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A load of symptoms and worried!

User
Posted 17 Aug 2018 at 12:48
I guess so Chris...still...it is a bit of a lottery but I do get the point about the impact on the NHS sadly!
User
Posted 17 Aug 2018 at 13:39

@MarkBerks

If I've helped lessen worry, I'm happy.

Your points about GPs and education are sensible...
GP awareness is lower than ideal.
Embarrassment is a deterrent to DRE.
DRE is increasingly considered less than effective and unnecessary.
Better education will be of benefit.


@Cheshire Chris...

> ...it would overwhelm the NHS to treat every man with prostate cancer, and in most cases such treatment would be unnecessary. I'm sure you can imagine the worry it would cause to a huge number of men to know that they have cancer, even when that cancer produces no symptoms and will never need treating.


As incidence and mortality of prostate cancer and breast cancer are relatively similar, is the lack of activity (education, diagnosis and treatment) similar to that undertaken for breast cancer (and likewise the smoking->lung cancer connection) acceptable in a relatively developed society? (I think not.)

Though less-than-ideally reliable, a PSA test as potential early detection is worthwhile... fast and cheap, it ought to be far more routine than it to-date has been.

The cost-benefit analysis is likely favourable... reducing the need for the expensive machines and meds which accompany later detection.

And socially, enabling people to live healthy lives... well, what price that?

The validity of 'needless worry' is questionable... although many instances of Pca require no treatment, enough do - and hence the value of the earlier-mentioned breast cancer-type programs, in which an important element is self-education and responsibility.


And, in closing, from a personal viewpoint... although vaguely aware of 'prostate cancer' for years, it's something to which I've not been sufficiently exposed to develop appropriate awareness.

I know far more about requirement and penalties for tv licence and car tax; that smoking causes cancer and other diseases; and that ladies are wise to get their breasts tested.

But, Pca... that it's common and often a killer? Nope, until recently that was something of which I was unaware beyond 'Isn't that where the doc sticks a finger up yer a**? No mate, I'm not into that.'

Edited by member 17 Aug 2018 at 13:41  | Reason: Typos

User
Posted 19 Aug 2018 at 12:36
Hi - I am still worried and will see the GP again in the week as the antibiotics have changed nothing and I still have pain after urination, a dull ache in my pelvis and a pain in my lower back (right above the tailbone I think). It bothers me that my level of worry seems out of kilter with the potential issue and even the reality that it could be cancer which is either treatable or at least has a 'years' prognosis rather than months (which my sister had with hers).

I don't want to be chided but has anyone else on here had similar symptoms and been ok with the whole process? Basically about 20 mins after going I get an urge to go again and a pain really where I think my bladder is! I also get perineal (sp?) pain and even rectal discomfort. Now the lower back pain which could be stress, bad posture or any combination! I also have muscle fatigue but have had that for years.

Sorry to keep harping on. I will see the GP, and I have an appointment with talking therapies hopefully to deal with my anxiety which seems out of control at times! I also really appreciate that many, indeed most, have very real struggles and make an effort to reply with sensible advice...whatever the outcome I hope to be as brave/pragmatic and considerate as the group on here...

Mark

User
Posted 19 Aug 2018 at 13:53
Still sounds like a UTI rather than anything else. Some are very resistant to antibiotics.
"Life can only be understood backwards; but it must be lived forwards." Soren Kierkegaard

User
Posted 19 Aug 2018 at 14:50
Mark, unless a culture is grown and the bug identified, it will be down to trial and error to sort out your UTI. This may be outwith your GP's capability. An urgent referral to your Urology Dept may bring you satisfaction. Hassle your GP!!

AC

User
Posted 19 Aug 2018 at 15:50
Thanks Lynn and AC - I will see him this week and ask for referral. Better to get checked and know the score than hope it goes away! I do have CFS (a bit like ME or Fibro) and read this can of thing can occur with both of those, but this seems very focussed in one area and the back pain and muscle pain has gone into overdrive...possibly as a result of stress too! I hate the unknown and the lack of certainty so you are right in that I need to get another check and see where we go from there. If nothing else, this is pretty uncomfortable and demoralising in its own right...stupid bloody gland!

