Starting Chemo in JAN 2007

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  • jonimb
    jonimb Member Posts: 900
    edited March 2007
    I'm so sorry that you are not feeling well, and especially on your birthday. I find that Gravol really helps on those really bad days, have you tried it? It also helps with sleeping. Another thing besides gingerale that helps my stomach is gingersnap cookies. My sister makes me a new batch each month. My #2 chemo made me sick for almost 2 weeks, and since I have been using the gravol I had a lot less bad days with #3 and #4.

    Try to enjoy part of the day....thinking of you...

    Hugs...Joni
  • Amera
    Amera Member Posts: 452
    edited March 2007
    Quote:

    Amera, don't tell me they gave you Zoloft *just* for a few days around in infusion?!!!




    Oh good gosh, I meant Zofran. Chemo brain has officially hit.
    Amera
  • NOLONGERREADINGORPOSTING
    NOLONGERREADINGORPOSTING Member Posts: 778
    edited March 2007
    Amera, try and just enjoy it...go into your fog and make it an excuse not to do anything you don't want to the next few days. Have a bubble bath. Think of it as a religious healing experience.

    Happy Birthday Lynn!!!! Sorry it's so gloomy. The next one will be better!!!
  • jonimb
    jonimb Member Posts: 900
    edited March 2007
    Hello all:

    I have an appt to meet with the radiation oncologist on April 2. It looks like now I will be done my chemo on April 16th...so that is good news. I had a long talk with my medical oncologist yesterday, and we went over all the test results from all of my scans & MRI's. I also have to have another MRI on May 1 to check those liver spots again..worry worry worry. I think I will adopt your slogan Mary, don't worry about things you have no control over.

    I also stopped by my office yesterday. It was really nice to see everyone, it's been 5 months since I have been in there, and 6 months tomorrow since I was diagnosed.

    We decided we are not going to Banff this weekend, we are going to start cleaning up the yard. My tulips are coming up, and so are my crocuses, so I'm pretty excited.

    Cindy, I'm glad you stuck around, and personally talked to your oncologist. I hope you feel better really soon, and with the lesser chemo for your next infusions, hopefully, you will feel much better.

    Amera, when do you start your radiation? Do you have to have radiation for sure?

    Mizsissy, your darn infections are taking way too long to heal up. I bet now that you are back exercising, and OFF chemo, your body will bounce back.

    Skye, that is so cute how you got your name, and kind of ironic!

    Hope everyone has a great day.....

    Hugs to all....

    Joni
  • meliaanne
    meliaanne Member Posts: 682
    edited March 2007
    Good Morning all,
    Lynn, I am sorry you are not feeling better ... baby yourself, and hopefully you will feel a bit better by tomorrow. Joni, I guess all we can do is not worry, but that's so much easier to say than to do! Glad your bulbs are coming up. Winter is depressing enough without fighting bc, so it's nice to see spring. Though living in San Diego, our weather is moderate all the time, pretty much.

    My final ac knocked me on my rear, have never felt so exhausted. My eyes burned from trying to keep them open, so I gave up early last night, went to bed, and slept nearly 12 hours. So of course I feel much better this morning. I am going to go to the library to find some nice, light books, and to the nursery for some seedlings for my window boxes. That will be the extent of my productivity for the entire weekend. My husband needs to spend the weekend getting our taxes ready for the accountant, so being lazy works for me.

    Stay strong everyone.

    Melia
  • Lynn12
    Lynn12 Member Posts: 1,008
    edited March 2007
    Thanks for all the birthay wishes! It's so cute that this site puts a little birthday cake next to your screen name. I've started a new puzzle and drinking my hot chocolate. The phone is ringing and ringing for birthday wishes and chemo 'are you ok'.

    Joni, I thought you didn't have to have radiation because your tumor was < 5cm. Was there something new that came up?

    Lynn
  • Amera
    Amera Member Posts: 452
    edited March 2007
    Happy birthday Lynn!

    This last AC has knocked me on my butt too. I am sooo tired and sooo just bleck. The yuck mouth has hit today too, and the steroid bloat. I can hardly button my jeans. I have a friend coming over in a minute. I hope I can stay awake. It's a play date for my girls and the mom is a really good friend but I'm not sure I have the energy to chit chat. It will be a nice diversion, hopefully.

