the rotten disease has come back, almost five years to the day. This is not to scare you, it is to say that I understand how you are feeling; how can this happen to our young girls. Mine has been vegetarian since age 15, didn't smoke, an occasional drink and not into drugs. No history in the family either.
The road is scary and rough, as mothers we do our best to smooth out the rough bits, reassure and lend practical support. Love is just there - its not negotiable!
Be assured that there are better treatments available than there were 5 years ago - lumpectomy and radiation is not so bad, its the initial shock that's hard.
My agony is why could I not protect her from this disease, as mothers we would do anything to protect our kids, I would swap places with her if I could. I too have been through the 'what did I do wrong' stage.
I honestly think that we have to look at environmental factors playing a role. We are exposed to so much artificial stuff in our homes and atmosphere. I got rid of all my plastic storage containers and replaced them with glass, NEVER heat food in plastic containers in the microwave, and try to eat only organic food as much as possible. Its all to do with exposure to artificial hormones. My daughter's neurosurgeon (we live in Australia) is deeply suspicious of mobile phone use, especially for young people. He sees too many youngsters with brain tumours - I agree with him.
Hang in there Mum - you will find the strength - and if you have good family and friends don't refuse any offers of help. A friend who had been through the same thing offered me some good advice 5 years ago, in response to offers of help, say 'yes please and thankyou' - sometimes its the only thing that folk can do for you but it means a lot.
My daughter is still doing treatment - we never give up hope! Sometimes I can't believe that this is happening to us. (and my husband has Alzheimer's disease, was diagnosed at age 59)
Best wishes to you and your daughter, I am sure that she will be fine
cxm
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Thanks, cxm -- you're the first mother I've communicated with who shares this agony . . . so many things go through your mind, don't they? So sorry for you with your daughter AND your husband . . . after crying myself to sleep last night, I can say you are absolutely correct, we never give up hope! It is still so new for us and I am trying so, so hard to be strong around my Lisa -- she is just so, so scared right now. I know this initial shock and fear will pass and we will be stronger!
I will keep you, your daughter and your husband in my prayers and thank you again for your kind, kind words!
Laura
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Although I couldn't imagine being in your shoes, I often thought of how I would act if this ever happened to my daughter. I am not a mother who had to watch my daughter go thru something that I couldn't help or take away the pain from. I AM the daughter that just survived breast cancer this summer and watched my mom on countless days look at me with such sadness in her eyes. It was hard to watch her. I am a very independent woman and don't usually ask people for help. Please just be there for her even if she says she doesn't need you there. There were days that my mom just sat with me - barely saying 5 words in the whole day - because I was so sick.
I was diagnosed with invasive ductal carcinoma in January of this year. I am 39 yrs old with 2 children no breast cancer in any of my family. I want to just say, that without my mother, I do not know how I would have survived. I have a husband and a wonderful family but some of my closest family couldn't bear to see me sick, they just didn't know what to do or say. I knew from the day the dr called and told me that it was cancer, I was going to be fine. I was usually better than some of the people around me.
This is an extremely scary time for her and no one can even start to understands unless they have been thru it.
I could go on and on with advice to you and her - from my personal experience, so I will end this by just saying I am doing wonderful now! I really feel normal - like I had just been thru therapy over the summer. I am back to work and feel fine. Diagnosed Jan 10, '08 -- lumpectomy in Feb --chemo started in Feb and ended in June--started radiation in July and ended in August. It is now October and I consider myself CANCER FREE!!!! May God Bless You and your CHILD - for he will bring her thru this.
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Thank you, Johnie -- and God bless you and yours also!
