|
Rank: Advanced Member  Groups: Registered
Joined: 11/20/2010 Posts: 244 Location: Cornwall
|
OK so the last couple of months have been a bit rough in various ways but of course everything will be alright next year! In the meantime though, not sure what to do next so could do with some pearls of wisdom.
Bottom of my middle finger on my left hand has been a bit iffy on and off before and after diagnosis 12 months ago. Its now been swollen for 2 months solid and the constant burning 6 inch nail jammed in it is getting a bit wearing. Showed the rheumy nurse a month ago and she said that if she asked the consultant to inject it he wouldn't because it wasn't bad enough, go away and get on with it. CRP's OK and tolerating the MTX which is clearly working, so you're fine. I'm now severely fed up with it, can't do any middle finger wiggling including typing, gripping or movement is pretty much out of the question and a slight knock has me on the ceiling or in tears. Its like having a useless painful, paw on the end of my arm rather than a hand!
So I rang the surgery this morning to see if the GP could recommend anything or did I really have to just put up with it. He's on holiday back in the week before Xmas but is triaging any requests for appointments. I've seen other GPs before and quite honestly its a waste of time.
I'm wondering then, do I put up with it because there really isn't much they can or will do? Do I chance getting an appointment with my GP and will he do anything about it anyway or just tell me to speak to rheumy? Do I ring the rheumy nurse in an attempt to change her mind or get some advice? Do I wait until my OT appointment on 3 January when I know that my consultant is in the room next door and I might be able to sneak in for a quick chat OR flaming well what??!! Could just get drunk I suppose, oh no forgot, I can't!
Take care all Sara
|
|
Rank: Advanced Member  Groups: Registered
Joined: 12/3/2009 Posts: 3,006 Location: Timperley
|
None of these things, Sarah. You ring up or write to your consultant, tell him how badly this is affecting you and ask for an IMMEDIATE appointment for a joint injection. These people make me so mad when they say "it isn't bad enough" How on earth do they know when they are not suffering the consequences?
I get stiff and iffy fingers and my consultant always injects and the relief in amazing.
Don't put up with this crap, Sarah. Sorry, but things like this make me furious, especially when there is no need for it and you so obviously need help.
Take care and please let us know what happens.
Love Jeanxx
|
|
Rank: Advanced Member  Groups: Registered
Joined: 12/4/2009 Posts: 1,524 Location: W. Yorkshire
|
I agree Sara-thius is not good enough. I would do what Jean suggested , I once weote a long letter to my consultant telling him exactly how i felt and it worked wonders. YES I'VE CHANGED, PAIN DOES THAT TO PEOPLE.
|
|
Rank: Advanced Member  Groups: Registered
Joined: 3/28/2011 Posts: 956 Location: North Preston
|
Hi Sara
I have only just read friday's posts. I agree wholeheartedly with Jean and Julie. You can't be expected to put up with this. Keep ringing until you get some satisfaction.
Sheila x
|
|
Rank: Advanced Member  Groups: Registered
Joined: 9/3/2011 Posts: 717 Location: Torbay
|
I am just posting to say that I agree with the others. You should not have to put up with this. keep fighting. I really hope that you get some relief soon. Best wishes from Naomi.
|
|
Rank: Advanced Member
Groups: Registered
Joined: 10/19/2010 Posts: 88 Location: Saddleworth, UK
|
I second everything that Jean wrote!
Unless they have RA etc they cannot say "its not bad enough" Argh it makes me so mad when they do this.....
Lxxxx
|
|
Rank: Advanced Member  Groups: Registered
Joined: 12/3/2009 Posts: 2,237 Location: nr Southampton
|
stupid people, how dare they say "not bad enough"!
Get onto that consultant and I find if they dont ring or contact you back their secretaries are very helpful!
Jenni xxhow to be a velvet bulldoser
|
|
Rank: Advanced Member  Groups: Registered
Joined: 11/20/2010 Posts: 244 Location: Cornwall
|
Thanks for the advice, I love it how we can get so cross on each others behalf! I really couldn't face the battle with the consultant and rheumy nurse because I go to a local clinic which is only held once a month and to actually see either of them at any other time would mean a 40 mile round trip. The one handed driving has got a bit scarey recently!
But the good news is I have been granted an audience with my GP on Friday afternoon. I had a brainwave and phoned a friend of a friend who has been through the mill with the RA and knows the ropes locally. She's in her 30s and already had a hip replacement, turns out she has the same GP as me and he's whiz with the old steroid needle. So I'm keeping everything I can cross, crossed for Friday.
I have worked out an answer for 'not bad enough' So would it have been bad enough if I were being treated in hospital after doing myself a nasty injury? It really is only a matter of time, so a jab would surely cost the NHS less in the long run!
Wish me luck Sara x
|
|
Rank: Advanced Member  Groups: Registered
Joined: 6/18/2010 Posts: 351 Location: Herne Bay Kent
|
Hi Sarah Hope all goes well for you and you get all you want from the GP to give you relief to enjoy Christmas Best Wishes Sue
|
|
Rank: Advanced Member  Groups: Registered
Joined: 12/3/2009 Posts: 3,006 Location: Timperley
|
Well done Sarah - will be thinking about you on Friday.
|
|
Rank: Advanced Member  Groups: Registered
Joined: 12/7/2009 Posts: 262
|
Good luck for Friday Sara!
Diane x
|
|
Rank: Advanced Member  Groups: Registered
Joined: 12/3/2009 Posts: 3,157 Location: Huddersfield
|
I think you are right there Sarah, and it would have been treated differently if it was an injury to your hand. Goodness knows what makes them think that, because we have RA, we can cope with any amount of pain!
Good luck for Friday.
Love Doreen xx
|
|
Rank: Advanced Member  Groups: Registered
Joined: 11/20/2010 Posts: 244 Location: Cornwall
|
Merry Xmas to you all
So saw my lovely GP yesterday to try to unravel the causes of the various swellings!
We concluded that some of my face symptoms and swelling is down to a sinus infection which has developed from my cold.
The jaw stuff is just the RA having a bit of fun in that area this week. Bring on the soup and smoothies!
Yes, he would have given me a steroid jab in my hand if I'd seen him a couple of weeks when I couldn't scratch my a**e, but we agreed that it wasn't as bad now and if I wasn't hanging off the ceiling with it then it was best to hold on in there. I really am a big baby where these things are concerned. But I now know that at least I can rely on him rather than the rheumy nurse for a jab if I need one.
And last but not least, the puffy swelling around my eyes on Tuesday and feeling like I wanted to crawl under a stone is an allergic reaction to taking the MTX. I've been telling them it makes me feel pants for 12 months now but must be another thing that's all in my head!
So lovely GP is going to write to my consultant for an emergency appointment and I'll be on the phone first thing Wednesday. The MTX was doing its job RA wise but now after 3 months of one infection after another and the allergic reaction, which apparently could turn into full blown anaphylaxis if I take it again, it is not for me anymore.
The next chapter has started! At least I can enjoy New Year just like in the old days.
Wishing you all a festive season full of laughs and jollity, you just gotta laugh (although along with chewing and snogging it hurts a bit at the minute)
Sara xx
|
|
|
|