General Medical issues thread

I use it now although I didn't to to begin with. Regret that as it's so easy to check on blood tests and anything else. Results are uploaded but can't be opened by me for 7 days after publication. I suppose that's to give the Dr time to see them without being hounded by the patient. I assume that's the same with everyone and not just some setting I have missed.
 
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I was talking to a friend last night and she said I should download the My Health Record app.
Where you can see all your blood tests, scans and results etc.
I seem to recall some chatter about it when it first came out.
Anyone have any opinions or experience?
Yep. I can check all the scripts I been have issued and dispensed. Some places don't upload to it which is disappointing. All of husband's hospital visits and results are there however the place we go for his bone scans have to be manually imported by the GP I believe as they don't upload to My health they have their own system
I am also a bit reassured that is something happens eg a car accident or suchlike , my GPs information is there , my meds etc
 
I was talking to a friend last night and she said I should download the My Health Record app.
Where you can see all your blood tests, scans and results etc.
I seem to recall some chatter about it when it first came out.
Anyone have any opinions or experience?
I've found that many providers never upload to it. I have to go to a specific lab and they always load up. I do have the breast screen results loaded, and the Covid tests that we were required to have during that time. And that's it. No recent X-rays. Annoying. Especially when they cost a heap but I have to go to the GP to get the results. Get them to print them and so on. It wasn't supposed to be like that.

Scripts filled are in the Medicare file which has always been available. Separate to my health.
 
I use it now although I didn't to to begin with. Regret that as it's so easy to check on blood tests and anything else. Results are uploaded but can't be opened by me for 7 days after publication. I suppose that's to give the Dr time to see them without being hounded by the patient. I assume that's the same with everyone and not just some setting I have missed.
That's the same for everyone, 7 days. Some results may need a Doctor to deliver them with counselling etc, also to prevent people self medicating when they see a result (as some on here seem to do a lot!)

I think there are a couple of tests available immediately but most is the week.
 
That's the same for everyone, 7 days. Some results may need a Doctor to deliver them with counselling etc, also to prevent people self medicating when they see a result (as some on here seem to do a lot!)

I think there are a couple of tests available immediately but most is the week.
Yes. Locked for 7 days. Covid and similar were available immediately.
 
Some new legislation has been passed in relation the MYHR

Productivity Commission report on digital health data

For those withAFR subscription
About time. S&N were supposed by law to upload pathology results to MHR by dec 2024. Still have not done it! QML no problem but S&N you have to go to website after tests and specify the day and time of the collection. Bloody ridiculous lazy company.

I know some diagnostic services and medical practitioners and specialists want to keep results from the patients and some practices still resisting disclosure. Should be fined for non compliance IMHO.
 
About time. S&N were supposed by law to upload pathology results to MHR by dec 2024. Still have not done it! QML no problem but S&N you have to go to website after tests and specify the day and time of the collection. Bloody ridiculous lazy company.

I know some diagnostic services and medical practitioners and specialists want to keep results from the patients and some practices still resisting disclosure. Should be fined for non compliance IMHO.
4cyte are very quick at uploading
 
About time. S&N were supposed by law to upload pathology results to MHR by dec 2024. Still have not done it! QML no problem but S&N you have to go to website after tests and specify the day and time of the collection. Bloody ridiculous lazy company.

I know some diagnostic services and medical practitioners and specialists want to keep results from the patients and some practices still resisting disclosure. Should be fined for non compliance IMHO.
But that’s not the only problem with S&N. They are the nearest lab for me to get my therapeutic venesections. But about 5 years ago they decided that they wouldn’t do them for people over 70. So now have to go to QML at Buderim.
 
Thanks to being able to see my MRI report in the QScan app, and to my physio, I understand more about my back pain than what the ortho explained to me.
He basically said my discs are degenerating/have degenerated, there’s no surgical answer and I should see a pain management clinic.

Severe dessication at L4-L5 and L5-S1 mild to moderate arthropathy and prominent L5-S1 discopathy. Moderate bilateral exit foraminal stenosis at L5-S1, mild mass affecting L5 nerve roots.

My physio says my lower spine will likely fuse itself over the next 10-15 years. And the MRI explains some thing about my back/body he was finding confusing.
In the mean time, calf and hip flexor stretches and pelvic exercises.
 
I'd like to ask a question on carpal tunnel syndrome management here as I know some have experienced it and some have clinical knowledge. Sorry for the length; I hope it's clear. 12 mths ago: symptoms began to worsen markedly (after 18mths of milder ones), with significant sleep disturbance from dead or tingling hands. Was waitlisted for surgery (public, in Melbourne, no PHI). Tried (competent) physio without benefit. Tried a course of prednisone 25mg which helped greatly, but only for the time taking it.