This long journey is just getting started. She asked me to take her for her MRI yesterday and today I will be taking her for her oncology appt. Her husband has to work and she wants me to go with her. I tell her that when she gets this behind her, it will seem like the time just flies by. But gosh, how long these days are -- that is what amazes me more than anything. The days, from getting up in the morning till going to bed at night, just seem so, so, so long --
I introduced her to this site and she found a young mother, like herself, diagnosed on the same day who lives very nearby - in Clearwater. She has had some wonderful exchanges with her in the past couple days. I can already see her confidence level picking up -- I know the Good Lord will take care of her, as does she, and as He does so many others, including yourself --
I pray that all continues well for you and your family and am very happy for you -- my best to your mom, it's a very, very difficult thing! And thank God for all the wonderful mothers, daughters, sisters, nieces, and all who provide support that is so desperately needed through this site!
Hugs to you!
Laura
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Laura,
I am impressed that you are on this site only because my mom refuses to turn on a computer:)
I am happy for your daughter that her prognosis is so good. Of the different treatments, I would take either over chemo. It is wonderful that you live near her and that you are so supportive for her. She is going to need that while she is going through this. Best wishes to you and your family.
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Hi, Jule -- and to all you wonderful supporters out there, thank you so very, very much! We were really uplifted today after meeting with her oncologist who spent close to two hours just talking to us about this terrible illness. Both he and her surgeon feel her best option at this point is to go through chemo first, kill any cells that may have strayed before she goes through the actual surgery. They don't normally do this first but they feel that considering her youth, her strength right now, etc., that is the best way to go. She will get some sort of scan first to check the surround lymph nodes, then if that checks out okay and there's no sign there, they will start the chemo. Then it's on to what appears she is going to choose, which is the mascectomy. She's pretty decided on it and felt SO VERY, VERY CONFIDENT when we left the oncologist today.
It was so good to see her spirits actually lifted and though she is just starting on her journey, she has so much support and we all just love her so much and her faith is so strong, I just don't see how anything could NOT go her way for a change. Thanks so much and not having been quite so aware of the turmoils of BC, as I'm sure many people aren't until it happens to them or someone they love -- you know all to well how it just changes everything. And I told my daughter there must be a reason for all of this at such a young age - it just puts so many, many things in perspective - things like our children, our day to day lives, those that aren't blessed in other ways that we are, just so many things it opens new doors to. So, I guess in reality, we never stop learning about life, do we?
All of you are in my thoughts every single day -- and hugs to all moms and daughters dealing with this!
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I am sorry to hear about your daughter. I know what has helped me the most is that my mom has just been there for me and for making me laugh. I can never imagine what you are going through.
Here is what my mom wrote to another mother with a daughter with BC.
"I know exactly what you are going through. My 39 year old daughter was diagnosed with barest cancer in April while stationed in Korea. it was so hard not being with her while she was going through the testing and not being there when she got the news. After having the lump and some tissue removed she ended up in Hawaii. My husband and I met her there the 14th of April. She had additional surgery but because of some problems (with her original oncologist) she and I were transferred to Travis AFB (my husband went home for a months and shipped her car to us). He as wace again joined us in CA.
The most important thing you can do is for you to be OK, that is the only way you can really help her. She has to know that you are OK, she has to much on her plate to worry about how you are doing. This first step did not come easy for me.
I made a practice of getting up before everyone, take my coffee and Bible and sit on the front porch. The beauty of the lush trees, flowers and the ocean gave me the peace and quite I so desperately needed. The trouble reality always reared its ugly head. One morning I flipped open the Bible and came to:
Isaiah 12:2 and 3. God is my Savior, I will trust Him and not be afraid. The Lord gives me power and strength, He is my Savior. As fresh water brings joy to the thirsty, so God's people rejoice when He saves them.
I wrote this on a card and took it everywhere with me. When those terrible thoughts entered my mind I would pull out the card and read those tow passages until calm and peace once again cane upon me. This is the kind of peace that only God can give.
I am now in the position to be able to be there for her. Laughter is so important, I make a practice to kiss her bald head everyday (she would not let me or my husband shave our heads).
