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Looking for suggestion of clinical trials for mCRPC
I have had SBRT (2007),
Chemotherapy
(2010/2011), ADT using Casodex/Lupron/Zytiga (2012-Current). Interested in joining trials that involve PARP inihibitors, immunotherapy, or other new/novel therapies. Can any of you suggest trials currently accepting candidates.
I have had SBRT (2007),
Chemotherapy
(2010/2011), ADT using Casodex/Lupron/Zytiga (2012-Current). Interested in joining trials that involve PARP inihibitors, immunotherapy, or other new/novel therapies. Can any of you suggest trials currently accepting candidates.
Cmdrdata
in
Advanced Prostate Cancer
2 years ago
Any advice would be appreciated
Three years ago my dear friend was diagnosed with metastisized prostate cancer. Stage 8. Cancer had spread to bone but not to lymph nodes or organs. HealthUnlocked helped me, as primary support person, to navigate options, to formulate useful questions for our medical team, to anticipate treatment side
Three years ago my dear friend was diagnosed with metastisized prostate cancer. Stage 8. Cancer had spread to bone but not to lymph nodes or organs. HealthUnlocked helped me, as primary support person, to navigate options, to formulate useful questions for our medical team, to anticipate treatment side
SupportP
in
Advanced Prostate Cancer
1 year ago
Kidneys are in trouble. Chemo delayed.
I was to have
chemotherapy
yesterday. Unfortunately, my creatinine level was up from 1.11 to 1.68. Also, filtration should be above 60. Mine dropped to 32. An ultrasound has been scheduled on February 16, and I see my oncologist the following day.
I was to have
chemotherapy
yesterday. Unfortunately, my creatinine level was up from 1.11 to 1.68. Also, filtration should be above 60. Mine dropped to 32. An ultrasound has been scheduled on February 16, and I see my oncologist the following day.
Sashay2020
in
My Ovacome
2 years ago
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Feeling sorry for myself
In bed most of day on a beautiful day like today !! Had my chemo on Monday and it has floored me again but at least it working sorry for the moan x
In bed most of day on a beautiful day like today !! Had my chemo on Monday and it has floored me again but at least it working sorry for the moan x
Cazy1010
in
My Ovacome
1 year ago
Husbands radiotherapy/chemotherapy
Hi, please can you tell me your experience after having the mould made. My husband has his first radiotherapy treatment 3rd of January. Scared is an understatement and any words of wisdom will be gratefully received.Jason has cancer of the left tonsil and of his mouth. He cannot open his mouth far at
Hi, please can you tell me your experience after having the mould made. My husband has his first radiotherapy treatment 3rd of January. Scared is an understatement and any words of wisdom will be gratefully received.Jason has cancer of the left tonsil and of his mouth. He cannot open his mouth far at
Ellafen
in
Glioblastoma Support
2 years ago
Advice on bloodwork after radiation treatment?
Hello all, I have been coming back to this forum since finding it a few weeks back, and am looking for some advice and thoughts on my father's case. He was diagnosed with prostate cancer (a very low PSA) back in 2016, underwent a radical prostatectomy that year, and then radiation a year or two later
Hello all, I have been coming back to this forum since finding it a few weeks back, and am looking for some advice and thoughts on my father's case. He was diagnosed with prostate cancer (a very low PSA) back in 2016, underwent a radical prostatectomy that year, and then radiation a year or two later
Hidden
in
Advanced Prostate Cancer
1 year ago
not working? Need help!!
