Anyone starting Chemo in Feb?
Comments
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Good morning all - hope you are enjoying your weekend.
Melanie - if you have internet access at the condo, hope you're having a great time and stayed dry yesterday! I'm sooo jealous!
Hillary - add me to the chemopause list. This is the one SE I'm truly enjoying! Had the last "one" right after A/C # 1, nothing since - so 2 1/2 months. I do have some night sweats, but they dont wake me. I notice them if I do have to get up in the middle of the night. If this is as bad as it gets, sign me up for changing the sheets more often! I'm really hoping that at my age the periods are gone for good!
I am starting to have a slight problem with the neurapthy. Particularly my hands. I over did it yesterday, and became overtired. That seemed to make it worse. It's barely noticiable today. hmmm...
Updated the bar reservations, shaping up to be a busy week.
Enjoy your day all!
Carynn
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Monday - Vegas
Tuesday - SammieKay (10th Taxol)
Wednesday - Karen (1st Taxol)
Thursday - Carynn (1st Taxol)
Friday -
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Belated Happy Birthday Terry!! Hope you had a good time. I have been struggling with 5 and 6 lb. weight flucuations. I actually came out of the hospital after surgery weighing 12 lbs more. It was fluid from IV's. But then when I started Taxol, I can gain 5 or 6 lbs between visits for chemo. It is very discouraging. But I keep telling myself when I start A/C I may drop back to my normal weight. My friend put it in perspective by saying she is so glad to see me looking healthy and not emaciated. My decadron puffy face caused my nail person to ask if I had had "work done" on my face. LOL. She asked if I had had botox. Guess that is the bright side of steroids, chubby face, fewer wrinkles. Keep your chin up. Remember we are all in this together. Hugs your way, Sammie Kay:)
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Alyson, hope you are feeling better. So sorry you had such a bad reaction. What a wonderful trip you have planned. How exciting. Will the trip be after your DD's wedding?
Vegas, I will let you know closer to Vegas trip. Would love to meet you in person. That will be after my 3rd A/C. I was concerned about being exposed to infection, with Vegas being such an international environment. But my onc said it was fine. I am not on DD, so maybe I won't be as immunosuppressed as the ones on DD.
I has a read bad case of shortness of breath on Thursday and my weight was up 6 lbs that night. I called the onc's office Fri. and they called me in some diurectics and potassium pills. I will have to take diurectics daily as my body is not handling the extra fluid. My question is what are they harming with chemo, my kidneys or my heart. Really scary, what damage chemo can do. I never had fluid problems before.
Hugs to all, Sammie Kay -
P.S. to my note to you, Vegas. My dh has to be in meetings during the day, but I am free. I always hang out in the room and read and rest or go down and donate to the slot machines. Will remind you when the time for a trip arrives and maybe we can meet f2f. Sammie Kay
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Hello All, I am reporting in for Theresa. Number 4 has been similar to what most of you have described....fatigue. Mild nausea and a slight dizziness has also been a factor. It doesn't seem to be as uncomfortable as number 3, but way more fatigued.
We are 66.6% complete....4 down, 2 to go. I noticed in an earlier post that suggested Theresa is on her last A/C. That is not correct. She is getting Taxotere, Adriamycin and Cytoxin in all 6 txs. The onc said when we are done....we are done. Looking forward to May 23, that's for sure.
I have also been reading with interest, the posts concerning SNB, sentinal node biopsy and the injections related to that procedure. Do a google on lymphosintigraphy. That has been the most interesting procedure I have witnessed during this whole BC experience. I was able to see it performed just minutes before my sweety went into surgery back in January. Made me wish I would have persued radiology and imaging when I had the chance 27 years ago.
Hang in there, everyone. Greetings hubbies.
Scott -
Fellow Cruisers,
No "last" chemo for me on Thursday. My onc. didn't want to take a chance with my shingles. They are drying, but I'd sure hate to irritate them any more than necessary. I'm kinda relieved, I haven't felt as well as I usually do 3 weeks after chemo.
I'm scheduled to go in Wednesday, and try again. I've finished my Valtrex, the nerve pain is alot less, and the lidocaine spray and hydrocortisone spray are helping the local pain....darvocet is my pain pill of choice and it along with advil work really well.
