Ohio Chemo Sisters

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  • ChickaD
    ChickaD Member Posts: 1,025
    edited May 2013

    Tx you Miss Kelly.....however Day 3 after chemo is NOT my day...the bone pain from the Neulasta shot is crippling for me....UGH...back to sleep and big drugs.

  • sewingnut
    sewingnut Member Posts: 1,129
    edited May 2013

    ChickaD, have you tried taking Clariton for the bone pain? I didnt my 1st nuelasta and never had so much pulsing pain. You can take the generic loratidine. I got mine at the dollar store. I think the first chemo is the roughest. Your body says "what the hell just happened here?".  

  • ChickaD
    ChickaD Member Posts: 1,025
    edited May 2013

    Yep...took the Claritan, but I think this part is just my "ugh"

  • leslie612
    leslie612 Member Posts: 17
    edited June 2013

    Help! I have just found out that my onc is no longer an in-network provider w/my insurance company so I am in the market for a new dr. This is a call out to all of the central Ohio sisters for onc recommendations.

    I know that I definitely have coverage at OSU/Stephanie Spielman and the Bing Cancer Center at Riverside. Thank you!

  • GirlPowerDebbie
    GirlPowerDebbie Member Posts: 213
    edited June 2013

    Leslie - I am in Canton, OH and my insurance is Anthem.  My onc is Dr. Dina Rooney, and she is awesome.

  • GirlPowerDebbie
    GirlPowerDebbie Member Posts: 213
    edited June 2013

    ChickaD - Day 3 was my worst, too.  Day 1 I felt pretty good because of the steroids.  Days 2-3-4 were my worst , and day 10 was really my turnaround day when I started feeling decent.  I had TAC x 6, every 3 weeks.  The day after my first Neulasta shot I felt like I got run over by a truck, but it was the worst one.  The Claritin seemed to help a little ... I figured "can't hurt, might help."  I think the Percocet helped too, LOL! 

  • leslie612
    leslie612 Member Posts: 17
    edited June 2013

    Debbie, thanks for sharing your drs name. Fortunately my situation has been resolved and I am able to stay with my MO. I'm not sure who made the mistake that resulted in my receiving the notification but I am certainly relieved it has be taken care of. Just to backtrack and vent a bit - I received a letter from Aetna (dated 5/28) on 6/6 informing me that as of 6/1 my onc was no longer in network. I could request transition coverage and would have to call them, request a form, fill it out and return it to Aetna all before 6/1. Argh! I think that dealing with the insurance co is more hazardous to my health than BC! At least my blood pressure has stabalized and I am breathing easier - at least til the next bump in the road. Thanks again.

  • GirlPowerDebbie
    GirlPowerDebbie Member Posts: 213
    edited June 2013

    Leslie - how goes the Arimidex for you?

  • angieinohio
    angieinohio Member Posts: 17
    edited July 2013

    Late to this boards but I'm a friendly neighbor.-Wooster !

  • jojo69
    jojo69 Member Posts: 26
    edited July 2013

    Thought I'd let everyone know I just finished chemo on June 29th!  Feels so good to be DONE!!  Now on to tamoxifen & watching the hair grow.  Angie, I'm a very close neighbor.  I live in Orrville:)

  • Kelloggs
    Kelloggs Member Posts: 965
    edited July 2013

    congrats jojo69!!!! That's a great feeling, being done with chemo! 

    Welcome angieinohio! 

  • munnybunni
    munnybunni Member Posts: 156
    edited July 2013

    hi everyone ...would like to know if anyone has heard anything about soy protein isolate i read where it is high in estrogen and i am er+pr+ her2-  i take arimidex now and am concerned about too much estrogen

  • munnybunni
    munnybunni Member Posts: 156
    edited July 2013

    after going through the surgeries and the mammosite radiation, and the chemo i feel a frustration with myself that i seem to think and worry about the bcancer coming back.

    it is always in the back of my mind....do others of you not think about it. 

    feel like i am always having a pity party for myself at times

  • ohio4me
    ohio4me Member Posts: 491
    edited August 2013

    Munny - I was told to stay away from soy products. I am 100%ER+/PR+ so it makes sense I want to saty from things that produce estrogen. I also stay away from alcohol - it has the same effect as soy (except red wine).

