Depression getting deeper, will to keep fighting getting stronger?

ManWithaMission
ManWithaMission Member Posts: 497
edited September 2012 in Breast Cancer #1
Sounds like a contratiction of fellings,don't it. Well,that's how I've been felling since my Hip Surgery in July. August,found a lesion to femer bone. July 3rd, rod in femer to stablize for rads. July 18th, 2 weeks radiation(low dose). Oncoligest changed my harmone treatment from Famera to FASLODEX shots. First (two) shots were July 19th, along with Zometa infusion. You get two shots in the upper buttocks,then come back in two weeks for two more and then it's two shots once a month after that.

Now,Sept. 23rd,found a new lesion in my neck. It started out as a stiff neck,tryed putting heat on it and that just made it worse. Then tryed an ice pack,that didn't help the pain either. So now I have to have more radiation to my neck and my onc wants to try another estrogen blocker or just start a new chemo.

If it isn't one thing with this "beast", it's another, all piling on top of each other at the same time. See,the wife and I had (non-trasferable & non-refundable) airline tickets to Pensacola,Fl to see my new grandson starting October 3rd through the 9th. ALL my Doctors said I can't go! I sure hope that fate or Karma or whatever are having a good laugh on me again!

What's that old saying from "HeeHaw";"If it wern't for bad luck,I'd have no luck at all! Gloom,dispair,agony on me." Laughing Way Out Loud!!!!!

Robert
«1

Comments

  • CypressCynthia
    CypressCynthia Member Posts: 4,014 Member
    I am so sorry to hear this.
    I am so sorry to hear this. I have missed your posts, but am sorry you are posting with this news :-( But I love your fighting spirit!!!

    BTW, I am on faslodex and xgeva. I was on zometa but I asked my onc about xgeva, because 1) no kidney worries with xgeva and 2) it is a subq (shallow) injection in the arm given once a month, so no iv's and no waiting. Studies have deemed xgeva as or more effective than zometa, but it is more expensive (not a big deal with most insurers).

    Also, my onc of 25 years mentioned that if faslodex is not working, he would next add afinitor, because he has seen really good results with this drug. He said main side effect was mouth sores, but they go away if you stay the course. Ask your onc cuz I admit I don't have any idea if the treatment for men is different.

    Wondering if you call the @#$% airlines if they might give you a break? Especially if you have documentation? Probably not, the @##$@%*'s.

    Big hugs and prayers!
  • CypressCynthia
    CypressCynthia Member Posts: 4,014 Member

    I am so sorry to hear this.
    I am so sorry to hear this. I have missed your posts, but am sorry you are posting with this news :-( But I love your fighting spirit!!!

    BTW, I am on faslodex and xgeva. I was on zometa but I asked my onc about xgeva, because 1) no kidney worries with xgeva and 2) it is a subq (shallow) injection in the arm given once a month, so no iv's and no waiting. Studies have deemed xgeva as or more effective than zometa, but it is more expensive (not a big deal with most insurers).

    Also, my onc of 25 years mentioned that if faslodex is not working, he would next add afinitor, because he has seen really good results with this drug. He said main side effect was mouth sores, but they go away if you stay the course. Ask your onc cuz I admit I don't have any idea if the treatment for men is different.

    Wondering if you call the @#$% airlines if they might give you a break? Especially if you have documentation? Probably not, the @##$@%*'s.

    Big hugs and prayers!

    PS
    Sending references separately because lately my computer has been freezing up when I copy and paste. Don't know what that is about, but it is really cramping my style...lol

    Denosumab Superior to Zoledronic Acid for Breast Cancer Patients With Bone Metastases

    http://www.aacr.org/home/public--media/aacr-in-the-news.aspx?d=2847

    Everolimus (Afinitor)

    http://www.cancer.org/Treatment/TreatmentsandSideEffects/GuidetoCancerDrugs/everolimus
  • Megan M
    Megan M Member Posts: 3,000
    I am so sorry Robert. I
    I am so sorry Robert. I hate cancer!!!! Maybe if you contact the airlines and explain all of this to them, they will make an exception with your tickets. I hope so and please keep fighting!

    Hugs, Megan
  • New Flower
    New Flower Member Posts: 4,294
    Megan M said:

    I am so sorry Robert. I
    I am so sorry Robert. I hate cancer!!!! Maybe if you contact the airlines and explain all of this to them, they will make an exception with your tickets. I hope so and please keep fighting!

