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Brain tumours (low-grade/mixed)
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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
1 year 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
1 year ago
New adult onset asthma
Hi all, I'm a man in my early 40s of normal weight and never smoked. I've just come out of hospital with what is assumed to be a severe asthma attack. I spent 10 days in respiratory ward. My o2 got down to 89% and my peak flow down below 200. It took me a long time to turn round but now back at home
Hi all, I'm a man in my early 40s of normal weight and never smoked. I've just come out of hospital with what is assumed to be a severe asthma attack. I spent 10 days in respiratory ward. My o2 got down to 89% and my peak flow down below 200. It took me a long time to turn round but now back at home
Particle32
in
Asthma Community Forum
11 months ago
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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
1 year ago
Asthma Drs do they know.
Hi There are times when I can’t breath, but when I check my Sats they are between 90 and 95. But I still struggle, the hospital Dr says it can’t be bad as I am between 90 and 95. I am usually 85 up my peak flow is 250 best and 150 in the morning. I don’t know why I struggle at that No but it’s scary
Hi There are times when I can’t breath, but when I check my Sats they are between 90 and 95. But I still struggle, the hospital Dr says it can’t be bad as I am between 90 and 95. I am usually 85 up my peak flow is 250 best and 150 in the morning. I don’t know why I struggle at that No but it’s scary
Eian59
in
Asthma Community Forum
11 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
1 year ago
treatment of prednisone side affects
I live in the USA I’ve posted before but have a question . My rheumatologist has not agreed to taper my 20:mg dosage of prednisone yet , ( 6 months on this dose) Ive had two doses of Kevzara and all labs are normal,but IL-6 is increasing . He says soon we will taper slowly . In the meantime my FBS are
I live in the USA I’ve posted before but have a question . My rheumatologist has not agreed to taper my 20:mg dosage of prednisone yet , ( 6 months on this dose) Ive had two doses of Kevzara and all labs are normal,but IL-6 is increasing . He says soon we will taper slowly . In the meantime my FBS are
GMA74
in
PMRGCAuk
1 year 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
1 year 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
1 year 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
1 year ago
How could AI help in asthma care?
Hi all! I have a question for you: as an asthma patient, how do you think AI could potentially help meet needs you have that aren't currently being met? For example, I have been reflecting on how doctors could potentially use AI to more accurately diagnose, treat, and educate patients. For me personally
Hi all! I have a question for you: as an asthma patient, how do you think AI could potentially help meet needs you have that aren't currently being met? For example, I have been reflecting on how doctors could potentially use AI to more accurately diagnose, treat, and educate patients. For me personally
hilary39
in
Asthma Community Forum
11 months 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
Early detection saves lives!
‼️ EARLY DETECTION SAVES LIVES! Check your skin monthly and seek immediate professional advice with anything NEW, UNUSUAL or CHANGING.BE WARNED! Skin cancer comes in many guises and not all types of melanoma follow the ABCDE rule!To LEARN MORE and TAKE CHARGE of your skin health and surveillance, install
‼️ EARLY DETECTION SAVES LIVES! Check your skin monthly and seek immediate professional advice with anything NEW, UNUSUAL or CHANGING.BE WARNED! Skin cancer comes in many guises and not all types of melanoma follow the ABCDE rule!To LEARN MORE and TAKE CHARGE of your skin health and surveillance, install
SkcinHQ
Partner
in
Skin Cancer UK
1 year 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
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
Newly Diagnosed and shocked
50 yrs old. Just got diagnosed with prostate cancer. Gleason 9. Spread to pelvic and vertebrae Took first casadex pill today. Will do injection (turpa I think) within 2 weeks Pretty down as you can imagine because of words like incurable!! Just saying Hi and will start checking out the site and
50 yrs old. Just got diagnosed with prostate cancer. Gleason 9. Spread to pelvic and vertebrae Took first casadex pill today. Will do injection (turpa I think) within 2 weeks Pretty down as you can imagine because of words like incurable!! Just saying Hi and will start checking out the site and
Yzinger
in
Advanced Prostate Cancer
1 year ago
PSMA PET 2 weeks after EBRT
So my MO scheduled a PSMA PET 2 weeks after the end of my EBRT. I didn't argue and did it. Im seeing her tomorrow and will ask why. Maybe she forgot I did radiation?? Ill ask for another in 3 months. Meanwhile, the report shows the lymph node is now mild uptake SUV 2.5 MAX. It was intensely radiotracer
So my MO scheduled a PSMA PET 2 weeks after the end of my EBRT. I didn't argue and did it. Im seeing her tomorrow and will ask why. Maybe she forgot I did radiation?? Ill ask for another in 3 months. Meanwhile, the report shows the lymph node is now mild uptake SUV 2.5 MAX. It was intensely radiotracer
Hidden
in
Advanced Prostate Cancer
1 year ago
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