    I'm not sure when I start radiation. I have an appt in a week or so to find out. I just hope I can avoid the exhaustion that I've heard comes along with it. I cannot imagine being this tired for 6 straight weeks. Maybe I'll get lucky though.

    Okay, off I go.
    Amera
  • Caya
    Caya Member Posts: 971
    edited March 2007
    Hello ladies,

    My cousin came over this afternoon and did a semi-manicure/pedicure on me today - no cutting of cuticles, just soaking, pushing the cuticles back, buffing and filing the nails, then polish - this was a great treat. We are very close ( our mothers are sisters ) and we both do not have sisters of our own, so our whole lives we have been very close ( she is 5 years younger than me).
    Tonight I am going out to a nice steak/seafood restaurant with some friends - this is a big deal for me because since the chemo started I haven't really gone out much, so I am looking forward to this. It's one of those places that has a couple of fireplaces, warm and cozy.
    Lynn - Happy Birthday, and many more. Hope you are feeling better this afternoon.
    You too Amera. Hope your day went okay.
    Mizsissy, glad you are enjoying your wig. A french braid sounds lovely.
    Skye - love the story about your name, sounds very "Hootery" - and like you said, how ironic.
    Joni - enjoy your crocuses and tulips. My dh reminded me that he already planted the lilac bushes last fall, so I should have lilacs in May - this will something to look forward to.
    Have a great day and evening everyone.
    Caya
  • jonimb
    jonimb Member Posts: 900
    edited March 2007
    Lynn, my tumour was 4.8 cm, so just under 5.0, also I did have 1 positive node, and my margins although they were clear were close, so my medical oncologist thinks that rads might be in order. I'm going to find out what percentage of benefit I will be able to get from them, to see whether or not I will agree. Does anyone have to do rads without positive nodes?

    Who in our group has to do radiation? MizSissy, did we keep track of that? I think we all agreed to stay on this board for all of our treatments, but I'm not sure of that either.

    I went out today, and bought some "yellow" shoes, then came home and we (Dan & I), cleaned up the whole front yard. Tomorrow we are going to tackle the back yard.

    Sitting back and watching golf and enjoying a nice cup of tea, with cookies.

    Hugs everyone...

    Joni
  • NOLONGERREADINGORPOSTING
    NOLONGERREADINGORPOSTING Member Posts: 778
    edited March 2007

    Joni, I'm doing rads...I think anybody who has a lumpectomy has to do rads. I had clear nodes. We can add Rads and dates to the list as people get scheduled. So, hey, you ladies with masts..here's something you DON'T have to do, no you don't have to drive 30 times to Radiation Oncology to get nuked!!!

  • Rebecca
    Rebecca Member Posts: 971
    edited March 2007
    Quote:

    Joni, I'm doing rads...I think anybody who has a lumpectomy has to do rads. I had clear nodes. We can add Rads and dates to the list as people get scheduled. So, hey, you ladies with masts..here's something you DON'T have to do, no you don't have to drive 30 times to Radiation Oncology to get nuked!!!




    Well, I had a Mastectomy, and my medical oncologist has sent me for a consult with a radiation oncologist because my margins were close. I may have to get nuked after all Keep your fingers crossed for me!
  • Lynn12
    Lynn12 Member Posts: 1,008
    edited March 2007
    Hi Miszissy,

    There are some of us with mastectomy that do need rads. Mostly women who have tumor over 5cm or 4+ positive nodes. I had a mastectomy and need rads becasue my tumor was 7.5cm. Also, I had a really close margin of 1mm. Looks like there are a few of us from the group.

    Lynn
  • mer1957
    mer1957 Member Posts: 534
    edited March 2007
    I am having a mastectomy on 4/27 and have rads starting about 3 weeks after that. I don't know if it's because it's ILC or Stage 3 but they say I definitely have to have (about 33 rads). It can't be as bad as chemo.

    This Celebrux seems to be helping with the Taxol leg pain more than Ibuprofen. I am taking it along with Tylenol. Day 1 of leg pain almost done ....
  • NOLONGERREADINGORPOSTING
    NOLONGERREADINGORPOSTING Member Posts: 778
    edited March 2007
    OK gals,

    Whew...sorry I spoke too soon about rads! Well, looks like I am going to get started soon. My first appointment with Radiology is a week from Monday. Geez, I'm not even over chemo yet or this infection and I've got to go through something else!!! Oy! It can't be as bad as chemo.

