Member Since: August 14, 2004
Last Login: July 8, 2008
Birthday: February 2, 1961
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| Diagnosis: | Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
| Diagnosed: | August 8, 2004 |
| Type: | Invasive or Infiltrating Ductal Carcinoma |
| Recurrent? | |
| Metastatic? | Yes |
| Stage: | Stage IV |
| Lymph Nodes Removed: | 20 |
| Positive Lymph Nodes: | 1 |
| Tumor Size: | |
| Tumor Grade: | Grade 3 or high grade |
| Hormone Receptor Status: | Tumor has both estrogen and progesterone receptors |
| HER2/neu Status: | Tumor has an excess of HER2/neu receptors or genes |
Posted in:
Support & Community Connections + Commemorating Loved Ones, Created: Jul 8, 2008 09:53 pm
Please Pray for Dawn & MenaI just mustered up the guts to read these posts, and I want to thank all of your for your compassion in this truly, life-, body- and mind altering tragedy that has yet to make any sense. "Thank you" sounds so simple but here the words are profound; and although my heart has never been heavier, I am lifted by your condolences and kind words. Miz, thank you for relaying news that I just could not put into words. It's all still so surreal and even typing this seems other-wordly. I know how much you loved Dawn. I just couldn't do what you did for me and I want you to know I do appreciate it even if I sound crabby. Shokk, I think it was you who remembered my son. He is not doing well and I am very, very touched that you remembered him. All of you have overwhelmed me once again with your solidarity and empathy. Marin! Yes, I got your call and saved your number. I can't say I'm doing a stellar job of getting on with life today, but I did get my hair done (despite the fact that I'll be losing it shortly) and I spent hours visiting with Arpy from Chat. I made myself shower, shave, makeup -- all of it. I guess you'd say I'm on a automatic pilot with God at the helm and my new special angel, of course. My niece had a quite detailed and happy, colorful dream about Dawn and this helped all of us. She said Dawn looked like a beautiful angel and said she was happier than ever. She was with me and we had our arms wrapped around one another. Dawn happily added that there was even a candy-land up there. She also told my niece that she can only visit every ten years. I'm hoping ten years is nanoseconds up there. I know dreams have all kinds of interpreters and interpretations, but I'm taking this for what it is worth. OK, I'm blathering and tearing up a bit. So once again, monumental, sincere, I've never been more honored to say, thank to forgot you to all of you. Please keep praying. I don't want to forget anyone and in my heart I haven't. I have to offer special thaks to Cheri. Man, she really knows how to get a girl through the night lol! Thanks for listening and sharing more about Dannyl. Everyone please be kind to one another and as John Mayer croons, "say what you need to say...." (but do it gently). Love, Mena xo Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
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Recovery, Renewal, & Hope + Moving Beyond Cancer: Time to Circle the Wagons, Created: May 25, 2008 04:23 pm
Update on Puppy... add prayersHey Pups...thinking of you always and hoping you are comfortable as can be...miss you...you're in my heart and prayers daily, Deb...Mena...xo Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
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Recovery, Renewal, & Hope + Growing our Friendships After Treatment, Created: May 25, 2008 04:18 pm
HUGS4HARLEY!!!!!!!Hang in there. It's all gonna be OK...Mena...xo Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 29, 2008 10:18 pm
Dealing with the ups but mostly downs ..Liz, you probably can benefit from therapy and/or meds for the depression, fear, anxiety and stress! I'm sure you are aware of "Caretaker's Syndrome"...cancer effects everyone. You need to take care of yourself so you can handle what's going on with Mom. If you think you need help, and that's why you posted...honey, you do. It's not a character defect or shortcoming. In a sense, you have cancer, too! You need your treatments as well. Even if it's just venting to a therapist. I wish I had more sage advice for you...a magic bullet...be kind to yourself and remember YOU are experiencing a trauma as well and may need professional help. No shame. Who wouldn't? Keep sharing...Mena...xo Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 29, 2008 10:00 pm