    Yes, I worry about the cancer coming back. I don't worry continually, but every time I have a cough or pain, I do a self assessment and wonder if it is something I should worry about. Maybe that goes away with time? Maybe I'm not far enough out to have the worry behind me.

    Best wishes to you.

    Diane

  • GirlPowerDebbie
    GirlPowerDebbie Member Posts: 213
    edited August 2013

    Diane - good to hear from you.  I just shook my head when you mentioned the cough, etc.  I am still not done over-analyzing every little ache and pain.  It has been over 2 years.  I guess this hangs over your head a long time. 

  • RetiredLibby
    RetiredLibby Member Posts: 1,992
    edited August 2013

    Good morning, ladies.  I am long-term resident of these boards -- an Ohio native living in Virginia for the last 34 years. 

    I am seeking Buckeye help for my 41-year-old niece who was just dx with cancer on Friday.  She lives in Dayton and lost her mother (my sister) last year to IDC and ILC.  We were never happy with my sister's medical team, so I am seeking recommendations from Dayton-area sisters who are happy with their surgeons and oncologists and other providers.  The doctor she has now is so bad that the office called her on Friday afternoon to tell her that her biopsy was positive but then said that was all the info they had - the nurse was out in training so there wasn't anyone to talk to.  They let her swing for the whole weekend! This morning the nurse said that the report was very complicated and technical and even she didn't understand some of it so she wouldn't read it to her over the phone -- she had to make an appointment to see the doctor IN A FEW DAYS!  Yell 

    SO -- help!  Does anyone have any recommendations I can pass along to my niece? 

    Thanks!

    L

  • sewingnut
    sewingnut Member Posts: 1,129
    edited August 2013

    Retired Libby, I tried to PM you but didn't have that option.  TonLee and Lilylady are from that area. TonLee was military. Lilylady has a very on top of things oncologist. PM her. She only gets on the boards a few times a week. Hopefully you will get others to chime in.

  • ohio4me
    ohio4me Member Posts: 491
    edited August 2013

    I would tell her to get a copy of her pathology report, her mammos for the last five years and make an appointment at the Stephanie Spielman Breast Center at Ohio State.

    To schedule an appointment, please call the James Line New Patient Referral Center at 614-293-5066 or toll-free 1-800-293-5066.

    1145 Olentangy River Road
    Columbus, OH 43212

    I would go there first and make sure she has the right diagnosis and the right treatment plan. They may be able to refer her to someone local in Dayton but she is close enough to excellent care - I would be heading to OSU.

  • RetiredLibby
    RetiredLibby Member Posts: 1,992
    edited August 2013

    Thanks, Ohio4me.  I already told her she needed her path report (and not to take "no, we really don't do that" for an answer), all of her mammo reports (she is only 41 and had her first mammo at 35 -- and maybe only once since then) and all of her imaging (either on disk or on film).  I also told her she needed to start a file with all her reports and make packages up to take to new doctors for consults. 

    I agree that OSU would be a good place for a consult and am going to recommend that, too.

    Thanks for responding!

    L

  • LakeGirl2
    LakeGirl2 Member Posts: 68
    edited August 2013

    I have been treated at OSU this year. Highly recommend my surgeon Dr. Agnese and also know many people who have seen Dr. Farrar, head of the department, highly regarded.

  • RetiredLibby
    RetiredLibby Member Posts: 1,992
    edited August 2013

    Great -- thanks!  I will pass that info along to my niece.

    L

  • travlmom
    travlmom Member Posts: 90
    edited August 2013

    Hello Ladies!

    I live in Mentor and meet with my BS tomorrow for my follow up after lumpectomy and SNB to get my pathology report and schedule my recission. I am being treated at University Hospitals. Chemo is in my near future.

    My mantra - Live like there is no midnight!

  • Eileenohio
    Eileenohio Member Posts: 460
    edited August 2013

    Travlmom--   Sorry you are here,however all the ladies here are wonderful and so very helpful.. I live in Solon Ohio.  I had my surgery at UH Main Campus ( Dr. M.Persons) chemo ,herceptin and radiation at Seidman Cancer  Center in Beachwood.   Do you have to have are excision to get clean margins? Private message me if you have any questions that I can answer.

