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Rank: Newbie  Groups: Registered
Joined: 2/26/2010 Posts: 2 Location: Coventry
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Hi, My name is Karen. I have been with my fantastic husband Wayne for the last 22 years and we live in Coventry with our 2 lunatic dogs Buster and Poppy. As a special treat for my 40th Birthday last year I was diagnosed with RA. It came as a shock but also as a relief as I had thought I was going crazy with the different swellings, aches and pains I had been getting! I am still trying to get my meds right, so at the moment I am on sulphazine, methotrexate and prednisolone. In addition to this I have also been taking fluoxetine for depression for over a year now as well as metoprolol for migraine prevention (for the last 10 years) and feel like I rattle when I walk with the amount of pills I seem to be taking I joined nras last year when I was diagnosed and have often read the forums but have never been brave enough to post on it..... until today! So what has changed today to make me feel the need to post on here? An appointment with my Rheumy Nurse. I went to see her today and came away and cried. Not because she was unsympathetic, didn't listen or any of the other things I feel when I see my GP but I cried with relief that she was exactly the opposite. For the first time in a long time I felt listened to, cared about and was given answers as to why I feel like I do as well as making future plans to help me feel better both physically and mentally. It was only 20 minutes of her time but it was the best 20 minutes of this year for me! I didn't realise how isolated I felt and how much I had shut myself off from everyone around me. It takes all my effort and energy to get out of bed in the morning let alone speak to friends on the phone or even worse face to face. I want this to change and know that I am the only one that can make it happen and today seems like the day where I can finally start to move forward. I feel so much better for just writing this, so if you have read this thank you for reading my little rant! Take Care xxxx
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Rank: Advanced Member
Groups: Registered
Joined: 1/23/2010 Posts: 100
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Hi Karen
Well done for plucking up the courage to post a thread. Welcome from me.
I joined the forum in January and was only diagnosed at the end of 2009. I'm 50 now and it certainly was a shock to the system finding out I had RA.
The people I have spoken to on here have been great, giving me some good advice. I shut myself away too and couldn't cope with the disease. Now I'm back at work my colleagues have been tremendous.
If ever you need to have a rant, then this is the place to do it. Everyone is so supportive and they know what you're going through so lets hope you join in and post as often as you can.
Take care Chris x
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Rank: Advanced Member
Groups: Registered
Joined: 12/4/2009 Posts: 2,127 Location: Thornton Cleveleys
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Hi Karen Lovely to read your post and a warm welcome to the forum. Great to hear that you have had such a positive appointment today, doesn't it make you feel a whole lot better when someone takes the time to really listen?! I know exactly where you are coming from when you speak of isolation and shutting yourself off; I do it myself sometimes it is so much easier than trying to explain to people who don't understand nor do they want to! You are in the right place here where everyone is so friendly and, of course, we are all in the same position, some a lot worse than others. It's good to know that such support is always available and there's always someone who has had similar experiences and can offer their thoughts and perspective on things. I'm sure you will really enjoy being part of the group. By the way, I'm Lyn, married to Mike, we have four children including twins (Abby 22, Ian 16, Jake 16 and Louis 15) all in various stages of education. We live in Thornton Cleveleys, Lancashire, near Blackpool but not too close ... really!!  I have had RA for 21+ years been through the gamut of medication and various surgical procedures and am now on Enbrel, Methotrexate, Prednisolone, Naproxen and a few other bits and pieces! Karen you are not ranting ... just expressing your feelings!! And this is exactly the place to do just that. Look forward to chatting with you again very soon but in the meantime keep smiling you have made a huge leap today. Do you know what? Having read your post again I too now feel a whole lot better about the day so thank you for that  . Lyn x
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Rank: Advanced Member  Groups: Registered
Joined: 12/5/2009 Posts: 48
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Hello Karen,
My name is Jayne and I live in Leicestershire not far from the A5/M69. There are a couple of us living locally so please keep coming on the site. Are you going to come to the lunch in April at Leicester to meet everyone?
I have had RA for two years and like you hate the illness. I live alone so sometimes it is hard as I have no help when things get bad. I have two cats at home and 16 pet sheep hence the picture. That is Daisy.
