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Treatment for 54 year old

User
Posted 20 Mar 2024 at 12:22

I am 54 and was recently diagnosed. PSA 34.6, no previous tests, T2A, Gleason 4+3. As per the forum topic, the cancer is localised although NHS do intend for me to get a PSMA scan. The oncologist strongly recommended the surgery option for me, primarily "because of my young age". At first I was resigned to this, and I have an uncle who had RP in 2011 with a good outcome. But after a lot of research online, admittedly including a lot of YouTube videos from "experts" who are usually in the US, I was strongly drawn towards RT which appears to have equal results but with reduced side-effects in all areas. However, the one great advantage of RP is the much lower chance of recurrance and I think that's where my age and life exptency come into it.

I'm left confused and it feels an impossible choice. I've mostly talked myself out of the surgery option, everything about RT nowadays seems better, although I understand 10+ years ago that wasn't always the case. Both RP and RT are offered to me, it was just that RP was the recommended route. If I take RT, I just worry that it might be a stupid choice that I will regret. Can anyone offer reassurance about RT? And especially, is there anyone here diagnosed in their 50s (or younger!) who can talk about the choice they made?

Although I don't have private medical insurance, I would consider paying for the procedure, within reason, if it was going to give me greater peace of mind. But from what I read on other threads here, the main draw would be a reduced number of RT fragments (5 instead of 20+), plus potentially no need for hormone therapy, but apart from that the outcomes would be pretty much the same.

User
Posted 20 Mar 2024 at 14:22
Most important for you at the moment is the PSMA scan. I would stop thinking about it until you have the results from that. Spend your money on a private PSMA scan if necessary NOT private RT treatment.

If the scan confirms your staging RP or maybe Brachy are probably your best options with RP having the proven best results (in terms of PC survival) for younger men.

User
Posted 20 Mar 2024 at 14:44

Hi RadicalRob,

I agree that you need to wait for ALL your tests as the choice might be taken away from you. I was all set for RARP but then at the MDT they changed my staging which meant it was taken off the table.

Both treatment have side effects, I wouldn’t say RT is the easy option, especially if you need  HT as well. Some men seem to get off lightly, but for others like me it is the spawn of the devil!

Good luck with your treatment.

Derek

User
Posted 20 Mar 2024 at 15:08

Reducing the number of sessions of RT (referred to as 'Fractions'), to 5 is a fairly recent innovation so there is not the long term assessment of it but going back some 13 or so years the same could be said of 20 Fractions largely replacing the 37 which was the previous standard as a result of the CHHiP trial.  Essentially each Fraction gives a higher dose of Gys with Hypofractioned RT than with the more frequent fractions but the total amount of radiation is less. Of course patients like the fact that there are fewer attendances for them and the people who set up the machines need to spend less time doing this over a the course of treatment a patient has.  In my lay view it is more important to have your RT on one of the state of the art linacs, rather than be concerned about fewer fractions.

It is true that younger men are more likely to be steered towards Surgery leaving follow on RT (should this be necessary) to deal with cancer cells that cannot be reached.  If you have RT first, getting RT to everywhere else that might need it could prove problematical so you can you save your RT for later spread.  Side effects may be a concern but I feel dealing effectively with the Cancer is the most important aspect.  There is also the possibility that a cancer may regrow even in a radiated Prostate - happened to me. Every case should be looked at individually and a decision taken with everything in mind.  Have a look at the 'Tool Kit' which goes into more detail.

https://shop.prostatecanceruk.org//our-publications/all-publications/tool-kit?limit=100

Edited by member 20 Mar 2024 at 15:09  | Reason: Not specified

Barry
User
Posted 20 Mar 2024 at 15:20

Hi RadicalIRob

I would wait till you get more information following PSMA. Ideally what you want to know is whether the cancer is confined to the prostate gland and also whether there is a clear negative margin. If this is the case the balance begins to shift towards RP but not definitely because targeted RT may still be a better option depending on how the cancer is distributed within the gland and other factors. If you have RP and than RT, if necessary, RT would be a good back-up. But generally speaking if you go for RT than RP as a back-up is not a good idea although there are consultants who specialise in prostatectomy after RT treatments. This is my reading of the situation about  RT versus RP but, of course, nothing is simple. I have probably confused you further!