I've taken an new job. I'm an old ER RN, but can't work with patients because of my white blood count, so I've taken a job as 'trauma coordinator in the hosp. I'll still be working closely with the ER staff, just not the patients.
I'm lucky to have gotten it really, but it's a little stressful at first, especially since chemo didn't go as planned. It's hard to plan your life around cancer sometimes, isn't it??
Hugs to everybody, I'll get back to you guys on Wednesday...Send some prayers and hugs please...
Tracy -
Tracy, this must have been so painful, and, as you say, making planning around BC a challenge. Wishing you to get rid of these shingles soon and to get used to your new job without too much stress. Sending hugs to you, take care,
CatherineH -
Leah, I was so happy to read your good news a few days ago that I forgot to answer your sweet (suger free) offer about Ricola drops. I have a good supply right now (sent by my sister). I try not to use too much of those (although the mint ones are really refreshing) because of the sorbitol they contain which gives you belly aches...
Have a beautiful sunday.
Hugs,
Catherine -
Good morning all!
We are having a lovely nor'easter here. My ds is bummed because it was the first day of T-ball season (dh is coach!). Yesterday, however, was nice and I managed two short walks, thinking of Catherine the whole time!
Tracy -- Thanks for checking in. Sorry about your shingles and delay in treatment -- very frustrating! Great news about your new job, however!
Scott -- Sorry I goofed about Theresa's treatment schedule --blame it on chemobrain! Send good wishes to her from us!
SammieKay -- I hope that the diuretics do the trick. Make sure that your onc does a full blood test next time -- they can look at enzyme levels to see if you are having kidney problems.
We still need to here from Kim and StephJ -- are you OK?
So far, taxol SEs have been very manageable. I'm grateful to the relative lack of nausea, which means less pills to take and less SEs from those pills. The bone pain can be treated with tylenol or motrin, so that's good. The bone pain is funny. For those of you "older moms" with small kids or grandmoms, you will appreciate this -- my body feels like I've been sitting on the floor for hours playing with my son. I think walking is going to help, and I might try some gentle excercise class through our local Wellness Community. I'm being very cautious with my hands, avoiding hot water (no dish washing for me!). Some of my nails feel as if they are almost recovered from being slammed by a hammer, but again, its manageable!
How are the rest of the taxol/taxotere girls doing?
{{Hugs}} to all ...
-- Hillary -
Good morning!
Tracy - hope you recover soon. I'm glad to hear that it's becoming more manageable. Congrats on the new job!
Hillary - you and I have to stop this getting up at 3:00 in the morning business! DH has learned to go back to sleep now as he knows I'm not sick, just wide awake. The dog and cats are another matter! Thanks so much for the SE update. Again, we seem to be on the same page. What has started with me is a tingling on the bottom of my feet that I can ignore. My thumbs and forefingers have that slammed in the car door feeling, but I can ignore it for the most part. But I'm starting to get the tingling in my hands too. Did you have any of that before the Taxol? I will let you all know if the Taxol makes it worse. If it stays at this level, I'll manage fine.
Oh! I almost forgot! I dont know if any of you use Philosophy skin care / make up. It is wonderful stuff. All of their products are made for extremely sensitive skin and those that are sensitive to heavy fragrances. Their products have a light clean smell and are not heavy or sicky sweet. I received their news letter yesterday and they have a new product called Shower for the Cure. 100% of all the proceeds are donated to the Womens Cancer Research Fund. Im seriously thinking of buying several bottles and using them for birthday gifts for my girlfriends this year. If you want to check it out, you can read about it here: https://www.philosophy.com/web/store/pro..._-shower%20cure
Enjoy your Sunday's all. Talk to you later.
Carynn
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Carynn -- I was up at 6 am -- East Coast time. You're the one who gets up in the middle of the night! By the way, as the hours advance this morning, I can feel more stiffness in my body and hands. This taxol is making me feel like an old lady, and I'm only 49!
-- Hillary -
Ahh - Thanks Hillary. Can one have a blond moment if they are bald? Forgot that by showing my time in MST it shows everyone else in MST as well. Guess it just shows that I really am a natural blond.
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Theresa, my big day is also May 23rd!! Taxol #4 that day is the last of it for me since I am not doing radiation. Got a big circle on it in my calender. We can celebrate together.
Tracy, glad to hear the shingles are doing better and great news on your new job.
