Starting Chemo in June 2005
Comments
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I like the Blue Album too. But it can make me feel blue too.
Especially that coming on Christmas song. I get puddles in my eyes over that one.
I had my mammogram yesterday. I was a mess.
a real mess.
I came home and napped twice. I was exhausted and depressed and as I said earlier a mess.
Maybe it was body snatchers or something.
Today I seem to be back to my regular old self again. I will have to remember that these tests make me crazy both before during and after.
Luckily there was nobody around to witness my behavior. -
I meant to write to Jen.....
Hooray about the house and having this all work out so well for you. Hooray, hooray, hooray... -
Thanks, Ladies!!
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I have my six months post-chemo exams on Tuesday. I'm starting to be a mess, too. Strange, I don't even worry about a recurrance in my breast, I had mammos and MRI's in December and wasn't worried. I'm worried about mets, just can't stop thinking about it. Tuesday I have a chest x-ray, blood tests, visit with med. onc and with rad onc. A full day. Last week my shin hurt and I was sure I had bone mets until after a couple of days I remember I had banged it on the trailer hitch of my car while loading groceries. My, oh my! I'm going to drive myself totally bonkers with irrationality!
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Brenda, I was getting myself in a frenzy one day due to an on-going ache in the upper part of my spine. I did some searching on the recurrance thread and found a post from someone with bone mets who described the pain as "on a scale of 1-10, the pain was a 47" and it put my ache into perspective (but then I felt horrible for what that woman must be going through - I still think about her). At least I have a better idea of what bone met symptoms must be like and when to call the doctor.
I go for my 6-month check in two weeks, but I want to call the onc's office tomorrow and have them schedule an ultrasound for me. I keep feeling a lump in the breast that had the lumpectomy, but I was able to dismiss it for the most part. Then yesterday I asked my husband if he could feel anything weird in the breast, and he stopped right over the lump and said he could feel something. It's about the 12:00 position, and my original lump was about the 2:00 position, so I don't think it's scar tissue (oh, I just accidently typed "scare" instead of "scar," how ironic is that??) It's just scare tissue, don't let it bother you...LOL!!
I ordered the Lance Armstrong book "It's Not About the Bike" from Amazon.com and so far it has been very interesting. I never knew how bad his cancer was before. It is amazing he was able to overcome it (but having the money to fly around the country for second and third opinions helped, I'm sure.)
Jen, I hope you and your family get settled soon!! It will be nice for you to be reunited and sleeping under the same roof.
Jo, I'm glad your mammo came out OK. I remember when I had mine and the radiologist who diagnosed me walked through the door to explain the results. My first thought was "what are YOU doing here....it's gotta be bad news" but he was just happy to tell me in person that it looked good. WHEW!
Hey, you other Junie patoonies drop a line now and then, would ya? Let us know you are OK!! -
Nancy let us know what you find out about the lump. It could be a cyst. I got one because the scar tissue had created a pocket of some kind. So anyway.....it was a lump but it was an O.K. lump. The ultra sound showed that it had clear fluid in it.
I am thinking that is what you have.
Awful news today about Dana Reeves. That has rocked me to the core.
She was such a lovely lady and boy, did cancer take her fast?
I got the all clear yesterday. I got the results of my six month mammogram and my pap test.
So I had wine for supper.
I think those of us who are still writing were all diagnosed with later stages than those that have gotten on with their lives.
Do you think that is true or am I over generalizing?
As the anniversay of the diagnosis approaches I find myself needed a "hazard suit". A friend suggested it is like mourning death. The first year after you loose a loved one the anniversary's are so hard.
I thought that was a good analogy.
Each all clear helps enormously but we all know year two is a "land mine".
Don't cha think? -
Nancy hope everything turns out Ok for you.
Jo it is awful about Dana Reeves, she seemed so upbeat and positive.
