Starting Chemo in JAN 2007
Comments
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I tried logging into the chat, but can't get it to work. I think this is the Internet's way of telling me to turn off the computer and go to bed.
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Chat didn't work for me either. I nearly fell asleep just now watching a program on TV, so maybe I'll call it a night early like Jan is.
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Well I can see it wasn't just me. I also tried 3 or 4 times to get into the chatroom, couldn't get on.
Jan - your girls are adorable. Also congrats on Em winning the blue ribbon in her horse competition. She looks great, very regal perched on that horse. She's brave, I could never do that. I hear you on the one boob thing in San Antonio. Try wearing a loose nightie/pjs with a loose robe overtop if that makes you feel more comfortable. I'm sure your business partner/friend won't care. It's more how YOU feel.
Debbie - you look great. The hair is growing in nicely.
I'm going downtown tomorrow to see the PS I saw last year who specializes in breast reconstruction. I saw her before my mastectomy to explore all my options, and I decided at that time to do nothing, just do the MRM, let it heal, do the chemo etc. So now that I am all healed up, I want her to look me over again and see what she thinks. I listened to the tape recording of the appointment I had last November with her to refresh my chemobrained memory.
That's in the morning. Then I have an afternoon appointment with my obgyn for a pelvic exam and to discuss taking out the ovaries. Sounds like a fun day, eh girls? OY!!!
I will let you know what happens with Cassie. Thanks again to all who voted for her. In the last few days a few more contenders showed up, so the competition is a little tighter. But even if she doesn't get it, it will look great on her resume that she was a finalist. We might not know for a couple of weeks.
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I couldn't get into chat tonight either. Guess we'll try for Thursday?
Caya, I can't believe Cassie won't get the job. I've looked at all the other candidates, and there are some good ones, but Cassie is still the best. Your girls are both exceptional. Good luck with your appointments tomorrow, and let us know how things go.
Robbin, congrats on quitting smoking, and I hope your back feels better soon. Bet you've got all kinds of hair by now.
Jan, the Halloween pic of the kids was adorable. What lovely little girls you have. I can't imagine that your friend would be uncomfortable with your single-boob status - it's not like it's news to her, right? It's more a matter of what is comfortable for you, and that's different for everybody. For me, it wouldn't be an issue. I figure I didn't ask for this, but it's what I got, and I'm not ashamed of it. Of course, it will be better when I have my reconstruction done, but for now, this is me. Really, though, I can't imagine your friend would be uncomfortable unless you were. When is your conference in San Antonio? Will you have any free time? Just wondering, not sure I could get over there anyway, but it's a thought.
Debbie, you're looking good, girlfriend! Your hair looks SO much better than mine does. Everyone's does, actually. I may just keep wearing the wig forever. I really, really look like Bozo, only gray. And gel doesn't help me one bit - it's too curly (except for the straight spots) for even the strong gel to tame it. Meanwhile, every day I get compliments on my "hair" with the wig. Even men notice and comment, and that's not a guy thing at all. Maybe I should just take the hint. On the subject of the comments about how "good" we look, though, I don't get too upset about it. I figure, considering what I've been through, I don't look all THAT bad, so I just say thanks and take it for what it is. Most people are just trying to be nice. Those who aren't, well, I know who they are and don't worry about them.
Tina, what day is your surgery? I hope it all turns out well for you this time, and that you are happier with your results this time.
Rebecca, please do post a pic of your hairdo. You have described it so well I can almost imagine it, but we still need a pic. I'm working up to going in to have mine shaped and colored, but I think I'm waiting until it looks better - I hate to even let them see me like this. I think it's hopeless, though. I need color.
Skye, maybe I can blame my chemobrain, but I can't figure out how to hear you on that psytalkradio site. Seems like I tried this before and failed also. What's the secret? I'd love to hear you talking about some of your stuff.
Joni, so glad your partner's surgery went so well. I can't imagine such a big tumor, even after radiation. Wish I could walk around the lake with you. I'd love to be around the ducks and geese. I used to buy 200+ lbs. of corn a week to feed to the geese and ducks (I lived right on the river). There were hundreds of them, and they got to know me and vice versa - I'd stand out there on winter nights until they all took off for wherever they spent the night, and I almost felt like I was part of the flock. This was when I lived in Kansas, where we really had a winter. It was really magical.
