TRURO Meet-Up Group: Just a reminder that we have... - PMRGCAuk

PMRGCAuk

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TRURO Meet-Up Group

Pollyanna16 profile image
32 Replies

Just a reminder that we have Dr Andy Pothecary, Specialist Rheumatology Pharmacist talking to us on Monday at 2pm, Truro Golf Club. He will be talking about common (& some not so common treatments) & possible future treatments for PMRGCA. Look forward to seeing you there.

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Pollyanna16 profile image
Pollyanna16
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32 Replies
jinasc profile image
jinasc

Would be interested in what he has to say 'on possible' treatments in the future. Will you be able to post what he has to say please?

Pollyanna16 profile image
Pollyanna16 in reply to jinasc

I’ll do my best !

PMRpro profile image
PMRproAmbassador in reply to Pollyanna16

Ask him if he has a summary sheet or a presentation he could send to one of us maybe.

Pollyanna16 profile image
Pollyanna16 in reply to PMRpro

Will do

PMRpro profile image
PMRproAmbassador

My husband doesn't believe him!!! I wish I could come - just to meet him ;)

Pollyanna16 profile image
Pollyanna16 in reply to PMRpro

He’s real ... honest 😉😉

PMRpro profile image
PMRproAmbassador in reply to Pollyanna16

I want to see his birth certificate ;)

HeronNS profile image
HeronNS in reply to PMRpro

I wondered whether it was his real name. Did his parents plan this? :)

PMRpro profile image
PMRproAmbassador in reply to HeronNS

It is his real name - now at least! He's on Linked-in.

I once saw a birth announcement:

"To Fred and Mabel Conquest: a son, Norman"

How could they?

Pollyanna16 profile image
Pollyanna16 in reply to PMRpro

Yes he is real! I know, he has treated me. When I first got the appointment letter I had to look him up as I thought it might be an error.

Pollyanna16 profile image
Pollyanna16 in reply to HeronNS

🤣🤣🤣🤣🤣

jinasc profile image
jinasc in reply to Pollyanna16

Pollyanna16, I looked at your profile and have no idea whether you have PMR, GCA or both. It would be nice if you could add more details please.

Pollyanna16 profile image
Pollyanna16 in reply to jinasc

Oops will do ! PMR since 2011, adrenal insufficiency prob forever 😬

Pollyanna16 profile image
Pollyanna16 in reply to jinasc

I hadn’t realised the conditions were “hidden from view” have corrected & filled in some detail. Thanks

jinasc profile image
jinasc in reply to Pollyanna16

Don't feel bad about it, loads of people do not realise that. So I thought I would just do a reminder.

Rugger profile image
Rugger in reply to PMRpro

My husband doesn't, either! He's gone off muttering "...nominative determinism"!

Truro's a bit too far from Yorkshire or Italy!

PMRpro profile image
PMRproAmbassador in reply to Rugger

The first time I saw it I said "Nom derm gone mad ..."

YuliK profile image
YuliK

Do you think that the chronic tiredness could be connected to the Chronic fatigue syndrome (CFS), also referred to as myalgic encephalomyelitis (ME)...

So many folks who have had pmr ,and are still coping with low doses of prednisone are suffering this dreadful tiredness.

Just a thought ?

PMRpro profile image
PMRproAmbassador in reply to YuliK

Don't think so really - not in my case. They are different. Autoimmune disorders are connected by the fatigue. And after long term pred- so are low doses of pred.

YuliK profile image
YuliK

Just thought that possibly pmr could be a trigger to CFS.

I wonder if the pmr researchers have looked into this possibility ?

Thanks PMRpro for your answer. 👇

PMRpro profile image
PMRproAmbassador in reply to YuliK

Mine would have been the other way round - ME came first. And I know there are a few others on the forums with the same sort of history.

YuliK profile image
YuliK

This link below is a quite interesting read. I know you have a medical mind, so it should be 👍 for your perusal..

mayoclinic.org/diseases-con...

Seems the symptoms are very similar to pmr. Just the treatment is different.

Curious to read what you think ?

PMRpro profile image
PMRproAmbassador in reply to YuliK

My ME was quite different to PMR - no pain for a start. Just mind numbing fatigue and nausea. And weight loss - never lost weight with PMR more's the pity! Gained because of inactivity. With ME I went down to about 8st in 6 months and kept if off until I was pregnant - and gained a ton because of pre-eclampsia.

YuliK profile image
YuliK in reply to PMRpro

I didn’t know that you unfortunately had first hand experience with ME. No wonder you are a walking encyclopedia. 🤗

PMRpro profile image
PMRproAmbassador in reply to YuliK

I was lucky - and it wasn't diagnosed as such that long ago, yuppy flu was a very new "thing". But it was typical: a viral-type episode with raised liver enzymes and extreme fatigue that lasted about 6 months as an acute thing. Then a slow improvement over the following few years.

tina-shelley profile image
tina-shelley

Looking forward to meeting you all.

Galloping profile image
Galloping

I wish we had a group in Warwick/Leamington area. Would be good to meet

up in person.

Pollyanna16 profile image
Pollyanna16 in reply to Galloping

Maybe HQ could help with that. I guess there is a regional contact.

PMRpro profile image
PMRproAmbassador in reply to Galloping

Nothing comes from nothing ...

A group starts from small beginnings - ask Rugger. All you need is to find a couple of others to meet for coffee informally and talk about how to go from there. Her group started with a few - and grew to 39 members.

pokeynokes profile image
pokeynokes

I'd like to attend - can I just turn up there tomorrow?

Pollyanna16 profile image
Pollyanna16 in reply to pokeynokes

Absolutely yes do come along any 2nd Monday is fine. No need to book! Do you know where the golf club is?

pokeynokes profile image
pokeynokes

Yes I do thanks. See you there!

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