A website for discussions about any type of cancer, including lung cancer, breast cancer, prostate cancer, laryngeal cancer, leukemia, lymphoma, multiple myeloma and others
+ Reply to Thread
Page 1 of 2 1 2 LastLast
Results 1 to 15 of 23
  1. #1
    Moderator Top User
    Join Date
    Feb 2006
    Location
    UK
    Posts
    1,082

    On the move again.

    Alas, my skin mets are not responding to hormone treatment, so I am moving into chemo again. Capecitabine is the one chosen.

    This was triggered as there has been a tumour development in the skin under one eye, and it is affecting the eye movement. Since the danger is that I will be stopped from driving - and I cannot at present afford to be in that situation, aggressive action must be taken to reduce these growths.

    For those that are interested, I am [with my oncologist's agreement] also trying this special honey from Israel which is supposed to mitigate the side effects and improve the efficacy of the treatment. I will let you know what happens.

  2. #2
    Top User
    Join Date
    Apr 2007
    Location
    Brisbane, Australia
    Posts
    575

    On the move again

    Hi Vee

    Sorry to hear you are back on the chemo road again! I hope this resolves the skin mets under your eye?

    I will be interested to hear about the Israeli honey treatment too!

    Thinking of you,
    Cheer, Angie.
    Brother diagnosed with GBMIV Feb 07
    Treatment: Radiotherapy, Temodal, Gliadel Wafers, Dexamethasone, Keppra, Dilantin, Clexane
    Went to our Heavenly Father after a 19mth battle,, 47 years young.
    23 Sep 2008
    http://cancerforums.net/viewtopic.php?p=19227

    "Without Faith We Have Nothing"

  3. #3
    Moderator Top User
    Join Date
    Feb 2006
    Location
    UK
    Posts
    1,082
    Hi, Angie - first round over - and my feet and mouth are killing me! However, fortunately this chemo is adjustable so it may be reduced slightly on the next one.

    I am taking the honey - the jury is out at present. I think I need to give it three months to be sure if it helps or not

  4. #4
    Moderator Top User
    Join Date
    Feb 2006
    Location
    UK
    Posts
    1,082
    Update:
    My blood counts have remained almost normal, and the nurses tell me they think that is the effect of the honey, so I am continuing it.

    However, I have the dreaded hands and feet syndrome, with cracking skin on the fingers and toes, on the edge of the nails. AGONY!!!

    Anhyone who has had the same problem - how did you cope??

  5. #5
    Top User
    Join Date
    Apr 2007
    Location
    Brisbane, Australia
    Posts
    575

    Re: Chemo side effects

    Hello Vee
    Thanks for the update, I've been meaning to check on you for some time now. Sorry 'bout that.
    The skin problems sound dreadful & soooo painful for you. I'm sorry you are having to endure this discomfort & pain. As I'm not familiar with the side effects of this chemo I cannot suggest anything? Terribly sorry.
    It's a real bonus to have your bloods so good & an added bonus to have recognition for the "honey", from the nurses.
    I hope someone will come to your aid soon, with some simple, staightforward advice.
    Thinking of you.
    Cheers, Angie.
    Brother diagnosed with GBMIV Feb 07
    Treatment: Radiotherapy, Temodal, Gliadel Wafers, Dexamethasone, Keppra, Dilantin, Clexane
    Went to our Heavenly Father after a 19mth battle,, 47 years young.
    23 Sep 2008
    http://cancerforums.net/viewtopic.php?p=19227

    "Without Faith We Have Nothing"

  6. #6
    Moderator Top User
    Join Date
    Feb 2006
    Location
    UK
    Posts
    1,082
    Update - Today we decided to stop the capecitabine. The toxicity outweighs the benefits. Sad, but frankly life has been pretty intolerable, with sore, cracking hands and sore, cracked feet making movement difficult. The last blood counts were against me, so the decision had to be taken. Onwards and upwards! Probably back to trying hormonals for a while. Fortunately it is a very slow cancer, so my onc. is hopeful.

    I have been taking the Lifemel honey, but clearly it has not really been of major help so I will probably stop that as well. Disappointing, but one alwys hopes for the best.

    I do wonder if there could be DNA tests developed to indicate how individuals might respond to chemos.

  7. #7
    Top User
    Join Date
    Apr 2007
    Location
    Brisbane, Australia
    Posts
    575

    Re: On the move again

    Dear Vee
    Sorry I haven't replied earlier Vee. Have been thinking of you & always follow your posts (even your replies to others) you are inspirational to me that through your pain & uncertainty you are such a "rock" to others on this forum.
    In regard to the DNA tests for response to chemo are you talking about the "gene deletions" test? 1P & ? (whatever the rest of the test is called?). Have you had this checked? I know Brainman talks about this test often on here.
    I do hope the hormonals will be kinder to your body & your skin affliction will clear up quickly once you stop the chemo.
    Keep on keeping on Vee.
    All the best, my prayers & thoughts are with you.
    Cheers, Angie.
    Brother diagnosed with GBMIV Feb 07
    Treatment: Radiotherapy, Temodal, Gliadel Wafers, Dexamethasone, Keppra, Dilantin, Clexane
    Went to our Heavenly Father after a 19mth battle,, 47 years young.
    23 Sep 2008
    http://cancerforums.net/viewtopic.php?p=19227

    "Without Faith We Have Nothing"

  8. #8
    Moderator Top User
    Join Date
    Feb 2006
    Location
    UK
    Posts
    1,082
    Thanks, Angie.