Well, yesterday was my last full day of freedom. I had a list a mile long to take care of. I woke up, turned on the coffeepot, and nothing happened. It just died. Then I opened the silverware drawer, and the front came off the drawer! I went back to bed. When I finally got up and tried again, first thing on the agenda was a new coffee pot, but since I hadn't had any caffeine, I couldn't think well enough to make a decision. Finally had to leave, go to Starbucks, then try again. I didn't end up getting much done with my day at all. Did manage to get my flu shot, though. It was miserably hot here, and that didn't help my mood or my productivity. Tomorrow should be better.
Work today was fine. I ended up staying the whole 8 hours, and although I felt pretty stupid, I was at least functional. I've forgotten a lot of things, but maybe some of them will come back. It did feel good to be back at work, but I'm also glad I'm not scheduled for tomorrow. I'll try to go in on Thursday and Friday, at least for a while.
Bedtime for me. Harrison and dh are already snoring.
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A 22 lb. tumor? Whoa, Joni, that's massive. Amazing that the guy is doing so well.
Jan, that's rough about the room sharing issue. It WILL be nice to not have weigh these extra considersations some day. I feel so relieved to not have to worry if my scarf matches or clashes with my shirt...it was like every day, one or the other had to be a solid. Just pain in the neck extra things to have to think about every day. It got old.
Rebecca, I've had that happen....trying to reverse directions and you get totally messed up. Don't beat yourself up. The streets in the northeast are often not "grid like" and you can get totally messed up. Boston is horrendous for that. I also found Orange County in So Cal hard initially as roads wind in and out of the canyons, east and west of the freeways. Once I learned my way, I was fine, but...
Debbie, your pictures are great. I like you in short hair. And the lighter color too. Shows off your eyes more. I just had my daughters hair cut last night into a chin length bob and it looks great. So much better on her tiny face. She, typically, wants long, flowing hair, but her hair just isn't that type...mine was never either, so I can relate, but.... she needs to do what works for her. I may just do chin length bob this time around too. Take my own advice.
I am taking all of yours and not letting scissors near it for a long, long time. My bangs are about an inch long (short). Looks like ruler head, but...beats a centimeter.
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Hi All,
Jan, great photo of your daughter. My girls rode, had their own horses, and now one is an equine vet. I think it's a great hobby; keeps them busy, out of trouble, sense of responsibility, etc. Plus so much fun.
Mel, glad the first day back went ok. Your job is so physically draining, in addition to the intellectual / emotional drain. Just do your best.
Just finished my big presentation. Now I am off to deal with my father and his social worker. But last nite I had dinner with my son, tonight my daughter, and HOME tomorrow nite. Cannot wait for this very high pressure trip to end.
When I was waiting for the presentation today, I was so nervous. Then I told myself I did 6 mos of chemo, I could certainly do this. It helped calm me down. The chemo was the most challenging thing I have ever had to do, no doubt. And it helps me keep all the work stuff in perspective.
Hugs, Melia
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Jan, I think you should go with what makes you comfortable when sharing the hotel room with your business partner. Wearing the prosthesis all the time doesn't sound like much fun, at all. I would hope that she would understand your situation. I would be comfy in PJs and a robe in the room; treat it like a home away from home.
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Jan, I agree with everyone else; don't feel you have to wear the prosthesis around your friend .... be comfy. Business travel is tough enough!
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Jan, I third that motion - wear a robe. I think we are more aware of it than others are.
Tomorrow I get my hair colored - wish me luck. I'm not going to let her cut it. Have another appt for that in 5 weeks. By then it should need some shaping.
Wow this time change and my changed working hours are tiring. This is the longest week ever! So Mel you are not alone in being tired. Hope Lynn is having a good vacation
Caya, let us know how your appts went. Hugs...
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Well, after waiting nearly 2 hours to see the PS, I was informed that she is leaving to go to UCLA, and is not booking any more surgeries. So I am thinking, then why I am here, I will need to see a new PS. Well, I figured I would see her anyways, to get her opinion. She says I don't have enough tissue for a DIEP - she recommended either the latissimus dorsi flap (moving the flap and muscle from the back) with an implant, or doing the tissue expanders with an implant. Because of the breast reduction I had already lost alot of skin, so my mast. scar is tighter than most (although it doesn't feel tight) - so there is only so big I could go. I am a 36D right now, after the reduction ( I was a G cup before), so they would have to reduce my left boob again. I just don't know if I want to do anything at all right now. My prosthesis is very natural looking, feels very comfortable. This PS suggested I go back to my original PS who did the reduction, as he is very adept with the expander/implant method. And I do really like him. So I will make an appointment to see him.