I had prostatectomy 12 years ago when RP was a clear choice for me because relatively speaking, RT options were not as advanced as they are now. Would I choose RP now?  I really don't know but with hindsight I am pleased with my decision not withstanding the fact that I suffer from very minor incontinence and ED which is due to my age and the surgery did not help! Generally speaking penile function post surgery - and possibly RT as well - is unlikely to be the same as pre-surgery. But there are many options to help one with ED if you happen to be unlucky.

If I were you I would closely examine the expertise and experiences of the consultants you have excess to and whether jointly they can help you to make a decision. 

I feel that much as I try to be objective about choices it is likely that I am biased towards RP because in spite of the side effects I suffer it has provided me a curative path so far!

Finally, you are young and fit therefore be optimistic about whichever treatment you choose and good luck.

 'Physics is like sex: sure, it may give some practical results, but that’s not why we do it.'                    Richard Feynman (1918-1988) Nobel Prize laureate

 

 

User
Posted 20 Mar 2024 at 17:48

Originally Posted by: Online Community Member
However, the one great advantage of RP is the much lower chance of recurrance and I think that's where my age and life exptency come into it

That's not right - if the cancer is contained, RP and RT have almost identical outcomes in terms of risk of recurrence. 

If you are leaning towards RT, you might be even more tempted by brachytherapy - risk of side effects is lower that with RT or RP while recurrence rate is almost the same. My husband was 50 at diagnosis and would hve had brachy if it had been available to him but he wasn't suitable - two of his mates have since had brachy and are very pleased with their decision so far!  

"Life can only be understood backwards; but it must be lived forwards." Soren Kierkegaard

User
Posted 20 Mar 2024 at 12:22

I am 54 and was recently diagnosed. PSA 34.6, no previous tests, T2A, Gleason 4+3. As per the forum topic, the cancer is localised although NHS do intend for me to get a PSMA scan. The oncologist strongly recommended the surgery option for me, primarily "because of my young age". At first I was resigned to this, and I have an uncle who had RP in 2011 with a good outcome. But after a lot of research online, admittedly including a lot of YouTube videos from "experts" who are usually in the US, I was strongly drawn towards RT which appears to have equal results but with reduced side-effects in all areas. However, the one great advantage of RP is the much lower chance of recurrance and I think that's where my age and life exptency come into it.

I'm left confused and it feels an impossible choice. I've mostly talked myself out of the surgery option, everything about RT nowadays seems better, although I understand 10+ years ago that wasn't always the case. Both RP and RT are offered to me, it was just that RP was the recommended route. If I take RT, I just worry that it might be a stupid choice that I will regret. Can anyone offer reassurance about RT? And especially, is there anyone here diagnosed in their 50s (or younger!) who can talk about the choice they made?

Although I don't have private medical insurance, I would consider paying for the procedure, within reason, if it was going to give me greater peace of mind. But from what I read on other threads here, the main draw would be a reduced number of RT fragments (5 instead of 20+), plus potentially no need for hormone therapy, but apart from that the outcomes would be pretty much the same.

User
Posted 20 Mar 2024 at 15:49

Like you I was in my mid-50s when I got my PC diagnosis, like you I agonised over which route to take, from HiFU, to RT to RP. My concerns were also the QoL and cure. I was lucky enough to have some sort of consultation with all the different consultants. I did however noticed that the RT consultant was trying push me towards the RP route, so it was easy to discount to discount her pathway! My choice in the end was between the RP and HIFU, I chose the surgery pathway.s This is coming up to 2yrs now, I do not regret my choice but however wonder if I could or should have waited a little bit longer before doing the surgery!

User
Posted 20 Mar 2024 at 17:50

Originally Posted by: Online Community Member
I would consider paying for the procedure, within reason, if it was going to give me greater peace of mind. But from what I read on other threads here, the main draw would be a reduced number of RT fragments (5 instead of 20 ), plus potentially no need for hormone therapy, but apart from that the outcomes would be pretty much the same.

I think you have been befuddled by google - the differences you have set out above are nothing to do with going private or NHS - they are just different approaches to RT based on a man's diagnostics and his onco's preference. 

"Life can only be understood backwards; but it must be lived forwards." Soren Kierkegaard

User
Posted 20 Mar 2024 at 19:03

Hi Rob, My diagnosis was worse than yours (but PSA was lower). I was 53 at the time, and I'm now 59. Click on my avatar view my profile and you can see my story which I would describe as successful (so far). Scroll to the bottom of my profile for links to useful threads. The good news for me was I had no choices offered, they said the only chance of a cure was HDR brachy and EBRT. I don't envy anyone who is offered a choice, after all I'm not an oncologist how am I supposed to know what's best?