Had my three month check with onco yesterday, least she become normal suddenly she asked me if I had had a mastestomy(sp).-that doesn't give me anymore confidence in her. And she declared my hair positively weird LOL LOL.
Jo I was a later stage too #2 per surgeon or #3 according to onco. going with surgeon, like her better. I have a mammogram at the end of the month. Not really worried about it yet. I feel good about things. But I do think about the day of my surgery. It is stamped in my brain like my children's birthday or my anniversary. I wonder how many years will pass before I go about that day and not remember it?
Thinking of all of you:)
Hugs
Bev -
Nancy...most likely it will be nothing, but of course you can't help but get scared. Sending good thoughts and prayers your way.
I think a lot of people just get too busy to post here any more, plus some people just want to put it all behind them. I like to check in now and then to see how everyone is doing. This was a place that was so helpful while dealing with treatment. I spend a bit of my free time on the internet so checking in here is just part of it.
I don't really think of my surgery day as the anniversary, but the day I was told I had cancer. Seems far away now and I am very glad to have the treatment phase over with. It was a rotten year...so it's time to start enjoying ourselves!
Liz -
Hi ladies, Thanks for your support! The rad onc said he thinks I have cellulitis in the breast, so I'm on Levoquin for 7 days. He also said this side effect should "settle down after 2 or 3 years," as this will probably happen a few more times. He didn't think the lump was anything to worry about, but if I can still feel it when I see the med onc on the 20th, I think I will insist on an ultrasound!
I was a wreck after hearing about Dana Reeve. I couldn't help think how life is so unfair sometimes. But they had one of her quotes on the news that I think was "life isn't fair, so you better quit expecting it to be." Wow, she was just the picture of grace, wasn't she?
Then yesterday I helped to evaluate this little guy who has autism, and his mom looks SO much like my ex-daughter-in-law. I felt so badly for this poor mom who has a very difficult child and a toddler to take care of. I guess I felt like I already knew her because of the resemblence, so I just wanted to hug her (but that's very unprofessional!!) Then I just felt so sad that my ex-DIL is not in my life anymore.
Today I have my yearly teaching eval...I better perk up...LOL
Sorry to have rambled. I do feel in many ways that I've moved on, yet this is still a place I can come when I'm feeling kind of rocky. (I was stage 2b, maybe you are right about those of us who still post?) Thanks for listening. I'm sure today will be a better day. I love you guys! -
Hey, everybody! I had med appts and tests all morning yesterday, and all is clear! I do have to go to the gyno later in the month for a pap, but that's routine, so, even though I'm worried, I'm not, ya kknow? And onc told me to go to my primary doc and schedule a colonoscopy since I've never had one. But all the tests were good.
Jo, you're probably right about stages in re who's still here. I was 3A, though my surgeon said 2B - right on the line. It's scary, isn't it?
BTW, while I wandering around in the cancer center, the onc's nurse saw me and hugged me. While I was in chemo, she was about a year out of chemo for ovarian (I think). She basically had the same treatment protocol as us. She has just cut off the rest of her curly "post-chemo" hair and now has her straight hair back. She was getting bloodwork done for a followup. She looks good! -
When I was diagnosed, I assumed I was at an early stage since my mammo/us six months earlier was normal. Not so...I had a very aggressive grade 3 cancer and am stage IIIC, borderline 4 according to my onc and stage 4 according to my primary...guess who I like better? Since I am NEDS now (HOORAY!!), all that means is that I am at a higher risk for reoccurence. Sure I worry about it sometimes, but not much...I figure someone has to fall on the good side of the percentages...why not me? Of course I freak out when anything strange is going on in my body...but I refuse to let this crappy disease take over my life. I am still not physically back to where I was before, but I'm a lot better each day and that's what counts. My doctor said my response to the chemo was amazing and I'm taking that as a good sign for a good future!
Liz -
I was diagnosed as a 2a. Whatever. All I know is that I had to have a part of my body cut off and my system flushed with something akin to pesticides. I'm not really afraid of a recurrence, but the thought is always there.
