Anyone starting Chemo in August 07?

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  • nash
    nash Member Posts: 2,600
    edited July 2008

    One of the other bc girls in VA found an obit with Kim's picture. It's really nice to put a face with our Kimmie. She and I were a month apart in age, so I enjoyed seeing her in her senior high school photo, b/c it reminded me of my high school days.

    Rest in peace, Kimmie. Frown

  • Harley44
    Harley44 Member Posts: 5,446
    edited July 2008

    Nash, thanks for posting that obit. for Kim...  Now I am feeling so sad!  What a beautiful young woman!  Oh, I HATE this terrible disease, taking so many young women with so many people who love them and depend on them!  Oh, it just SUCKS!

    On another note, I didn't get the biopsy, because this gyn I saw yesterday was a total jerk!  He refused to even examine me!  He wants me to see a gyn onc, and just the idea of seeing yet another onc scares the HECK out of me!  I may not be able to get in to see him for months, and then what happens??  I don't want to think about that!  I am willing it to NOT be ca...  I can not even type that word!  

    But, I AM seeing my onc's P.A. tomorrow for my 6 month check up, so I'll discuss this with her.  Maybe my onc can get me in sooner.  I think I will just ask for a hysterectomy, because I don't want to keep these parts that have never worked properly anyway, and could turn against me in the future. 

    Harley 

  • katoMato
    katoMato Member Posts: 645
    edited July 2008

    Thanks, Nash.

    Pretty girl. Young mom. (sigh.) Ok everybody. Kiss family members today.

    Harley, there was a day i used to say - no, keep your own body parts...and there is an argument for that, true. But THESE DAYS i say TAKE 'EM OUT BEFORE THEY TAKE YOU OUT.

    Of course, taken to it's logical conclusion, with my new rational we'll all eventually be reduced to nothing but typing fingers with no bodies. Like "Thing" on the Addams Family.

    (and the problem with that would be.......?) 

  • DGHoff
    DGHoff Member Posts: 624
    edited July 2008

    Nash, Thanks so much for posting that obit with the picture. It somehow gives me a small feeling of peace to see what she looked like. I don't know why, but it does.

    June, so sorry about the fall. No fun! I hope nothing is broken.  Those freak accidents do pack a punch. A friend of mine broke his ankle last year at my 40th b-day party by taking his turn at the pinata, of all things. You just never know. One minute you are trying to get candy, and the next minute you are lying in the back of your friend's minivan being carted to the ER. Life is plain crazy. 

    But, I hope not terribly crazy for you, Harley. Let's hope your onc's PA can get this all sorted out for you. 

    Kaye, I tried some savory smoothies this week. I don't prefer them over the fruit ones, but I'm still tweaking the recipe to get it right. Any good recipes to share? I think I need a better blender.  

    Oh, and I think I'll hang on to all my body parts for awhile still. I kind of like them all! Actually, I had a follow-up with the plastic surgeon today and he pronounced himself "very happy" with the result. It is a darned good match size-wise. I'm pretty impressed myself. Now, I just need the nipple, and I'll be ready to go. 

    Oh, and one last thing... I'm going to color my hair tomorrow. Yes, yes, I know the gray looks nice, and I get lots of compliments, and "people pay lots of money to get this kind of look" blah, blah, blah. I figure I'll have the rest of my life to wear the gray. Why not have fun with it while it this short. I found a stylist who does all totally natural coloring - no ammonia and no other nasty chemicals. All botanical stuff. I'll let you know how it turns out!

    DeAnn 

  • katoMato
    katoMato Member Posts: 645
    edited July 2008

    ripe tomatoes,
    cucumber
    celery, with leaves included

    handful of chopped fresh parsley
    chopped fresh chives or green onion w/ green part
    fresh garlic, minced
    red wine vinegar
    olive oil (optional)
    freshly squeezed lemon or lime juice
    Salt and fresh ground pepper to taste
    Tabasco sauce to taste
    Worcestershire sauce (omit for vegetarian option)
    tomato juice (optional)

    And because i live in Avocado-Land i put half an avocado in it. One time I ended up with what tasted suspiciously like Guacamole...no fat, but so killer. And another time, i put some black olive tapenade (chopped black olives in olive oil...) and thought i'd literally gone to heaven. (Dh still hasn't stopped twitching...i made him taste it. He thought i was trying to poison him. So get a chip and pretend it's a dip, duh.) I don't do the olive oil much because i'm trying to cut WAY back on fat/oil in general.