I never wanted to post here, but what do I do now??Oh Deb...it's a dark place where you are right now, for sure. I understand and so do too many of us. It takes a while to adjust to this new living-with-cancer. And that's what you're going to do. Live with it. It's not easy and harder for some of us given our life circumstances, but you have always been so upbeat and optimistic and kind and gentle and helpful. Now it's time to let us help you. First, get another opinion. Get two. Do what makes you feel like you are doing everything you can. Have your cancer tested again to see if anything has changed (ER/PR/HER2). This does happen. I am so sorry. You will grieve the loss of your health and that is perfectly normal; don't let anyone tell you otherwise. You are such a fighter! Mourn this news and then you will get on with tx and life! I don't think you have to tell your girls you're dying. You're not God and you don't know what's really in store for you. It's another battle that you will fight galantly and with good humor once you adjust. I've been living nearly 4 years with mets, Deb! And you know my personal life has sucked since that dx, but here I am. You can do this. You will grieve and cry and probably lose sleep for a while (took me about 8 mos!) And then you will pick up and live one day at a time, as we all should. Please check you pm's and know that you will now form bonds stronger than the ones you've had (and they are plentiful, right?). I'm just so %^^%$#( angry at this disease. You need to talk to metsters and refuse to give up, which I know you will when you're world stops reeling. I will pray for you and I understand every thought you are having. Many of us do. Lean on us now, Deb. You deserve it and we owe you! Love, Mena...xo Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
Posted in:
Recovery, Renewal, & Hope + Moving Beyond Cancer, Created: Feb 29, 2008 06:31 pm
Has anyone ever tried Topamax?Hey LU...chiming in here...I was on Topamax for nearly three years...no side effects to complain of! Great drug for knocking off a few pounds, too (in the beginning)... You've gotten great feedback here; it is an anti-seizure med that is now approved for a plethora of other uses. Truthfully, you don't have to fear s/e's from this...xo Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
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Connecting With Others Who Have a Similar Diagnosis + HER2/neu Positive Breast Cancer, Created: Feb 29, 2008 06:28 pm
Herceptin questionPreventative. I've been one it for about two years and it is slowing the progression of my disease, so they say... It is not a chemo; it does not directly kill cancer cells...But if you are a candidate for it, by all means, do it!...xo Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 29, 2008 05:54 pm
Triple Negative Now In Brain - AdviseYes! Get on bcmets.org and talk to the ladies there. I know a few who have had brain mets for 2-3 years and still lead more exciting lives than healthy folks...Please post over there. You will get lots of feedback from women with the same and similar dx's, tx's, etc. It's a great site for metsters, since everyone is a metster and lots have gone thru things already and will help with info and support. I've been thinking of you since I first read about your difficulties earlier this week. I continue to wish you comfort and peace and commend your composure. Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 26, 2008 10:21 pm
Anxiety Meds DilemmaAtiman hahaha just saw that...how funny...xo Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 26, 2008 10:11 pm
Abraxane and famaraBonnie, by all means, go where you are comfortable... As a seasoned metster (3-1/2 years), I've learned that you don't fix what ain't broken! You need to hold whatever you can in your arsenal. However, trying a different hormonal just might be the kick you need; but I'd stay with the Being comfortable with your care is half the battle, no? I wouldn't settle for convenience. Is there anything convenient about mets? Nope. Just chalk it up to the ordeal we endure, much as it sucks. Good luck to you. I'm anxious to see what you do...Mena...xo Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 26, 2008 10:05 pm
statis of mets survivorsHeather, STATS ARE FOR BRATS (HA!)...seriously...I was dx'd with lung mets in Aug/04 and told not to expect more that 18 months. I'm still here, functioning, fighting, and...eating anything I want (in other words...fat!). One day at a time. It's difficult, I know. You're not alone. Keep sharing...Mena...xo Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 26, 2008 10:01 pm
Anxiety Meds DilemmaWatson, you're so funny. I think every bc patient I've ever met has had at least one anti-anxiety med and most take antidepressants, too...well, most of the fricken population does that...except for Scientologists, of course... Anyway, I also use ativan at 1 mg tid. I hope this helps. Oh, you know, this will help your pain, too!! Definitely, I have noticed that. Try to keep track of when you take it, what pain meds you have in you and see if you don't get some relief with the ativan instead of the breakthroug pain meds. Just up that Fentanyl and you'll see a big difference...good luck, sister...Mena...xo Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 26, 2008 09:55 pm
Fentanyl patch questionOh don't be afraid to up that Fentanyl...I started at 25 mcg and now use 150 mcg and nothing but Tylenol 3 for breakthrough pain. Just tell your onc. There's no reason why you can't have more that 25 mcg; you'll just have to minimize the other drugs you take for pain, especially the morphine. But don't increase anything without asking or telling (ha!)...Also, some patches (generics/brand) are better than others. I've had good success with the Sandoz brand. I hope you feel better. Pain sucks...Mena...xo Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 26, 2008 09:49 pm