My gyn. examined me, says it all feels/looks good down there. We talked about getting my ovaries out - she agrees with my onc. - not necessary based on my age - 49 - and my BRCA status - negative - and family history - nothing to speak of. I will go back to the gyn. onc. again to see what she now thinks, although she did tell me that the standard of care at her hospital,PMH, the #1 cancer hospital in Canada, is to yank the ovaries out for all premenopausal ER+ BC patients under age 50. I will ask my onc. about this again when I go for my next herceptin in 2 weeks.
I am doctored out tonight. OY!!
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Hi Ladies, Just logging in to say hi. I have kept up with everyone's news and I am glad you are all doing well. I am pretty much going through the motions. I have to say that with all the anti depressants I have been on in my lifetime, this effexor is not doing it for me. Look at me cross-eyed and I'll cry. I am putting in a full week at work, but after I am going to see my Dr. I have got to do something, I am just not happy. And my family has had it with me. Don't blame them. I try to explain how this experience has devastated me inside, but they don't understand. They say it's over and I should get over it too. It's so hard, I am reminded of it several times a day, when I dress, look in the mirror, take a bath, etc. I am thinking of getting professional help. The bad thing is, it is the year end and my HSA will renew and my deductible is huge! I need to try and recover financially from this, too. I was doing fine, until I started this med, I really think it doesn't like me. My hot flashes are just as frequent also. My hair is approx. 3 inches long. I look like a man who needs the barbershop, but after reading everyone's experience with cutting, ummm... naw I'll wait.
Tina, that e-mail you sent me on the JC Penney's catalog brought tears to my eyes. I am still laughing, Thank you!! Poor Jeff said it reminded him of his childhood Christmas's. E GAD!
Were we all crazy or something back then? Loved the barrel dining room set. Tee hee, If the other sister's haven't seen that e-mail you seriously need to forward it to them. Girl's it was hilarious!
Well that brought a smile to my face, you all are so good for me.
*Hugs*
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Hi all,
I finally moved back home. I can’t believe all the stuff we schlepped there. My cottage is down a big hill- around 40 steps. It is okay going down, but going up with lots of stuff is a b****h. We lost electricity during the Saturday storm for 24 hours. Luckily it did not get too cold. Being back feels good but Comcast could not hook us up until today. I missed all of you.
I have been trying to trace my family roots before I go for genetic counseling. Apparently no one knows how my grandmothers died. My mother never wanted to know about death or how anyone died. When she heard the word cancer, she never asked any questions. Everything was always a big secret in my family. Trying to find out now is impossible. The hospitals cannot find the medical records and the death certificates would take over a month to obtain. All my grandparents were born in Russia, and their actual date of birth was also a secret. My appointment is next week, so I will have to wing it. We know neither grandmother had breast cancer and I will have to assume they did not have ovarian cancer.
Even though it is rare to have both the Her2 protein and the BRCA gene, the geneticist told me it was still possible. What am I doing? I have become obsessed. I should just let this whole thing go- but the FORCE website spooked me. My daughter does not want to know, and I do not blame her, but if there was a chance that I was BRCA positive, I would feel so guilty not finding out for her.
To do or not to do--I do not think there is an answer. Wait a minute- ATIMAN------I haven’t taken that little pill in a while. Maybe time to pop one.
Caya,
If you are not sure, I would wait. You have to be 100% ready before you take on another surgery. You have plenty of time and it is a very big decision. You will know when you are ready.
Nancy,
Please hang in there. This is all so hard. No one but us sisters truly understand what we have been through. When I went for my bone density today, I was in the room with all the ladies waiting for mammograms or the results. This was the same room where I was told my results last November. It kind of freaked me out. I wanted to run away, but I couldn’t. It IS hard. You are not alone. We are in this together and we are always here for you. Maybe you can try something else if Effexor is not working for you. Lots of hugs.