Sammie Kay, has the water retention been going on the whole taxol treatment? Hang in there, the easiest weight to lose is suppose to be water weight!
Hillary, well I was doing good at first with #1 taxol then Friday night I wore myself out with that dang survivor walk and yesterday was the pits. No energy, bone pain, and yesterday evening got up to get something to drink and about blacked out. Had to sit down on the floor and let it clear. Went straight to bed hoping to sleep off whatever that was. Feeling OK this morning. My hips ache and couldn't get comfortable with my legs last night.
About the periods. Started chemo on Feb 7, was expecting "on time" Feb 12 and never came. So completely in chemopause. My onc said I might get it back and might not. I wonder if that will change up the tamoxifen for me? Isn't that for premenapausal? Very confusing.
Carynn, when exactly to you sleep?? LOL
Vegas and Sammie Kay, I am jealous, I want to go to Vegas!! Somebody go put a chip on 23 at the blackjack table for me. That seems to be Theresa and my lucky number!
Love to all, talk to you soon.............Marsha -
Just sitting here beside the fireplace, the rain slapping the roof and skylights, and reading your posts. Sounds like a few of you are dealing with the Taxol SEs...I'm sorry to hear this but hope they remain manageable. Marsha, Hillary, others -- I keep telling myself that whatever SEs pop up, this too shall pass. I'm up 3 lbs this morning so I'm thinking, like you SammieKay, I'm starting to retain fluids...ack! My bones are okay - no aching, no sore fingers. I have a sore baby toe (which manifested pre-Taxotere) and that seems to have intensified since Thursday. My eyes are making me nuts...watery, stinging...my lashes are pretty sparse as are my eyebrows. I skipped two of the decadron tabs, one because I didn't get the prescription on time the day before Tx and the second because I figure I can do without too much in the way of steroids. My appetite is good I just don't want to gain a bunch of weight right now. One of the few good news items for me lately has been my weight and if that changes I feel like I'll go into a downward spiral. Terry, hope your birthday was a pleasant as can be. Vegas, thanks for the info. I'll email back later today. I don't feel like doing much of anything today. Carynn, I don't sleep very much either...I wish I had the energy though to be doing something productive, like work. Instead, I surf, write, chat...generally waste time. Actually, I find it therapeutic....mindless. Catherine, I'd go for a walk today but I might just get washed down the street.
Hugs all around. -
Ditto on the subject line Twink - beautiful weather in PA! I guess it beats the major nor'easter we were supposed to get tho!
Melanie - I sure hope you're enjoying your Nascar weekend. Not sure I'll watch today since Ward didn't get to try to qualify.
Karen & Carynn - I'm sure you're excited about your first Taxol - just one more thing off the checklist. I won't say it's a pleasure but it sure may be after the AC (and I didn't think that was all that bad except for the bout of the flu I picked up after AC#3.
Happy belated birthday Terry. My husband's bd was April 12th and I'm up April 19th. Heading to Quaker Steak and Lube in State College for dinner Friday night with some other April birthday'ers.
Tracy - sure hope you last chemo works out for you Wednesday. Good deal with the new assignment.
Leah - that is absolutely awesome news. I hope you're breathing easier now!..You may even be able to relax a bit during your tests Wednesday.
Linnie - where are you?
Catherine - was Denver spared a bit with the snow last week? I saw Colorado City and Monument got over a foot but it appeared Denver wasn't hit quite so hard.
Marsha - was wondering where you were. Thought maybe you started walking and never came home.
Hillary - Yea, I think I can agree with you on the 'sitting on the floor' thing. I think it was on the January discussion someone referred to it as 'cement legs'.
Vegas - Tx for the sizing info. I was wondering how I was going to establish precisely what size I wanted to be. I knew there had to be a 'technical' analysis tool for it - I like the Mardi Gras bead thing.
Update on my Taxol SEs - tx was Monday (the 9th) - Wednesday night - very, very mild leg bone aches (no drugs necessary). Thursday, Friday and Saturday, leg bone pain more pronounced but nothing beyond Motrin plus more Motrin and a sleep aid at night. Today's pretty good. The leg bone thing makes me think it may feel kinda like I would expect Restless Leg Syndrome to feel - it's not an excruciating pain but ya sure can't get comfortable. As with Twink, my eyes are burny and watery. No tingly fingers or toes, but the skin on the palms of my hands and fingertips feels like it's stretched to the max. It's not pain and really not even uncomfortable, just annoying, but they felt like that prior to the Taxol so it may be just a chemo or steroid SE in general. Otherwise, it's life as usual and I almost feel normal although still more tired than pre-chemo.
