Recurrence
Ladies I received the news that my one solitary nodule that they took 1/2 my middle lobe out for was a recurrence of UPSC. So now I wait to see my oncologist this coming Thursday. I've been reading all the recurrence posts seeing what line of defense is used. Has anyone went on Social Security disability with this? I am also interested in maybe an integrative oncologist....All questions and comments encouraged.
Comments
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So sorry
So sorry to hear this. No one wants to hear those recurrence words. I had a recurrence in Dec, 2013. With mets to my neck, liver and several in my abdomen. I change Cancer centers, for many reasons, and was blessed with the wonderful oncolonist that I have now. We went back to the Taxol/ Carbo chemo and it did work bringing my CA 125 back down to 7 and tumors shrunk small enough that they couldn't be detected on a CT scan. I was already old enough for Social Security at this time, but I think that stage 4 and maybe stage 3 cancer would qualify a person for Social Security.
Sending you Hugs and prayers, Lou Ann
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immunology?
Tayers, have you looked into immunology? My husband needs to do chemo again (he had chemo, then surgery and now they want him to do chemo again). He is looking into immunology. If I find anything out on it, I will let you know. He meets with his oncologist next week.
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Sorry to hear that this was
Sorry to hear that this was indeed a recurrence. You might consider working with a board-certified naturopathic oncologist as well as your conventional medical team. A list can be found here: http://fabno.org/membership.html Many specialize in complementary care working with your medical team to enhance chemo, radiation, etc. and reduce undesirable side effects while strengthening your body's own self-healing mechanisms. In my experience, naturopaths or integrative doctors take a more whole patient approach to healing that could include diet, exercise, supplements, meditation, yoga and other types of self-care.
CheeseQueen57 applied for and got Social Security Disability. I remember this because I was considering on applying earlier this year. If she doesn't come along, you might send her a message about that.
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Disability
So sorry you are going through this. Yes, I got SS disability and it was approved very quickly. It's worth a try to apply.
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Tami, I am so sorry to hear
Tami, I am so sorry to hear your news. I can't add anything on SSD, but it is worth a try as CheeseQueen said. Please let us know what the doctor said is his thoughts on attacking this. Hugs
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Tami,
Tami, I join the other ladies in expressing how sorry I am to hear of your reoccurence. I will keep you in my prayers as you continue your treatments. It just shouldn't happen again....(HUG)). Lori
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Tami, Hate the news and I'm
Tami, Hate the news and I'm sorry you are having to deal with it. Please let us know the plan of attack once you get it. Sending you loads of support.
I hope you are able to get on Social Security. I bet you can!
Love and Hugs,
Cindi
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Dear Friend
Hi Tami,
I'm so very sorry to hear the news. I echo what everyone has already said, this board is wonderful and a wealth of information. I hope that this Thursday goes well and you leave with a clear direction and path.
God Bless and keep us informed. You will be in my prayers.
~Laura
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Chemo again
My oncologist said since it sbeen 31/2 years since chemo we can use carboplatin and pacilitaxol again. He was presenting my solitary nodule to the tumor board at Magee's Womens Hospital in Pittsburgh. Usually it doesn't come back as a solitary nodule? I get my port put win on December 30. I asked at a clinical trail and he didn't think there were any available right now.... I had to call twice to get my port set up. Isn't that weird?
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I'm sorryTAyers said:Chemo again
My oncologist said since it sbeen 31/2 years since chemo we can use carboplatin and pacilitaxol again. He was presenting my solitary nodule to the tumor board at Magee's Womens Hospital in Pittsburgh. Usually it doesn't come back as a solitary nodule? I get my port put win on December 30. I asked at a clinical trail and he didn't think there were any available right now.... I had to call twice to get my port set up. Isn't that weird?
you have to face this again. Did you save any of your headgear from last time? I think I should donate my wig, caps and scarves but then I think twice and don't. I liked what I had and would hate to shop all over again. Also, I might be a touch superstitious.
Did you tolerate the chemo pretty well last time?
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Tami, I am sorry to hear youTAyers said:Chemo again
My oncologist said since it sbeen 31/2 years since chemo we can use carboplatin and pacilitaxol again. He was presenting my solitary nodule to the tumor board at Magee's Womens Hospital in Pittsburgh. Usually it doesn't come back as a solitary nodule? I get my port put win on December 30. I asked at a clinical trail and he didn't think there were any available right now.... I had to call twice to get my port set up. Isn't that weird?
Tami, I am sorry to hear you have to go through the chemo again but if it kicks it than that is the road to go. Please let us know how you are doing. I didn't know you were in Pittsburgh - I am originally from there. Hugs, Tami!
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So sorry you have To go back to the chemo
but if it will get you back to dancing with NED, it will be worth it. You caught this early, that has to be a good thing. It does seem odd that you had to call more than once for an appointment to get a port put . Maybe the holidays have something to do with that.
My advice to everyone would be to leave that port in for a really long time and keep your head gear.
Hugs and prayers, Lou Ann
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Sorry to hear that it's chemo again.TAyers said:Chemo again
My oncologist said since it sbeen 31/2 years since chemo we can use carboplatin and pacilitaxol again. He was presenting my solitary nodule to the tumor board at Magee's Womens Hospital in Pittsburgh. Usually it doesn't come back as a solitary nodule? I get my port put win on December 30. I asked at a clinical trail and he didn't think there were any available right now.... I had to call twice to get my port set up. Isn't that weird?
I'm hoping that you have few side effects, and most importantly, that it kicks the cancer to the curb.
Peace and strength,
Chris
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