    Hugs, Megan

    Robert sending you positive thoughts
    Robert,
    Having 10 lesions myself, I think I understand. There are many options to treat these conditions. Ask for Xgeva , which suppose to promote bone growth.
    Please ask your doctors why they did not want you to go? And if you do what precautions should you take making your trip successful.
    Hugs
  • MAJW
    MAJW Member Posts: 2,510 Member

    Robert sending you positive thoughts
    Robert,
    Having 10 lesions myself, I think I understand. There are many options to treat these conditions. Ask for Xgeva , which suppose to promote bone growth.
    Please ask your doctors why they did not want you to go? And if you do what precautions should you take making your trip successful.
    Hugs

    Robert...
    So sorry to hear this news.....yes, cancer is the "gift" that keeps on giving....it sucks! If you feel up to it, why are the docs saying you can't go? I've gotten to the point I tell my docs what I AM going to do and not do...after all, it's our life and we make all final decisions concerning what we feel is best for us...my oncologist actually calls me "Sassy".....I have scans coming up in October (scanxiety) I told them fine but I wasn't going to drink that awful, two bottles of "stuff"...if you do go get a letter from your onco detailing the "metal" you have...and don't go through the scanner...let them pat you down, if needed...

    We have a trip that's been planned for months, for Feb....to the Dominican Republic, tickets secured, etc...but since we didn't know if I will be okay to go, I think I will, providing the scans are okay, we spent an extra $180.00 for trip insurance...my brother law and wife are going too, they're both healthy but also bought the insurance....as we all know life can change in the blink of an eye....I have a port and since it sticks out like a sore thumb due to my losing 36 pounds, those pesky security people may think ut oh we've got a problem....so I will take a letter with me....

    Robert, are you taking anything for the depression...if not, please ask for something...no shame in asking for help....I'd bet at least 80% of us on this board take something....it helps...

    Please keep us posted, we care, our brother in pink....
    Hugs, Nancy
  • Frankie Shannon
    Frankie Shannon Member Posts: 457
    Oh Robert i am so sorry with
    Oh Robert i am so sorry with all your problems but more so that you don't get to go and see your new grandson,lets pray the new regiment works for you.It's been a long time since I've heard that old saying it's like when it rains it pours and that's what it sounds like it's doing for you.My thoughts and prayers are with you.
    Hugs Frankie
  • ManWithaMission
    ManWithaMission Member Posts: 497

    I am so sorry to hear this.
    I am so sorry to hear this. I have missed your posts, but am sorry you are posting with this news :-( But I love your fighting spirit!!!

    BTW, I am on faslodex and xgeva. I was on zometa but I asked my onc about xgeva, because 1) no kidney worries with xgeva and 2) it is a subq (shallow) injection in the arm given once a month, so no iv's and no waiting. Studies have deemed xgeva as or more effective than zometa, but it is more expensive (not a big deal with most insurers).

    Also, my onc of 25 years mentioned that if faslodex is not working, he would next add afinitor, because he has seen really good results with this drug. He said main side effect was mouth sores, but they go away if you stay the course. Ask your onc cuz I admit I don't have any idea if the treatment for men is different.

    Wondering if you call the @#$% airlines if they might give you a break? Especially if you have documentation? Probably not, the @##$@%*'s.

    Big hugs and prayers!

    @#$% airlines
    Yea, my wife called them and they said if we get a Doctors note explaining the situation,that we can re-schedule our flight dates without an additional charge. Only problem right now is that everything is up in the air. I see the Rad Onc monday @ 8am(didn't anyone tell them I don't get up till 11am)(LOL) when I will find out how long and how much radiation.

    Also,won't see my Onc till my next appointment on October 11th,when she will have decided what she will do with me? Like you said, treatment is different for men. I told her I would LOVE to be her gunnie pig!LOL!

    Thanks for the web sites,too. I don't know if I will go to them right now because too much knowledge makes me too nervous and worry way too much.

    Pink Bro
    Robert
  • ManWithaMission
    ManWithaMission Member Posts: 497

    Robert sending you positive thoughts
    Robert,
    Having 10 lesions myself, I think I understand. There are many options to treat these conditions. Ask for Xgeva , which suppose to promote bone growth.
    Please ask your doctors why they did not want you to go? And if you do what precautions should you take making your trip successful.
    Hugs

    Doctors Said "NO!" to Trip
    Their only comment was that if something were to happen(like if my disks were to move suddenly,pinching the spinal cord),I would only have strangers to treat me and not someone who knows my coditions. It kind of makes sense.