Once we get moved and settled I am going to have a prophylactic right mastectomy and reconstruction. Partly so I don't have the worry of more breast cancer - though it won't stop mets. But also I want the plastic surgeon to earn his money. If all he has to do is match my one remaining small and droopy boob, then he'll be done in a matter of minutes! lol. I want it to be worth the hassel!
I saw my gyn a couple weeks ago and my pap came back clear. I also saw my endocrinologist (swollen right thyroid with nodules) and he said that everything looked great. That one was really a relief because there's the risk of the nodules becoming cancerous. I had half of my thyroid removed when I was 23 (DANG! That seems like such a long time ago!) because they thought I had a malignancy. Thankfully it wasn't.
I see my onc tomorrow. And how funny is this? I'm really looking forward to seeing my lab techs. I loved them! They were so much fun. I'm a little sad that it may be the last time I see them since we'll be moving in June.
I, too, am glad that we all seem to be getting on with life. But you ladies have become so precious to my heart and I always want to know what's going on with each of you!
Jen -
i have not been on the boards for awhile, but decided to stop back in last week. i had mt second reconstruction surgery a week ago today. i can;t go into details because it is still hard to type. i'll post more next week when i'm more flexable, but wanted everyone to know that all went well and cross your fingers that the staph does not come back.
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Hey Scout!! I hope you are feeling better today, it's good to hear from you! I'll be praying for you that you never have to deal with the staph crap again.
Liz, Jen, and Brenda, I'm so glad that your appointments have all gone well!! YAY for normal results!!!!
I called my GYN yesterday to set up an appointment for my annual pap - she's taking a WAITING LIST for AUGUST and they won't even set the stupid appointment up! The receptionist said they will call me in July to make the actual appointment. I knew she gets booked up quickly, which is why I called in March for a June appointment. I usually see the nurse practitioner, but after bc I want to see the MD for everything. But August? Gee whiz. I think I'll see if I can find someone else.
I hope everyone is doing well. Have a great week! -
Nancy I know what you mean about getting everything checked out. I was skipping my Pap smear..going every other year, but this year called for my appointment before I got the reminder card! I see my onc again 3/20, but then will go on a 3 month schedule. Also have to go for mammo/us on my remaining breast every six months and I'm due for that in April. I have a follow up with the rad/onc in May...and I'm assuming that will be the last visit there. Because my cancer was very aggressive my onc wants to keep my port in for a while to be on the conservative side...so I have to get that flushed every six weeks. Finished PT therapy for lymphedema on Friday. I have a very mild case...hasn't gone to my arm...just in chest area. The massage and exercises are helping and it doesn't take that long to do it each day.
At least now there are long breaks between doctor's appointments and that feels like a vacation!
Scout...good to hear from you ... hope you post when you are feeling better.
Jen...I like staying in touch with all of you even though thankfully we are moving back towards more of a normal life. We've all had a tough year and it's good to hear good news from everyone!
Liz -
I'm just checking in. I went to a party for two friends who turned fifty last night. Lots of jokes aobut growing old. Needless to say they weren't really jokes to me.
I thought "I wonder if I am the only cancer survivor in this room". Kind of a lonely place to be. Then a friend came over and rubbed my back and I could tell "he got it" I don't think my face gave me away . I think he was just knew......
I continue to paint everyday and am loving the results. I've gotten so much better.
I can't wait to see what I do tomorrow.
At some point I have to photograph this stuff and put it on the web site. For now I am doing it just for me.
I took off my rubberband. I realized I wan't snapping it anymore. I don't know if it worked or not.
I'd say it helped.
That is something.
I don't think I ever said that I am stage 3a. That scares the heck out of me.
I know if my stage was lower I would be less anxious.
For now I am using drugs and wine at night. Otherwise I get really morbid. -
Jo...wonderful to hear you are enjoying painting again!