Viddie -
Viddie, I hate that deja vu feeling you get when you walk into the places where you were delivered the news that changed your life, etc. That's how I feel every time I go to OSU. I realized last night I will be having my surgery at the "University Hospital" portion of the building and not the "James" Cancer Hospital. I hated even BEING in a place called "cancer hospital". I am the mega multi-tasker. I am asking to have my herceptin infusion while I'm admitted vs. going in Thursday, the day before my surgery. I figure if I'm gonna be lying around for 3-4 days... speaking of herceptin, I have it today.
Caya, that IS annoying that the dr. is moving to UCLA. I think they should have told you that prior to your visit. Why take on a new consultation when you know full well you aren't taking on new patients? I am happy to hear about PMH's policy on under 50 ER+ patients. Makes me feel better about what I'm doing.
Nancy, sorry you're feeling so crappy still. That Effexor is working wonders for me, but I'm a newbie on it. I hear it can stop working or not be as effective. Maybe a switch is in order. Yes, that JC Penney email was by far, the funniest thing I'd seen in years. I woke up laughing even the next day. My favorite part was the man in the striped polo shirt/dress w/the matching coffee mug..."when he puts that mug down". LOL! Anyone that wants a good laugh, PM your email and I'll forward it to you. I only had Rebecca's, Nancy's and Mel's.
OK...gotta get ready for a 9:30 Herceptin. I see the NP too, which is odd. Usually it's every 6 weeks. Maybe due to my recent mental crack up they want to see me more frequently.
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Nancy - I hear you. It's far from over. Some days I feel like this is the beginning. Between waiting for a recurrence and the constant reminders every time I pass a mirror, get dressed, take a shower, or collapse in bed at 9 instead of 11 I can't put it behind me. And if my mangled body wasn't enough of a reminder there's the meds and hot flashes! I am still very angry. I know exactly what you mean about family and friends thinking that it's over. But we understand that it is not. If you think you could benefit from professional help - go for it. I know it's a financial hit - but if you can get in better shape emotionally you'll be able to focus better on work - so maybe there would be a long term financial benefit as well.
Viddie - Glad you are back home. I haven't been back to the mammogram waiting room yet. I know I'll be terrified on that day. I actually made my appointment at a different office so that I won't have to see the exact same room again.
Tina - I've seen that JC Penny email. Hilarious. But the really funny part is that what we are wearing right now will look just as ridiculous some day.DH has been out of town all week. He gets back today. I can't wait!
The chat room seems to be working again - I'll try to make it tonight.
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Nancy, I'm so sorry you're having such a hard time. I hope you will call your shrink ASAP and schedule an appointment. We've all got our issues to deal with, but I suspect with you it is a matter of being on the wrong meds, since you were doing so well before you changed. Maybe you can get back on the Lexapro. There are no easy answers, but you need to look at quality of life, and right now yours seems to be lacking. You can't go on like this, for sure. We all love you, and are here for you, regardless. Big hugs to you, and please let me know if I can do anything to help you.
Viddie, glad you're home and settled back in. I hear you about it being so much easier to move in, downhill, than to move out uphill! Can't tell you how many times I've had that experience. How are you feeling now - pretty much back to normal? Did you try the ATIMAN cure for your obsession? Maybe you should stay away from the FORCE website, huh? I don't know how I'd feel if I were in your shoes. I suspect I'd want to find out everything possible, just as you do. Since you seem to be stuck on it, maybe that's a sign you need to go ahead and be tested, I don't know.
Caya, that's a drag about your PS leaving, but at least you got an unbiased opinion, since she won't benefit financially. Did she mean you didn't have enough tissue for one D size boob, or were you asking about bilaterals? I've had a couple of friends who had lovely dieps done, who had very little excess stomach. Everybody's different, I guess. Fortunately, I have no problem in that regard.
Mary, hope you're getting through your work week ok. Maybe if enough people are unhappy and express their opinions, they will consider changing back at some point. I know, doesn't sound likely, but we can always hope, right? My first day at work went fine, although I have definitely forgotten some stuff. Some is coming back slowly, but some is just flat gone! I don't remember being this out of it last time I was out of work for a while. I found out yesterday that my Disability insurance will allow me to work part time for a while and they'll make up the difference - woohoo!! I was very surprised that they volunteered that, although they have been very good to work with. That definitely takes the pressure off me. I'm working half a day today, probably also tomorrow.