    In the meantime, I have to do taxes, clean up the yard, sew up a jacket for a design contest, and hopefully do what I enjoy most, do some plein air painting!!!

    Mizsissy
  • sharon56
    sharon56 Member Posts: 220
    edited March 2007
    good evening gals
    caya have a good nite out
    joni I have to get rads 33 have and appointment on May 11th for my ct scan and tatooing marks . then its 6 weeks 5 days a week of driving down to TO for me . We live about 60 kms away from the nearest radiation center . I have to pay for parking too which will cost about 70.00 a week . But I am going to use this a gauge for going back to work as it is the same route I used to take to work everyday just a little father down the "404" our local hwy . The only thing is traffic so I will be trying to get in the earliest I can . My plan is to drive my hub to work drop him off then onto rads . Soooo I should be done the beginning of July .......
    Lynn happy birthday ! I can feel for ya hang in there I too have really struggled with the nausea , if it wasn't coming out the top with Fec it's coming out the bottom with the Taxotere .
    Iowacindy i have 2 more Tax's to go too my last april 23rd . So far I am just darn TIRED ..... good one day like a slug the next as rebecca says .
    Ladies watch out for the sun .... use lots of sunscreen .... I was out on my deck yesterday with a hat on but must have had a little too much . My lips are swollen and my face a little red .
    Oh and I have a brillo head , can feel it ..... just can't see the hair yet ..... my eyelashes are GONE
    So how do you do your eyes with no eyelashes ?????
    We also booked our holidays today for the beginning of aug we are going camping at one of ontario's provincial parks for 2 weeks ..... we take our boat and truckcamper and set up and relax ...... Then in Sept my plans are to go back to work ....
    Feels good to have spring here .... tomorrow I am staying in the shade
  • MrsShakur
    MrsShakur Member Posts: 18
    edited March 2007
    A man I've never saw before came to me standing over my bed and said to me, it's time to take him home and I don't want you to be affraid you need to be strong for your mother because she's going to need you. At that time my
    father was in the hospital with kidney and live failure, yellow jondus as well. The phone rang early that morning about 6 and I was so affraid to answer it. When I did the person on the other end, ask me who I was to Albert Perry which was my father's name, I stated his daughter and he than said, this is Dr. Walker and I'm sorry to tell you that your father passed away early this morning at 5. Well I didn't put things together at that moment because I was shock. My mother was just coming in from a night out with my brother that has now passed on and I had to be the one to tell her, they was together for 20 years. She lost it and from that day forwarded she took a nose dive into depression, she tried to kill herself several times, drank more than I ever seen her drink. I had to hide medications and actually every chance I would get I would take her alcholol and pour it in the sink. I stayed by her side day and night, missing school, missing friends and I was only 14 this lasted for a few months until she met my stepfather. One day I was going through some old picture I have never seen before and I came across this old picture of a man in a grey brim hat and long dark coat. I said to myself, I seen this man before, and than realized it was the man that was standing over my bed wearing the same thing, the brim hat and long dark coat, the man that said it was time to take his son home and be strong because my mother was going to need me. I asked my mother who was the man in the picture, she said that is your grandfather, your father's dad she said you have never met him because he passed away before you was born. I asked her have I ever seen this picture before she said no, because she just received it from my grandmother, my father's mother which at that time was still alive. I was blown away by it all.

    Goes to show you that the dead do communicate with us, in one form or another at least that's what I believe.

    Chey
  • IowaCindy
    IowaCindy Member Posts: 341
    edited March 2007
    Hope it was a very lovely Spring day!

    Cindy
  • IowaCindy
    IowaCindy Member Posts: 341
    edited March 2007
    Yep, your story gave me goose bumps.

    I believe also believe that the dead have a way of communicating.

    It was a habit for my mom to flick her porch light at us as we would leave her house, a kind of final farewell. The morning she died at home, we all sat with her and waited to leave her home until the funeral home had removed her body. As the hearse pulled away from her drive, all the lights in her house flickered three times. Once for each of us kids??? We always thought so.

    Cindy
  • viddie
    viddie Member Posts: 547
    edited March 2007
    Mrs. Shey,
    Wow, that is quite an eerie story. A few of my friends have told me stories of their departed mothers or fathers coming to them in their sleep, so I am a believer.
    The night my father died 23 years ago, and they were taking him out of the house, I was holding my 3 year old son in the next room with the door closed. We were looking out the window. It was night and my son waved out the window and said goodbye to Grandpa. He did not know that my father had just died. I will never forget that.