Everyone here is very kind and will do what they can to help you if you have any problems. Welcome to the site.
Jayne
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Rank: Advanced Member  Groups: Registered
Joined: 12/3/2009 Posts: 690
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Hi Karen,
A big warm welcome to the forum, and pleased that you plucked up the courage to post. I'm 50, married and have 23 yr-old daughter and 2 cats. I was diagnosed last year with RA, and understand how isolating it can feel with this illness. Unfortunately for many of us, RA and depression seem to go hand-in-hand, especially during the first year of diagnosis. I am glad that you have found such an understanding nurse they can make such a difference to our care and are worth their weight in gold.
Take care and keep posting,
love,
Barbara XXXXXX
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Rank: Advanced Member  Groups: Registered
Joined: 12/3/2009 Posts: 3,006 Location: Timperley
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Hi Karen
Welcome to the forum - another one here glad you decided to join us.
I promise that you will never feel isolated again. This forum is full of warm, caring and some completely mad individuals (of course, I'm not one of them!!)
You'll make loads of friends on here and find there is always someone to talk to.
How great that you have a supportive rheummy nurse - they're worth their weight in gold.
Oh - and never apologise for anything on here - we all have a rant from time to time.
Take care
Love Jeanxxxx
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Rank: Advanced Member  Groups: Registered
Joined: 12/3/2009 Posts: 3,157 Location: Huddersfield
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Hi Karen,
Welcome to the forum, where you will never be alone again. We all know what you are going through. I am 60 and have had RA for 9 years, now on mtx and humira. Hope you can get the right meds for you soon. Don't worry about the tears, I am like that when anyone is kind to me! Looking forward to getting to know you.
Doreen xx
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Rank: Advanced Member  Groups: Registered
Joined: 12/3/2009 Posts: 1,110 Location: London
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Hi Karen, welcome, glad you decided tol post. Its amazing when someone understand isnt it? I found it was with the private consultant I saw in January. It made me feel so much better, previously I felt like they were saying, "just get on with it" pain is part of life, so thats it!! After seeing him I knew more could be done,for me personally I want to keep working as long as possible. I was diagnosed in July 2009. Having more tests for other auto immune diseases too. Dont worry anbout the tears, thats normal!! Good to see you here, everyone is very supportive. BARBARA
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Rank: Advanced Member  Groups: Registered
Joined: 12/3/2009 Posts: 2,237 Location: nr Southampton
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Hi karen and a BIG welcome from me too!
I am Jenni and if you have been reading the forum you will know all about me and the others so I will not bore you with it again but you are dead right that you need as much support as you can get with this rotten disease.
I am so pleased that you have posted today, it is the first big step forward in getting to grips with the RA.
Jenni xxhow to be a velvet bulldoser
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Rank: Advanced Member  Groups: Registered
Joined: 12/4/2009 Posts: 856
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Hi Karen- a big welcome from me. I'm 52- had RA for almost 3 yrs- was a nice 50th prezzie for me!
I'm glad you had such a positive appointment- I know what you mean about the relief. I've found from bitter experience that people just don't understand RA and I've felt so alone at times.
I've been going through a very down phase recently and some days I've cried for ages. I've got to see the rheumy nurse so hopefuly I will get the same support.
Take care
Maria x
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Rank: Advanced Member  Groups: Registered
Joined: 12/3/2009 Posts: 1,689 Location: Durham
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Hi Karen, Welcome to the forum I`m glad you decided to post, there are many benefits to be gained from this forum. It certainly helped me when I joined, as I didn`t know another soul with RA. Tears are normal - we all shed them from time to time, so don`t worry about that. I`m Kathleen, married to Nick for 38 years, two sons & two grandsons. We live in Durham, and have a lovely Golden Retriever called Flynn. Keep posting, Kathleen x
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Rank: Advanced Member  Groups: Registered
Joined: 3/8/2010 Posts: 914
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HI Karen I'm Lorna married to Ken for 28 years and have 3 grown up daughters. I developed RA almost 3 years ago, like you I had never known anyone with it. It was a massive blow as I am so active. I just joined the site this week I should have joined a long time ag, everyone is very nice and you don't feel you have to cope on your own. My meds are stable now so try to be positive it does get easier. Hope you find comfort on here, thinking about you. Lorna x
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Rank: Advanced Member
Groups: Registered
Joined: 12/3/2009 Posts: 1,035 Location: in a house
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Jayne G wrote:Hello Karen,
My name is Jayne and I live in Leicestershire not far from the A5/M69. There are a couple of us living locally so please keep coming on the site. Are you going to come to the lunch in April at Leicester to meet everyone?