Dear all! What did do ur doctor if after 3 chemos there is some changes for mts they became smaller but some bigger and some the same size? Do they immediately change chemo or try more the same? Ca125 went down… thank u
Dear all! What did do ur doctor if after 3 chemos there is some changes for mts they became smaller but some bigger and some the same size? Do they immediately change chemo or try more the same? Ca125 went down… thank u
Inguc_is
in
My Ovacome
1 year ago
CA 27-29 has your tumor marker test ever gone into normal range
Update to my last update: the people who ran my blood said they mixed up the vials of blood with another patient. They offered to retest me at no expense. I go in tomorrow for my bloodwork retest. I can’t imagine how often stuff like this happens and how often it goes unnoticed. It says Mayo Clinic
Update to my last update: the people who ran my blood said they mixed up the vials of blood with another patient. They offered to retest me at no expense. I go in tomorrow for my bloodwork retest. I can’t imagine how often stuff like this happens and how often it goes unnoticed. It says Mayo Clinic
CatLady2022
in
SHARE Metastatic Breast Cancer
1 year ago
Please tell me your success stories
So in short, I was diagnosed stage 3c back in Oct 2016 and had surgery followed by chemo. Had 1st recurrence summer 2021 so had surgery followed by chemo but during chemo the cancer started to grow again. So in Jan 2022 I was put on Rucaparib and then had surgery again in the summer. But now the cancer
So in short, I was diagnosed stage 3c back in Oct 2016 and had surgery followed by chemo. Had 1st recurrence summer 2021 so had surgery followed by chemo but during chemo the cancer started to grow again. So in Jan 2022 I was put on Rucaparib and then had surgery again in the summer. But now the cancer
Kouyate
in
My Ovacome
1 year ago
Hello Everyone ...6 year anniversary
Morning everyone ....well it was 6 years ago I was here online telling you had been diagnosed with Breast cancer ...worried, panicking, upset and very worried ....and here I am now after operation chemo and radiotherapy and finishing 20th June my 5 years doing a trial ...Happy and content living my best
Morning everyone ....well it was 6 years ago I was here online telling you had been diagnosed with Breast cancer ...worried, panicking, upset and very worried ....and here I am now after operation chemo and radiotherapy and finishing 20th June my 5 years doing a trial ...Happy and content living my best
jackearls1000
in
My Breast Cancer Community
1 year ago
Treatment plan
Hi, could anyone tell me if this amount of chemo sounds right as all posts I read are more, I have stage 2b nsclc adenocarcinoma, plan is 6 weeks radiaton with week 1 cisplatin and vinorelbine, week 2 vinorelbine, week 3 just radiotherapy, week 4 same as week 1, week 5 same as week 2, week 6 just radiotherapy
Hi, could anyone tell me if this amount of chemo sounds right as all posts I read are more, I have stage 2b nsclc adenocarcinoma, plan is 6 weeks radiaton with week 1 cisplatin and vinorelbine, week 2 vinorelbine, week 3 just radiotherapy, week 4 same as week 1, week 5 same as week 2, week 6 just radiotherapy
Stayp0sitive
in
The Roy Castle Lung Cancer Foundation
1 year ago
trial stopped working
Hi ladies. So six months in on weekly taxol and catequintanib at the marsden it was going so well I had partial response which was good. Then a month later I started to get pains in my stomach and rising ca125 the next scan showed I had progression and some new spots, so was referred back to my usual
Hi ladies. So six months in on weekly taxol and catequintanib at the marsden it was going so well I had partial response which was good. Then a month later I started to get pains in my stomach and rising ca125 the next scan showed I had progression and some new spots, so was referred back to my usual
Duvin1
in
My Ovacome
1 year ago
BC metastasizes to dermis
Hi everyone, I would love to hear if any of your diagnosis’ are a local recurrence presenting itself as a lesion in your dermis as metastatic disease. As I have shared, I have been diagnosed with BC 3 times. First was triple negative at 44 with a lumpectomy, chemo and radiation. I was cancer free for
Hi everyone, I would love to hear if any of your diagnosis’ are a local recurrence presenting itself as a lesion in your dermis as metastatic disease. As I have shared, I have been diagnosed with BC 3 times. First was triple negative at 44 with a lumpectomy, chemo and radiation. I was cancer free for
CalGal56
in
SHARE Metastatic Breast Cancer
1 year ago
Holiday inspiration!
I am from the UK, and was crushed when I had to cancel my planned silver wedding anniversary trip to New England twice, the first time because of the pandemic, and in October last year because of progression and switching to oral
chemotherapy
(Capecitabine/Xeloda).