Lung Mets NOW starting pain on chemo?Watson, that cough can be asthma related -- lungmets-induced asthma. Don't you have Albuterol and Advair or anything for relief. I've had the damn buggers since Aug/04 and still do not have a cough (except when I smoke my cigars)...xo Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
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Connecting With Others Who Have a Similar Diagnosis + Palliative Therapy/Hospice Care, Created: Feb 26, 2008 09:44 pm
I am also now officially "Palliative"Hi J...haven't stopped thinking about you and praying since I first read your post. Just dropping by to say "peace"...love, Mena...xo Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 23, 2008 06:27 pm
lung metsLung metster weighing in here. Dx'd August, 2004...still kicking...and screaming...pain is only symptom of mets...that is controlled with fentanyl patch...no sob, no coughing...actually the tx is worse than the dx...hang in there...Mena...xo Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
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Connecting With Others Who Have a Similar Diagnosis + Palliative Therapy/Hospice Care, Created: Feb 23, 2008 06:11 pm
I am also now officially "Palliative"You are amazing to share this. It's hard to find anyone who really wants to talk about this side of it all. So brave of you. I pray you are surrounded by angels who keep you pain free and unafraid. God bless. Many warm and gentle hugs, sister...Mena...xo Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Jan 13, 2008 04:07 pm
Sigh...your input pleaseWow you guys are great! Thanks so very much for all of your responses. On RFA, I asked about that last year and I believe I have too many tumors or because my disease is systemic, it won't help much? I will ask again. I see my onc on the 24th. Thanks for bringing that up again. I think I was told that RFA is used for localized, not metastatic disease, but I will doublecheck. I have meds for everything except insomnia hahaha...that's why I'm off to take myself a lil nappy right about now. Just popped in to say thanks for all the love and support. Have a wonderful evening. I will talk to my angels for you as I drift off into the Land of Nod for an hour or two...xo Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
Posted in:
Recovery, Renewal, & Hope + Moving Beyond Cancer, Created: Jan 13, 2008 04:06 am
MENA NEEDS US!!!!!!Mena is OK! Just hit another bump in the road. Scans reveal more suckiness and onto another tx which has me puking already so here I am...hahaha...fear and vomit are great motivators! Thanks you sooooo much for all of your support. Yes, my Gramma is still in critical condition, and yes, I adore her and vice versa. So it will be a great loss. She is 99 and one helluva woman. I got rather run down running back and forth to the hospital and think I picked up a bug. Then I got the results of my scans last night and yuck. I'm refusing chemo for now and opted for what I just figured out is my fifth hormonal. Aromasin. So for the next three months it's Aromasin (and Herceptin which I've been on for about 2-3 years now; have to look that up). Then scans again. I appreciate everyone and all thoughts, posts, calls, cards, everything. Thank you. I feel better just being here at this absurd hour. My family is becoming more supportive...don't know who what when why or how -- all of a sudden but I'm happy about it. This is the second Saturday in a row that my brother has taken me out for breakfast. Of course today I had to run to the Ladies' room to vomit and couldn't eat, but nonetheless it was pleasant. Hey, one thing about cancer -- I know where all the public restrooms are and I can get there fast! I can even get in the ones that store owners claim they don't have hahaha...I mean, they get scared when you get that vomitous look...Besides, is it really going to kill them to let you use their damn toilet? Absurd. I do have to get over to the hormone thread and find out why I am puking from one day on Aromasin. And hot flashes, too...I suppose it could be all the running and upset over my Gramma. She's decided she wants nothing if she goes into cardiac arrest and doesn't want to be intibated (sp?) any more. They just extibated her yesterday. So, we are all preparing for the worst and we were all called there a few days ago "to say our goodbyes" and after 36 hours she rallied. Then we were told she took a turn for the worse again. So, it's going to be a touch and go situation from here on out. I'm sure many of you have experienced similar situations. This is going to be a huge loss to our family. She is a true matriarch and the creator of so many traditions and such legacy. All the preparation in the world doesn't make it any easier. She has, however, been the maker of my fondest childhood memories for which I am eternally grateful. Like I am for all of you. All of you...xo Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Jan 13, 2008 03:33 am
Sigh...your input pleaseBut you have helped, Ravdeb...just by being here! Thanks for dropping by...I love your pic...great glasses... Renzo...hmmm...you love my voice?....ahahaha...well, then...I think you'd love America hahaha... Dx 8/8/2004, IDC, Stage IV, Grade 3, 1/20 nodes, mets, ER+/PR+, HER2+ |
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