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Brain tumours (low-grade/mixed)
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New MRI finding
Yesterday I had an MRI due to some back pain. I had an MRI, pet scan in February and clean CAT scan in June. Plus all of my labs have been perfect. Now they’re telling me that they see a 2.1 CM metastasis on my L2 area of my spine. I am a bit freaked out but I’m trying to wrap my head around this.
Yesterday I had an MRI due to some back pain. I had an MRI, pet scan in February and clean CAT scan in June. Plus all of my labs have been perfect. Now they’re telling me that they see a 2.1 CM metastasis on my L2 area of my spine. I am a bit freaked out but I’m trying to wrap my head around this.
Flavia100
in
SHARE Metastatic Breast Cancer
11 months ago
Radiation for Salvage Treatment
I am about to start salvage treatment after a failed surgery and a rising PSA value of 0.1. However, I would like to know if weeks of external radiation with ADT, is the best treatment option here. The idea of blindly radiating pelvic area with a re-recurrence a few years later does not appeal to me.
I am about to start salvage treatment after a failed surgery and a rising PSA value of 0.1. However, I would like to know if weeks of external radiation with ADT, is the best treatment option here. The idea of blindly radiating pelvic area with a re-recurrence a few years later does not appeal to me.
Rams91
in
Prostate Cancer Network
11 months ago
LU-177 I&T, FAILURE?
Just received PSA results from 4th Infusion of LU-177 I&T, as part of the Eclipse Study. It increased from 0.1 to 0.2. PSA baseline was 2.0. Following 1st infusion PSA dropped to 0.3. Following 2nd infusion no PSA was taken. Following 3rd infusion PSA 0.1. Following 4th infusion PSA 0.2. Having
Just received PSA results from 4th Infusion of LU-177 I&T, as part of the Eclipse Study. It increased from 0.1 to 0.2. PSA baseline was 2.0. Following 1st infusion PSA dropped to 0.3. Following 2nd infusion no PSA was taken. Following 3rd infusion PSA 0.1. Following 4th infusion PSA 0.2. Having
john4803
in
Advanced Prostate Cancer
11 months ago
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Lymphoma or unconnected New Tumour.
Hi All, further to my recent 'post' re the Bells Palsy' that never was, I want to thank you all for your support and advice. I am still waiting on a 'Biopsy' date, followed by the three week wait for results. After which I will know better, where I stand. I have received my recent Bloods from my
Hi All, further to my recent 'post' re the Bells Palsy' that never was, I want to thank you all for your support and advice. I am still waiting on a 'Biopsy' date, followed by the three week wait for results. After which I will know better, where I stand. I have received my recent Bloods from my
Vindicatrix
in
CLL Support
11 months ago
EBRT SE after Brachytherapy
Well, I can say the last 3 weeks after brachytherapy have been, medically, the worst of my entire life. QOL was poor at best. Maybe I have lived a sheltered life all these years and didn’t know what it is like to really be ill or have medical issues. I do now. Brachytherapy dose was 85 Gy, 60 seeds.
Well, I can say the last 3 weeks after brachytherapy have been, medically, the worst of my entire life. QOL was poor at best. Maybe I have lived a sheltered life all these years and didn’t know what it is like to really be ill or have medical issues. I do now. Brachytherapy dose was 85 Gy, 60 seeds.
electronics-guy
in
Prostate Cancer Network
11 months ago
Helperwifey
I am the wife of a husband who has advanced prostate cancer. He has just finished 6 rounds of Taxotere chemotherapy. He has taken Orgovyx and Nubeqa since his diagnosis. I am exploring holistic adjunctive therapy for him.
I am the wife of a husband who has advanced prostate cancer. He has just finished 6 rounds of Taxotere chemotherapy. He has taken Orgovyx and Nubeqa since his diagnosis. I am exploring holistic adjunctive therapy for him.
Helperwifey
in
Advanced Prostate Cancer
11 months ago
Dad actively dying , can't breathe. Horrifying. Need support after today if anyone available to reach out.