    Robert
  • SIROD
    SIROD Member Posts: 2,194 Member
    Bad Luck
    Dear Robert,

    Wondered why you were not posting and I have missed your posts too. I know how you feel. On my second time around with Faslodex, driving to the cancer center, I kept telling myself that I did not have to do this again, an again. I could just not show up. I am in my 12th year metastatic and just past my 18 year from diagnose. There have been times, that I was very discourage.

    Faslodex is a slow hormonal drug, it might not have reached the point where you would have seen results yet. Sometimes it does take 6 months to work on some people.

    CC has a good suggestion of Aromasin with Afinitor that has shown a lot of improvement for those of us who are ER+. Might suggest the combo to your oncologist.

    I've been reading and participating with online bc boards since 1997, In those years I have come across with men who have this disease. They all seem to be ER+ as they do the hormonal thing, then go on to the chemotherapy. More than likely the chemo will be Taxol if you haven't yet had this drug or Xeloda.

    Radiation at this point is palliative, to kill the lesions. You might have 10-15 treatments. It is never as long as the first time around when they hoped to cure you.

    "If it weren't for bad luck.... I have used that line myself over the years as so many of my prescription drugs (15 in all) are from side effects from the hormonal drug therapies that have beget other conditions that require other drugs and there is no end to it.

    Wishing you the best on the road ahead,

    Doris
  • CypressCynthia
    CypressCynthia Member Posts: 4,014 Member

    @#$% airlines
    Yea, my wife called them and they said if we get a Doctors note explaining the situation,that we can re-schedule our flight dates without an additional charge. Only problem right now is that everything is up in the air. I see the Rad Onc monday @ 8am(didn't anyone tell them I don't get up till 11am)(LOL) when I will find out how long and how much radiation.

    Also,won't see my Onc till my next appointment on October 11th,when she will have decided what she will do with me? Like you said, treatment is different for men. I told her I would LOVE to be her gunnie pig!LOL!

    Thanks for the web sites,too. I don't know if I will go to them right now because too much knowledge makes me too nervous and worry way too much.

    Pink Bro
    Robert

    Please also know that
    Please also know that anxiety and depression are much more common in all cancer patients. Your oncologist knows this and, if you are too down, let him know. He/she will know what meds to take to help and will also know what meds are compatible with your teatments.
  • CypressCynthia
    CypressCynthia Member Posts: 4,014 Member

    Please also know that
    Please also know that anxiety and depression are much more common in all cancer patients. Your oncologist knows this and, if you are too down, let him know. He/she will know what meds to take to help and will also know what meds are compatible with your teatments.

    P.S. Here is the link re
    P.S. Here is the link re cancer and depression/anxiety from the NCI. The fact that depression is occurring in about 1 in 4 survivors is a mind-boggling statistic to me. Do not let it get out of control.

    When I finally went to see a psychiatrist, I was boo hooing, anxious, and down and had no idea what was wrong with me. It just couldn't be the most obvious diagnosis-depression. Two weeks after treatment, I swear the sky looked physically bluer and I don't think I was hallucinating. I shared this with my psychiatrist and we laughed, but she said she understood exactly what I meant and others had shared the same sentiment.

    If you do start an antidepressant (which are actually the treatment of choice for most anxiety disorders), know that there can be an adjustment period of 2-4 weeks where you feel a little worse and you may need additional medication coverage for this period.

    If I sound like an authority, I'm not. But my older sister is a psychiatrist in Seattle and she really knows her meds! Feel free to pm me. Big (((hugs))) and I am glad you are back with us, even though, as I said before, I am so very sorry for the reason. Hang in there!
  • camul
    camul Member Posts: 2,537

    Doctors Said "NO!" to Trip
    Their only comment was that if something were to happen(like if my disks were to move suddenly,pinching the spinal cord),I would only have strangers to treat me and not someone who knows my coditions. It kind of makes sense.

    Robert

    Robert
    So sorry to hear this news. There is no other way to describe this disease it sucks and sometimes no matter how hard we fight the tumors just don't respond. I was so disappointed in March when I was told I could not go on the trip with my family. I was so looking forward to it.

    This really is a roller coaster ride. I am on Xgeva every 4 weeks and will be most likely starting the chemo combo that CC mentioned. This was the option given to me. The doctor feels it will be easier on my immune system. I was also changed over to Evista for the blocker as Tamoxifen was toxic to my system. Every-time I walk through a doctors door, I feel as though something has changed!

    I hope all of this goes well for you and you get to Pensacola so see that new baby soon!!