    Can't give you amounts because i just throw things in there.

    (the last family gathering, stories of my culinary experiments were the entertainment. They mock what they do not understand. Pity the poor mortals.)

    The rest of the time i just start with a banana and go from there. Sometimes it ends up sweet, sometimes not. (and then there was the time the wooden spoon was clipped by the blades...well. That is another story, for braver souls than these.)

    All i know is that i've lost 5 pounds. I have decreed that i WILL look like something in that dress.Yell

  • katoMato
    katoMato Member Posts: 645
    edited July 2008
  • nash
    nash Member Posts: 2,600
    edited July 2008

    Well, I just may have to whip one of those up soon. Smile

    Today is Mi Muy Grande Fiesta, being held because of the Muy Mal Ano we all went through.  Wish you all could be here--I'll toast everyone with a margarita, with special thoughts towards Kim and Stacey. 

    Hope everyone has a good weekend.  

  • katoMato
    katoMato Member Posts: 645
    edited July 2008

    Nashie - you have a GREAT TIME for all of us.

    I hope the weather is good for you - it's icky here. (hot, humid - looks alot like August.)

    Wish I was there to toast the NEW year, and celebrate your BIRTHDAY with you!!! 

    Give my regards to...Kathy (? is that her name? i forget. I'm sorry!)

    Love to all - have a good weekend! 

  • nash
    nash Member Posts: 2,600
    edited July 2008

    Yes, her name is Kathy. Smile Good memory! It's humid here, too, but not as hot as the last time we had people over, so it's pretty pleasant.

    Off I go to chop up some limes..... 

  • DGHoff
    DGHoff Member Posts: 624
    edited July 2008

    Kaye - I never thought about putting worchestershire sauce in a smoothie, but what a great idea. Did you know Annie's makes a vegetarian version, by the way, that is quite good! I'm not a vegetarian, but  tend towards it (not tonight, however. We are having shrimp on the grill).

    Nash, have an awesome party! And may this be the start of a very good year for you! Welcome to 40! 

    Oh, by the way. I love my new colored-hair! She did an amazinginly subtle job, and it looks so much like my original hair color, that I feel like my old self (you know, minus the one boob and all). 

    DeAnn  

  • chemomom
    chemomom Member Posts: 171
    edited July 2008

    Hey girls.  I am in a bit of a funk...  A word to the wise... now is not the time to watch "The Bucket List."  It was a good movie but it has made me melancholy.  I am just a few days from my 1-year mark.  My mind is in a tumult.  So much going on in there.  Hope mixing in with fear, mixing in with I don't even know what  But it makes me cry.  It is warn here, so warm that my boys (3 and almost-6) are sleeping in their undies.  They fell asleep on the couch with my DH and I, while we finished watching our movie.  So I am crying at the end of the movie with this beautiful little boy on my lap.  A perfect specimen of a little boy.  I smile and love him all the while I am haunted by the fact that poor Kimmie went on with her life for 11 years and then was taken away.  My heart is breaking thinking of those kids crying for their mom.  Going to sleep knowing that mommy will never come back.  It is eating at me-- It could be any of us!  I am pissed and freaked.  I am angry at myself for watching this stupid movie.  i didn't realize the characters had cancer.  i thought it was just about 2 old guys.  But I watched this stupid movie and got my mind running in all directions.   thank you, thank you, thank you for being here.  I am so f-ing sick of people telling me to "keep thinking positive!" and "those thoughts should fade with time!"  It's freaking BS!  My mom tells me that crap and I smile and pretend it doesn't freakin piss me off when she does it.  No one knows but you.  This crap never really goes away.  We can move on and live our lives, but the next ache or pain, or feeling too tired, or watching the wrong stupid movie on a Saturday night, and it's all right back here.  Messing in our heads.  Ugh. 