    Happy Birthday Lynn,
    I hope you feel better tomorrow.

    Amera,
    All done now with chemo! Congrats! I hope you feel better tomorrow.

    Robertin,
    It sounds like you are having a great time in Utah!

    Rebecca and Caya,
    I also usually have the Seder at my house. This year my sister will have it. I asked her to have it on Tuesday because my last A/C will be on the Thursday before and Monday will be more difficult. Hopefully I will feel alright enough to go. I intend to go. I will definitely take my ativan and whatever else I need to take to get me through the night. All that food though-----I love it all, but eating it all might mean trouble the next day- another challenge!

    Caya,
    I will also be starting herceptin in the end of April. Luckily they have it for us. A few of us on this board will be getting herceptin and taxol, so we can compare notes.

    There are so many posts to read and enjoy when you are away for a few days,, I forgot who asked about stomach reliefs. My doctor put me on Omeprazole (protonix) 2 weeks ago and it seems to be working. I will see how I feel after my next A/C on Thrusday. Previously I mentioned that my PCP gave me a rx for Librax which is supposed to relax both my stomach and me. I have not taken it yet b/c I want to ask my onc about it first.

    We just got back Maine. We had a wonderful time. Friday's weather was spectacular! It was sunny and it felt like it was in the 70's. We sat out on our private deck in our B & B and read and relaxed. We also did a lot of walking and enjoying the scenery. I totally enjoyed our time away and am looking forward to another mini time away before I start my taxol & herceptin.

    Have a nice night everyone,
    Viddie
  • IowaCindy
    IowaCindy Member Posts: 341
    edited March 2007
    I had an appointment with the surgeon on Monday, October 30th to get the results of my excisional biopsy from the week before. I woke that morning at 4 AM to empty my bladder and when I went back to sleep I had the dream.

    There was a gorilla sitting in the comfy chair in my living room. Very quiet, just sitting. I loaded it into my car (it was very cooperative) and drove it somewhere out in the country and released it to the wild.

    When I drove home and walked back in the house, there was the gorilla sitting in my comfy chair again.

    I woke right up and knew that although the lump had been removed, it was cancer. After the surgeon told me "Cindy, you were right to be concerned about that lump, it was cancer." I told her about my dream. She told me I was the first gorilla dream she'd heard but she's had more patients share some kind of fore-warning dream about their cancer.

    Cindy
  • IowaCindy
    IowaCindy Member Posts: 341
    edited March 2007
    several years ago. I was there for a folk music festival at the university. I loved the hills. My friend and I went to Grandfather Hill (I think that was the name) and looked out over the convergence of the three rivers. I thought it was beautiful. I even briefly considered moving there I like it so much. I've just stayed in Iowa though.

    Cindy
  • jonimb
    jonimb Member Posts: 900
    edited March 2007
    Hello all:

    I too had a mastectomy, but I may have to do rads. I will find out after my appt on April 2. Rebecca, I'm the same as you...close margins, and I did have 1 positive node, although, there is not a significant difference in prognosis for anything under 3 nodes.

    For all that had mastectomies...does anyone have a divot. It seems like the closer to my sternum, I have a divot, maybe because they had to go so close to the chest muscle...then under my armpit, I have a bit of a pointed flap? Also, after chemo..usually around Day 5, I actually hurt along my mastectomy scar...anyone else? I got my oncologist to check everything out again on Friday, and he says I have healed well, and that everything looks good.

    Those dreams you guys have had really make a person think, and I truly believe they are trying to help each of you, or tell each of you something.

    Shorti....keep all your receipts...we can't claim the interest on our mortgages in Canada, but we can CLAIM mileage (anything over 40 kms), and we can claim all parking costs. Keep your receipts. I know in Calgary, you can buy a pass for the week.

    Up late watching the curling from Japan. Hope all are well.


    Cheers...Joni
  • horsegal
    horsegal Member Posts: 103
    edited March 2007
    Hello Jan group! I am actually from the Feb chemo group, but have been reading your thread. I started chemo 4 tx AC on Feb 6th - so found much info on your thread and have totally enjoyed and learned from all of you!

    I will be finishing my AC on Apr 9th - and then on to rads. I meet with my rad. onc this Monday, so will see when I will officially start and what's next I guess.