I have had RA for two years and like you hate the illness. I live alone so sometimes it is hard as I have no help when things get bad. I have two cats at home and 16 pet sheep hence the picture. That is Daisy.
Everyone here is very kind and will do what they can to help you if you have any problems. Welcome to the site.
Jayne He he Ha ha Spoted the Leiscestershire so please come to the lunch ( please let monty know as we have to book you in ) its £15 and i you can use the pool for a fiver ( think what i paid last year ) our 3rd get togetor . see you then Christine chockers chrissy christina The chocolate eating housewife ...The washer woman .....naughty lady
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Rank: Advanced Member  Groups: Registered
Joined: 12/3/2009 Posts: 327
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Hi Karen and welcome to the forum. I'm so sorry you've had such a rough time and have felt so isolated, but glad you've finally got someone listening to you. We all rant on here from time to time, so you're in good company, and will always find people who understand exactly what you're going through.
Anthea
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Rank: Newbie  Groups: Registered
Joined: 2/26/2010 Posts: 2 Location: Coventry
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Thanks everyone for the warm welcome. Today has been another fairly good day (if I discount falling flat on my face when I went to the bank at luchtime). Not too much damage other than to my pride and the poor pavement (a new pothole I made for the council to fill in  ) although, I dare say the stiffness will hit me more in the morning! It is good to know that I am not alone and I promise to continue to both read and post on the forum. Take care Karen xxxx
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Rank: Advanced Member
Groups: Registered
Joined: 12/4/2009 Posts: 2,127 Location: Thornton Cleveleys
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Hi Karen Hope you are okay after your fall; do make sure you get properly checked over if you've any worries. Sometimes potential problems can have a habit of lurking in the background unseen for a while then strike when you least expect them! Have a restful weekend, keep your feet up and stay warm. Hope you're not too stiff in the morning Think the council make as many potholes as they fill in so another one won't matter .... they won't even notice! Actually, you didn't fall in a pot hole did you? Round here there are more holes than even pavement at the moment Lyn x
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Rank: Advanced Member
Groups: Registered
Joined: 12/4/2009 Posts: 336
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Hello Karen and welcome,I tend to cry when someone understands me and is nice to me I think that we put up this hard shell and joke about things to help us cope and the understanding breaks through. I have a Rhenmy nurse who is lovely and I can talk to her much easier than the consultant and often feel better having talked with her and got some things of my chest. I'm Glenys from Notts, 56, married with 2 daughters and 3 grandchildren, I've had RA for 10 years now. x
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Rank: Advanced Member  Groups: Registered
Joined: 12/4/2009 Posts: 312
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Dear Karen, nice to meet you! I am Fiona, 52, living in Plymouth and diagnosed with R.A at age 38. The first year is tough after diagnosis, at least that is how I found it to be, especially as I refused all medications at that time! I have been on Hydroxychloriquine Sulphate for many years now and it has helped me tremendously. I will look forward to reading your posts. Best wishes, Fiona
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Rank: Advanced Member  Groups: Registered
Joined: 12/3/2009 Posts: 872
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Hello Karen, sorry to read about your RA but really glad u posted, Im Liz 39 (40 this year...) Im married to Paul, we have two daughters Sophie 16 and Jess 13 RA turned up suddenly for me at 27, same time as when my mum died, i think its so true someone said about the hard shell we make for ourselves but on here we can be really true to ourselves with people who really care and understand - i think we can all empathise with your experiences in one way or another, this forum is SUCH a great help xx i have had a bit of a "duvet" day today, feeling bit down in the dumps today and came on here to cheer myself up a bit, its nice to "meet" you, please keep posting and take care, love Liz xxxxx
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Rank: Advanced Member  Groups: Registered
Joined: 12/3/2009 Posts: 872
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Hope you're ok after your fall? xx
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