Had some sad news yesterday - a dear friend passed away suddenly. She was in her 70's, but as sharp and energetic as someone half her age. She lost a lot of weight last year and was diagnosed with kidney cancer, and after surgery was on oral chemo and doing well. She worked Monday, Tuesday morning was unresponsive and died Wednesday. She and I were going through the cancer thing together, so it's a real blow. I didn't get to say goodbye...really makes me think. You just never know - we should all keep our relationships in good repair, and be sure people know how we feel about them. This lady did...but I'm just feeling bad that I didn't get to say goodbye, I guess. I could have gone by Monday to see her, but was overwhelmed with the b ack to work issue and decided to wait till Friday. Damn.
Melia, are you home yet? How did the presentation go, and the talk with the social worker? Hope you can relax now that you have this trip over with.
Better get to work. Later, girls. Will try to remember chat tonight.
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Hi Nancy...I've heard a lot of very bad things about Effexor; one of my friends turned into a kind of zombie for a while and even lost her bladder control...are you taking it because you're on tamo? Why not have an oophectomy and take an AI like femara? I am taking Prozac and Femara with minimal SEs except for flashes and even those are tapering off. I feel just great too!!
Viddie..your new quarters sound romantic...down a hill and living by candlelight for a while...where are you?
Caya..I say, if you are comfortable the way you are now, why submit your body to more surgery.
Jan...I know what you mean, now that we're done, this crazy business of waiting for recurrence!!!??? I've been checking around the site and my attitude about this whole business has always been, OK, I'll get the lump out, go through treatment and do everything they tell me to do, and then I'm going to forget about it and get back to my life. Now I find out that being ER+ without being PR+ is very bad for recurrence, that along with my high oncotype score. I just don't even want to think about it....except....maybe a quickie double mast to be on the safe side...?
I think I may need to stay away from this site...
RobbinJaye, Joni...where are you?!!!
Mizzy
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Tina,
Tha J C Penney's email sounds like fun. I sent you a PM with my email. It sounds like you might be a bit busy the next few days so there's no rush, send when you get the time.
My husband's cousin sent me a cute video clip from Jenny-O Turkey this morning. If anyone wants to see it, just send me your email addy in a PM. It really was a rofl moment.
If I remember this evening I'll try to join in the chat.
See you later.
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I'll look for the PM, Deb!
Mel, sorry about your friend. 70 is way too young. I did my Herceptin today. 3 more to go: Nov. 29, Dec. 20 and one in Jan. I feel like everyone in there is 70+ lately. The older people look at me like what the heck are you doing here? Some can't help but ask if I'm waiting for someone or... I don't mind. Mel, excellent deal about the reduced work hours. Good for you!
Got my vein with one stick today! Wahoo! Still took from 9:30 to 1 pm to get through the infusion as the pharmacy was backed up.
Jan, the more thought I gave to your prosthesis sitch, I'd say to hell with it... I'm sure it's not hugely obvious under big jammies. Plus, put the shoe on the other foot. Would you care? Definitely not. Be comfortable and do what's best for you.
Viddie, not sure what the FORCE website is....will have to google it. Welcome "home".
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Hi Gals,
I'm finally out from under that deadline crush...emailed the final bits in at three minutes to five yesterday and didn't want to even look at my laptop again until today. I still have to deal with the editor's requests but that is much easier.
Debbie, I love your hair the new way. I think it is more flattering than your pre-chemo do, truly!
Viddie, welcome back to your main domicile. It must have been such a nice break for you in the cottage however. And on the gene test, I know I'd want to know if it were me but that's just how I am.
Melia, so did you get back ok? Your trip sounds like a marathon but one you handled well. Now you can relax all weekend, right?
Tina the chin length bob sounds darling for ds. I long for the day my hair is chin-length again, though I don't think I'll let it get longer than that.
Jan i fourth the wear a robe and let one hang recommendations. It's just how you are, if it were me I'd make a joke about it and lounge in comfort.
Nancy yes we are all with you. Does your oncology dept. have breast cancer specialty nurses that you can talk to? Mine has one on staff at all times, and they can recommend counselors, programs, etc. because I guarantee you are not the only one to feel this way.