Thanks again for listening - it helps massively...

Mark

User
Posted 24 Aug 2018 at 08:10

Well, GP still didn't suggest PSA as it could be variable if still an infection but he has referred me to a Urologist who I am seeing today in London. In the referral letter my GP says that the Prostate feels 'normal' but cannot work out where the post-peeing pain and pressure in the bladder area is coming from so asking for a second opinion. 

Waiting and worrying is a nightmare! I am not very good at this at and am now tending to withdraw and get very quiet which also has my wife worried...

Thanks as always for any support and encouragement...

User
Posted 24 Aug 2018 at 08:24

@MarkBerks...

> 'I do have CFS (a bit like ME or Fibro) and read this can of thing can occur with both of those...'

 

With CFS, 'all bets are off' and the body can behave unpredictably and erratically... scenarios with which many GPs are unfamiliar (and many still 'resist' CFS, wrongly considering it a psychological rather than physiological issue).

Without negating the obvious good intent and value of most GPs, there's a suggestion (which I've heard from specialists) they should increasingly more-quickly hand-off cases for appropriate follow-up.

And, although 'you don't need a weatherman to know which way the wind blows'... a 'feels ok' from a GP is bl**dy useless - only a small area can be felt, and it's as valid as 'assessing wind by sticking a finger in the air'.

The potential for prostate cancer (and various other things) is often not appropriately considered (by patient and/or medic), and hence disregarded, to the detriment of the patient's health (and the NHS budget).

 

User
Posted 24 Aug 2018 at 14:51

So, been to Professor and now really worried. Prostate hard on one side so he will book me in for an MRI. I suffer terrible anxiety and am now feeling very low. I know it is early days but I can’t help thinking the pains in the back and now a firm prostate is bad news. Feel like crying

User
Posted 24 Aug 2018 at 15:08

Sorry to read this Mark, the wait for the MRI plus results will compound how you feel.

Take care,

Ian

Ido4

User
Posted 24 Aug 2018 at 15:21

Thanks Ian. I don’t think I have ever felt so alone

User
Posted 24 Aug 2018 at 16:20

@MarkBerks...

 > Feel like crying.

That's understandable.

Crying often helps - so don't hold back.

 

> I don’t think I have ever felt so alone.

 Again, that's understandable.

 

So, 'prostate hard'... could be relatively minor or indicative of something more significant.

Either way, whether tests deliver an 'ok' or not... 'only way out is through'. With luck, any Pca gets diagnosed sufficiently early to be easily handled. Worst case, it's not.

'Nothing I can do about it now...', it-is-what-it-is and no amount of worrying, guessing, or anything else will influence that - but will cause you unnecessary and draining dis-ease.

So 'saddle-up for the ride' and relax as best you're able. Remember, however bad it is, things could always be worse.

 

:-)

 

Edited by member 24 Aug 2018 at 16:23  | Reason: Indecision and inability.

User
Posted 25 Aug 2018 at 08:48

Thanks Gulliver. I am to have an mpMRI and CT scan of the abdomen in Guildford once I get the appointment through. Back pain becoming immune to painkillers now and fear still there. Any tips on working through that appreciated. Also itching skin which seems an odd symptom. 

Mark

User
Posted 25 Aug 2018 at 09:23

>...I am to have an mpMRI and CT scan in Guildford. Back pain becoming immune to painkillers now and fear still there. Any tips on working through that appreciated. Also itching skin which seems an odd symptom.

 

Ah, Guildford... I once passed a relatively pleasant (yes really, things can always be worse than what's happening at the time) half-day in a locked-door pysch ward there. (Those questioning my use of 'relatively pleasant' should try being married to a 'texan, redhead, lawyer'... even though I loved her dearly.)

Anyway...

There might be further painkiller options... to slow tolerance I used to do a month of Dihydro and then a month of Tramadol. For non-opioid, Diclofenac is stronger than Naproxen. (I'm told smoking heroin is quite good, and relatively un-addictive.)

GPs vary in 'willingness to prescribe', but the H should be easy to get.