I could not discuss my stage anyone other than my husband and a few friends until recently. I don't think I've ever even told my children..didn't want to worry them. Now that I am "dancing with NED" it seems different. You will eventually become less anxious as time goes on. Glad you were able to get rid of the rubberband! Every stage of cancer is scary and subject to reoccurrence. I just don't dwell on the numbers, as it doesn't change a thing. Just remember Spring is just around the corner and you have a lot going for you...that's all most people have no matter what their situation is.
You are already getting better and that's what's important!
Liz -
Hi Girlies!
I read your posts often... I just lurk here sometimes though these days. I've been pretty busy with getting back to work and scrapbooking and stuff. I don't read anything else though... just not ready, ya know?
Last Monday, I had my first mammogram since being diagnosed last April. It was NORMAL! Woohoo! But I do have a pretty large lump of scar tissue right where my tumor was removed. It freaks me out daily, but I'm learning to ignore it a bit better! My breast was sore for about 5 days or so after the squishing I received... Wow! DOES THAT HURT! But, I'll keep doing it!
Anyhow, I'm happy to read that you all are doing well. It's a tough road we've traveled and we'll never be the same, but hopefully we'll all gain something positive from the experience.
My hair is growing ok... it's pretty curly and doesn't do what I want... so I still wear my wig. I'm not ready to give it up yet! Soon... I'll post some pics for you.
Hugs to you all! Be well!
Dana -
Another "lurker" checking in....I read the posts almost everyday and then can think of nothing really to say. I am very tired of wearing my wig but it is still too cold and my head gets cold...plus my hair is really ugly! Not that it was cute before but oh well....My hospital job is a stress right now and the gal who was going to take over my position at the college resigned last week so trying to balance those plus home is busy, but did go to state girls basketball tournament this weekend and enjoyed!!!And my grandchildren are moving back to Montana this month (happy to have them back but don't know that it is the best move for them)...Seems like since finishing chemo I over analyze everything and then get stressed....some times I think I spent so much time focusing on chemo and all that went with that that I now have to keep my brain racing about "stuff"....and then I ramble. Better go...
KimB -
HI everyone!
I realized when I started reading that it's been a month since I've been here. Life is really taking over again...but in a good way. At least it's not cancer taking over my life.
Things seem to be really moving along for folks. Folks are painting, houses are selling, folks are moving.
Nancy...are you ready for spring with all the snow SLC has had in March? I'm ready for a change of season....I guess it's so I can see the rebirth of nature. Just a self healing process.
I don't remember if I posted or not, but went to my PCM at the military hospital for yucky eyelids, he put me on Elidel (used for eczema) and proceeds to tell me that studies have shown that if it's ingested it could cause leukemia, so don't ingest it. I came home and immediately called my onc. He thought it would be ok. I didn't think it would work to begin with, but used if for 2 weeks just in case. It didn't work. Decided to use a steroid cream which the PCM told me was the next step, and it cleared it up.
I've been trying to get back into the routine of exercising. At least it's on my mind. I pulled a muscle in my back that set me back for about three weeks. I'm having a massage tomorrow to see if I get rid of the pain. I haven't been to the doctor because I know he'll put on muscle relaxers, and I figure I've spent enough time knocked out, that I'd rather try massage first. Hopefully it'll help. If not, I'll probably go into freak overload.
My hair is continuing to grow. My neighbor told me how thick it was starting to look. It's as straight as ever...and can't make up it's mind about being dark or gray. I LOVE the t-shirt that says I paid my oncologist a lot of money for this hair cut. I thought a better one was "My insurance didn't pay my oncologist enough money for this haircut!"
Oh, my big crisis is my 17 yo daughter has been having best friend and boy issues. I just wish I could understand why girls at that age feel like they are incomplete if they don't have a boyfriend. She spent the month of February grounded--no car, no cell phone. My husband spent his first month of terminal leave (he's retiring from the Air Force) having to haul her to and from school and work.