    I would like to keep up with all of you, so thought I would introduce myself! I was dx in Dec '06; lumpectomy Jan. 07. 1.0c tumor, right breast, IDC with one Sentinel Node micromets (opted NOT to do the axillary dissection).

    I live in Ohio, have a son in Iraq - and a 6th grade daughter at home.

    I honestly have to say, that without these boards, I don't think I would be able to handle all this as well! Everyone here and on Feb boards has been sooo helpful getting each and everyone of us thru!!

    Jen
  • Amera
    Amera Member Posts: 452
    edited March 2007
    Good morning gals and welcome Jen. I'm just going to throw this one out although it's probably old news. I have been absolutely *forcing* myself to get liquids in, which as we all know, is pretty tough after the swamp mouth comes around. I have gotten those add ins that you get for water bottles--I think someone mentioned Weight Watchers or Crystal Light. I swear, they have worked miracles. I am not constipated at all like all the other times. I feel sooo much better. I just cannot stand plain water or anything out of a can. Why didn't I listen to you all sooner?

    Okay, for the question: What have you all been told about your risks for lymphedema? I don't think we'ver ever mentioned it on this board. I posted a question on the lymp. board and was directed to a very helpful website but frankly, it scared the heck outa me. I had a snb but because so many nodes were removed (9!), I feel that this puts me at bigger risk and was essentially a dissection. My onc agrees but my surgeon said I'm cleared for everything, even blood work on that side.

    I originally asked because I want to schedual a massage but am worried that I need to ask them to avoid that arm. Turns out, I need them to avoid the entire side.

    The nurse at DF told me they used to think women were at risk for life. They then changed it to 15, then 10, now 5 years out for risk. It's all so confusing. What can you tell me?

    Thanks,
    Amera
  • mer1957
    mer1957 Member Posts: 534
    edited March 2007

    Welcome aboard Jen, I agree these boards are a God-send. I finished my AC and my last Taxol is 4/5 then surgery then rads, so I'm not far behind you.

  • Dar1
    Dar1 Member Posts: 146
    edited March 2007
    Hi all - sounds like most are feeling well this weekend! I'm feeling good. My energy is not quite there, but I bought a step-counter on Friday and logged 10,600 steps yesterday! No wonder I was tired last night.
    Canadian girls, you can claim a mileage amount for travel - you don't need to claim by receipt. The amount per km is varies by province. You can also claim meals without a receipt (if memory serves) - parking needs a receipt. Last year I was immersed in this stuff - I'm trying to get my brain cells working again! Also, either spouse can claim the expenses - it's better for the one with the lower income to claim them. Please feel free to pm me if you want - if you have specific concerns.
    Amera, I have lots of questions about lymphedema as well. My sister has had primary lymphedema in both feet for about 15 years now. She did nothing to treat it early on - didn't know what it was. She wears compression stockings most of the time now, but her feet are permanently swollen - look like little sausages. Makes me feel sad - and scared. I don't want an arm like that! I thought that light massage was OK on the effected arm. I'm going to ask the oncologist for a referral to a specialist when I go this week. I used to do weight lifting, but I'm scared to start that without guidelines. And you read and hear such conflicting information.
    Hope everyone has a good day.
  • horsegal
    horsegal Member Posts: 103
    edited March 2007
    Amera -
    I had only one Sentinel node removed, and my surgeon says he rarely has a patient with major lymphedema issues with the full axillary dissection. My onc nurses will not touch my right arm/hand however. Not for blood pressure or needle sticks - like I said, even with only one node removed.

    I talked to a "survivor" who uses acupuncture to deal with both the fatique and the lymphedema and she swears by it - she plays tennis! I will be checking into the woman she goes to before I start rads for the same purpose. Better to be preventive than reactive she said!