Seven year aggressive fight against stage four cancer from the start which after treatment turned to cll. His pca never changed but very slightly until of all meds and five weeks of hospice..chronic lymphocytic leukemia presumably from treatment is what's taking his life . "Gene's laughter and positive
Seven year aggressive fight against stage four cancer from the start which after treatment turned to cll. His pca never changed but very slightly until of all meds and five weeks of hospice..chronic lymphocytic leukemia presumably from treatment is what's taking his life . "Gene's laughter and positive
Daddyishealing
in
Advanced Prostate Cancer
11 months ago
New to the forum Peak Flow questions
Hi and thank you for allowing me to join your forum. Q: So I've done a peak flow diary over 22 days before I speak to GP tomorrow. My average readings are between 250 and 290. Is this poor? I have a complex health history, many battles with health pros, lots of investigations and some firm diagnoses
Hi and thank you for allowing me to join your forum. Q: So I've done a peak flow diary over 22 days before I speak to GP tomorrow. My average readings are between 250 and 290. Is this poor? I have a complex health history, many battles with health pros, lots of investigations and some firm diagnoses
Sallybones
in
Lung Conditions Community Forum
10 months ago
Bells Palsy that never was
Hi all, I mentioned a few weeks ago that I was diagnosed with Bells Palsy', and put on prednisolone for 10 days, it didn't work, and I was sent to an ENT man, who did an MRI which confirmed that I did not have the Bells Palsy, but they found a small tumour active and moving in my left facial area. I
Hi all, I mentioned a few weeks ago that I was diagnosed with Bells Palsy', and put on prednisolone for 10 days, it didn't work, and I was sent to an ENT man, who did an MRI which confirmed that I did not have the Bells Palsy, but they found a small tumour active and moving in my left facial area. I
Vindicatrix
in
CLL Support
11 months ago
Really positive respiratory review
I know I've moaned a lot on here about the difficulties I've had in getting the right care since diagnosis, but I had an annual respiratory review this week and it was really good - so thorough, and the nurse really listened to what I was saying and was working with me to keep the asthma well managed
I know I've moaned a lot on here about the difficulties I've had in getting the right care since diagnosis, but I had an annual respiratory review this week and it was really good - so thorough, and the nurse really listened to what I was saying and was working with me to keep the asthma well managed
Mandevilla
in
Asthma Community Forum
10 months ago
Pet scan vs CT scan
Hi fellow warriors, I've just had a phone appointment with my Oncologist my PSA is 0.7 and started to go up but not high enough to warrant having a Scan at the moment.My problem is she doesn't think she will be able to put me forward for a Pet scan as I have already had a couple in the past and with
Hi fellow warriors, I've just had a phone appointment with my Oncologist my PSA is 0.7 and started to go up but not high enough to warrant having a Scan at the moment.My problem is she doesn't think she will be able to put me forward for a Pet scan as I have already had a couple in the past and with
Chubby42
in
Advanced Prostate Cancer
11 months ago
excuse me asking. Brain fog.
Just a quickie, and excuse me for treading over old ground. Re starting Tapering , from 10 . My Dr called me whilst I was away, for an update on my Cancer Op, how was I feeling etc……. Mentioned to him about going back onto Pred, due to my fingers & hands . Long story short, wanted me to try and taper
Just a quickie, and excuse me for treading over old ground. Re starting Tapering , from 10 . My Dr called me whilst I was away, for an update on my Cancer Op, how was I feeling etc……. Mentioned to him about going back onto Pred, due to my fingers & hands . Long story short, wanted me to try and taper
Stifffingers
in
PMRGCAuk
11 months ago
A update on treatment/ and more.
I went for number two of a short three BCG course for my BC. The liquid BCG is inserted into bladder from a huge syringe into a catheter. A student nurse was present and my Urology Nurse a=said to het I had Muscle Invasive Bladder Cancer. news to me, I said and don't know why - I will now
I went for number two of a short three BCG course for my BC. The liquid BCG is inserted into bladder from a huge syringe into a catheter. A student nurse was present and my Urology Nurse a=said to het I had Muscle Invasive Bladder Cancer. news to me, I said and don't know why - I will now
Ern007
in
Lung Conditions Community Forum
11 months ago
Medication potential
Hi, I feel like an alcoholic, my name is Johnny, this is my first time here, I’ve had life changing FM for 4.5years and no days sober. I would like to know has anyone tried the following drugs and if so what were the results? Low dose Naltrexone, Milnacipran or Sunosi…..