Hope you all enjoy your Sunday. Hugs to all!
Phyl -
Good morning everybody (9:45 am, Denver time)... stay dry out there, in the East...
Phyl: Denver was completely "missed" by the storm... a few flurries, no real hard freeze (I had covered everything I could for nothing), not even some needed rain... The weather people were very much on the defensive, since a lot of people had taken the day off for not being stuck in this expected foot of snow...:) It's going to be in the low 70's this afternoon...
Abraxane SE's: even if the method of administration is different and pre-meds not needed (no steroids, no benadryl), Abraxane is definetely a taxan (from ew trees, right?)... I am following exactly the same pattern as you Hillary, Marsha, Phyl: skin feeling tight (like old leather) in fingers, not as bas as "slammed in the door" finger pain, but definitely "nettle burning/tingling" (although much milder today). Bone pain has settled in (hips, lower back, mostly), uneasy legs at night (deep in the legs, like some blood circulation issue, but went away). No tingling in toes, but tender feet when I walk barefoot. I still slept fine with all this, not taking anything. Even though I get up at least 4 times to go to the bathroom since I drink so much, and from night sweats (chemopause here, too...:)), I manage to go back to sleep relatively fast. I hesitate to take too much advil, so I decided to wait to see how bad it will get (I feel it easier to "pace" yourself when you stay aware of the SE's... nothing unbearable so far. The nose SE's are better (less runny, less watery eyes, less puffy), but nose bleeding (light) from Avastine (the other tx I get with Abraxane).
We are expecting beautiful weather today again. Yesterday I raked the leaves protecting the few rose bushes (thick layer) and cleaned all the dead stuff from the roses (not much left, as it turns out) and from the lavender, and I found the exercise extremely tiring, although I was sitting on the ground, warming my back in the sun... I feel less energetic this time around, as if I did get Neulasta (but did not)... I have been walking everyday, though, and will go soon... I believe it helps me, but these SE's are different from AC's... Also, my tongue is really sore and my mouth is uncomfortable (do not taste much, but not the metallic taste post-AC, something different this time... go figure...).
I see that you mention Motrin a lot: dear nurses out there, could you tell me what the difference between Motrin and Advil??
Well, hoping the healing fairy will have taken the opportunity to ride the jetstream and go around swiftly to make your day pain free...
Hugs to all,
CatherineH -
Hi to all you Fabulous Feb. Chemo Cruisers,
It is a beautiful sunny Sunday here in So. Texas. I send sunny thoughts to all in areas of "wintery weather". It was extremely windy and cold yesterday, but today is great.
Tracy, Congrats on the new position. Hope it isn't too stressful. Sometimes new jobs are at first. I'm an "old Pacu RN"(17 years in PACU). I am working parttime, 2 days a week. Perfect for me, covers my insurance premiums with a little left over for fun money. I was scheduled to retire in Jan.'07 and then cancer struck in Oct.'06. I concur about life revolving around cancer. I must stay on until I am through with ca treatment because my hospital employee's insurance is primary. In a way it is a blessing. Getting up and going to work is good for my mental health and my spirit. From what I read here on this board, employers have been really supportive of our health issues. It is very heartwarming to get that support.
I need to go and get ready to go out to eat with friends. I will post more later. Hugs to all, Sammie Kay -
Hello All,
So I hear everyone talking about SNB. I am so glad that I had mine done the day of my surgery and my surgeon before hand explained to me the procedure and I was dreading the pain. Good thing for me the anesthesiolist was in the room when she was about to start and said that he was ready to start my IV an if she waited 5 minutes I would feel anything. Thank God for him.
Regarding the fingernail soreness, I too experienced it. I could hardly close my buttons it hurt so bad. I keep my nails short for this reason. On the fingernails of my thumbs around the cuticles I have dark streaks. Anyone know what this is from?