    Jen
  • sharon56
    sharon56 Member Posts: 220
    edited March 2007
    Amera I had 16 lymph nodes removed and 8 of them were cancerous one being 4 cm big . I am at high risk of lymphedema . But I have not had issues yet with it,of course I cannot have my blood drawn or any blood pressure done on my left side . I have exercised my left side my arm has full motion there is a spot that I cannot feel but it does not bother me . I do believe that we are not supposed to go into hot tubs etc . It may or may not affect us , I am not worrying about it right now i just remind the nurses to stay away from my left side . One other reason i have a port .
    welcome jen
    Yep I am going to claim my medical expenses on my taxes next year gas , parking and all. Could not get it this year as I worked most of the year and made too much $$$ , but being on unemployment benefits and long term disability this year will help with my 2007 taxes .
    As for dreams yep lots of em ..... the drugs we get help with the Technicolor
    I think we all believe in higher powers here and the existence of our angels and spirit guides . There is alot of research being done right now with cancer and new age healing . Me my dad is my traveling guide he used to be a traveling salesman and passed away when I was 19 , I can feel him beside me when i am driving .
    I meditate and visualize my body healing itself at night , having all those nasties getting eaten up by the dope and my body returning to "normal" . Pretty sure I posted a bit back a Link to this Dr website http://www.healingjourney.ca/main.htm
    The power of the mind and spirit for anyone ..... me i am a nature nut so my connections are like my sign Virgo earth related ....
    This stuff is real and it helps us to heal yes our loved ones are here ..... angels are watching us I have a "willow" angel beside me on my bedside table her arms outstretched
    Keep the faith ladies ... everyday is a new day ... we are going through or spring rebirth here
    whoooo whoop .... the blue jays are back in the trees , daffodils are appearing ...
    There is a reason we are all winter chemo girls beat this @#$%^ BC
  • jonimb
    jonimb Member Posts: 900
    edited March 2007
    Good Morning all:

    Amera, I had 16 nodes removed, 1 positive for cancer. Do NOT let them give you any needles (especially IV's on the side you had lymph nodes removed). My surgeon, and my onc both said to make sure you protect that arm. Also, be careful when having manicures, as you will not heal as quickly on that side. You should always have your blood pressure done on the opposite side also. Lymphedema can come up quite a bit later after your operation, according to my docs. You should be diligent to watch for it.

    With the weather warming up, I want to get out to the golf driving range, so what my doc recommended, was take a tape measure and measure, by your shoulder, by your elbow and by your wrist. After you are back from golfing wait a few hours and measure...this will tell you if the strain was too much. Also, with flying you should purchase a compression sleeve, as the pressure can cause swelling even if you never had it before.

    Most surgeons nowadays are pretty good, and protective of hitting or cutting the nerves in your axilla that would cause this. It should also be noted in your post operative report, as the surgeon will make specific note of them. They usually say something like, "the intercostal brachial nerve and the long thoracic and thoracordorsal nerves were visualized and protected. These are the ones that in the old days if a surgeon didn't watch he could damage them.

    Hope this helps.

    Greetings Jan...welcome to our group.

    Love to hear the Blue Jays are back Shorti....are you coming out West for any of your holidays...stop in to see me if you are coming to Calgary, as I'm only just off the Trans Canada Highway. Let me know.

    Joni
  • NOLONGERREADINGORPOSTING
    NOLONGERREADINGORPOSTING Member Posts: 778
    edited March 2007
    Hi Gals,

    Nice to see all these posts, and Chey, thanks for posting that story about meeting your granddad from the otherside..that was such a fascinating story!!!

    Welcome Jen...we have a great group here and we feel complimented by your presence.

    I have a new worry today, it came in form of a message I received last night from a dear friend who has been a wonderful help to me all through this BC journey..
    Quote:

    My aunt had a difficult bladder infection and her doctor kept giving her more and more antibiotics until all the good bacteria in her body was killed and it allowed a very virulent type of bacteria called C. diff to take over her body. She died horribly in a matter of days from this--it literally ate her form the inside out. The entire time she had refused to try some of these more natural remedies and felt the doctor knew best by giving her mega doses of antibiotics.




    She wasn't aware that my infection had gotten worse, so now I am really worried. I have had this bladder infection since January 10 and have been off and on antibiotics since then without success. My doctors have not been coordinated; each one who has treated me has done so in a rather offhand way and passed me along to someone else when the infection didn't go away. The last time I talked with the NP in my PCP's office telling her the latest prescription wasn't working, she said, "Linda, well What do you want us to do. Do You have any ideas? We've done what we can. Is there anything We can do to make you happy?!" All this was said in a sarcastic tone of voice. I told her I had no idea what to do because I'm not the doctor. I just didn't want this infection. I've had many urine cultures, and they tell me that each time it is a new bacteria, but they haven't told me what.

    I am seeing a new female Chinese urologist on Monday...I really don't know what is going to happen next, but I certainly don't want to end up like the aunt..hoping this is a false alarm!!!!

    Mizsissy

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