  • travlmom
    travlmom Member Posts: 90
    edited August 2013

    Dr. Persons is my surgeon too.  I love her.  Yes she did not get clear margins on the back side towards the chest wall. Initially she thought I had 1/3 nodes involved but luckily that was not the case after futher look.  This was such a bummer - the day she called me and gave me the news I was going to my OBGYN to schedule my hysterectomy.  So that will come later and he will remove my ovaries too. 

    I will post tomorrow once I know more.  

  • travlmom
    travlmom Member Posts: 90
    edited August 2013

    I have a question... did anyone seek a second opinion on treatment after surgery?  

    I really like my surgeon and have not met any additional staff yet for my treatment plan.  Part of me would like to compare the 2 hospitals thoughts once I am at that point - when ever that is.  I have a soft spot for the Cleveland Clinic due to the fact that last year the doctors saved my fathers life. 

    How did/do you go about it? I really want to look at the overall complementary/intergrated therapies along with the traditional treatment plan.

  • Eileenohio
    Eileenohio Member Posts: 460
    edited August 2013

    Travlmom,  I did not get a second opinion. I went to UH because of the long standing excellent rating of the Seidman Cancer Center ( formally the Ireland Cancer Center).  I was very pleased with the doctors,nurses and support staff. I hated going down to the Main Campus and was thrilled to be able to have chemo,herceptin and radiation at the Beachwood Seidman Cancer Center.. Only 10 minutes from my home which meant a lot to me . I can not begin to imagine how hard it would have been if I had to go to the Main Campus,especially for the  33 radiation treatments.  I will be 75 yrs old in October and live alone so treatment close to home was important to me..

    I was very lucky-- minimal side effects from the chemo,no side effects from rads and minor hereptin side effects  brittle fingernails and slow growing thin hair.. I don't think that I could have done better anywhere else.  

    Good luck -- the decision making process is  difficult..      Hugs  Eileen

  • ohio4me
    ohio4me Member Posts: 491
    edited August 2013

    Travlmom - I did not seek a second opinion. But, I have a medical background, my sisters are both nurses (one is an oncology nurse), we asked lots of questions and felt very comfortable with my surgeon and oncologist. I went to the Parkview Cancer Center at Summa Barberton Hospital and saw Dr. sprance and Dr. Hazra. They are both wonderful ladies. I was diagnosed March 2011, finished treatment March 2012, have been on Aromisin since then. There is no evidence of disease so I continue to be happy. I know I made the right decision for me.

    Maybe you need a second opinion to know you are on the right plan of care. That's okay. I would probably ask my family doctor where to go for a second opinion, or if you have a doctor in mind, call and say you want a second opinion. Take your pathology report and your mammo images (last five years).

    I always say 'no regrets'. I need to make the decisions I know are right for me so I can look back on life and not have reqrets. If you want a second opinion - go for it.

  • ohio4me
    ohio4me Member Posts: 491
    edited January 2014

    Is there anyone going to Mercy Hospital in Canton for treatment? And has a doctor from Mercy that they really like? I'm looking at Mercy but don't know any of those doctors. I am looking for the (Mercy) doctor that comes highly recommended by a patient. My insurance does not cover Aultman or the doctors I wanted there - I'm waiting to see what the Yes, You Can program offers me at Aultman.

  • GirlPowerDebbie
    GirlPowerDebbie Member Posts: 213
    edited April 2014

    Diane - at Mercy that would be Dina Rooney.  She is a rock star.

    I have not been on the boards for months.  Are you doing OK?  I thought you liked Barberton?

    Deb

  • ohio4me
    ohio4me Member Posts: 491
    edited April 2014

    I love Barberton and love my onc, Dr. Hazra. But she did not want to be part of Summa Physicians she had to give up her office space at Barberton. She moved to UHC Wadsworth on the corner of 18/92 (?). I really didn't want to make the drive out there. I went to see the 'new' doc at Barberton once, nice guy, but really wanted Dr. Hazra. So I made the trip to see her.

    Yes - I am doing well. Still getting good reports. Have other aches and pains but they are not associated to breast cancer.

    Thanks for asking.

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