I can not think why you will have to go private for any treatment, the NHS has many faults, but it does reasonably well with cancer treatment, but it is appalling at diagnosis. Do you know what hospital you will be treated at? I was treated at The Christie, they have all the state of the art equipment. If you are not being offered brachy it may be because your nearest hospital does not do it, but you could be referred to one further afield if it were the best choice for you.

As others have said a PSMA scan will give you much more information about what is the best treatment. If it shows spread in the pelvic area it would probably rule out RP, so there is a strong argument for not doing anything until you have that scan. The NHS is pretty bad at organising scans, so emailing the oncologist and saying you will take a short notice scan, maybe enough to get your oncologist to pick up your file and remember they are supposed to be treating you soon.

Don't go looking at RP thinking, oh well if it fails I can have backup RT. You want whatever your first treatment is to be the right one. If RT does work as a backup treatment it would have been better to have had it as the first treatment and skip a pointless RP.

Dave

User
Posted 20 Mar 2024 at 19:18

Thanks so much for this Dave. I haven't gone through your story yet but I shall. Yes, the choice does seem impossible. It feels empowering to have a choice, but then the choice becomes impossible.

I shall enquire about Brachy. It sounds like as you say I should push for the PSMA quicker. I have chased a couple of times, but only in an enquiring kind of way. I'll see if it can be brought forward.

I am in the Birmingham/Sandwell area, the QE would be the best in the area and that was already mentioned I think in relation to RP but I'm not sure about where was intended for RT. Luckily my diagnosis was handles pretty speedily (although I had pestered for a PSA scan in the past and pretty much talked out of it. And this time around was chasing a PSA since Sept but took multiple pushes till Jan before it actually happened). The PSMA and treatment were promised speedily also, but like I say, still waiting on the former.

Regarding the private route, it was only something I looked into in the past 24 hours and looked very tempting, particularly in relation to the MRIdian machine. Since discovered it's £32k - £42k though.

User
Posted 20 Mar 2024 at 23:51

Originally Posted by: Online Community Member

Yeah those are the parts that scare me 🤢

Hi Rob.

Welcome to the forum.

 It seems that generally there is very little difference in the outcomes between the various radical treatments. However in each radical treatment there are often enormous differences in outcomes to individuals. If you see what I mean?

 

 

 

User
Posted 21 Mar 2024 at 00:58

Originally Posted by: Online Community Member

Hi Rob.

Welcome to the forum.

 It seems that generally there is very little difference in the outcomes between the various radical treatments. However in each radical treatment there are often enormous differences in outcomes to individuals. If you see what I mean?

That is probably the most eloquent post this forum has ever had.

Dave

Show Most Thanked Posts
User
Posted 20 Mar 2024 at 14:22
Most important for you at the moment is the PSMA scan. I would stop thinking about it until you have the results from that. Spend your money on a private PSMA scan if necessary NOT private RT treatment.

If the scan confirms your staging RP or maybe Brachy are probably your best options with RP having the proven best results (in terms of PC survival) for younger men.

User
Posted 20 Mar 2024 at 14:44

Hi RadicalRob,

I agree that you need to wait for ALL your tests as the choice might be taken away from you. I was all set for RARP but then at the MDT they changed my staging which meant it was taken off the table.

Both treatment have side effects, I wouldn’t say RT is the easy option, especially if you need  HT as well. Some men seem to get off lightly, but for others like me it is the spawn of the devil!

Good luck with your treatment.

Derek

User
Posted 20 Mar 2024 at 15:08

Reducing the number of sessions of RT (referred to as 'Fractions'), to 5 is a fairly recent innovation so there is not the long term assessment of it but going back some 13 or so years the same could be said of 20 Fractions largely replacing the 37 which was the previous standard as a result of the CHHiP trial.  Essentially each Fraction gives a higher dose of Gys with Hypofractioned RT than with the more frequent fractions but the total amount of radiation is less. Of course patients like the fact that there are fewer attendances for them and the people who set up the machines need to spend less time doing this over a the course of treatment a patient has.  In my lay view it is more important to have your RT on one of the state of the art linacs, rather than be concerned about fewer fractions.