So I went for my 2nd Taxol Thursday and I was unable to recieve treatment. My liver enzymes were elevated so I have an appoitment on Monday for new lab work and hopefully Thursday I can reciev treatment. I was really upset that I am now a week behind. I was looking forward to having my last treatment on my wedding anniversary- May 10th. Now it will be hpefully May 17th. The pain in my legs has gotten better. I have taken Extra strength Tylenol. I figure with all the drugs in my system, I don't want to add anything more.
I'll update you all on what is going on.
Good Luck to all.
By the way is anyone doing the Avon Walk for breast cancer near their city?
Kim -
Hi all. Just checking in, finally. I had a couple of down weeks. You all are finishing up some of your tx, and I am so happy for you all. Moving on to taxol, and then soon to be done. Yay!! I had to stop visiting here for a while because I was feeling sorry for myself. I am supposed to be on my chemo and hercepting indefinitely. I have weekly visits to the bar and while, my chemo is pretty endurable, I feel crummy for 4 out of seven days. But not bad, I still work, walk and go to aerobics at least twice a week.
the weather got really cold here, colder than even Christmas week, in fact. And that brings me down. I just started thinking negative thoughts about how I will have to feel awful "forever".
I"m doing better now. Visiting here and reading your posts really helps me, even though soon, I will continue on my journey alone.
Thanks for reading and still thinking of me.
Oh, yeah, and I get this week "off". Yay! -
Tropicmom --
So good to finally hear from you, but sorry that you're feeling so blue. You know that your February sisters are here for you. We'll continue the journey with you and with Leah.
{{{{{HUGS}}}}}
-- Hillary -
Kim, Tropicmom, good to hear from you and to know you are still visiting this forum... Tropicmom, you won't continue your journey alone... we will continue to communicate, I hope, and there are other threads for support, as, I am sure, you know. I will go to the bar until December 11 for Avastine (every 3 weeks), others will move to rads, others will have their normal routine back,, but I think we'll keep in touch...
Keep coming back and let us know about how you're doing.
Hugs to both,
CatherineH -
Leah, I am a bit behind with the Easter stuff: a dear friend of mine dropped by last Sunday, with Easter goodies which I have "sampled" slowly all week... and today was the turn of the chocolate Easter bunny... and as I was munching at its ears first, I was thinking of you with a big silly smile on my face...
CatherineH -
OK, folks, new SE from taxol. I now have a rash on my face. It matches the 2 x 3 inch rash on my belly that appeared a few days ago and appears to be immune to cortisone. I'll phone doctor's office tomorrow.
I'm now also worried about another SE that I was ignoring -- racing heartbeat.
-- Hillary -
Monday - Vegas
Tuesday - SammieKay (10th Taxol)
Wednesday - Karen (1st Taxol)
Thursday - Carynn (1st Taxol)
Friday - -
Hi all just checking in before settling in to watch the Sopranos. (Quite the ritual at our house)
Marsha to answer your question, I dont much! Not since tx started anyway. I was always a great sleeper; at least 8, maybe 9 hours all the time. Since tx Im lucky if I get 6. I dont let myself nap during the week, or on Sundays in hopes of sleeping thru the night, Saturdays I try to catch up. Oh well, probably more info that you wanted. :P
Twink I mentioned on the triple neg board that I had a chance to peruse your blog today. It really looks good. BTW I love your hats!
Phyl I have the watery eyes too, but it seems to come in spurts, so its manageable. I quit wearing mascara tho.
Catherine raking leaves??!!! You are putting me to shame. Does it count that I did some housework today?
SammieKay are you far from DFW? It looked like a beautiful day at the track today in Fort Worth. It was 80 here and just beautiful!
Kim Im sorry to hear that you will be a week behind in tx. Its funny how we all have our dates and are counting them down. Bet we could all rattle them off without checking the calendar. BTW, I have streaks that just appeared this weekend on my thumbnails. I wasnt too surprised to see them as I guess its a pretty common SE with chemo.
Karen you will NOT be here alone. Look at the main index of the chemo forum. People who started threads two years ago are still posting and keeping in touch. I would imagine it is no longer a daily post, but the threads are still very active. As Hillary said, we will be here for you and Leah. You both are stuck with us.
Hillary Im so sorry to hear about the rash. I heard its pretty common. I think I read on another thread that there is something they can give you for it. Does it itch or anything? BTW please dont ignore the racing heartbeat. If it continues, call the Onc. Remember, they work for us, and always have someone there for us. It doesnt sound like something you should ignore.
