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DONT ASSUME IT’S LONG COVID

14 replies

FixTheBeak · 16/10/2022 09:10

DONT ASSUME IT’S LONG COVID

My mum had what we thought was long Covid. We looked after her and took her to appointments etc . As a family we are well informed, articulate and proactive so quick on managing symptoms and and getting appropriate medical help.

Her consultant thought she probably had cancer of the bowel or Polymalgia RHEUMATICA and she underwent scans etc - so far all clear. Bowel and bladder cancer referrals were put in at this time.

Eventually her energy levels were soo poor that we had to have her admitted to hospital for tests and to manage severe anaemia. While there she had episodes of tunnel vision which they hospital were completely uninterested in. I ended up calling an optician for advice as I didn’t understand why they were not fussed. In fact one of the consultants recommended that my mum go and see an optician when she got out.

DO NOT IGNORE VISION DISTURBANCES
DO NOT LET THEM FOB YOU OFF

My mum lost the vision in her eye a few days later and she is completely devastated.

it turned out she has a disease called GIANT CELL ARTERITIS which means steroids indefinitely. It is a medical emergency. I am putting the symptoms
at the bottom if this post because I had never heard of it before. To be fair she didn’t have any of the symptoms really so I understand why it wasn’t diagnosed on time. But I will never forgive them for ignoring episodes of tunnel vision - her eyesight could easily have been saved.

ADVOCATE FOR YOUR PARENTS BECAUSE THEY ARE REALLY VULNERABLE TO BEING FOBBED OFF

BE AGGRESSIVE ABOUT MANAGING SYMPTOMS

CHECK THAT ANY REFERRAL HAS BEEN PUT IN - my mums bowel cancer referral was delayed by two weeks because of incompetence

SYMPTOMS DONT ALWAYS FIT exactly - my mums only symptom was tunnel vision.

PLEASE PLEASE DONT ASSUME ITS LONG COVID

SYMPTOMS OF GIANT CELL ARTERITIS
(Inflamed temporal arteries)

The most common symptoms of giant cell arteritis are head pain and tenderness — often severe — that usually affects both temples. Head pain can progressively worsen, come and go, or subside temporarily.

Generally, signs and symptoms of giant cell arteritis include:

Persistent, severe head pain, usually in your temple area
Scalp tenderness
Jaw pain when you chew or open your mouth wide
Fever
Fatigue
Unintended weight loss
Vision loss or double vision, particularly in people who also have jaw pain
Sudden, permanent loss of vision in one eye
Pain and stiffness in the neck, shoulders or hips are common symptoms of a related disorder, polymyalgia rheumatica. About 50 percent of people with giant cell arteritis also have polymyalgia rheumatica.

When to see a doctor

If you develop a new, persistent headache or any of the signs and symptoms listed above, see your doctor without delay. If you're diagnosed with giant cell arteritis, starting treatment as soon as possible can usually help prevent vision loss.

THANKS FOR READING

OP posts:
Letsrunabath · 16/10/2022 09:23

Thank you.
Never heard of this but glad you have made me aware.

AnApparitionQuipped · 16/10/2022 09:26

Thank you Flowers

Mariposista · 16/10/2022 09:34

This is very true, for the elderly and also for young students. The latter group always seem to be being fobbed off with ‘ahh they are always ill anyway/freshers flu/they just drink too much and get run down’ and on some occasions they are actually sick and need treatment they have to really fight for it.

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FixTheBeak · 16/10/2022 20:30

Yes that’s very true - I remember thawing glandular fever very badly and they actually forgot to see me in the surgery- just left me asleep for hours @Mariposista

OP posts:
Buteverythingsfine · 16/10/2022 20:37

Sorry about your mum. One of my friends kept getting told her extreme exhaustion was depression by her GP, but she wasn't depressed and had no signs of depression except sadness she felt so shit, it was a brain tumor. Doesn't mean drs should assume that, but they do need to keep an open mind (eventually she had a seizure and it was discovered). Still think about her.

BringMeTea · 16/10/2022 20:39

Thank you and all the very best to your mum. Flowers

Sagaris · 16/10/2022 20:50

So sorry to hear about your mum @FixTheBeak - I was diagnosed with the same condition recently, hopefully before any long term damage has set in. There is a good support group on Facebook and the GCA PMR UK organisation is also very helpful - I rang their helpline last week for advice. There is also information on the Versus Arthritis website, and I've also just found a book by Kate Gilbert which is a mine of information. Please PM me if you'd like to chat - it's not a nice condition to have at all.

Badger1970 · 16/10/2022 20:53

My poor Dad had Covid in July. He was already unwell but we'd struggled to get him a face to face appointment and he got confused at times so when the GP phoned him (even though we'd asked them to phone me or my sister), he'd just mumble he was fine and this had been going on for weeks. In the end, I had a complete meltdown at one of the receptionists (not my finest moment) and he was given an appointment and the GP agreed to do bloods. They mumbled about Long Covid (even though Dad had been barely unwell with it) and did some bloods. 2 weeks later, he collapsed and was taken to hospital - where he was diagnosed with terminal liver cancer. All the symptoms - weight loss, no appetite, sweating, fever, confusion, pain in his shoulder - all fobbed off as long covid. The surgery rang back about another 2 weeks after this to say that Dad's bloods showed some issues... no shit, Sherlock.

I'm so unspeakably angry still. You're very right that Dr's are assuming way too much about bloody Covid.

BringMeTea · 16/10/2022 20:57

Oh Badger I am so sorry. That is horrific. And so wrong. Flowers

Namealreadyinuse1 · 16/10/2022 20:58

Sorry to hear this💐My mum was diagnosed with this a few years ago & then developed polymyalgia. As a general rule this develops in females over 70 (though there are of course exceptions). The steroids of course also do damage but must be taken.

Namealreadyinuse1 · 16/10/2022 21:01

Also, if you watch Doc Martin, this is a condition that was highlighted & is an ongoing storyline as Ruth was diagnosed with it.

ChocFrog · 16/10/2022 21:02

I agree the elderly are particularly vulnerable to this because they trust the doctors to do what checks/referrals are appropriate and don’t understand quite how badly the nhs is broken.

gmailconfusion2 · 16/10/2022 21:40

I've been told it's long covid. I've asked about CF, ME, MS, post viral fatigue and a selection of other things and been fobbed off each time, they seem to be so fixated on covid.

I work in a lab, we regularly get temporal arteries as specimens marked as routine, and always upgrade them even though the protocol is start patients on steroids immediately if it is suspected. I'm sorry you have been failed.

FixTheBeak · 17/10/2022 08:48

@gmailconfusion2

Can you get a full range of bloods done?

she was started on steroids stating away but only after the she lost vision.

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