Caya, I think it's great you still got the opinion from your PS, too bad she is moving. Sounds like you have so many factors to consider that it is really worth taking your time anyway. And yeah, your DS so deserves that position!
I wonder if chat will work tonight, it sounds like tech problems Tuesday night so maybe that is resolved. I will try to pop in and see.
BTW I did call the puppy breeder to see how Grendel is doing and they said he's walking and drinking a little water and eating bits of solid food so he is coming along. This weekend I am for sure going there with dh.
All those of you who are back to the office, tomorrow is TGIF and you made it! - Skye -
Hi all!!!
It's been a very busy week. I've been working at painting my living room and kitchen by myself and I've been working so it's been a slow go. It's taken all this time but everything is fresh and clean. And I did more retail therapy after the living room was done. I've a new area rug, chair, lamp and set of nesting tables being delivered next Thursday. Yeah.
Saturday night I went to a concert with a couple of friends. We saw Midori, the world class violinist. It was magical. I don't know how to describe the music but I sat near tears. That music managed to hit all the emotions of the last year. In two hours I experienced it all again through her music. What a gift.
I've been reading everyone's posts. I know I've already forgotten topics I wanted to respond to but I do know that Nancy's post resonated with me! I've not had any problem with the Effexor and have found it helpful for my hot flashes. But I do have this sense of waiting, waiting, waiting....it's a huge part of the reason I've decided to have the other mastectomy.
And Caya, I'm so sorry about the MD moving away. How frustrating when you've had this plan in mind all along.
Tuesday morning - 9AM central time. I've bought some temporary tattoos to decorate my breast. They're butterflies. Couldn't find anything else that I liked. The butterflies seem a little lame but hopefully it will bring a smile to the faces of the staff.
The t-shirt I ordered to wear home from the hospital has arrived. I ordered it very oversized so I can slide it on. It says "lost my boobs - not my sense of humor". I'll see if my daughters will take a picture of me with it on. Maybe with my doctor who is totally awesome.
Gotta go continue to put the house back together and put things away and pay a couple of bills. Sheez, maybe I can rest under the anesthesia.
On to the weekend!!!!
Woohooo!!! I'm going to see Tori Amos with my daughters. They want to see her and want me to go with them. I don't really know her music but how can I turn down my daughters if they want my company?
hugs to all the sisters here....I think about everyone often and hope that everyone is reaching forward and feeling better every day!
Cindy
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Jan, I agree with everyone else about your prosthesis…be comfortable. Remember that you will not be judged by how many breasts you have…it is what is UNDER them that counts! I am sure your friend will be fine with it. Cozy pajamas it is!
Tina hooray on the needle stick. I am sooooo sick of needles….I can only imagine what you herceptin gals feel like. That JC Penny email was absolutely hilarious. I sent it to DH, and he was mad at me because he WORE those things when he was a kid LOL
Skye I am so glad you are done with your book!
{{{Nancy}}}
I agree with Skye. I think it is time for the big guns. Your quality of life is really suffering and it is time to find your happiness again. I think it very likely you are not reacting well to the Effexor and anyway it does not appear to be doing what it is supposed to do. You need to have your meds adjusted….there are other meds that can be taken for hot flashes, and there are many great antidepressants out there. CALL YOUR DOC! You should not be feeling this miserable. Oh, and may I recommend frequent use of icepacks to help with the hot flashes? At the first sign, slap one on the back of your neck…I find that this keeps them short.
Viddie welcome home! And do not stress about the BRCA. I think that you have to do it for yourself, even if your daughter does not want to know…..particularly if you are feeling distressed about it. Remember that the internet tends to magnify things….BRCA is not as common as it would seem from reading things on the FORCE website. Do not catch Google-itis.
Caya ditto on the waiting. I think that you got a wonderful, honest opinion from that PS since she had nothing to gain with her recommendations. If you are comfortable, however, there is no need to rush into more surgery.
Mel I am glad that you did so well at work. Do not worry it will all come back. Sorry to hear about your friend.
Cindy I can not wait to see the result of your diligent decorating (hint hint). That concert sounds so wonderful. It is amazing how music can reach inside and touch you in such an individual way. I think butterflies work very well….you are transforming yourself after all! T shirt sounds hilarious. Oh, and Tori Amos is wonderful!
