As promised: Jane’s account of how the condition changed her life.
PMR (polymyalgia rheumatica) is a painful, debilitating condition which affects
the muscles. Symptoms and the condition’s severity vary from patient to
patient.
GCA (giant cell arteritis) can occur on its own but about 25% of patients with
PMR suffer from GCA. As the name suggests enormous cells form in the wall of
inflamed arteries. This affects the normal flow of blood to many areas of the
body. A patient’s sight is particularly at risk and this may occur unless
treatment is started quickly. The condition may cause headaches and
tenderness at one or both sides of the forehead, blurred vision, and (in my
case) jaw pain when chewing. It makes you feel very unwell generally.
I became ill, suddenly, seven years ago in August 2012. I was a fit and healthy
68 year old. Peter (my husband) and I had just completed an eight-mile strenuous walk along a coastal path in Wales when pains developed in my hands, then my shoulders. Within a few hours I was in agony. I couldn’t climb into bed. I couldn’t even switch on a light.
My GP was very quick to act. Blood tests showed my CRP (inflammation
marker) was 168 (normal is less than 5.) However, despite seeing a very senior
rheumatologist, diagnosis was slow. By now I was in a wheelchair. Strong
painkillers had very little impact on my symptoms. The rheumatologist was
unsure whether I had Rheumatoid Arthritis or PMR. He gave me a 60mg
steroid injection and within a few hours I could move and the pain subsided.
GCA was diagnosed five months later. I was lucky. As I was taking steroids
already, my risk of sight loss – in one or both eyes – was very much reduced.
PMR and GCA are auto-immune diseases. Although the majority of patients suffer with just one condition, some patients develop other auto-immune diseases. For the past seven years I seem to have a new diagnosis about once a year. The worst of these is Rheumatoid Arthritis. I have a severe form of this.
The good news is that new drugs are being developed all the time. I am on a
trial for a biological drug. It is hoped that, in the future, steroid-sparing
treatments such as this, will prevent the devastating side effects of conditions
such as GCA. In my case, I have had no GCA flares since starting the bio drug
twelve months ago. Even more importantly, I feel so very much better and, best of all, I am off steroids – they can have long-lasting side effects when
taken for many years at high doses. I am also able to walk about a mile without
suffering from overwhelming fatigue.
Much more research is needed to find treatments (such as the bio drugs) and
research any potential long-term problems with them. At present, the bios are
very expensive, so doctors have to ration their use. There’s a nice irony that
having so many auto immune conditions has worked in my favour.
Ninevoices is a group of nine enthusiastic writers. We met nearly twenty years ago, and have got together every fortnight for most of that time. We have organised several writing competitions and the members decided to donate any profits to the little known charity: PMRGCAUK. (Yes, terrible title. The organisation is trying to find a better one.)
I was delighted and so was the organisation. Each of you, who entered our
competition, has taken PMRGCAUK one tiny step further to finding affordable
treatments and, hopefully one day, a cure.
Thank you all so much.
Jane Dobson
Jane is too modest to mention how bravely she has fought this condition, her consistent good humour even when in pain, and her determination to keep writing wonderful poetry and short stories – if, perhaps, at a more stately pace than previously. We are so lucky to have her as one of our voices.
Really glad to hear the bio drug is helping, Jane.
Jane’s story is almost identical to mine, although I was one year younger and am only three years into this journey. I had recently walked a thirteen mile charity walk and was still working. One day I awoke to find I just could not get out of bed. Nothing worked. Everything hurt. I was diagnosed with PMR. Followed shortly by GCA. Followed after six months by RA. Now I have insulin dependant diabetes as a direct result of taking high doses of steroids. I take many medications and also have Lupus plus numerous other auto immune conditions. I look back to the days I only had PMR almost with longing. I too, am in a wheel chair and when well enough, use a buggy. I can only walk a few steps with two sticks.
There are worse things to have and we mustn’t forget that. But it would be a help if people could see the pain involved. If they could understand that one can’t open ones eyes in the morning (sjogrens) and cant lift ones arms to put eye drops in (PMR) or turn over in bed, or indeed get in and out of bed and feel very ill and tired all of the time. Meanwhile I shall try hard not to scream the next time some well meaning friend says they too have a spot of arthritis …. and have I tried hot wax ? ………….
So very sorry to learn of how difficult things are for you Jayne. It sounds as if, with so many auto immune conditions, you are a suitable candidate for a bio drug. Tocilizumab (which I take by injection once weekly) has been a life saver for me, mentally as well as physically. Perhaps it would be worth exploring whether you a suitable candidate for this, with your Rheumatologist?
Kind regards,
Jane Dobson
Hi, what bio drug were you able to use it off prednisone? I have both PMR and GCA and I’m on prednisone and I’m really struggling. Thank you
No longer take Prednisolone. The bio drug is Tocilizumab.
Regards
Jane