    Ladies, I will try to get some sleep.  I am sure I will feel better in the morning.  nash-- I am hoping you are still up partying.  DeAnn- will we get a new pic with the new hair color??  Kato, Jackie, June,Tami & Lilith-- hi to all of you as well!!     I am so glad to have you all.  Hugs to everyone.  Angie

  • katoMato
    katoMato Member Posts: 645
    edited July 2008

    Oh Angie - {{{{hug}}}} I'm sorry...what a drag. (BTw: Thank you for the heads up re the movie. I'd heard it was "good", but "good" means a lot of different things to a lot of different people. I'm NOT watching a movie about cancer anytime soon. Period. And a warning to you too, for the record - don't see "The Family Jewel" either.) We don't need to think about that crap now. I may never watch a movie like that again if i can help it. I don't need it - I'm not watchin' it. It's comedies for me. I want to laugh so hard i snort soda through my nose. Period.

     One day at a time Angie. All anybody has (cancer or not) is one day, and we live them one at a time. We can be grateful for today. (It doesn't hurt as much as all the other emotions that run through my mind at any given time...& it actually feels kinda good.) So. We look at our kids, and we're grateful that we HAVE them. And we look at our DH's and we're grateful that we HAVE them. And we wake up in the morning, and we're grateful we DID. Then we go to bed at night and we're grateful we had THAT day. We'll worry about tomorrow, TOMORROW. And it will just have to stinkin' take care of itself.

    You're right. So far it hasn't "gone away"...it does ebb and flow, and I'm HOPING your mom is right about it fading in time...What's so unnerving is having some little thing happen, a minor thing - and bingo - it all comes back. It makes it so hard to live consistantly. It was my habit to live "thoughtless-ly" about the future - taking it for granted. No more. And being conscious of one's mortality is not a bad thing. It makes us THINK, and become wise.

    It's awful that Kimmie had to go. Her family can be grateful that she had ELEVEN years that she wouldn't have had, if she would have gone the first time. So if this is the start of my eleven, I'm going to be grateful for EVERY ONE OF THEM, starting TODAY. Even the miserable ones.

    And for starters, I'm so grateful for you girls...and you know exactly what i'm talking about. We could be doing this alone. THAT would be miserable. 

     I love you girls. Hang in there, Angie.

  • DGHoff
    DGHoff Member Posts: 624
    edited July 2008

    Boy, you said it, Kaye! We could be doing this alone and that really would be harsh! Angie, I hope that you will feel a little better once the actual one-year mark is past. It was much harder than I imagined it would be to face that "anniversary" but now that it is a few weeks behind me, I feel like I have just a little more distance.  I think about Kimmie being cancer-free for 11 years too, and I know there are many others like her who had thought it was behind them, and then bam! there it is back again, but with a vengeance.  Every ache and pain makes us wonder if "IT" is back. I felt a pang of recognition when you described looking down at your perfect little boy and what it might feel like to not be there for him.

    So, I'm really trying to stay in the present moment. It is not easy, but I cope by doing yoga, meditating, eating carefully and consciously, and writing songs.  I send  the gunk in my head out into the universe in a song so that I don't have to bottle it up inside.  Its also easier to tell people how you feel in a song format than in person. At least it is for me.  We're having a big party next week to celebrate being into a cancer-free year, but I'm going to sing some of my songs for the party-goers. They think I've been so care-free. Wait until they hear what was really going on in my head!

    DeAnn 

  • Monkeygirl61
    Monkeygirl61 Member Posts: 49
    edited July 2008

    Hello Everyone.  Well it was a beautiful weekend on the Eastern Shore of Maryland.  DH and I finally got to go out on the boat.  Only the 2nd time this summer (and we won't even talk about last summer. Sealed.  Anyway being on the water, enjoying the sunshine and feeling the breeze got me out of the funk I was in. Hey maybe there's a song in there DeAnn.  I know it's cliche but sometimes we really do need to "stop and smell the roses".  Chin up Angie, dear.  Kaye's right it does ebb and flow.  Nash I was partying with you in spirit.

