Newly diagnosed : I’m a retired lecturer in English... - PMRGCAuk

PMRGCAuk

21,303 members40,394 posts

Newly diagnosed

Sibelius5 profile image
13 Replies

I’m a retired lecturer in English at Hull university. I was diagnosed with PMR in August 2023. My wife Les was diagnosed with rheumatoid arthritis in the mid 1980s in her mid 40s and then developed lupus and later diverticulitis and cauda equina after I retired in 2013. She was severely ill for the last years before she died during lockdown in June 2020. Thankfully I was with her in the nursing home. I’ve been in deep grief since then and at the same time I have been being very busy and active, taking up abstract painting at a local alternative art school and culminating in a three month trip to revisit Australia this year, where Les and I had two lengthy trips in the 1990s for my academic work. During the trip I felt stretched to my limit and beyond, and three years on from Les’s death, I think my body just said that’s enough, you need to stop now - and the PMR has certainly done that. I have been sitting quietly recuperating, reading and watching the birds and flowers in the sun in our garden ever since and finding out from various sources, including the very helpful Kate Gilbert book, what it is I am experiencing. I am beginning to feel the steroids are starting to manage this condition more effectively, so I’m beginning to slowly reactivate and try out activities I used to take for granted but do them on a smaller, more careful scale.

Written by
Sibelius5 profile image
Sibelius5
To view profiles and participate in discussions please or .
Read more about...
13 Replies
SheffieldJane profile image
SheffieldJane

I am so sorry that you lost your wife after a long and challenging battle with health problems. I am not surprised that PMR brought you to a halt, as it does with may of us, following extreme stress. Your story is heartening in that you have found the sun poking through the clouds in aspects of your life. Finding an artistic expression and getting intimate with nature. You are wise to get to know this tricky condition and to learn to manage it in a mindful way. Acceptance is tough and necessary, you are well on the way. Wishing you joy and health in your future. You do seem to have found the path. 🌷

Sibelius5 profile image
Sibelius5 in reply toSheffieldJane

Thanks

PMRpro profile image
PMRproAmbassador

Hi and welcome. Yes - it isn't at the time it hits you physically. I had had PMR for years but during Covid and my husband's final illness I needed more pred to function physically caring for him. Six months after he died - I had a massive flare and needed even more pred.

But this too shall pass. I have only just decided it is time to do something - but it won't be revisiting the scenes of past academic-related excursions. I shall gently explore the bits of Europe that were neglected in favour of the Pacific rim!!!

Artandpoetry profile image
Artandpoetry in reply toPMRpro

I love “this too shall pass” . Have some wonderful adventures. Please share them with us. You so deserve some treats having given so much of your time to fellow sufferers! 💖

Sibelius5 profile image
Sibelius5 in reply toPMRpro

Thanks

DorsetLady profile image
DorsetLadyPMRGCAuk volunteer

Hi and welcome….many of us know how long and in many difference forms bereavement can take.

Wishing you all the best with your PMR and your different way of life.

Sibelius5 profile image
Sibelius5 in reply toDorsetLady

Thanks

piglette profile image
piglette

What a sad time you have had. As the late queen said “Grief is the price we pay for love.” She was right.

If you have not joined yet you may be interested in our PMR and GCA Gardening group. facebook.com/groups/6288051...

Sibelius5 profile image
Sibelius5 in reply topiglette

Thanks piglette

S4ndy profile image
S4ndy

Welcome to the club no one wants to join. So sorry for your loss. I too lost my partner of 45 years a year ago. It is getting easier though as I am rebuilding my life and doing the things that make me happy. I know my late hubby would want me to get on with life. Sorry you are suffering but this too will pass.

I've had PMR for many years and now on a 5mg a day maintenance dose. Just recovered from a lumbar decompression to free up my nerves and relieve pressure on my cauda equina. It's been life changing for me.

So hang on in there, take one day at a time and embrace the way you are now as the past is just that, the past. Sounds like a cliche but being in the moment really works for me.

Sibelius5 profile image
Sibelius5 in reply toS4ndy

Thanks S4ndy

Body_bonkers profile image
Body_bonkers

Sorry to hear your story Sibelius5 and wishing you a smooth recovery. Grief and PMR are similar in that they will do they're own thing so continue to take each day as it comes

Sibelius5 profile image
Sibelius5 in reply toBody_bonkers

Thanks

Not what you're looking for?

You may also like...

4 First Cousins Diagnosed in a Year!

I was diagnosed with PMR in June 2018. Since then, 2 first cousins (women), one a retired doctor,...

Newly diagnosed with PMR

I have just been diagnosed with PMR after a good number of months of increasing pain and...
Patricia157 profile image

MGUS Newly diagnosed

I'm 61, 2 years ago I was diagnosed with GCA and PMR, which was wrongly diagnosed as fibromyalgia 5...
Lindilooo profile image

In need of information as newly diagnosed

Hello, I'm 57 and was diagnosed with giant cell arteritis three weeks ago. Initially my GP put me...
Rainemaris profile image

Newly diagnosed with PMR

This is my first time on here. I’m 63 years old and was recently diagnosed with pmr. Rheumatologist...
Dejon73 profile image

Moderation team

SophieMB profile image
SophieMBPartner

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.