Hi, I feel like an alcoholic, my name is Johnny, this is my first time here, I’ve had life changing FM for 4.5years and no days sober. I would like to know has anyone tried the following drugs and if so what were the results? Low dose Naltrexone, Milnacipran or Sunosi…..
Hidden
in
Fibromyalgia Action UK
1 year ago
Biopsy results
I received my biopsy results today. Last week the doctor took out a 2cm polyp in my sigmoid colon. My symptoms were blood in stool and rectal pressure. It came back as having some high grade dysplasia (precancerous) so I will need to repeat a colonoscopy in three years. If anyone is concerned about
I received my biopsy results today. Last week the doctor took out a 2cm polyp in my sigmoid colon. My symptoms were blood in stool and rectal pressure. It came back as having some high grade dysplasia (precancerous) so I will need to repeat a colonoscopy in three years. If anyone is concerned about
Hidden
in
Colon Cancer Connected
1 year ago
Clinical Trial with Abemaciclib and Olaparib
Hey Queens! I am reaching out to see if anyone is participating in this clinical trial. I am having a hard time deciding if this is a “favorable” option for me. I’d love to get some type of feedback from an actual patient. It’s fairly new, so any findings seem impossible to come by. Also, I’
Hey Queens! I am reaching out to see if anyone is participating in this clinical trial. I am having a hard time deciding if this is a “favorable” option for me. I’d love to get some type of feedback from an actual patient. It’s fairly new, so any findings seem impossible to come by. Also, I’
TealBlooms
in
My Ovacome
1 year ago
Constant green phlegm since March 2023
Hello. I was diagnosed with asthma in 2019 after a nasty chest infection where the GP said my chest was very wheezy and suggested that she thought I had asthma. It was confirmed over the next 2 months by spirometry and peak flow with the asthma nurse. I was given Fostair 200/6 and used it until February
Hello. I was diagnosed with asthma in 2019 after a nasty chest infection where the GP said my chest was very wheezy and suggested that she thought I had asthma. It was confirmed over the next 2 months by spirometry and peak flow with the asthma nurse. I was given Fostair 200/6 and used it until February
Rhirhi234
in
Asthma Community Forum
10 months ago
Reaction when first diagnosed with APCa
When I heard I had APCa I was not happy of course, but also not surprised too much since it runs heavy in my family. It took a while to realize it was the first day of the rest of my life, And if I didn't make some changes it could be a short one. I went mostly vegetarian, committed to daily exercise
When I heard I had APCa I was not happy of course, but also not surprised too much since it runs heavy in my family. It took a while to realize it was the first day of the rest of my life, And if I didn't make some changes it could be a short one. I went mostly vegetarian, committed to daily exercise
Derf4223
in
Advanced Prostate Cancer
1 year ago
Acoustic Neuroma - MRI Report After 1.5y of Surgery
Hi All. My wife(28y) was diagnosed with 1.3cm large Acoustic Neuroma and it's surgically removed in 2022 March. after surgery she is having deafness in right side and weakness of facial movement on right side. but those are manageable and now she is working as usual. only few symptoms are noticed
Hi All. My wife(28y) was diagnosed with 1.3cm large Acoustic Neuroma and it's surgically removed in 2022 March. after surgery she is having deafness in right side and weakness of facial movement on right side. but those are manageable and now she is working as usual. only few symptoms are noticed
siva_s
in
Acoustic Neuroma Support
1 year ago
Orserdu
After almost 6 years of being stable on Ibrance and letrozole I now have some very small progression into both my hips. My initial metastatic disease was in my lungs. I also tested positive for a mutation that frequently happens. That being said I am eligible to take the brand new drug Orserdu/elacestrant
After almost 6 years of being stable on Ibrance and letrozole I now have some very small progression into both my hips. My initial metastatic disease was in my lungs. I also tested positive for a mutation that frequently happens. That being said I am eligible to take the brand new drug Orserdu/elacestrant
HopeinNJ
in
SHARE Metastatic Breast Cancer
1 year ago
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