I don't think I posted, but he was hired by the company that gave him his first interview. We are in Utah to stay...at least for the next several years. What a joy to have good news in our lives.
Enough of this post. Keep your spirits up! -
This was a very social week. It was good to be out and about. Today I stayed home and got all my recent paintings photographed in preparation to enter some shows and post on my web site.
I still need my drugs at wine in the evening. I have a two week reprieve before three month blood tests again.
So it seems that there is room to breathe and then it is "here we go again".
The concept I am trying the hardest to work on now is to make nu7mber meaningless.
I have attached to much power to my stage of cancer, number of weeks between tests, weight on the scale , how many minutes I walk each day.
I have used number to find safety and control but the truth is I need to make number meaningless because it is and I need to learn to live comfortably in the "gray, fuzzy " areas.
MY daughter is home from college for the week and that is a total joy.
I like looking at here.
I am glad to hear others are moving on with their lives in positive ways.
I'm working on it, I'm working on it........ -
I started walking on the treadmill today. It's been 12 days since the surgery and I'm still "staph free"..yea! I was stupid enough to ask the PA (dr had emerg. surgery) if he has seen staph come back twice. His answer? "Oh yea".....shoot! I asked him if they go ahead and have reconstuction AGAIN, and he said yes. Why did I ask him this???
Anywho....no infection as of now. I'm still on 3 antibiotics because I found out I was a staph carrier (wish I had known) so I'm taking heavy duty antibiotics. Now I'm scared to go off of them!
I had some plastic "bandaids" sort of thingies...don't know what you call them, but they covered some stiches I had. I must be allergic to the tape because now I have what looks like poison ivy all around the stiches...ouch! I haven't called the office yet but I can't wear the "bra" they give you because it rubs too much on the rash. I did wear it while I was walking on the treadmill, but took it off after that. I'm just sitting around the house, so I don't think it should matter too much. I see the PS tomorrow and hopefully can get my drain out...it's such a pain! Last Friday the drain on my right side just fell out, so I only have one now. It's still draining 50mm so I'm going to pray that it slows down by tomorrow. It has to be 30 to 25 before they take it out. Bummer.
I went to an estate sale this weekend with my SIL and bought a really, really, cool potting hutch for $60! I am sooo excited! DH is going to put wheels on it so that I can just wheel it out of the garage and pot away!
I have some plants growing using the "winter sow" method, but wasn't able to keep up with all the warm weather we have been having, so it seems some died, I want to plant up the annuals next week which should give them plenty of time to grow.
It's good to hear that everyone is moving on. BC is such a beast that took over my life for way too long, and I'm still fighting to take it back..some days are better than others. -
Diana, Kim and Rebeccah...good to hear from you all!
Jo...sounds like you are doing it not just working on it! You just sound so much better in your posts lately..and that is great!
Scout...we all have good days and bad days. You've just had major surgery after all the other fun stuff of the past year and it sounds like you are going full speed ahead with your recovery.
Nice to keep this group going...you are all a wonderful bunch of ladies!
Liz -
Thanks Liz. I would like to feel like I am making some progress.
Scout......You are one tough cookie.
Treadmilling with the drain in....wow!
I hope this infection stays dormant and you can get on with the healing.
You have had enough complications.
I too am looking forward to gardening season.
I am going to find someone to do the heavy lifting so I can enjoy the easy parts.
It is snowing tonight so I don't think I have to get anything organized in the next few weeks.
In the meantime I have my indoor tulips and paperwhites blooming.
They make the house smell like the florists.
