Hi, has anybody else been told they can't have their blood test due to the shortage? I've been on, since the pandemic, a 3 monthly test cycle, and due now but the doctors are saying no blood tests for at least a couple of months. I'm on Methotrexate and Rituximab and feel OK but the tests have bought a problem up in the past!!
Blood test capsule shortage: Hi, has anybody else been... - NRAS
Blood test capsule shortage
Not yet but I expect a delay next time round. But luckily mine is also done by my Nephrologist so that has to be done and I'll go to the Renal hospital and they will share results.
There’s a National shortage of vials. Only emergency tests for a few weeks I saw in the newspaper today.
Yes, mine was booked for the 7th but I had a text saying that they were allowed cancelled until the 17th. I went online and rebooked for the 17th so we shall see...
I must be living under a rock, I had my blood test on Thursday (every 3 months) this is the first time I've heard of a shortage of vials, my dermatologist also requested my full bloods last month before my skin biopsy and requested more this month for connective tissue disease and coeliac screening, I don't have my bloods checked at the Drs, I go to a rheumatology clinic. I will be seeing my rheumy consultant in September and she's already said I'll be having a full blood screen (which they always do anyway).
My blood tests are organised by my Doctor's, it changed that way about 2 years ago. I have my tests done at the hospital but need my Doctor's surgery to "put it on the system". I have seen a reference to the vial shortage on the news, and wonder if it's just starting to go down hill!!
I've had mine done twice in the last 3 weeks but I'm having problems with my BP, liver and HB, so I assume that's why.
bbc.co.uk/news/health-58374553 Article about shortage
I had heard but not been informed officially. Mine aren't due for two months so wouldn't expect to hear yet anyway. Another worry to add to the collection.
I need to book mine this week for 2 weeks time so I’ll see what happens. At the beginning of the first lockdown last April I was told by the surgery that they weren’t doing blood tests but once I’d missed 2 (every 6 weeks) they stopped issuing my methotrexate - without telling me why.
Had my monthly bloods taken last Thursday and no mention of any shortages, but heard about it in the media.
Not at all.no problem at my surgery
I’ve recently had to add Sulfasalzine to my MTX and should be on two weekly bloods for while - I’ve had the first set on Friday and when I go online I see my next two lots of bloods have ‘blocked’ next to the dates and I can’t do my usual online booking for the one due after that so I will have to see what my bloods look like from Friday and make a decision wether to keep upping the Sulfasalzine as prescribed by rheumy or to sit tight on what I’m on until bloods can resume.... getting hold of rheumy clinic has always been impossible (short opening hours, phone rings and no one answers or it’s engaged!)
Hey ho, what can you do but carry on - at least I’m not running for my life!!
All the best
Ali
Yes, I can make an online booking at the hospital, but I know from experience if it's not booked on the system by the surgery then they won't /can't do it!!I found an email address for my rheumy help line on my last visit, I can't believe they all don't have one. Its not quick but I have had a telephone response from them using it.
Just have to keep pushing your way through, and hope for the best!!
I had bloods done last Thursday when there was some bits in the press re shortages of vials, by my nurse appointment on the Friday it had gone to essential bloods only. Was told 2 monthly instead of monthly and can no longer book on the NHS app, have to ring my surgery
This is a very worrying time, No Vials! I wonder if they come from abroad? I’m glad I’ve just had mine done. My haematologist insists I get them done at the hospital but my GP also contacts me every 3 months to get other ones. I have lymphoma and wouldn’t like the bloods getting delayed as it’s a kinda relief after they are done telling me that everything still the same and my condition is not getting worse. I’m sure everyone feels like that after getting bloods done. Fingers crossed the situation improves as it will create another backlog.
I have a blood test tomorrow 🤞which my GP and I organised to see how my body is accepting the increase of mtx.
Yes, I had mine booked for Thursday and had the doctors cancel it. I also have them every 3 months but my white cell count is very low. It’s a real worry!
I have heard about the shortage of vials in the news. I have blood tests booked for tomorrow morning and still going ahead as had a reminder text this morning. Feel guilty being able to have my blood tests done when other people are not able to have their critical blood tests done. Hoping it is temporary and everyone who needs their blood tests can get them done very soon. x
Definitely no need to feel guilty!Mine is definitely not urgent and I'm sure that there are plenty in the same situation whereas you need monitoring!