    Okay, now for my dumb question.  When is one's anniversary? Is it the day of the surgery?

    I been trying to help my neighbor the last several days.  He was in an accident.  The lady ran straight through the red light. He hit her and she died.  He just got a few cuts and bruises.  The lady's son is one of the big wigs at work so that's kinda of how I got involved.  The son has been very gracious and compassionate to my neighbor.  It's going to take alot to get my neighbor through this.  Life can change in an instant.

    So I've been doing some reading on survivor's guilt for him and I think I had a touch of it myself after Kimmie's death.  Why Kimmie and Stacey and not me?  I don't have children.  Oops, enough of that...this was supposed to be a happy post.

    Thanks again for everyone here.  I wouldn't have made it through this without each and everyone of you.

    Hope you're felling better June.  

  • yellowtownhouse
    yellowtownhouse Member Posts: 142
    edited July 2008

    Hey all,

    DH and I have been talking about seeing The Bucket List since it first came out months ago.  Long story short we finally rented it about 3 weeks ago and settled into the den with lots of snacks to enjoy.  Well Angie, I lasted about 10 minutes and told my DH to enjoy himself but I was all done!  I really thought I would be okay with it and we so enjoy Nicholson and Freeman.  NOT SO!  Hubby refused to watch it either so it went back unseen.  It was the early dx and hospital scenes that got to me.  So, Miss Angie I think we're both pretty normal in our reactions.  It's just a little too soon and a little too close to home, right? 

    DeAnn, good for you for throwing an anniversary party....you go girl.  Wish we could all be there to celebrate with you and hear you sing.  Your songs reflect all of our feelings you know.  Let us know how it goes.  BTW, I can't wait to see a picture of the "new do." 

    Speaking of parties Nash...did you have a blast???? 

    My foot and ankle are doing much better thanks.  I did manage to get a tennis shoe on this morning after I put the compression anklet on.  First time in 5 days.....I was really sweating going to work in flip flops.  LOL

    Kaye, congrats on the weight loss......you are going to be smashing.

    Harley, anything new happening?  What happened with the PA? 

    Hugs to all,

    June

  • Harley44
    Harley44 Member Posts: 5,446
    edited July 2008

    Hi everyone,

    I had my appt. with my onc's P.A. on Friday.  It was my 6 month check up, and we discussed the trans vaginal u/s results.  She thinks it isn't anything to worry about, but said IF it were HER, she would se Dr. Gaejowski, and he is the gyn onc that I am going to see.  The appt. won't be til July 22nd.  I will insist that he do a hysterectomy, because I don't want to have a biopsy and then still need surgery.  Besides these parts have never worked right, and as Kaye said, I don't want to wait for them to turn on me.

    I'll let you know what happens, but I'm sure that next week's appt. will just be to talk about what to do next. 

    I was telling my DH that I can't take ONE more thing happening!  My nerves are just shot, I can't take anymore medical problems! 

    I just got back from an opthalmologist appt., to check for cataracts.  He was fishing for more money, because he asked me "why do you have TRICARE PRIME?"  I told him that it is the least expensive plan for me.  There is a STANDARD plan, but you have to pay deductibles and all kinds of things... in fact, my drs. can charge me for the difference between what my insurance pays and what they charge...  Then he ordered all sorts of tests, because he said "my optic nerve looks weird..."  I think I will go to an independent Opthalmologist and pay out of pocket for another opinion, but I am just too overwhelmed by all this!  I think I'll wait til March, when it will be time for my next eye exam.  Can you believe that a dr. would just order tests for more money?

    Well, it's time for dinner.  Thanks for asking how I'm doing.

    Take care everyone!  Sending HUGS to all!

    Harley

  • nash
    nash Member Posts: 2,600
    edited July 2008

    Hi, girls. Just checking in for a minute--the party was a blast. Wish you all could've been there.