I like that. -
JoMac----you are doing great.....I read your posts and don't echo enough that I often feel like you....for sure good days and not so good days, but returning to your painting is such a joy....I can tell and just that makes me feel better...as far as gardening wow...I'm thinking that for a little while anyway we could keep a secret here--we'll do the fun stuff and have hubby or children do the weeding and heavy stuff! We were "planning" to low-maintenence our garden area, but with the grandkids being back at least "close" we are looking forward to our "Perfect Winnie the Pooh Garden" for Jozlynn and Tannin. Don't know if I told you that last year our garden produced doughnuts and Candy Bars one Sunday morning and I don't know who was more tickled Jozlynn or my husband. I'm excited just talking about it....and we are supposed to have snow tonight (here garden goes in in May and if we are LUCKY we have corn before the first hard freeze). Better go. KimB
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Dana - my daughter (11) and I are planning on starting scrapbooking once we get moved and settled. I've done a couple scrapbooks and it was fun. But I'm really excited to get to share this with Katie.
KimB - I'm very excited for you to have your grandkids nearby. What a blessing!!
Rebecca - Great news that you get to stay in Utah!
Jo - Can you give us your website addy again, please? I'd love to see photos of your paintings. I'm just so in awe of people who can make beautiful things like that.
Scout - Very glad to hear there's no infection. I'll keep up prayers for you. And I'm powerfully jealous about you going to an estate sale. I LOVE antique shopping and estate sales, but I haven't been to one in forever. I'm afraid I'll find something great that I'd love to have, but with our move just around the corner I think it might be silly to purchase something else. So I guess I'll wait until I get up to PA.
Things are still moving forward with the house. Yesterday we thought we were going to have to pay $800.00 to have some dormant fungus under the house sprayed and killed. My husband asked if I wanted to shell out the money or if we wanted to take our chances and have the buyer back out. It made me cry - and I'm not a cryer. I told him that $800.00 is nothing compared to the anxiety of trying to sell this house again. I honestly don't think I could take the stress. Which is really odd when you consider I handled the stress of dx and tx quite well. But I think it's more because I'm just about at the end of the rope I've been on for the last year and to have this sale fall through would pull it completely from my grasp.
We were to meet our parents for dinner last night and I told Todd to please, forget about the house for a little while so we could enjoy our dinner. He asked how I could forget about something like the fact we may have to pay a lot of money and I told him (with no small amount of righteous indignation) that I went through cancer and treatment and everything that goes with it. THIS IS FREAKIN' NOTHING! He just looked at me like everything all of a sudden made sense. He was such a pleasure at dinner. lol.
After the dinner we went to our daughter's talent show and she sang "The Voice of Truth" by Casting Crowns. I was in tears by the time she finished. It was beautiful. I don't know where she gets the talent or the gumption to be so calm in front of 200 people. But she was phenomenal. And yes, I do realize I may be a tad bit biased.
When we got home from the show the realtor called and said the buyer decided not to go through with the treatment. WHEW! So now it looks like there's nothing else to stand in the way of the sale. Of course, I won't breathe completely easy until the closing at the end of the month.
The kids' spring break is next week and on Saturday we're flying up to PA to spend the week with Todd. We're going house shopping, too!!! I haven't had any problems with lymphedema, but my onc prescribed me a compression sleeve for air travel. I really, really, REALLY hope I remember to take it out of the drawer and put it on before we leave Saturday. Oh. And I've been doing well on Weight Watchers - counting points and getting at least some exercise. But I'm not counting points when we're in PA. I mean, we're going to tour the Hershey factory, for cryin' out loud! Like I'm going to worry about points??? I don't think so. I'm just hoping that all the walking we'll do will counteract the overload in calories and that I'll break even by the time we get back.
As usual, my post is long-winded. Sorry. Here's to a great rest of the week for all of you!!
Jen -
I'm literally waiting for the paint to dry on a picture before I put on a second layer. So I decided to come check out the board.
Jenster.....Talk about saying the right words at the right time!
good for you.
I hope you have fun house hunting. I'll write in on Friday and remind you to put on the sleeve.
Kim Be....I have an idea for your garden of treats.
Once when I was little someone hung donuts from string on the trees outdoors.
We had to catch our own breakfasts in our mouths like young birds. It was so much fun!