    I was meaning a test to establish what treatments will suit an individual with the minimum of dangerous or uncomfortable side effect. Maybe genetic testing is a better term.

    An Oxford company has been working on this idea, but it still costs a horrendous amount to implement, and has not been properly tested.

    A major breakthrough has been achieved to do with HIV, where the leukocytes have been altered to recognise all forms of the virus and to attack it in any form. It seems to me that this could also be a first step towards developing cells that will recognise cancer in any form and that will then attack them. Maybe not in my lifetime, but a real small glimpse of a possible future.

  9. #9
    Administrator Top User brainman's Avatar
    Join Date
    Oct 2005
    Location
    Tennessee
    Posts
    6,641
    Vee, I am also sorry to not have replied sooner . I am so sorry that the capecitabine is doing more harm than good. How are you doing on the emotional level?

    They are indeed looking for ways to check a person's DNA to taylor make a chemotherapy for that individual but I am not sure how close they are to finding those for all cancers.

    Big hugs for you {{{{{Vee}}}}}}
    Jim
    Administrator and long-term cancer survivor
    1992 Astrocytoma grade 2, left motor strip
    2005 Recurrence this time said to be an Oligodendroglioma grade 3, same location.
    http://cancerforums.net/viewtopic.php?t=2405
    My Story Part 1: http://cancerforums.net/viewtopic.php?t=2528
    My Story Part 2: http://cancerforums.net/viewtopic.php?p=7350
    My Story Part 3: http://cancerforums.net/viewtopic.php?t=8029
    Twitter: @JimHawkins54
    FaceBook: http://www.facebook.com/James.Hawking54?ref=profile

  10. #10
    Moderator Top User
    Join Date
    Feb 2006
    Location
    UK
    Posts
    1,082
    Hi, Jim - coping is the best way to put it. Constant pain is so wearing, and of course failure of a treatment is always a disappointment. However, my Onc. is not giving up and is looking at other ways of handling this.

    It is an odd situation, to be categorised as terminal, but feel well, eat well, can think and act!

    Thanks for the hug - much needed.

  11. #11
    Quote Originally Posted by Vee Smith
    Update - Today we decided to stop the capecitabine. The toxicity outweighs the benefits. Sad, but frankly life has been pretty intolerable, with sore, cracking hands and sore, cracked feet making movement difficult. The last blood counts were against me, so the decision had to be taken. Onwards and upwards! Probably back to trying hormonals for a while. Fortunately it is a very slow cancer, so my onc. is hopeful.

    I have been taking the Lifemel honey, but clearly it has not really been of major help so I will probably stop that as well. Disappointing, but one alwys hopes for the best.

    I do wonder if there could be DNA tests developed to indicate how individuals might respond to chemos.
    Sorry to hear you are having to endure all of this all over again, Vee. If you want to try natural things, as well as treatment, you may want to look into curcumin (Turmeric), which is suppose to help protect from skin and lung cancers. It has to be taken with bioperine (black pepper). Also, change your diet to include any unnecessary glucose from simple carbs. Also look into putting more omega 3 in your diet (fish, fish oils, etc).

    They already have test that will tell how well a person will respond to chemo or if it will be of any benefit to them, or not. I can't remember the name of the test, however. My best to you.

  12. #12
    Moderator Top User
    Join Date
    Feb 2006
    Location
    UK
    Posts
    1,082
    Thanks for the suggestion. Turmeric has not worked for me.

  13. #13
    I'm sorry to hear that, Vee. I don't want to get on your nerves, so I will just make one last suggestion. Have you tried IP6 with Inositol Hexaphosphate. I took it in powder form, as it is easier. I got mine from iherb.com. Also, Oxygen Elements Plus. Read up on them when you get some time.

  14. #14
    Moderator Top User
    Join Date
    Feb 2006
    Location
    UK
    Posts
    1,082
    Thank you - but at present I am resting from everything.

  15. #15
    Moderator Top User
    Join Date
    Feb 2006
    Location
    UK
    Posts
    1,082
    Well, the next step has been decided. A scan to check on what's going on inside, then onto methotrexate - either on its own or as part of a cocktail. We mutually agreed not to go for Taxol+Avastin following my neuropathy, which to be honest is a relief. And hormonal treatments would be too slow acting.

    So there we go - a little more hope than before, and maybe not too taxing a chemo for a change.

Posting Permissions

  • You may not post new threads
  • You may not post replies
  • You may not post attachments
  • You may not edit your posts