  • nash
    nash Member Posts: 2,600
    edited July 2008
    Tami--I'm really sorry to hear about your neighbor's accident. You're right--life can change in an instant. Frown
  • nash
    nash Member Posts: 2,600
    edited July 2008

    It's just me again. Completely random post, but it's bothering me and had to share. I requested copies of my medial records from the onc's office to take with me to a new gyn office next week. I was reading through the onc's notes, and first off, almost every visit my BP and pulse rate were identical, which I find hard to imagine, but then she has things in her notes about results of examinations that never occured. For example, she says she palpatated my liver, etc, to check for enlargement, listened to my heart and lungs, thumped on my chest, checked for rashes, etc, at each visit. The reality is that she's never done any of those things, with the exception of listening to my heart once b/c I asked her to check a murmur that I have. WTH?

  • Monkeygirl61
    Monkeygirl61 Member Posts: 49
    edited July 2008

    Nash that is just so wrong.  My onc listened to the heart and lungs, checked my reflexes, checked my feet and legs, checked my port area at every visit.  I think I'd have to report substandard care.

    Hang in there Harley girl.  I'm thinking about you.  Thinking healing thoughts and I asked God to send an angel your way. 

  • DGHoff
    DGHoff Member Posts: 624
    edited July 2008

    Nash - That sounds very fishy. What, is she just filling in the blanks on the chart to make herself feel better?  I know you said there weren't many options around you in terms of oncologists, but man, there must be SOMEBODY that is better than her. Sheesh. Hopefully, you won't need to visit her much anymore.

    Glad to hear you had a good party though! I wish I could have been there!

    June, glad to hear the foot is better!

    Tami, I counted my anniversary as one year post day of diagnosis. I've kind of been marking off all the milestone though... one year from surgery, one year from the date of the "all clear" on my scans that revealed I was NOT stage 4 as feared. I just keep celebrating something every day!

    Harley, I can understand the feeling of just wanting to go ahead and remove stuff so as not to worry about it! I'm glad you have an appointment next week to talk to somebody who has been recommended.

    I just saw a cardiologist yesterday. As reported before, my last MUGA showed that I've dropped from 67% LVEF to 55% since starting chemo and herceptin. That's a pretty big drop so she sent me to the cardiologist to see what could be done. I don't have high blood pressure (which is basically what the beta-blocker drugs they have to help with this do is lower your blood pressure), and I don't seem to have any sign of damage, and the cardiologist said that the MUGA isn't the most reliable indicator. She did say, however, that she has seen the beta blocker drugs used as a preventative in some herceptin patients, so she wrote me a  scrip for a low dose and said I could try it to see if I can tolerate it.  I'll be going in on the 30th for an echocardiogram so we can get a better picture of the heart. I just don't know about taking more meds. But yet, I don't want to damage my heart either, but I don't really think I should stop Herceptin until I've done the full course which won't end until October. Sigh. Drugs suck. 

    DeAnn  

  • Harley44
    Harley44 Member Posts: 5,446
    edited July 2008

    Nash,

    That is just SO WRONG!  How can your dr. say that they did things that they didn't do?  Hope you can get them straightened out.  Yes, Tami is right.  That sounds like sub standard care.  My onc listens to my heart and lungs, the P.A. always feels my new breasts, and last week, she felt my abdomen/pelvic area too, because of my abnormal tv u/s.  I think that my onc only feels areas if I say that I have noticed something weird or pain, or whatever.  At least, I'm pretty sure that he would. 

    Thanks Tami for the healing thoughts and prayers.  I can feel that Angel by my side.  Next week, my dh will go with me to the gyn onc, but he won't go in when he examines me, and I'll just close my eyes and think of that Angel next to me. 

    DeAnn,

    What a dilemma, to have to take MORE drugs, just to protect your heart, while you are getting Herceptin.  It sucks that you won't be finished Herceptin til October!  I'll be thinking of you on the 30th, and praying that your pics of your heart show that it is in PERFECT health!!  I'll be seeing my ps one last time, for a photo shoot of his art work... if I'm not having that hysterectomy sooner, which I would prefer.  You know, I don't want more surgery, but I just can't see keeping these parts which never worked right anyway, and then having to worry that they will turn cancerous.  Now I am worried that I will have to get chemo again & radiation this time.  If I knew that just taking it out would be all that was necessary, I would be ok.  The latest development is that I am now bleeding, it is just spotting, but now I am getting scared again.  Seems every day there is a new development.