It is true that younger men are more likely to be steered towards Surgery leaving follow on RT (should this be necessary) to deal with cancer cells that cannot be reached.  If you have RT first, getting RT to everywhere else that might need it could prove problematical so you can you save your RT for later spread.  Side effects may be a concern but I feel dealing effectively with the Cancer is the most important aspect.  There is also the possibility that a cancer may regrow even in a radiated Prostate - happened to me. Every case should be looked at individually and a decision taken with everything in mind.  Have a look at the 'Tool Kit' which goes into more detail.

https://shop.prostatecanceruk.org//our-publications/all-publications/tool-kit?limit=100

Edited by member 20 Mar 2024 at 15:09  | Reason: Not specified

Barry
User
Posted 20 Mar 2024 at 15:20

Hi RadicalIRob

I would wait till you get more information following PSMA. Ideally what you want to know is whether the cancer is confined to the prostate gland and also whether there is a clear negative margin. If this is the case the balance begins to shift towards RP but not definitely because targeted RT may still be a better option depending on how the cancer is distributed within the gland and other factors. If you have RP and than RT, if necessary, RT would be a good back-up. But generally speaking if you go for RT than RP as a back-up is not a good idea although there are consultants who specialise in prostatectomy after RT treatments. This is my reading of the situation about  RT versus RP but, of course, nothing is simple. I have probably confused you further!

I had prostatectomy 12 years ago when RP was a clear choice for me because relatively speaking, RT options were not as advanced as they are now. Would I choose RP now?  I really don't know but with hindsight I am pleased with my decision not withstanding the fact that I suffer from very minor incontinence and ED which is due to my age and the surgery did not help! Generally speaking penile function post surgery - and possibly RT as well - is unlikely to be the same as pre-surgery. But there are many options to help one with ED if you happen to be unlucky.

If I were you I would closely examine the expertise and experiences of the consultants you have excess to and whether jointly they can help you to make a decision. 

I feel that much as I try to be objective about choices it is likely that I am biased towards RP because in spite of the side effects I suffer it has provided me a curative path so far!

Finally, you are young and fit therefore be optimistic about whichever treatment you choose and good luck.

 'Physics is like sex: sure, it may give some practical results, but that’s not why we do it.'                    Richard Feynman (1918-1988) Nobel Prize laureate

 

 

User
Posted 20 Mar 2024 at 15:49

Like you I was in my mid-50s when I got my PC diagnosis, like you I agonised over which route to take, from HiFU, to RT to RP. My concerns were also the QoL and cure. I was lucky enough to have some sort of consultation with all the different consultants. I did however noticed that the RT consultant was trying push me towards the RP route, so it was easy to discount to discount her pathway! My choice in the end was between the RP and HIFU, I chose the surgery pathway.s This is coming up to 2yrs now, I do not regret my choice but however wonder if I could or should have waited a little bit longer before doing the surgery!

User
Posted 20 Mar 2024 at 17:48

Originally Posted by: Online Community Member
However, the one great advantage of RP is the much lower chance of recurrance and I think that's where my age and life exptency come into it

That's not right - if the cancer is contained, RP and RT have almost identical outcomes in terms of risk of recurrence. 

If you are leaning towards RT, you might be even more tempted by brachytherapy - risk of side effects is lower that with RT or RP while recurrence rate is almost the same. My husband was 50 at diagnosis and would hve had brachy if it had been available to him but he wasn't suitable - two of his mates have since had brachy and are very pleased with their decision so far!  

"Life can only be understood backwards; but it must be lived forwards." Soren Kierkegaard

User
Posted 20 Mar 2024 at 17:50

Originally Posted by: Online Community Member
I would consider paying for the procedure, within reason, if it was going to give me greater peace of mind. But from what I read on other threads here, the main draw would be a reduced number of RT fragments (5 instead of 20 ), plus potentially no need for hormone therapy, but apart from that the outcomes would be pretty much the same.

I think you have been befuddled by google - the differences you have set out above are nothing to do with going private or NHS - they are just different approaches to RT based on a man's diagnostics and his onco's preference. 

"Life can only be understood backwards; but it must be lived forwards." Soren Kierkegaard

User
Posted 20 Mar 2024 at 17:58

Thank you guys for some great input. I would reply to all of you but there's a lot to take in. I understand what you mean about getting the PSMA results first, but it doesn't feel like (via NHS) that I have that luxury. They aren't pushing for my decision but it's been 12 days since they said they would line me up for a PSMA, but no sign of a date yet. Conversely it sounds like they might start pushing for my treatment decision if I leave it longer than another week or so.