Vegas thinking of you tomorrow. Be sure to check in and let us know how youre doing.
Good nite all!
Carynn -
Hillary, I will definetly check with doc about lab work for kidney function. Tonight I believe the shortness of breath is related to asthma. I used my inhaler and it is better. Now I have the back "heebeegeezies", that is what I call it when my back hurts and my legs feel like they have to move. Several people speak of taking tylenol and motrin. For some reason, the pain doc doesn't want me to take much tylenol. Something to do with it being hard on the liver. Along with the chemo etc.
BTW, someone ask about the difference between motrin and oops chemo brain. Can't remember the name of the other drug, but I do remember they were the same, both were ibuprofen. Stay warm with that nor'easter blowing.
Catherine, glad you missed the big snow. I am having the same back issues as I mentioned above. I am sitting with an ice pack on my back. Took my pain pills. Walking seems to make my back pain worse, but I need to do it for my peace of mind.
Marsha, do be careful. Don't want to add concussion to SE of Taxol LOL. Seriously, take care of yourself. Will remember the number 23 when in Las Vegas.
Twink, hang in there, as Marsha says the water weight will be easier to lose. Since I am not dense dose, I only get small dose of decadron the day of Taxol. LIke 2 milligrams. So I am thinking maybe it is the Taxol that is causing the weight gain.
You are all amazing. I share with you what someone told me, " don't be hard on yourself about not being productive, not having energy etc." Just give yourself some slack. We are all doing amazingly well. I hear from all of you, the things you do, work, walk, play with you children, take care of family, go to events and on and on.
All this while taking toxic chemicals into your body and fighting cancer. That is pretty awesome in my book. God bless all of you and be very, very kind to yourself. Love, Sammie Kay -
Carynn, I am quite a distance from DFW, about a 6 hour drive. The weather here was beautiful. Tomorrow we will return to the 15 to 25 mph winds. Couldn't sail today because no wind. Yesterday and tomorrow, too windy to sail. Oh well guess I will straighten my closet. I moved all summer clothes in and winter clothes out two weeks ago. I have been having to go back to the winter clothes closet and pull out warm things to wear. We set a record low here this am, I think it was 40 degrees. It was a record for this date. We get down in the teens some winters, but 40 for April was a record. Take care. You are an inspiration. Hugs to you, Sammie Kay
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Can you believe we are in the middle of a Nor'easter in Boston? It has rained over 4 inches, (would have been like 40 inches of snow) and the winds are fierce. I don't know how the runners are going to run in the Marathon.
Had a nice weekend for the first time in a long time. Went with DH Tom up to Burlington VT to see DD Lauren. It was cold and cloudy up there too- they actually got more snow yesterday. Winter seems not to want to give it up. I had put away winter clothes whe we had a spate of warm weather, but they are all dug out again. Even needed gloves on Saturday! Sheesh..Carynn, your description of 80 degrees makes me jealous. Obviously, vacation is just a memory!
Anyway, we were home for dinner on Sat, and then Sunday morning had company for pancake breakfast. My favorite brotherinlaw and sister in law. It was the most normal we have been in a long time. **Sigh**. I can handle this!
I started reading the radiation thread too. That seems to be next. Same range of "no SE" to "many SE"- still reflecting the differences in our bodies in treatment.
Thought you might want a report of 1 month after treatment and what is still/not happening:
-hair fuzz is growing! it is not white anymore- it is brown. I think the white was the roots from my old hair, but that seems to have been replaced by brown fuzz. It is sticking straight up and I love to rub it. Kind of prickly. Interestingly enough, it is not growing in uniformly. Seems to be more in the back, and the pieces framing the face seem to be growing differently than the top. Weird, but interesting.
-nail streaks are new, thumbs and index finger. Guess that keeps happening
-nose still dripping somewhat, though I seem to see cilia in the nose
-metabolism has totally changed. I am hungry a lot, but can only eat small amounts at a time. Back up to starting chemo weight (I had lost 5 lbs during AC). Oh well.
-vision still not totally right. feel eye strain after reading. Could my prescription have changed since September due to chemo?
-all other "systems"- bowels, etc. back to normal.