I am from the UK, and was crushed when I had to cancel my planned silver wedding anniversary trip to New England twice, the first time because of the pandemic, and in October last year because of progression and switching to oral
chemotherapy
(Capecitabine/Xeloda).
LibraryGeek
in
SHARE Metastatic Breast Cancer
1 year ago
Advice needed recurrence
Had a brilliant response by the oncology team…
chemotherapy
c &p, followed by debulking surgery. Started Niraparib in July 2022. Was doing really well, in February 2022 my CA125 was 5 and no symptoms but two weeks ago I started to feel breathless. Thought it was a side effect of the Niraparib.
Had a brilliant response by the oncology team…
chemotherapy
c &p, followed by debulking surgery. Started Niraparib in July 2022. Was doing really well, in February 2022 my CA125 was 5 and no symptoms but two weeks ago I started to feel breathless. Thought it was a side effect of the Niraparib.
Skyeplus
in
My Ovacome
1 year ago
Prolia and Blood Disorder
I am currently 61 years old. I was diagnosed with osteoporosis when I was 54. I chose Prolia because a known cancer doctor in my area told me to take that option. I took 4 shots over a two year period with no side effects. My next Dexa scan showed improvement to osteopenia. However, I developed a blood
I am currently 61 years old. I was diagnosed with osteoporosis when I was 54. I chose Prolia because a known cancer doctor in my area told me to take that option. I took 4 shots over a two year period with no side effects. My next Dexa scan showed improvement to osteopenia. However, I developed a blood
LadyDi2
in
Osteoporosis Support
1 year ago
xeloda or nothing?
I don't want it to disintegrate even more from adding in a new
chemotherapy
. I've signed up for Hospice, although death is not imminent but because of the great support and services. But, if I go on Xeloda I will have to step back from hospice since you can't be on any kind of treatment.
I don't want it to disintegrate even more from adding in a new
chemotherapy
. I've signed up for Hospice, although death is not imminent but because of the great support and services. But, if I go on Xeloda I will have to step back from hospice since you can't be on any kind of treatment.
lynnhbtb
in
SHARE Metastatic Breast Cancer
2 years ago
Hearing problems
After 14 infusions of chemo over the past 2 years I am beginning to think that my hearing problems may be related. My oncologist also believes this. Awaking each morning they seem pretty clear but as the day goes I have to yawn to help clear them, which doesn’t seem to help. My right ear continues
After 14 infusions of chemo over the past 2 years I am beginning to think that my hearing problems may be related. My oncologist also believes this. Awaking each morning they seem pretty clear but as the day goes I have to yawn to help clear them, which doesn’t seem to help. My right ear continues
docbulldog
in
Advanced Prostate Cancer
1 year ago
Afinitor side effects
I have been in treatment for breast cancer since 2006 and have done the drill - lumpectomy, lymph nodes removal, chemo, radiation, herceptin, Arimidex for six years… then in 2019 a mastectomy, more hormone blockers, and three years of various combinations with Ibrance, which has sadly stopped working
I have been in treatment for breast cancer since 2006 and have done the drill - lumpectomy, lymph nodes removal, chemo, radiation, herceptin, Arimidex for six years… then in 2019 a mastectomy, more hormone blockers, and three years of various combinations with Ibrance, which has sadly stopped working
Whitaker
in
SHARE Metastatic Breast Cancer
1 year ago
Hello all, hope you are doing well
I had my last chemo on may 4th, scan on the 8th and confirmation that my cancer is gone on the 10th by my Dr. She has chosen not to put me on naparibib at this time due to the side affects. She had a patient develop leukemia after take it and doesn't want me to develop it. Has anyone had side affects
I had my last chemo on may 4th, scan on the 8th and confirmation that my cancer is gone on the 10th by my Dr. She has chosen not to put me on naparibib at this time due to the side affects. She had a patient develop leukemia after take it and doesn't want me to develop it. Has anyone had side affects
Jacquiemoo
in
My Ovacome
1 year ago
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