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I can't take it anymore Options
natbabe1980
#1 Posted : Monday, April 07, 2014 9:11:43 AM Quote
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Joined: 7/2/2013
Posts: 41
I am so sorry to be moaning again!!!

I don't know if I can take much more. I have been in full flare for last 6 weeks and everything I do short of sitting on my fat behind is causing pain. I walk, I climb the stairs I try to do house work, I stretch in the bath under the water and still faced with so much pain.

I have had chest pains since last Wednesday, went to a & e did all the tests, nothing wrong with me its just the RA! still having them and palpitations along with them. I walke out the ward in agony sobbing on my own basically just felt like a fraud.

I am being referred to the pain clinic which I didn't even know was an option until I had a complete breakdown in the hospital, they think I may have fibromyalgia overlapping the RA.

I can't function, I have 2 children and I cant even get to work at the moment.

Really don't know what to say anymore, can't seem to bring myself to talk to anyone and when I do its just I have to be patient and wait, can'tdo it anymore x
Paul Barrett
#2 Posted : Monday, April 07, 2014 11:02:35 AM Quote
Rank: Advanced Member


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Joined: 4/24/2013
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Location: Hexham
So sorry to hear that you are struggling. It's just not fair is it?

It's good that you have been referred to the pain clinic, they are the experts in this field. Have you talked to you rheumy nurse / consultant? Maybe a short course of high dose steroids will help you? It's what A&E prescribed for me when I pitched up in their ward with similar problems - but we are all different.

The pain is debilitating isn't it, and it makes you feel so low. If you can summon the energy you should talk to your GP too see if there is anything he can do in the short term for the pain, and in the longer term to deal with how you feel mentally. Don't be surprised at feeling low. Pain will do that to you.

Keep posting to let us all know how you are getting on and we'll all help you through this.
Paul Barrett

Hexham - Northumberland - Loads of spectacular walks - all I need now are the joints to go with them! :)

Enthesitis (2012)
Ulcerative Colitis (1990)
natbabe1980
#3 Posted : Monday, April 07, 2014 11:14:32 AM Quote
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Posts: 41
Thank you so much for your reply Paul,

Unfortunatly the steroids didn't work and the side effects were horrendous and the pain relief I have been on since last year (tramadol and paracetamol) will not touch the pain so the doc in the ward basically made me feel like that's the only thing they could do for me, until I broke down then they were putting forward other options which they ended up giving me a suppository which took the pain down somewhat, but of course as they do not prescribe these things for home my sight relief was short lived and I am now taking ibruprofen, which hasn't touched the pain at all an a new tablet called pregabalin 25mg for neuropathic pain but no relief yet. I have rang my nurse this morning so waiting to hear from them and asked doc to call me back.........just feel like I am wasting everyones time x
JayneM
#4 Posted : Monday, April 07, 2014 11:37:12 AM Quote
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Joined: 10/20/2013
Posts: 7
Location: Hampshire
How awful for you to be in so much pain. You mustn't think that you are wasting
peoples time, they are there to help. In my experience, you need to be pro active in asking
for help sometimes. Not always easy when you feel so poorly.
Keeping my (rather lumpy!) fingers crossed that you get some relief soon.
take care, Jayne xx
Angiecha
#5 Posted : Monday, April 07, 2014 12:08:02 PM Quote
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Joined: 9/5/2010
Posts: 185
Location: Lowestoft, Suffolk
Hi Nat

So sorry to hear what a lot of pain you are in. I have Fibromyalgia as a secondary to RA and I know the type of pain is very intense. I wish I had an answer for you. I know you say you don't want to talk to anyone but have you tried the NRAS Helpline? 0800 298 7650 Even if they can't cure your physical pain they may be able to offer other options?

As Paul says, keep us informed on here as much as you can and we'll do all we can to support/help/advise.

Angie X
Be yourself - everyone else is taken. XX
gogs
#6 Posted : Monday, April 07, 2014 2:30:22 PM Quote
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Joined: 10/20/2012
Posts: 304
Location: Cheshire
Oh Nat, I'm so sorry you are in such a mess.

Only those of us who have really suffered this never ending onslaught can understand just what you are going through and how you are feeling at this
precise moment.

You are certainly not a fraud, never think that, ever. You didn't chose this illness and you certainly haven't welcomed it's attentions.
Sometimes the medical staff can be so insensitive. What you are going through needs ASAP care. Have you phoned your rheumatology dept?
I know you say that steroids don't work for you, but they can help a little, have you/they ever considered joint injections? I had them in my wrists last week (first time),
the right one is great, the left is still a bit painful, but it is relative and I am better than last week. You mentioned side effects from the steroids - are these worse than the pain?

Try really hard to enlist anyone you can to help you, if the pain clinic works that will be a real bonus. You also sound a bit low in mood (it is very understandable) so why
not speak with your GP and see if you can get some help. We are all so helpless to support one another but sadly it is you that will have to find the energy to instigate
some sort of help for yourself.


