NRAS Logo
Logged in as: pedro-pmc Search | Moderate | Active Topics | My Profile | Members | Logout

New Topic Post Reply
Hello Options
RAC1964
#1 Posted : Monday, February 25, 2013 8:25:50 PM Quote
Rank: Newbie


Groups: Registered

Joined: 2/16/2013
Posts: 1
Location: Abingdon
Hi all, My name is Rob, I'm 48 years young and live in Oxfordshire with my wife Debbie and our lively 5 1/2 year old springer spaniel Dylan. I was diagnosed with RA on 15th February but have only just started my treatment today. I look forward to being involved on this forum and chatting with you all.
Kathleen_C
#2 Posted : Monday, February 25, 2013 9:23:41 PM Quote
Rank: Advanced Member


Groups: Registered

Joined: 12/3/2009
Posts: 1,689
Location: Durham
Hallo Rob, and welcome to the forum, though I`m sorry you`ve been diagnosed with RA. You will find info and empathy on here, from members who know what it`s like to live with RA, so do keep posting.

What meds have they started you on? You should be able to access a specialist nurse, physio and OT if you need it.

Your Springer will indeed be lively - we used to have a Springer called Rory. He died when he was 11, but in truth, he never really grew up, and was as daft as a brush sometimes! Our next dog was a Golden Retriever - totally different. We`ve just lost him, at the ripe old age of 15, but no more dogs now.

Take care,

Kathleen

Naomi1
#3 Posted : Tuesday, February 26, 2013 1:16:51 AM Quote
Rank: Advanced Member


Groups: Registered

Joined: 9/3/2011
Posts: 717
Location: Torbay
Hi Rob, welcome. Sorry you've been diagnosed but glad you've found us. there's a lot of support and wisdom available here. I'm the same age as you and was diagnosed 20 months ago so my memories of the post diagnosis period are still quite raw and I can empathise with what you must be going through. if you're like me then you'll have plenty of questions. Feel free to ask anything you want. There's usually someone on here who has the same symptom or drug or whatever as you and everyone is willing to offer help where they can. I look forward to getting to know you better. best wishes from Naomi.
sylviax
#4 Posted : Tuesday, February 26, 2013 7:06:44 AM Quote
Rank: Advanced Member


Groups: Registered

Joined: 5/28/2012
Posts: 665
Location: Newton Abbot
Hi Rob - welcome to the forum - but sorry you've got to have RA to be here!

I'm Sylvia, 55, and was diagnosed last May. What a rollercoaster ride those early days were, so much to take in and so many questions - if it's the same for you then do feel free to ask away. - the good news is that the drugs do really help.
My DMARDS are methatrexate and hydroxychloroquin, plus various other meds for this and that - you will quickly get an entire cocktail of drugs if you're being started on the standard Triple Therapy, which most people do.

Have you been given steroids? That's very common to get the inflammation under control quickly, although it's usually only given as a temporary fix. When I started treatment, I had a jab (in my rear!!!!) followed by 4 weeks of tablets, and that was total bliss as no pain!! It might be different for you as we are all individuals and care does vary depending on who your consultant is, but there's a lot of people on this forum and between us we have experience of most things.

Let us know how you're getting on - with very wishes - Sylvia
Be kinder than is necessary because everyone you meet is fighting some kind of battle
mazza59
#5 Posted : Tuesday, February 26, 2013 8:20:52 AM Quote
Rank: Advanced Member


Groups: Registered

Joined: 5/7/2012
Posts: 149
Location: S E London
Hi Rob,
Welcome to the forum, I was diagnosed in March 2012.

What meds are you taking?

Lots of well informed people of the site, I found their advice very helpful when I was first diagnosed.

Hope to hear more from you in the future.

Mary
jenni_b
#6 Posted : Tuesday, February 26, 2013 9:08:44 AM Quote
Rank: Advanced Member


Groups: Registered

Joined: 12/3/2009
Posts: 2,237
Location: nr Southampton
Hey rob!

Welcome
I'm jenni
I'm 37
I'm married to Richard and have Michael Gemma and Bernice
The older two are teenagers
Bernice is 5!

We have a cat called kipper
I'm just waiting for a canine partner

Lots of doggy fans on here... (Mainly bonkers!)

Off to london today doing some research for hereditary ra prevention

Look forward to chatting more

Jenni

Ps what treatment are you on?
how to be a velvet bulldoser
suzanne_p
#7 Posted : Wednesday, February 27, 2013 11:30:29 AM Quote
Rank: Advanced Member


Groups: Registered

Joined: 8/25/2010
Posts: 1,289
Location: Buckinghamshire
hi Rob,

welcome aboard.

it's really daunting when first diagnosed, i really went through the wringer with it all .. and then the meds you have to face!

i am guessing you have started on Methotrexate? do let us know.

i've been diagnosed almost 3 years now, started on Methotrexate then added Hydroxycholoquine .. this combination didn't work for me, so i was put onto an Anti-TFN August 2011. i do pretty well now.

you will find this forum very helpful, there is always someone to listen or help you.

do keep posting so that we can get to know you,

Suzanne
sylviax
#8 Posted : Sunday, March 03, 2013 9:01:01 AM Quote
Rank: Advanced Member


Groups: Registered

Joined: 5/28/2012
Posts: 665
Location: Newton Abbot
Hi Rob - hope you come back and post again - we need more blokes to balance out the discussions here! RA is not just a disease for women - Sylvia
Be kinder than is necessary because everyone you meet is fighting some kind of battle
Users browsing this topic
New Topic Post Reply
Forum Jump  
You can post new topics in this forum.
You can reply to topics in this forum.
You cannot delete your posts in this forum.
You can edit your posts in this forum.
You cannot create polls in this forum.
You cannot vote in polls in this forum.

SoClean Theme By Jaben Cargman (Tiny Gecko)
Powered by YAF 1.9.3 | YAF © 2003-2009, Yet Another Forum.NET
This page was generated in 0.712 seconds.