Our daughter has just finished chemo and will start radiation in four weeks. Since coming to CA we realized that having a doctor who is not to busy to take the time to listen, and is upbeat is so very important. After her first treatment I took her back to the clinic 4 times just to make sure everything was still OK. She took it all in stride and never once made me feel like I was going out of my mind but that I was doing a good job watching her. If you daughter is not comfortable with her oncologist urger her to find another one.
Ursula"
I hope this helps. Since the 14th of April, my mom has gone to every appointment...she says she will not leave until I am totally done with my treatments. If you ever want to talk to my mom just let me know.......They live in Fort Walton Beach FL.
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Laura,
I had chemo first before surgery because of my age as well. I agree it wasn't as typical, but I have good results so far. I had bilateral masectomy at the end of September. The chemo is tough, but after that everything seems easier.
Good luck to her.
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Hello!! I was diagnosed with breast cancer last Aug.21,2007. I was 30 years old. It didn't run in my family,as well. You are indeed right,it was a HUGE shock to us all BUT I am like your daughter..I have strong faith,am surrounded by sooooo much love from my husband,family,and friends,and after the initial shock was over I had an amazing attitude about everything! I can tell you right now that you will be in awe at the blessings that will be poured over your daughter and family! I never really realized how much I was loved until my diagnosis!! I had my lumpectomy first and it was caught early and hadn't spread to any of my nodes. After that I had my port placement. I started my chemo the first week of October last year. I had 8 rounds of that...the first 4 were Ellence,Cytoxin,and 5FU and the last 4 were Taxitere. I lost my hair and all that not so fun stuff. Chemo is pretty harsh BUT once you get through that radiation is a breeeeeeze!! I had 35 rounds of radiation. Zapped everyday for 6 weeks. I finished my radiation June 9,08.I have to take the Tamoxifen(chemo pill)for 5 years b/c my cancer was hormone positive,which has put me into early menopause at 31 years old...uugghh! My husband and I don't have any human kids yet..just our precious dog and cat...so we just leave it to the good Lord to do whatever is best after I am finished with all my Tamoxifen. Since everything,I have got to make 2 speeches,one was at a fundraiser and the other was at the Relay for Life,which I got to walk as a SURVIVOR!! I have had my story used on several different websites and I have had a chance to do a few more projects. If I can help you,your daughter,her husband,or anyone else please let me know. There is another website you should check out too. It's www.carepages.com I have a page and my page's name is fighting. You can post everyday or whenever you have time and you can keep alllll of your family and friends informed without having to repeat everything over and over again. There is also a couple of pages where you go and request prayer. I have "met" some AMAZING people through those pages that I have grown to love so much!! It's a really really neat place! If you make your daughter a page please stop by mine and let me know so I can keep up with you guys. Until than you all will be in my prayers. God bless and keep your faith strong and God will get you all through this. I promise!! From a breast cancer SURVIVOR!!
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Thanks, Stephanie -- gotta' say you look great!
And I'll check out carepages.com.
Haven't posted or checked but thank you also, Sunshine -- things have been so, so busy! I do now know that Lisa is triple negative ER, PR and Her-2, which was not good. Grade II, but I still don't understand the stage thing and can't figure that out off the path report - Lisa gave it to me, she didn't want to know the size. She only knows it was larger than originally estimated. The tumor itself is actually measured at 4-5 mm, which is also not good. BUT, some good news, they did surgery this week to check the lymph nodes. The first two sentinal nodes were cancerous so they removed a total of 29 lymph nodes. 11 of those were sentinal nodes (doc said that was a new record that she knew of for the number of sentinal nodes); however, only the first 3 were cancer, the rest checked CLEAR which I was so, so happy to hear today! They will do a PET scan to be safe, next week, but there is absolutely no sign that it has spread any further, as we greatly feared!
They placed the port during Tuesday's surgery also, so she got a double-whamo! She is already healing well and today's news will just help her heal better. The sooner she heals up, the sooner they can start the chemo, anywhere from 4-6 months of that, and then bilateral mascectomy with reconstruction at the end.