They are still monitoring me for RBC, and I had to get a procrit last week due to a 11.7 reading. Hopefully this week it will be 12 and I will be done with that.
Not sure if we ever talked about the fact that one of my main supporters is a guy who is also my boss/colleague. Well, 2 weeks after my diagnosis, he was diagnosed with pancreatic cancer, stage IV with 6 months to live (age 49). Well, he found some great doctors, and just finished a course of chemo with drugs that were just approved in the last year for that type of cancer. He will have a CT scan on Tuesday (no blood tumor markers for that cancer). I am so hopeful, yet so fearful for him. He has really been there for me, though he has basically taken off for the whole course of his treatment. But, as he says, we are in the club, and can talk to each other about things that no one else can really understand. So as we go through the restaging thing together this week, there seems to be a bittersweet layer on it all as I already got a sneak peak at my results, but he won't know anything until Tuesday afternoon. If you have any prayers left, could you add Jeff to the list?
Well out into 60 mph winds. Hope I (and my wig!) don't get blown away!
Have a great week all! -
Good morning!
We woke to 3" of snow (well, really slush) here in Southeastern PA. How are all my other PA girls doing?
Other news -- the hives on my face disappeared overnight and I haven't had any heart racing for 36 hours. I'm wondering whether these SEs were more psychosomatic or anxiety driven.
Leah -- My best wishes for your colleague! It's amazing some of the new drugs that are available now. Sounds like you had a great weekend! How come you have to work today -- I thought it was a MA holiday ...
Catherine -- We still have Easter candy left, mostly bags that I had bought to fill the plastic eggs. Every few days, my husband opens a bag, eats a bunch, and puts the rest in a bowl. I then munch and munch all day. This could explain why I've been putting on weight the last couple of weeks. Unlike some of you, I can't claim that it's water weight -- my onc doesn't have me on any extra decradron besides the premeds in the IV!
Sammiekay -- Motrin is ibuprofen. My onc nurse said that I could take up to 4 at a time for pain. So far, one or two is enough. I've been trying to limit them to nighttime, so that I don't toss and turn too much and disturb dh. He's been operating on all cylinders, working full-time, taking care of me, and doing most of child-care and house work. It's a little better now that I'm off AC-- I'm more available for playing with ds, who is very high energy.
Yet more fingernails feel like they are recovering from being slammed in a car door. My back, legs, and hips feel arthritic (or at least what I guess arthritic would feel like). But other than that, I'm actually feeling calm today. Monday's are my day to regroup, after chasing dh and ds out the door! I might actually tackle the mess on my desk!
Cheers to all, and a big hug for Vegas today!
-- Hillary -
Hillary, you could be describing me in the above. Other than the fingernail things (so far!) My 24 hour rash was on the left hand. My DH is also doing what you describe. I am so lucky, he has taken on everything in the household, working, shopping (doesn't want me in grocery or drug store LOL germs) and says he just wants me to concentrate on getting better and giving me the luxery of doing that. On my good weeks he would rather I be doing things I've always enjoyed in the past, you know, normal stuff! So I realize how very lucky I am and tell him and others just that every opportunity I have. Yesterday he dressed in a tux (tails no less) and helped our catering friend at Taste of Ocala which is 50+ local restaurants competing for the best awards. WOW Jim looked really hot and my friend won for Judges Best All Around! Great fun had and lots of tasty samples to try.
I find it very interesting how we are all falling into line with each other. From the very beginning we've all seemed to experience the same or similar SE at the same time. Sometimes I get a little panic attack when I think about what is being pumped into my body. Anybody else can't get that off their minds at times?
Leah, this is not a short term friendship! You will not be continuing on alone. As we all know, once you are affected by BC, you are for always. I for one would be disappointed to lose contact with all of you! So sorry about your friend, at least you have each other. My friends love me but will never understand what I am truly living with 24/7 now. And unless you have been there, you can't truly know.
Sammie Kay, yes, I agree with you, we have to give ourselves a break. Baby ourselves if you will. Who wouldn't be fatigued, achy, and all the rest with what we are going thru and having put in our fragile bodies? At first I wanted friends and family to think "Wow, she is so strong, she's handling this so well" and now, well hell, I'm tired, I ache and I'm just counting down! LOL
Thinking about everyone visiting the bar this week. Hugs all around.......Marsha
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