Itching skin could be who-knows-what - often a stress-related symptom. Simple over-the-counter anti-histamines might help, and those which induce drowsiness should help you better deal with your fears... not much use if you're about to go on The Krypton Factor, or have nuclear bombs to defuse, though.

MRI should be easy (somewhere onsite I've a post - can't remember what it's called - about mine), I fell asleep.

CT is 'over before you know it'. So brief I didn't get the chance for a snooze.

You may at some point also get a bone scan... if so, ask 'em to 'lift the plate, so it's not scraping your nose' - it was only after mine that I learned how some techs have it lower than necessary, thus increasing chance of claustrophobia.

User
Posted 28 Aug 2018 at 13:32

Feeling awful now. Bad back pain, pain after I pee and this morning I went to A&E just to get some relief and maybe some reassurance. Bloods taken and normal outside of a slight elevation on an inflammation marker. 

 

So, now I have some inflammation, one side of my prostate is firm and I have the pain and symptoms. I am such a bad worrier and my total inability to deal with my emotions is really hard. 

 

I know I am supposed to man up, but I cannot move my brain in that direction at all! I will be having an mpMRI and CT scan of my abdomen at some point but I feel dead already inside. I lost my beloved sister two years ago and have not even moved on from that. 

I know symptoms are not a real indicator but I feel after zero help from antibiotics there is only one other thing left that it could be. 

Has anyone else felt as desperate as this? I may see the GP for something to reduce the anxiety but how do you all seem to get on with life and roll with the punches? 

Sounds pathetic I know, but just need some support and maybe some similar thoughts to know I am not alone. 

 

Thanks

User
Posted 28 Aug 2018 at 16:44

Mark, getting panicky while you're waiting for tests and results is completely normal, but it WILL pass. I was diagnosed with both prostate cancer and kidney cancer in May, and all I could think about from the moment I woke up in the morning until I went to sleep was cancer. At that time I couldn't imagine that I'd ever enjoy life again. Three and a half months later and the prostate cancer is in hand, the kidney tumour is being surgically removed this coming Saturday, and life feels good again.

No matter how bad the results might be, you'll feel better when you know what's wrong with you and have a treatment plan in place. I guarantee it.

In the mean time, do go and see your GP and get some medication for the anxiety. My GP put me on a drug call Sertraline which helped tremendously.

Chris

Edited by member 28 Aug 2018 at 16:46  | Reason: Not specified

User
Posted 28 Aug 2018 at 17:37

Thanks Chris - your reply has helped me relax a little! I think it is the fear of the unknown and also the fear of my usual route of withdrawing when I get depressed...I just don't want that to happen. I am already on Venlafaxine for a long standing depression but the mornings are hell and I seem to be in a lot of pain, which could even be mainly my own brain working against me (along with fatigue, bad posture etc).

But I appreciate your reply - it helps!

All the best,

Mark

User
Posted 29 Aug 2018 at 02:17

Hi Mark,

I’m a worrier too - still awake at 3am as usual. Just sending you a hug to let you know you’re not alone. 

Fingers and toes crossed for good results xx 

Vicky 

Broken crayons still colour 

User
Posted 29 Aug 2018 at 07:15

Thank you Vicky. Sending one back x

User
Posted 29 Aug 2018 at 07:26

Strange, I don’t think I have had any psychological reaction from my raised PSA, to being diagnosed with cancer, subsequent operation and biopsy results. Maybe because I read stuff like this below, and bear in mind, survival rates are increasing year on year.

In contrast, with lung cancer, 96% of sufferers die within five years. Don’t know if these statistics will give you any solace, I hope so.

From an American cancer website:

According to the most recent data, when including all stages of prostate cancer:

The 5-year relative survival rate is 99%
The 10-year relative survival rate is 98%
The 15-year relative survival rate is 96%
Keep in mind that just as 5-year survival rates are based on men diagnosed and first treated more than 5 years ago, 10-year survival rates are based on men diagnosed more than 10 years ago (and 15-year survival rates are based on men diagnosed at least 15 years ago.

https://www.cancer.org/cancer/prostate-cancer/detection-diagnosis-staging/survival-rates.html

Cheers, John

 

Edited by member 29 Aug 2018 at 13:58  | Reason: Not specified

 
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