So, though she has been up and down, she is VERY POSITIVE today which is just awesome! Her girlfriends are taking her out tomorrow and we're walking in Making Strides Against Breast Cancer in Pinellas next weekend, the 25th. Doc says she will be able to do that and you can bet she isn't going to miss it! She, of course, signed up and got all of us signed up on it -- my daughter is such a fighter and I have absolutely no doubt she will get through this! We look at it as a very bumpy road but it will have a good ending, we're sure! Her attitude just never ceases to amaze me though, of course, she does have her occasional downs -- thank you so much, everyone, for your kind words, your thoughts, and your prayers! You are all such wonderful, wonderful ladies!!
XOXO - Laura
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Laura....Hope you are well. How is everything going? Both my mom and I are thinking about you and your daughter.
I am very glad that I got a port. This way when she gets chemo or blood work done they don't always have to find a vein in her arm. Since getting chemo my veins are really bad.
If she has problems with sores in the mouth or a really bad taste (I called it the hairy tongue) tell her to try Biotene mouthwash.
kim and ursula
p.s. PLEASE don't forget to take care of your self!!!!!!
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Thanks for the advice and well wishes and we are doing just that, well . . . Lisa has now started chemo, virtually no side effects other than a change in her taste buds?? Her PET scan came back clear and her oncologist called her on a Friday night at 9:30 to let her know that - can you imagine a doctor that caring to take time on a Friday night for that? He is absolutely wonderful!
She plans on shaving her head in the very near future since she was told she would start losing it after the second treatment. This girl of mine is just a real trooper and is blessed now with so many small miracles it absolutely amazes me!
As for me, all I have to do is go around her and another small miracle happens - it just pumps me right up all over again! She is such an inspiration!
She organized a team to walk in the Making Strides Against Breast Cancer and raised $1000! We will have many more of those now, I'm sure --
Bilateral mascectomy will follow chemo in a few months but so far, so good --
Again, thanks for thinking of us . . . there are so many kind thoughts out there and they are all so appreciated. How are YOU faring? Please let me know -- btw, how are things going with the military? My husband is retired USAF --
My best to you and your mom! XOXO Laura
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Hi Laura,
I was just reading through some threads and happened upon this one- first let me send your daughter, you and your entire famil my love and support.
I then noticed you are in Tampa and you mentioned Clearwater as well. I live on Indian Rocks Beach.
I was DX in 06 (46 years old), have had a coures of treatments, and just underwent bilat mastectomy on 10/17.
You sound as those you all are doing quite well thus far through this journey, I am very close to you both, if you need anything, to talk, just anything - PLEASE do not hesitate to contact me - PM me at anytime .
Hugs - and Love - Cathi
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SoTpaGrl - I know exactly how you feel - my 33 year old daughter was diagnosed in late July. I have gone through all the emotions you have described. My daughter has 2 young children, a beautiful 11 year old girl and a very active 3 year old son. We are a little ahead of you in the process, she has had all the testing, a mastectomy, and is now doing chemo. I am fortunate that she lives 5 minutes away and I have been able to be part of the whole process. She was very scared at first, as were we all - she especially was upset about the loss of her beautiful long hair--but she took the initiative and she and her husband shaved her head. She too has a strong faith and after the initial shock has been so brave and positive. God bless you and your family.
Cathy
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Thanks, Cathy - it's amazing that these "little girls" of ours can have such strength and fortitude, isn't it? Sounds like you are well - we just absolutely have to keep up that positive "I CAN DO IT" attitude!!!
Hugs to you and yours!
Laura
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There are times when Angie puts me to shame! I try to always be positive around her - but I do have my low moments. What I hate most is feeling helpless - not being able to fix it or make everything better as her mom. Its a very long road for us, she has HER2+ so its 6 sessions of chemo (they told her she would start loosing her hair around day 15 - and they were right!), a year of herceptin and she is in an avastin study for a year.
My daughter posts here and I started reading at first - there is so much support and I am so thankful we have both found this board!
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