It feels like I've talked myself out of the RP option and it would be difficult to get back into that mindset. Although, unless RT goes perfectly, having years of follow-up hanging over me with even worse side-effects does sound like the worst. If I could get a transplant with crystal balls, at least I'd be able to predict the future!

Some snippets in relation to various replies..

  • Yes, avoiding HT would be great if at all possible. Although they have said it would only be a short-term (4 month) course.
  • Having RT in a state-of-the-art machine would be great, as I don't have insurance, I think I would have to pay through the nose for it. I've already enquired on the cost. It's possible, but uncertain if it's worthwhile at that cost.
  • ED - a subject in itself. Yes, many options to help, but many that I don't like. And shrinkage! Am I correct in saying that this is entirely limited to RP patients?
User
Posted 20 Mar 2024 at 18:00

@Gee_Baba It's good that you got a good outcome and that you don't regret it. Strange though that the RT consultant recommended RP. Since you mention HiFU also, was this private? I don't think that's an option for me.

User
Posted 20 Mar 2024 at 18:05

LynEyre You are correct, I am very much befuddled by Google and overloaded with details. I did see that the reduced RT fragments could be done on NHS but it certainly wasn't mentioned to me, and I think I'm right in saying wouldn't be directly available in my area. Travelling for treatment wouldn't be a problem if it was necessary. I can certainly enquire on that.

Yes I am aware of Brachy and it was mentioned (in passing) at my diagnosis. Possibly they didn't think it was suitable in my case but I'd have to check on that. I think it's still listed under "clinical trials" though? I could certainly look into it further. It's good to know you've heard of successes with it.

User
Posted 20 Mar 2024 at 18:09

Just to let you know, I've just found the "reply" option 😄 Sorry, I'm new

User
Posted 20 Mar 2024 at 19:03

Hi Rob, My diagnosis was worse than yours (but PSA was lower). I was 53 at the time, and I'm now 59. Click on my avatar view my profile and you can see my story which I would describe as successful (so far). Scroll to the bottom of my profile for links to useful threads. The good news for me was I had no choices offered, they said the only chance of a cure was HDR brachy and EBRT. I don't envy anyone who is offered a choice, after all I'm not an oncologist how am I supposed to know what's best?

I can not think why you will have to go private for any treatment, the NHS has many faults, but it does reasonably well with cancer treatment, but it is appalling at diagnosis. Do you know what hospital you will be treated at? I was treated at The Christie, they have all the state of the art equipment. If you are not being offered brachy it may be because your nearest hospital does not do it, but you could be referred to one further afield if it were the best choice for you.

As others have said a PSMA scan will give you much more information about what is the best treatment. If it shows spread in the pelvic area it would probably rule out RP, so there is a strong argument for not doing anything until you have that scan. The NHS is pretty bad at organising scans, so emailing the oncologist and saying you will take a short notice scan, maybe enough to get your oncologist to pick up your file and remember they are supposed to be treating you soon.

Don't go looking at RP thinking, oh well if it fails I can have backup RT. You want whatever your first treatment is to be the right one. If RT does work as a backup treatment it would have been better to have had it as the first treatment and skip a pointless RP.

Dave

User
Posted 20 Mar 2024 at 19:18

Thanks so much for this Dave. I haven't gone through your story yet but I shall. Yes, the choice does seem impossible. It feels empowering to have a choice, but then the choice becomes impossible.

I shall enquire about Brachy. It sounds like as you say I should push for the PSMA quicker. I have chased a couple of times, but only in an enquiring kind of way. I'll see if it can be brought forward.

I am in the Birmingham/Sandwell area, the QE would be the best in the area and that was already mentioned I think in relation to RP but I'm not sure about where was intended for RT. Luckily my diagnosis was handles pretty speedily (although I had pestered for a PSA scan in the past and pretty much talked out of it. And this time around was chasing a PSA since Sept but took multiple pushes till Jan before it actually happened). The PSMA and treatment were promised speedily also, but like I say, still waiting on the former.

Regarding the private route, it was only something I looked into in the past 24 hours and looked very tempting, particularly in relation to the MRIdian machine. Since discovered it's £32k - £42k though.

User
Posted 20 Mar 2024 at 20:57

Originally Posted by: Online Community Member

@Gee_Baba It's good that you got a good outcome and that you don't regret it. Strange though that the RT consultant recommended RP. Since you mention HiFU also, was this private? I don't think that's an option for me.

