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AIBU?

Share your dilemmas and get honest opinions from other Mumsnetters.

AIBU to warn you NOT TO ASSUME LONG COVID

29 replies

FixTheBeak · 16/10/2022 09:55

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:
FixTheBeak · 16/10/2022 17:15

@Banrockmystation @stayathomegardener

Are you both saying that you developed Giant Cell Arteritis after Covid? I has
wondered this too as she had Covid in March and by May had developed a weak voice and gastrointestinal issues

OP posts:
FixTheBeak · 16/10/2022 17:17

itswonkylampshade · 16/10/2022 10:56

So sorry about your Mum. I totally endorse your OP, we had the same with our beautiful Mum who was fobbed off again and again with visual disturbances, being told she had vertigo. One of her GPs actually became palpably irritated by her going back to him a second time because of them.

She turned out to have a brain cancer which killed her.

Her treatment by the NHS pre-diagnosis was unforgivable and we only found out there was something serious going on because a close relative has a senior position in the local hospital and insisted she was scanned.

I’m sorry about your mum, you just be devastated about the lack of care she experienced

OP posts:
stayathomegardener · 17/10/2022 11:44

FixTheBeak · 16/10/2022 17:15

@Banrockmystation @stayathomegardener

Are you both saying that you developed Giant Cell Arteritis after Covid? I has
wondered this too as she had Covid in March and by May had developed a weak voice and gastrointestinal issues

In my experience autoimmune conditions are not uncommon post any serious immune challenges which Covid obvious is.

I developed ME and RA after a live flu vaccine C2003.

Just recovered from it after lots of hard work C2016 only to have it re triggered by Covid 03/20.

My last Covid infection this summer has seemingly triggered TA symptoms, however the neurologist dismissed this on Friday because I'm apparently too young (not so at 53) but referred me to a specialist eye clinic, appointment tomorrow so we shall see.

It's exhausting researching and pushing everything, so hard when not well.

Really sorry about your Mum.

Zott · 17/10/2022 11:50

Sorry to read this. Thanks for the information. I agree completely we have to advocate and not worry about being nice. NHS is very hit and miss with the quality of its care unfortunately. Just seeing a GP face to face within 3 weeks of wanting is seen as an outrageous request in my area.

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