I don't have anything new on my site yet. I took old slides into the photo shop to be put on a disc. The new stuff is still in the digital camera.
I already don't like my old stuff. It isn't brave enough.
Also there are many many florals.
I don't do floral's anymore.
Peonies have lost their hold on me. I like solid trees and landscape now.
I need the feeling of being "rooted" to the earth.
As the Tom Petty song goes....
" I won't back down". That is my theme song these days.
I'm not the pussycat I used to be.
I think my animal transformation is more like a mountain lion than a kitty these days. -
Thanks for the doughnut idea JoMac---will have to try it. I think maybe I was just lurking on the bottom of the sea for awhile because I so enjoy the posts this week!!! Such a transformation for all of us. Think most of you were like me...don't rock the boat and try to make everyone else's life as easy as possible, and now I don't have a problem telling anyone I think they are sweating the small stuff and need to realize that chemo and cancer are doable so don't bother me with things that are easy to deal with. I am probably walking a thin line a work (the hospital) but I really don't care--I know how to do my job, I know what's right and that is what I do. If you don't like it tell me straight up--and so far no one has. My son and daughter in law that are moving back are sure I am going to back down---I'm excited about having them back but don't think it is a good move (her father had a melanoma removed in August and they are coming back to run his business-BS but I told them that I am not going to contribute car insurance, rent, cash anything other than being there for them and the kids (okay I will babysit...)I will be 50 on Monday and a year ago was looking forward to being out of town but nobody has said anything except my brother and his wife were here from AZ 2 weeks ago and we went out to dinner but the kids will be here for the weekend and I just feel blessed!
KimB -
Kimbe I think we all are just feeling blessed after the year we've been through. And Jen I can related about your husband-My dh and I were relaxing on the couch(did I spell that right?) and he started rambling about things-things we can't even change, and asked me how I could just sit there and not worry about all this. I told after the year we've been through how COULD he worry about that kind of stuff. Afterall the sky is blue(Brenda don't tell me about the weather here in NE Ohio ) But what I was trying to tell him was don't sweat the small stuff.
It was to wonderful to read everyone's posts. I love the idea of the candy garden and doughnuts, I want to borrow it. I think even Sir Grumps-A-Lot will get a kick out of that.
Scout I hope you get that drain out soon I remember those
Jo my son was home last week, it was so nice. I think I can make it until he comes home for the summer. He did tell us this may be his last summer coming home. He is planning ahead and thinks he may study abroad or take summer courses in the future. I told him to get a real job this summer(works at BK when home).
Jen can I come to Hershey with you? Sound YUMMY. We have THREE different spring breaks this year so are planning a big trip for June as soon as everyone is out of school. I want to go to Disney and visit Jeff's folks for the weekend while there. Youngest ds wants to go to Hawaii and see volcancos LOL. Dh spoils the kids so we will see who wins this one. But I know Hawaii is out$$$ LOL.
It is a suuny day here I think I will go on a long walk. Maybe I'll find a doughnut garden or a pot of gold since it is almost St. Patty's Day That would help the volcanco dream come true.
Bev -
Bev, where are you in Ohio? My DS is at Xavier and this is his second year. He didn't come home for spring break. He wants to go to med school so he went to Seattle for a week. My sister is a doctor and he wanted to follow her around for a week. He got to observe in several op rooms (yuck!) and he thought that was cool.
DD came home for spring break but only for the weekend. She left for Chicago (to visit a friend) and will be back this weekend.....I guess I should be happy that she is here for 2 weekends. It's hard when the kids are away!
I got my drain out...yea! The dr wasn't going to take it out since it was still draining quite a bit, but since I didn't have any swelling, she took it out...what a relief! I've had sooo many drains since this is my 4th breast surgery! I feel so much better without it!
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- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
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- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
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- 7.4K Waiting for Test Results
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- 4 Survey, Interview and Participant Requests: Need your Help!
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- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
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- 7.9K Chemotherapy - Before, During, and After
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- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team