Please do keep 'talking' on here, and phone NRAS helpline. They phoned me when I was at my lowest a couple of months ago, at the time I never thought I could get so low
but I did, and even now I'm not back to 'normal'.

Do please become your own best friend, shout out your needs to anyone who will listen, and please keep us posted - we want to knwoSmile

GogsLove
Paul Barrett
#7 Posted : Monday, April 07, 2014 3:08:06 PM Quote
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Joined: 4/24/2013
Posts: 703
Location: Hexham
natbabe1980 wrote:
...they ended up giving me a suppository which took the pain down somewhat, but of course as they do not prescribe these things for home....


What was the suppository? There's absolutely no reason why you should not have suppositories for home use. I have steroids that was when my Ulcerative Colitis flares. In Frnace they are regularly used and they are an accepted treatment. They just aren't that popular over here for some reason.

You are NOT a failure and your are NOT putting people to trouble. The people who you think you are troubling are there to help so never, ever, think that you should not bother them.
Paul Barrett

Hexham - Northumberland - Loads of spectacular walks - all I need now are the joints to go with them! :)

Enthesitis (2012)
Ulcerative Colitis (1990)
Paul Barrett
#8 Posted : Monday, April 07, 2014 5:45:29 PM Quote
Rank: Advanced Member


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Joined: 4/24/2013
Posts: 703
Location: Hexham
Just reading your posts gain and I see you are on Tramadol. That's an opiate based med like the codeine and morphine mix I take, and I think one of the problems is that your body gets used to it after a while. I wonder if a different opiate might help you? Talk to your GP or the pain clinic, whichever you can get to earlier
Paul Barrett

Hexham - Northumberland - Loads of spectacular walks - all I need now are the joints to go with them! :)

Enthesitis (2012)
Ulcerative Colitis (1990)
Jane.
#9 Posted : Monday, April 07, 2014 10:35:06 PM Quote
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Joined: 5/2/2012
Posts: 670
Location: where the sun always shines :o
Hello lovely

Sorry to read about the pain/crap time you are experiencing.
Ra effects us all differently, I will echo what has been wrote on here & contact bras helpline.

I've had moments of tears, but I've not felt low.....don't like loosing my independence having operations.

Keep talking on here as well so we can give you love & reassurance.

Gentle hugs
Jane
Xxxx
natbabe1980
#10 Posted : Monday, April 07, 2014 11:27:08 PM Quote
Rank: Advanced Member


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Joined: 7/2/2013
Posts: 41
Thank you all for your lovely and supportive replies, it helps so much to talk to people who know what I am talking about! a very lonely place this RA business sometimes.

I did speak to my GP today over the phone and he seemed very supportive of me, I am going for an appointment tomorrow and also the rheumy nurse rang and she is going to try and speak to the rheumatologist asap to try and sort things quickly for me.

I finally felt like they were listening today but by god I had to kick up a fuss to be heard!

Thank you again you are all such strong caring people and it is very appreciated xxxx
jewelsh
#11 Posted : Tuesday, April 08, 2014 7:54:02 AM Quote
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Joined: 9/15/2013
Posts: 125
Hiya
Have just caught up on your posts and feeling so sorry you are in such a lot of pain and feeling so low. It's a vicious circle, pain and depression and so hard to get back on top of everything. Pleased to see your GP was supportive on the phone yesterday and hopefully your visit today will produce some positive results. Will be thinking of you.
It is such a shame that we have to shout so loud to get ourselves understood about just how much pain this disease causes but sadly it does seem to be a common problem.

Take care and keep in touch

Julie xx
gogs
#12 Posted : Tuesday, April 08, 2014 4:57:37 PM Quote
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Joined: 10/20/2012
Posts: 304
Location: Cheshire
Well done Nat, you may not have won the war but you certainly won that battle!!ThumpUp

Please don't let any of those medics rest on their laurels - keep them alert at all times - your well being depends on it!!
Really pleased that you have a GP on your side - they are worth their weight in gold if you get a good one. Let him be your
go between when things seem to be slowing down.

Please use us as the need arises, never feel you are a nuisance, we're here to help one another and the people on this forum certainly do that -they're amazing.

GogsLove
Louisa
#13 Posted : Tuesday, April 08, 2014 5:00:45 PM Quote
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Joined: 2/7/2013
Posts: 71
Location: Suffolk.
I'm really glad you are finally getting some support. It is hard, and you mustn't let anyone make you feel like you are just making a fuss.

I hope you get some relief and feel a bit better soon x
Ailsa-H
#14 Posted : Tuesday, April 08, 2014 9:41:29 PM Quote
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Joined: 3/4/2010
Posts: 576
Hi Nat - just catching up and so sorry to hear you are struggling so much. Hope your GP appointment is helpful and he can come up with some other strategies to make life more manageable. Thinking of you xx Ailsa
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