Hope you get some answers soon 🤞😊
Err you need yours .. you’ve had major infections. Don’t feel guilt. I do worry some people may not feel they need their tests when they do. I will have more immunity ones I am recommended to by my rheumy as I’m getting bronchitis and pneumonia every other month now. That needs to be monitored closely. I think in a few weeks the shortage of glass will improve. 🙏🏻 It’s not right I agree if some people are left without vital blood tests. The rheumys will need to adjust re proof of the blood test results to be able to approve RA meds though if the shortage continues. Just as they had to last year. xx
I am very relieved to be having my blood tests and it is important as you say to monitor my recovery from pneumonia. Just wish other people have not had their much needed tests cancelled but hopefully things will get back to usual service for everyone as soon as possible. So pleased you are having your much needed tests too. xx
Have had some but need to have more in depth ones. Immunology phone consultation next week so I’m sure there’ll be some more they want me to have. Hope you’re feeling some improvement even if small steps. 🙏🏻💗 xx
Brexit strikes again 🙄. I hadn’t even heard of this one…totally insane…
gponline.com/gps-forced-spe...
Not Brexit this time. It's a global issue.
My husband who works in manufacturing, says there's a shortage of materials across many industries due to lockdowns, furlough and redundancies.
Yay 🎉…..I think the next few years are going to be arduous in different ways 🙃…Roll on 2025……😓
Saw my gp last Friday and I've booked a blood test for this Friday, he didn't mention anything about it, but I have seen it mentioned. It is very important to have regular blood tests when on methotrexate, my doctor used to get cross with me when I didn't have them done regularly when I took them. I would keep on to them, best wishes
You can’t usually get approval for RA meds and not Mtx if you don’t have your bloods done. My requirement on Rtx and Mtx is 3 monthly bloods or no approval for those meds. Last year some people had to go longer though re blood testing but I was told still 3 monthly.
Yes I'm 3 monthly and due a new biologic prescription so I'll have to check with my nurse if bloods are considered necessary during the current problems.
I would think they are. You’ll need to know where your bloods are before starting a new biologic. I’m due to change meds later in the year but hopefully the glass shortage won’t be an issue then to me or anyone. I’m currently having my immunoglobulins investigated as well as the usual blood tests for Rtx, so I would hope they will continue as my side effects are not improving.
Sorry wrote it wrong I meant to say repeat biologic prescription 🙄Hope a change of meds works out for you- asap 🤗
I’m due to phone up for an appointment tomorrow for my mtx bloods. In my favour I was told to do so by the dr I spoke to on Friday as well as my rheumatologist, and my liver results have been a bit dodgy over the last few tests my liver results have been decidedly dodgy.
I would hope that you will get a test, mtx is not a nice thing to have to take and does need monitoring for that exact reason.
I have mine booked In for Wednesday, I haven't had a text reminder yet though, so we will see.
Yes there is a global shortage so they are reserved for cancer patient and major bleeding etc. More stock should be available mid term late September.
I went for my blood tests this morning and the nurse was saying to me that they have cancelled all routine blood tests until the end of September in my GP surgery but said to me I will continue to have mine. Asked if they had heard anything about the booster vaccine for Covid but they are still waiting to hear what the government advise. Flu jabs will start mid to late September too and I’ll get a text to book my flu jab. Appreciate that this is just the advice for me from my GP surgery though. I feel very lucky to have such a good GP surgery in that they prioritise my blood tests and any vaccines etc. Just wish the care was the same for everyone x
I had mine done today but am pregnant as well as having steroids / flare up so lots to look at. She didn’t think it’s be too much of an issue having them going forward 🤞🏼
My hospital trust is saying restrictions are in place until the 18th September, only book if it's urgent or you have a clinic appointment before the 25th September. I'm due my 12weekly ones for my mtx and biologic next week so I'll probably contact the rheum nurse and see what she advises, as I've been having a flare this last week.
Yep I had an email and text this mirning from hospital this morning cancelling blood test booked for 13th, the email also said no re bookings available for blood tests at the moment.