    Thanks everyone!  Sending hugs to all of you!  You have all given me so much support!

    HUGS
    Harley 

  • nash
    nash Member Posts: 2,600
    edited July 2008

    DeAnn, I hope the beta blocker helps and that the u/s doesn't show anything amiss.

    Harley, I hope all your stuff goes well with the gyn onc. You've got a lot going on right now--hugs to you.

    Yes, I think the time has come for me to accept the fact that I'm going to have to drive a distance to get to an onc who is competant. Up until now, the need to get my mom to her appointments and the fact that my kids got out of school at different times, leaving me with limited blocks of time available, kept me from switching my care to the university hospital here (it's a hour away without traffic). But now that my mom is gone and my kids will both be in school all day in the fall, I think I can cross proximity off my list of important features in an onc's office. The univerisity hospital isn't perfect, either, but I think I need to give it a try.  

  • katoMato
    katoMato Member Posts: 645
    edited July 2008

    Good Grief, Nash, that is insane.

    Last year your life was quite a bit more complicated, and you had your mom's appointments to consider driving to and from onc appointments for two... do you still feel another onc some distance away might be too far? I'm worried about you and wish i could trust that woman. (UCLA is in the top 3 or 5 IN THE NATION...City of Hope is 30th and i LOVE them there.  We're probably not supposed to name places, but oops.)

     DeAnn, the beta blockers they've tried me on are Atenolol and the other one was Propranolol (Inderal) They're used for regulating certain cardiac arrythmias, migraines and other things. Mine were prescribed for vasovagal fainting. They lower your blood pressure, and since my blood pressure was so low anyway, he had me check it every day. He told me if it got too low to eat some fast food french fries! (He was amused because he never gets to tell anyone that!) I took it through the surgeries so if i were to have a problem with anesthetic induced nausea my heart would keep pumping. I didn't notice a collateral side effect to speak of...maybe felt kinda draggy...but under circumstances at that time it could have been half a dozen other things. I eventually took myself off of them because like you, i didn't want to be on anything else. My blood pressure seems to be a little higher now (good thing) and all seems to be well. I don't think you need to fear them if you need them...Inderal (for one) has been around for 30 years and has been well studied.

    Harley, keep us posted on that new development. Try not to stress...I will be praying for you. 

  • katoMato
    katoMato Member Posts: 645
    edited July 2008

    Nash - we were posting at the same time! you beat me!

  • chemomom
    chemomom Member Posts: 171
    edited July 2008

    Hey all.  Today is my one year anniversary from my diagnosis.  SO I consider myself a 1-year survivor.  Tomorrow is my LAST Herceptin (at least I am pretty sure).  It's crazy to think of what a whirlwind I was in last year-- I got a cancer diagnosis and somehow, within 2 weeks I had found a reliable cancer center and had my first chemo. I was getting weepy up until today, but so far, today has been OK.  I occasionally think to myself that today is the day, and I feel myself tense up a bit and then, luckily it goes away.  I had a follow-up with my horrible Rad Onc on Monday and just driving there got me feeling physically ill.  Sitting in that office again made me terribly uncomfortable.  I HATE that place!!

    Nash-  I work in a hospital and help support our medical records computer systems (among other things). What happens here is that docs sometimes have their "typical" note format and our transcription people are supposed to edit a canned statement that matches what that doc likes in his or her reports.  I am wondering if whomever types their reports just always throws the typical header in and never takes out what isn't mentioned in the doctor's dictation.  Of course, in this day and age, it may not even be a person doing the report, it could even be just a computer program that spits out a report based on the doc's words and a generic template.  I think you should report it to the Medical Records department.  It could be a crappy transcriptionist, not necessarily the doc.  But then, I am sure the doc signed the report, so the onc isn't completely off the hook.  And... I'd be interested to see how they are charging your insurance company, since the time they spend with you and the evaluations they do are supposed to be the basis for the charge.  So they could be over-billing you to top it off.  So I'd report it, get an explanation, and probably still be on the market for a new onc.