7 mths ago: Middle finger tendons started catching in the wrists, leading to ultrasounds, steroi_ injections, and updated referral for surgery. Still triaged as "routine". The injections mainly made good sleep possible, with gradual (perhaps unrelated) fading of the tendon-catch problem.

Last four mths: increasing sleep disturbance again, plus daytime "buzzing" in the hands (very strong after exertion), occasionally dropping things, some difficulty gripping hard, then recent occasional jolts of nerve pain with certain movements and strong morning stiffness of hands. I have tried taking a single 25mg prednisone about every 10days just to give me a night or two of full sleep. The GP reluctantly agreed to this approach.

Fortnight ago: I've been on the hospital waiting list for 11 months. I went back to the GP to get referred for repeat steroi_ injections. GP also updated referral to hospital given established functional impairment. As there usually has to be a gap between steroi_ injections and surgery ( the literature indicates more than 30days is clearly advisable, but various surgeons/services seem to say anywhere between two and six months), GP told me to wait until triaging was clear, then call the hospital to talk about the necessary injection-to-surgery gap. Alas, the hospital does not appear to have completed triaging in the fortnight since.

In the intervening fortnight I've had two new symptoms: (1) one morning where an attempt to close my hand caused intense tendon pain across one hand (became milder over the day and abated by evening). No obvious unusual use in the day prior. (2) The following night I was woken by excruciating nerve pain across the fingers of the same hand, lasting perhaps 30minutes (I didn't quite reach full alertness, but by the end of the doze/dream state I was contemplating whether I'd need to go to Emergency if it went on much longer). Thankfully this has not yet recurred.

I'm seeing the GP in a few days' time, but I feel I need to be better prepared for various planning and symptom management scenarios. AND I'm travelling for three weeks from late August, so the window for (hypothetical) surgery-plus-travel-safe-recovery is now effectively closed.

If updated triaging means I might actually get surgery in the next, say, four months, then injections may be unwise, leaving me with no previously-tried management options, and some clearly more serious symptoms popping up occasionally. If I'm still a "routine" case, then the injections would presumably give me a few months' amelioration (and make travel more pleasant). To be clear, I do still have reasonably good use of both hands most of the time. Any suggestions/thoughts welcome.
 
Sorry to hear @aspro2.

Carpal tunnel syndrome can be quite bad. I have it in both but right is worse than left. Unfortunately the right thumb and forefinger also have osteoarthritis and I cannot extend them to grip anything. Even putting something in right hand is hard to hold. The right thumb feels dead. Constant numbness. I get tingling feeling in fingers of right hand. On the left hand the forefinger, middle finger and ring finger feel tight from palm to fingertip.

I have intermittent swelling of both hands/arms all the way up to elbow. The tightness can be uncomfortable. I've been known to wake up in middle of the night with either or both hands numb. Stressful. Can take 15-20 seconds, sometimes more, to return to normal.

There are other issues but too many to remember and I have not documented them. I try not to take any medication. I have been known to take 15-20mg prednisolone if inflammation in body feels bad and occasion I've taken similar dose a second night but never 3 nights in a row. Last time was about 4-5 weeks ago.

One thing I noticed is that it can affect my golf. Struggled last trip in April until I decided to take 2 x Panadol Osteo, Mobic 15mg and Tramadol 100mg in the morning about 2-3 hours before golf and made me feel better and golf actually improved last 3 games as opposed to first 5 games. I'll do same in September and see how I go.

I'm not considering any sort of surgery. I'm also not considering any type of cortisone injection as every single joint in my body has severe issues and I'm not going to choose which one to treat and which one to leave alone. Just put up with pain and discomfort for as long as possible.
 
My experience only of course and it may have no relevance for you and is obviously not medical advice.

I had Carpal Tunnel Syndrome about 5 years ago. It started with a sharp electric pain if I knocked my fingers against something or twisted my wrist at an unusual angle. It then progressed to pains that would wake me in the night. I ended up lying on my back and sticking my hand vertically upwards and for some reason that would ease the pain. The finger and thumb were also becoming a bit numb.

I had a nerve conduction study that resulted in a diagnosis of severe CTS. My GP had a go with acupuncture which worked as well as I thought it would - not at all. But it was interesting to see how it was done and cost me nothing. My pain was never severe enough to require medication.

So I booked surgery. I have private health cover so there was not too long a wait. The operation was done under local and was no more painful than a tooth filling at a dentist. The scar is imperceptible. Recovery was without any complications with just a small amount of pain for a few days. The CTS has completely disappeared but the affected finger and thumb still have a slight feeling of numbness but it is only just detectable. This ongoing numbness is a known possibility. A friend of mine had a similar operation but it was more complicated due to arthritis and the post operation phase has been a lot more painful.

Now I have a 'trigger finger' and finger stiffness (different hand) that has been treated by physiotherapy. But while that has improved it somewhat it appears almost certain that I will require a steroi_ injection.
 

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