To be fair, the consultant was a bit dismissive of my request, she mumbled something about the size and thickness of my prostate, she did however (grudgingly) said if that is what you want, then you can have it. I did not like her attitude and that was the last time I met her.

With respect to the HIFU, I was lucky enough to be referred to UCLH, who were trialling HIFU at the time. Again the decision was left to me.. I decided to opt for surgery in the end. The question is would I chose surgery knowing what I know now? I think I would would be a bit more cautious (as I feel the incontinence and ED were under played before my surgery). I foolishly thought, all I would need to combat ED post surgery was the tablets, and incontinence would be a matter of weeks and not years!

User
Posted 20 Mar 2024 at 23:10

Originally Posted by: Online Community Member

To be fair, the consultant was a bit dismissive of my request, she mumbled something about the size and thickness of my prostate, she did however (grudgingly) said if that is what you want, then you can have it. I did not like her attitude and that was the last time I met her.

With respect to the HIFU, I was lucky enough to be referred to UCLH, who were trialling HIFU at the time. Again the decision was left to me.. I decided to opt for surgery in the end. The question is would I chose surgery knowing what I know now? I think I would would be a bit more cautious (as I feel the incontinence and ED were under played before my surgery). I foolishly thought, all I would need to combat ED post surgery was the tablets, and incontinence would be a matter of weeks and not years!

Yeah those are the parts that scare me 🤢

User
Posted 20 Mar 2024 at 23:51

Originally Posted by: Online Community Member

Yeah those are the parts that scare me 🤢

Hi Rob.

Welcome to the forum.

 It seems that generally there is very little difference in the outcomes between the various radical treatments. However in each radical treatment there are often enormous differences in outcomes to individuals. If you see what I mean?

 

 

 

User
Posted 21 Mar 2024 at 00:58

Originally Posted by: Online Community Member

Hi Rob.

Welcome to the forum.

 It seems that generally there is very little difference in the outcomes between the various radical treatments. However in each radical treatment there are often enormous differences in outcomes to individuals. If you see what I mean?

That is probably the most eloquent post this forum has ever had.

Dave

User
Posted 21 Mar 2024 at 11:15

Originally Posted by: Online Community Member

LynEyre You are correct, I am very much befuddled by Google and overloaded with details. I did see that the reduced RT fragments could be done on NHS but it certainly wasn't mentioned to me, and I think I'm right in saying wouldn't be directly available in my area. Travelling for treatment wouldn't be a problem if it was necessary. I can certainly enquire on that.

Yes I am aware of Brachy and it was mentioned (in passing) at my diagnosis. Possibly they didn't think it was suitable in my case but I'd have to check on that. I think it's still listed under "clinical trials" though? I could certainly look into it further. It's good to know you've heard of successes with it.

Two responses - 

 

(i)  At my information meeting the oncologist said that although this major London hospital had in fact been part of the trial that had been done with the five fraction delivery and it had - in their limited lights - proved successful - the NHS had/has yet to approve it so it is not a 'publicly offered' procedure on the NHS.  This particular oncologist kept telling me what I could have done privately - which I thought at the time was a bit rich being my NHS 'information appointment'.  It made me question the whole thing from this particular aspect.  

(ii)  I wasn't offered LDR Brachytherapy at the time of my diagnosis - and I was very much in the same PCa numbered category as you.  It was offered to me by the oncologist at the time of my information meeting.  I was then pressed for an answer.  I went in twice for a urine flow test.  The outcomes were forwarded and I was told that the determining result from the oncologist would follow in a few days.  Over a month later - after having written in any number of times to the CNS nurses - I was told that the named oncologist had been away and that if I wanted to pursue Brachytherapy I would have to forfeit my RP date and start again re-doing all the information meetings.  That would put me over the six month marker and it was the very oncologist himself who told me that I 'couldn't wait that long'.  Go figure.

On Monday this week - totally unrelated - I was on the phone with a doctor at my GP surgery for a mid-back muscle strain.  The doctor told me that I should have 'an x-ray to see of the cancer had spread'!  I replied that I had had both a PSMA PET CT AND PSMA PET MRI scan and it had been shown to be contained on 20th December of last year.  'Yes, but now it is March' he replied.  THESE PEOPLE ARE DANGEROUS.  The very idea that he thought you could see if cancer had spread with an x-ray was laughable.  No wonder the UK death rates are so high.  

 

 
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