Tribute to Shirlann
Hi all,
Whenever I get really discouraged, I always look for Shirlann's posts. Not only is she incredibly positive, she's unflaggingly kind and conscientious in her responses to all those of us who are still traveling the dark road and worried about our different symptoms and side effects.
What I find truly remarkable is that Shirlann has been disease-free for over nine years, yet still spends time every day on these boards reassuring and comforting all of us. How many women would feel compelled to give back, day after day, for so many years?
Shirlann, thank you for everything you do. You are one in a million -- you've undoubtedly given hope to hundreds of women like me, and I love you for it.
Annie Armpit Lump
Comments
-
Hear hear!!!!!! You've been a beacon of light for so many newbies. I don't follow the other forums very much (I just have LCIS), but I know you are so incredibly helpful to newbies. Thank You So Much!!!!!
-
Leaf, just what I was going to say, "hear, hear!!!"
Shirlann, you are just the best! And adventurous, too -- besides your kindness, insight, positivity, and all-around help -- your world travels are an inspiration! Hugs, Ann
-
I agree! I remember when I came to realize what it meant to be triple negative (I was so clueless and such a newbie six months ago), I cam across Shirlann and it gave me such a tremendous amount of hope and really made me feel better when I needed it most. I have noticed that she is always there when someone new has a question.
Lisa
-
Ann and Leaf,
Absolutely!! Even though I haven't been here that long, Shirlann has stood out from the start, as a caring, supportive voice of rational advice. She always has a thoughtful, non-judgmental answer for anyone she posts to.
Your tribute is well placed and well deserved!
Susan
-
We are lucky enough to have Shirlann in our San Diego BCO Lunch Bunch...she is a sweetheart!!
-
Yes, for sure! She's helped me may times. Thank you, Shirlann!
-
Hi, I'm new; just registered. I was dx last week. I have IDC pretty rapid growth. went from quarter-size lump in July and now my left breast is almost totally a mass and feels like it weighs 10 lbs. I will have a porta-cath placed this Thurs and my first chemo on Friday. I'm going to have Taxotere, Adriamyan(?) and Cytoxan. Can anyone tell me the side effects of these particular drugs? We're doing chemo first to stop growth and hopefully shrink. Then surgery followed by radiation. I would love to hear any advise anyone can give me
-
-
AMEN TO SHIRLANN!
My first two weeks she calmed me.
Thank you for sticking around for us!
Laura
-
-
I agree. Shirlann, I love your posts. They always bring comfort.
Sandee
-
Absolutely! She always gives a reply.
And it is always appreciated.
-
You were the first person who was there for me.
I needed that
-
Yes , yes! Tribute indeed! Shirlann is my angel. She made me laugh when I never thought I would again. And she is such a comfort and an inspiration. We are soooo lucky to have her here. Love you Shirlann!xxxx Melody
-
Hi Ladies:
I finished my Rads one year ago. This great Lady "Shirlann" has helped me beyond belief. What a gem this person is. In my opinion she has so many "ANGEL POINTS".
How privileged we were to have her share her wisdom and kindness with us. I'll always remember how much You've helped me, you have absolutely no idea what you have done for me. Would love to meet you in person, who knows.....anything is possible.
With love and the greatest respect,
Erika -- Canada
-
Dear Dee811,
Hi there sweetie - it's too bad you had a bc diagnosis but this is a great site for support and information. I wonder if you posted your question somewhere else, because it might have gotten lost on this "Tribute to Shirlann" thread. You could re-post on the chemo thread. Anyway, I had ILC and went through treatments with the 3 drugs you list. I didn't have any side effects for the first couple of days, but after about day 2 (I think- maybe day 3) I was tired and the main thing that happened with me was that I couldn't taste anything - my taste buds were affected and everything tasted gros. I was sick only after one treatment - they give you anti-nausea drugs so hopefully you won't have any of that either. I lost my hair (all over the body - not just on the head!!) at about days 17-18 after the first treatment. I did have some mouth ulcers but vigilantly rinsed my mouth with salty water....you could ask whether to do that right from the beginning or wait until you have a problem...you may never have them develop. I had 3 weeks between treatments and by the third week I was more or less back to normal - not as tired and able to eat no problem. I had a port too and it was wonderful - made it all a lot easier.
I hope this helps and that you hear from others too. You might be lucky and just have minimal side effects. Good luck to you! Just remember it is worth the side effects to be killing the cancer...that is how I looked at it - like the chemo was a positive thing!!
Peggy xoxo
-
Absolutely! I'm so glad you started this thread. I have often thought about how much Shirlann's experience, wisdom and humor have helped me. Thank-you!
Lisa
-
Yes, Shirlann, you are one of the most beautiful people, inside and out and I want to thank you for helping me and so many others.
-
Shirlann, you are very special!!! Thanks for being you!!
Harley
-
Bless you, Shirlann, for sticking around here and offering your mind and heart to all of us!
-
Oh my, I am in tears. I can't believe all these wonderful sisters. You are such a treasure to me, everyone of you.
I can't tell you how much your kind words have cheered me up. So kind, so sweet.
Hugs and kisses to everyone, Shirlann
-
Thanks Shirlann, for all you do for our bc sisters.
Hugs and prayers,
Candie
-
This time last year, when I first started my bc journey, Shirlann was one of the first ladies to respond to my frantic post. God Bless you Shirlann, for being such a wonderful and loving person. You've given so much encouragement and hope to so many of us. You are truly one of a kind. I love you, Shirlann!
-
Thanks from me too Shirlann! I can always feel your "gentle" hugs. You give us newbies hope and inspiration. It's so scary to get a cancer diagnosis, but your words of wisdom always bring comfort. You have truly found your ministry
Thanks a million!!!!
-
I am fortunate to be another one of Shirlann's monthly in-person BCO-Lunch sisters. She has, from the beginning, always been compassionate and concerned with each and every one of my questions, upheavals, and mild panic.
I have, over the months, seen her welcome new BCO lunch bunch members with the same caring and concern.
She's every bit as much of a treasure in person as her posts convey. Shirlann, thank you for your voice of calm and reassurance. Don't ever feel like you are a 'broken record' (I've seen you write that) for suggesting antidepressants, for advising anti-anxiety meds, for explaining post-traumatic stress disorder, etc. to the newcomer. You always are our voice of experience, of survival, of support. Definitely one of a kind.
xoxox
Lisa
-
Let me chime in here and add that when I was new and scared I got a kick out of reading her posts, especially the "gentle hugs" at the end
Even though, they were not meant for me, I loved them.
Shirlann,
you are so very appreciated!!!
-
Shirlann ..... I love you with all my heart and soul xxx
-
I think what makes us love Shirl is that she is not perfect. She gets silly, pissed, down and even dumb from time to time, which I think makes us feel her closer because none of us is anywhere near perfect. She is just like us, yet would never ever spare time and effort to offer help and support. That's why we love you Shirl.
xo
Fumi
-
Shirlann was a major reason that I got through the first few weeks of breast cancer. She is an angel who offers great encouragement and guidance. We are all lucky to know her.
-
Hi I agree Shirlann You are such a beautiful person with a heart pure as gold.You gave me hope and joy with every post.I'm 15 months out and Ned and doing well.All the women on these boards are wounderfull.When i get down or have a bad day i come here and read your post.I just want to say thank you for being that strong voice of courage.Godbless you and many many more years of health.....Love ya roxy
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 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