So many symptoms....: It’s hard to know what... - PMRGCAuk

PMRGCAuk

21,324 members40,436 posts

So many symptoms....

Paula-kent profile image
19 Replies

It’s hard to know what symptoms are PMR, side effects of medication, or something completely different. Anyone else suffer with any of the following:

B12 deficiency

D3 deficiency

Tinnitus

Iritis

Sweating

Fatigue (understatement!)

Confusion

Anxiety

High blood pressure

Dark raised spots on backs of hands

Thinning hair (on head)

Transforming into a brown bear (elsewhere)

???

Written by
Paula-kent profile image
Paula-kent
To view profiles and participate in discussions please or .
Read more about...
19 Replies
PMRpro profile image
PMRproAmbassador

Many of those are associated with autoimmune disorders - has your low B12 been checked out? Is your doctor confident you have PMR rather than anything else?

Can't say I've transmogrified into a bear of any colour recently...

Paula-kent profile image
Paula-kent in reply toPMRpro

I have b12 injections every eight weeks and take a D3 supplement.

Never get chance to remind GP of all my ailments in order for them to (potentially) make a connection.

Spend my life on google trying to find conditions I might be suffering from as I’m not convinced PMR is correct diagnosis. Time will tell, I guess....

PMRpro profile image
PMRproAmbassador in reply toPaula-kent

Is the low B12 due to pernicious anaemia? That is an autoimmune disorder too.

DorsetLady profile image
DorsetLadyPMRGCAuk volunteer

Hi,

I’m sure many will read your list, and nod their heads to a great number of them!

Most can be addressed with a little (more) help from medication - as if we need more! Plus as you get lower on the Pred most side effects diminish.

Oh boy..... Yes, yes, yes, and yes!

rantingsofamadwomanblog.com...

fmkkm profile image
fmkkm

8 x yes at some point in the last 3 years!

fmkkm profile image
fmkkm

Add

Mega bruising, sore wrists, muscle weakness, foggy brain and insomnia 😏

PMRCanada profile image
PMRCanada

Yes to sweating, anxiety, confusion (I call it pred head), and just recently fatigue as I taper down to 10mg (transitioning this week from 11 to 10).

Longtimer profile image
Longtimer

Yes to 6 of those....and others too.....very difficult some days....😕

scats profile image
scats

Yes to 6. Hair not only thinned went curly.

Islandgirl50 profile image
Islandgirl50 in reply toscats

Ohhh , a few curls , I would love that .. always been dead straight , used to try perms ,, disaster , either didn't hold or went frizzy !!!

scats profile image
scats in reply toIslandgirl50

You know I felt robbed, I had always loved my straight hair but I'm getting used to the curls and may even miss them now if they go.

Pennythedug profile image
Pennythedug

Hi Paula

Yes to almost everything that you mention and more! It really is impossible for family and friends to

Understand this strange this disease.

Still we don’t have a choice and just have to keep on reducing!

SheffieldJane profile image
SheffieldJane

Every single one at some time or another. Except the dark spots on hands, I expect they’ll be along presently. Don’t ignore anything especially troubling. My GPs try to treat anything I complain of in isolation.

Qubbie profile image
Qubbie

All indictments of my prednesoon reactions

Pongo13 profile image
Pongo13

Snap 🐊 (almost!). Club pred is a great holiday from normal isn't it?!

CT-5012 profile image
CT-5012 in reply toPongo13

Like that “holiday from normal “ 😂

Maryis80 profile image
Maryis80

I can relate to some of the symptoms stated in these posts, but also have the added problem of a DVT in my right leg which is being treated with Warfarin. This drug is very susceptible to other drugs so when I change the Pred dose, it upsets the blood reading for the Warfarin! Going through a flare at present so have upped my Pred so goodness knows what the blood reading will be for the Warfarin next week!

daworm profile image
daworm

Yup, and that’s the confusing part..PMR, pred side effects, tapering side effects, adrenal fatigue/problems...who knows, I don’t...

Not what you're looking for?

You may also like...

So many questions

Tomorrow I have my second visit to my GP since he started me on prednisolone three weeks ago, after...
Zebedee44 profile image

So many questions..re PMR

Hello from Canada..1st post..full disclosure I am a Retired Registered Nurse who up until three...
Knitwit2020 profile image

Starting PMR journey. So many questions/fears

First off, I want to say hello. I'm thankful that I found what seems to be a very caring and...
Scooter4645 profile image

After blood results, so many new things.

Just had the phone appointment with the Rheumy ~ finally. Blood glucose 7.7 (which indicates...
Missus835 profile image

PMR Life changing in so many ways

In early December 2020 I was suddenly immobilized by chronic left/right shoulder,hips and hands...

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.