Whew…all that in responding to posts! I am going to stop there for now, and then post again later with what I have been up to….have to go work out now. I think that the Tamo is starting to affect my metabolism because a few pounds have creeped on. ARGH!
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Hi All,
Got home last night from a very tough business trip, way too much driving, too many appointments. At least it's over. I am going into work late today and leaving early. Just making an appearance and updating my boss on how it all went. Hopefully that's the last trip for a few months, and the last one ever with so many meetings crammed into so few days.
Nancy, Sweetie, please call your doctor. You should not be suffering like you are. I know that many of our families just want us to move on, and I also know that we are trying. But no one but those of us who have been through it know how traumatic it has been. And it isn't like an illness that goes away with no reminders. All we have to do is look in the mirror. I seem to remember that you have had more than your share of difficult experiences to deal with in the last few years. You need some relief. You deserve it. Please call your doctor.
Viddie, welcome home. Sounds like you had a good summer. Isn't it hard to believe that it is almost Thanksgiving?
I was able to see my son and one of my daughters on the trip, which was a treat. I also saw my father who, for the first time, did not recognize me. That was such a shock. I spoke with his idiot of a social worker, who wants to do a psychiatric workup. For those of you who don't remember, my dad was taken against his will by the County and put in a nursing home. This is a legal manuever called conservatorship. We fought but lost. We are now refiling the papers to gain conservatorship ourselves (my brother and I). So the social worker is "concerned" that he is depressed and deteriorating. I had to use all my restraint not to scream at him. Of course my father is depressed. He was yanked from his home of 20 years and slapped into a bed. He is paralyzed, deaf, nearly blind. He refuses to cooperate with the nursing staff; sort of his version of civil disobedience. I kind of admire that. It is a very sad, very frustrating situation. It will take months and lots of money to win this case, and by then, I think my dad will be gone.
Oh well, we all have our crosses to bear. And in between all the daily crisis, we have to deal with our recovery. And find joy in there somewhere. Whew.
Melia
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Melia, glad you are home. That is so dreadful about your father. There is something seriously wrong with a system that would encourage a situation like this....you should not have to go to court to win the right to have your father pass his final days in the care of his children. Of course he is depressed and deteriorating in a situation like that. I am raging for you right now.
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Just a quick check in - I'm having 12 people here for Shabbat dinner - both my DDs are in for the weekend and requested a homecooked meal - so I'm doing the whole deal - chicken soup with matzah balls, chicken, sweet and sour meatballs, bean salad, steamed veggies, couscous, steamed red potatoes, challah, wine etc. You get the picture. Gotta go...
I will look over the posts later. TGIF have a great weekend everyone.
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Caya you are making my mouth water, sounds wonderful! DH and I are going out tonight, somewhere. Being in Wisconsin and it being Friday, that means fish.
Cindy I love the symbolism of the butterflies flying away with your breast, and the gentleness they imply. I'm sure coming home to your newly decorated digs will also be a huge lift (no pun intended).
Melia, I can't even fathom that nightmare with your father. But you are so right that there is always some joy in between. It's there somewhere. Hope and pray things get sorted out right quick.
I had to see Dr. Clapper today for my post-rad checkup. He diligently checked over everything relating to the sore breastbone and told me he thinks it is not the bone that is inflamed but the cartilage. He put me on 600 mg ibuprofen (3 tablets) 3 x a day for 10 days to see if it can dampen the inflammation down to where my body can handle it. I am so glad to have something to try! Plus it is bound to make all the other aches and pains feel better. I do like that Dr. Clapper.
Hope everyone has a good weekend, I'll be taking and sending more Grendel pix. - Skye -
Skye, I'd have been taking at least that much ibuprofen already if I had been dealing with what you have been - did nobody suggest that to you before now?? I sure hope that helps you. I know a lot of people have inflamed cartilage after rads - somehow that doesn't sound as bad as inflamed bone, to me at least.
Caya, you must be a wonderful cook, because you seem to enjoy it. No wonder your girls come home wanting mom's home-cooked food. Hope you have a great weekend with them.
Melia, I don't understand this conservatorship at all - can you explain it to me/us? I've heard the word, but I don't understand the point. It certainly doesn't seem to have benefitted your poor father, or you and your brother. I'm sorry you're having to deal with this.
Hope you all have a good weekend.