    Harley- I wish you could get a break.  And I understand your wanting to have prophylactic surgery.  I was all set to have the whole lot of "girlie bits" removed if my BRCA tests came back positive.  But please be sure to think this thru.  You are still young-- for one thing, make sure you are positive you are done having kids.  And then consider whatever hormones someone would normally get after a hysterectomy.  Can you even have any?  My onc said nothing with hormones, just to be on the safe side.  I will keep you even closer in my thoughts and hope good things for you.

    Deann- I was thinking you had said you have had migraines before.  Was that you?  If so, beta- blockers are supposed to help those, as Kaye mentioned.  So that could be the bright side?

    And finally, thanks to everyone for bringing me back to earth after my tirade.  Kaye, when you said something about "If this is the start of my eleven" then I will be grateful for every one of them.  That was what I needed to hear.  Well put.  Thank you.

    Well... this is a long post and I am still AT WORK, so I will end here.  Love to all.  Angie

  • nash
    nash Member Posts: 2,600
    edited July 2008

    Angie--thanks for the input on the medical records--you're probably right--the report is some canned version someone or something spit out. Still disconcerting, though, as it is completely inaccurate. Also, on one of the first visits, they had my family history completely wrong--I'd caught that before and had the onc correct her notes, but the records are still wrong. It's just sloppy.

    And hugs to you on your diagnosis anniversary. I know my diagnosis anniversary day was really tough.

    This week is the anniversary of my surgery--I honestly can't remember the exact date; it's either the 17th or 19th.  Yesterday was exactly five months since my mom died, and today is my late father's birthday. So fun all around this week. On the other hand, my dd is testing for her brown belt in karate today, so that's kind of exciting. 

  • DGHoff
    DGHoff Member Posts: 624
    edited July 2008

    Hugs to you Angie on this anniversary day and to you Nash, too on this day of many memories.

    Thanks to everyone for the supportive comments on the beta-blockers. I actually don't get migraines, so no bonuses there.  The cardiologist did say if I felt light-headed while on them I could eat pretty much any salty thing I wanted which would raise my blood pressure.  So, free license to eat chips! Too bad I never eat chips anymore. Part of me wants to say, hey, you know what, I'm healthier now than I have ever been. I eat something like 13 servings a day of raw fruits and vegetables, I eat meat maybe once a week, I don't do dairy, I don't do sugar, I exercise every day, I don't use any chemicals. Why am I still doing this Herceptin thing anyway if it is toxic to my heart? But then I see the "statistics" that show that my odds of having heart problems are overshadowed by the odds on getting cancer again and that Herceptin is the "wonder" drug, and I'm right back in the chemo chair every three weeks.  I guess I'm doing it because I would probably kick myself if I didn't do everything I could to keep it from coming back. No easy answers I guess.  I just appreciate you all being here for me to vent to! 

    Hugs to all! Just an FYI that I may be in limited touch for a few days as we get ready for the big party on Saturday. I'll let you all know how it goes and try to get some good pictures! And then figure out how to share them!

    DeAnn 

  • nash
    nash Member Posts: 2,600
    edited July 2008

    Have a wonderful time with the party, DeAnn! Can't wait to see pictures!

  • Harley44
    Harley44 Member Posts: 5,446
    edited July 2008

    Thanks Nash, Kaye, and Angie

    I am trying not to stress out about this, but it's hard.  Now that I'm bleeding, a little, after I went for a slow run on Tuesday.  Stupid of me, to think I could try to help deal with this stress by exercising...

    Angie,

    I could never have children because at age 35, I was dx'd with premature ovarian failure.  So there is no sense keeping these defective parts, in my opinion.

    Take care, all.  I'll try to post next week, after my gyn onc appt... just the idea of ANOTHER onc scares me!   I don't mind having a hysterectomy, but I don't want to have to get chemo again or radiation... I just don't think I can do it again.

    Harley

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