    Prayers,
    Carol
  • laughs_a_lot
    laughs_a_lot Member Posts: 1,368 Member
    Robert
    Considering all you have been through a case of depression is practically a neccessary element of your life or we might begin to think you were Spock from Star Trek. So if you need some help in the form of medication don't hesitate to ask. Depression is something you do not need to "tough it through". The fact that you are alive and wishing to kick with that messed up leg of yours is something you should probably get a purple heart or at least the medal of honor for. It's just that we don't get them in the cancer battle like they do in the military.
  • survivorbc09
    survivorbc09 Member Posts: 4,374 Member

    Doctors Said "NO!" to Trip
    Their only comment was that if something were to happen(like if my disks were to move suddenly,pinching the spinal cord),I would only have strangers to treat me and not someone who knows my coditions. It kind of makes sense.

    Robert

    Sending lots of hugs to you
    Sending lots of hugs to you Robert. I'm sad and so sorry that you can't go on your trip as planned.


    Hugs, Jan
  • mom62
    mom62 Member Posts: 604 Member
    Sorry to Hear
    Robert,

    Sorry to hear about your recent problems. I'm not sure I understand why you can't travel? Is it because you might miss your shots? Can't they arrange them so you can get them before you go and right when you come back? Just me blabbing on. Anyhow, that cloud above your head has been following me for some time. It's always one issue with me after another, can't catch a break. I too suffer from depression and it's not always easy to cope. I try to take it one day at a time, but sometimes it does overwhelm me. I see a therapist but it doesn't always help. Keep your chin up and don't forget we are all here for you.

    Terry
  • mom62
    mom62 Member Posts: 604 Member

    Doctors Said "NO!" to Trip
    Their only comment was that if something were to happen(like if my disks were to move suddenly,pinching the spinal cord),I would only have strangers to treat me and not someone who knows my coditions. It kind of makes sense.

    Robert

    My Opinion
    I know that I am totally off key in saying this as you should trust your doctors but I feel I have to for some reason. I think they are fear mongers, perhaps with good intention but fear mongers none the less. It would be a cold day in $$$$ when someone would tell me what to do, but that is just me. They couldn't recommend anyone in the area where you are going????? I'm sorry if I offended you or anybody else but as I said it is just my opinion.

    Terry
  • sea60
    sea60 Member Posts: 2,613
    mom62 said:

    Sorry to Hear
    Robert,

    Sorry to hear about your recent problems. I'm not sure I understand why you can't travel? Is it because you might miss your shots? Can't they arrange them so you can get them before you go and right when you come back? Just me blabbing on. Anyhow, that cloud above your head has been following me for some time. It's always one issue with me after another, can't catch a break. I too suffer from depression and it's not always easy to cope. I try to take it one day at a time, but sometimes it does overwhelm me. I see a therapist but it doesn't always help. Keep your chin up and don't forget we are all here for you.

    Terry

    Sorry to hear this Robert :(
    I hope and pray they nip this in the bud and you can be on your way to see that new baby soon!!

    Sending prayers,

    Sylvia
  • Alexis F
    Alexis F Member Posts: 3,598

    Doctors Said "NO!" to Trip
    Their only comment was that if something were to happen(like if my disks were to move suddenly,pinching the spinal cord),I would only have strangers to treat me and not someone who knows my coditions. It kind of makes sense.

    Robert

    Oh Robert, I am very sorry
    Oh Robert, I am very sorry to know how you are feeling and to read that you can't go see your grandbaby. I've missed you on the site. You're always the first to post happy birthday to everyone.

    Just know that I am cheering you on and praying for you.


    Hugs, Lex
  • VickiSam
    VickiSam Member Posts: 9,079 Member
    sea60 said:

    Sorry to hear this Robert :(
    I hope and pray they nip this in the bud and you can be on your way to see that new baby soon!!

    Sending prayers,

    Sylvia

    Robert --
    My hear goes out to you my brother in PINK -- my heart goes out to you and your family. Our CC offered some good and sound advise. There is hope, always hope.

    You get those 'pink' boxing gloves on .. kick some as$%%% !!!

    Continued positive thoughts, and prayers for you.

    Strength, Courage and HOPE for a Cure.

    Vicki Sam
  • Angie2U
    Angie2U Member Posts: 2,991
    sea60 said:

    Sorry to hear this Robert :(
    I hope and pray they nip this in the bud and you can be on your way to see that new baby soon!!

    Sending prayers,

    Sylvia

    I pray that you will start
    I pray that you will start feeling better Robert. I hope you know that the pink sisters are all praying for you and rooting you on!


    Hugs and prayers,

    Angie