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Hi Dear Ones,
Finished a marathon week at work, put in over 40 hours for the first time since last Nov. I'm pooped but feeling accomplished. I never thought I would be able to work those kind of hours again.
I have a Dr.'s appt. Wednesday for the effexor issue. and I "took the bull by the horns" and contacted the Y Me helpline to get my feelings in perspective. They also said it was normal feeling the way I do, but how to I make my family understand that? They just think I am nuts. Oh Bother!
Rebecca, that's how my DH felt when he saw those 70's clothes! He said it made him re- live his childhood Christmas'. He was scared! It was a nightmare to him. I am still laughing!
I plan to blow leaves this weekend, yippee! I wish I had the energy like Cindy to paint, I know once I got started it would be ok, I just can't take that first step. It's my kitchen that needs it and having that messed up for days is a scary thought! I am going to go back to my brother's in Atlanta for Thanksgiving, Laura and her boyfriend Andrew and Jeffrey of course will be coming too. I wanted my other daughter Kelly (who lives in Phoenix) and her hubby to fly in but she works retail and we all know the day after is a "don't even think of asking off day". She is an asst. mgr. at American Eagle.
What is everyone else planning for Thanksgiving? I don't even remember last years, I was numb from getting the BC news. Literally!
Oh yuck, had to help Laura with her rabbit this evening, he somehow broke off a nail and it was bleeding like crazy, I tried corn starch, cold water & pressure to get it to stop. She has had this rabbit for years...how in the heck long do they live? He is a really sweet bunny, but I thought they lived like hamsters, (in short term). He is definitely the "energizer" bunny. Geez. Course, We have a turtle at the office I work at that is 16 years old. I would of never thought a turtle could have a personality, but this one surely does. I have grown very attach to her. Isn't that crazy??? But I really like that turtle.
I have taken an ativan the last two nights and I have slept so good! Not once did I wake up hot flashing. But I know that is not the answer long term, but sure helps!
Everyone have a lovely fall weekend.
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Caya, can I come for leftovers???
Robbin, your hair is gorgeous!
Nancy, I am so glad you called your doctor!
Mel, conservatorship is a very scary thing. The govt can take control of you if they can prove to the judge that you are unable to handle your affairs. This even means that they can negate your right to vote, any dnr you may have in place, any decision making at all. I had an older brother who was brain damaged in a car accident years ago . My parents, and later, my younger brother, were his conservators. In this case, the county decided my dad was incapable of self care. My brother and I disagreed. The county took us to court, lost in the first round, won in the appeal. So they have control over my dad, including his finances. We were able to get his dnr reinstated, but now we are contesting the decision and are trying to get appointed consevators. We did not ask to be conservators originally since we felt he was competent and were sure the judge would rule in our favor. Oops, we were wrong. You can actually google it and scare yourself if you want. It is very disheartening and upsetting. One more issue in a year full of tough issues.
Ok, ladies, sweet dreams, and good weekend to all. I am going to do my best to sleep well and relax!
Melia
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Robin your hair looks great curly.
Viddie I am off for genetic councilling in Wed just my first interview and my onc says it will be the first of many as they go through a pretty intensive process . I had all my family history done a while ago and now am going to see if I can find out exactly what happened to my sister , what stage she was at , what her chemo regime was . If I do check out + it will be more for my family as I am menopausal any way .
Nancy good to hear that you are taking the bull by the horns and not getting yourself into real trouble . Family can be a b sometimes and maybe they are trying to forget themselves . It seems easier for them when they see that you are "looking" normal again . I have to remind mine sometimes that just because I am working does not mean I still will not get tired . And man do i , took Friday off work as i woke up dizzy , nauseated and weak . I spent the whole day in bed sleeping until 2pm . I figure I needed it .
Caya wow yes your dinners sound scrumpious .... yum yum enjoy your weekend .....
I am off today to the Royal Winter Fair in Toronto . I am a volunteer for the provincial OSPCA . I am helping at their booth with my youngest DD . The kids here have to have 40 hrs of sevice to graduate high school so we do this . I also before I got sick walked dogs and socialized them at the shelter . This fair is the biggest agricultural fair in Canada . Big horse show , lotsa animals and competitions . We are going to see alot today will be taking pics !
So I am off to get ready .....
Everone have a good weekend !
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