'Hello Everybody' - I Have Just Found Site So Thought... - NRAS

NRAS

37,219 members46,055 posts

'Hello Everybody' - I Have Just Found Site So Thought I would Say Hello And Introduce Myself.

Sophie123 profile image
11 Replies

I am a 46 year old woman who has recently (June 2012) been diagnosed with with RA.

After struggling along for nearly 3 years with well intentioned doctors scatching their heads (no RA positive bloods) to not so well intentioned doctor saying I had middle age burn out! Now as you can image as a busy working mum who really does not like to make too much of a fuss this one really did knock me for six! So I went away for two and half years and battled with pain in my hands, knees and elbows along with the awful tiredness that after busy days would leave me exhausted to the point of almost not having the energy to get up the stairs as my muscles burned with the extreme fatigue.

Eventually my family said 'no more, you have to go back to doctors'. I have to admit I was reluctant to go back with how I had been treated in the past - they made me feel I was either wasting their time or even making things up! I did go back though, and this time bloods now showed a positive RA.

Now I have a very sympathetic consultant who immediatley put me on Sulphalazine - unfortunatley these gave me the most terrible headaches so have now switched to methotrexate. They also gave me the long acting steriod injection that was a god send. After being in pain and feeling so awful for so long I actually felt quite eurofic, I had genuinely forgotten what it felt like to be pain free and full of energy! My husband said there was such a transformation in my whole being. Unfortunately as great as this was it was only a relatively short term fix (although I was very thankful for that time).

Thinking positively though for what the future may hold.

Many thanks for reading and I hope to chat to more members soon.

Written by
Sophie123 profile image
Sophie123
To view profiles and participate in discussions please or .
Read more about...
11 Replies

Welcome Sophie,

Once the MTX takes effect which is about three months you should start to feel better, if not there are other DMards out there that will help you. In the meantime take a look at some of the blogs on here including the archive ones, and you will see that we are a happy and friendly bunch, even though we are in pain most of the time.

Take care,

Sophie123 profile image
Sophie123 in reply to

Hi Georje

Many thanks for reply. I will, as you say delve into the archives. I feel I need to learn as much as possible at the moment in order to move forward and manage this illness in a positive way.

Thanks again.

sylvi profile image
sylvi

Welcome Sophie, you have found us and we will support you through the good times and the bad times as well. If you want to rant and rave feel free to do so and if there is anything funny happening please share with us as we do need to laugh with this disease.

Look forward to hearing more from you. Sylvi.xxx

Sophie123 profile image
Sophie123 in reply tosylvi

Hi Sylvi

I already feel welcomed by your post so thankyou for that. x

allanah profile image
allanah

hi Sophie

Great that you have blogged and that at last they have sorted you out a diagnosis, bet you are relieved now.

I got RA in March 2011 and it has definitely been a steep learning curve!! but theres always someone on here to give advice or cheer u up, i know i wouldn't have done so well without this site, so hear from you soon, lots of love Axx

Neverwell profile image
Neverwell

Welcome Sophie this site is great I've not long been on here and the lovely peaple on here helped me loads hope you feel better soon take care

Karen x

helixhelix profile image
helixhelix

Oooooh it makes me so cross to hear of people who waited ages to get diagnosed...I don't have the RA factor either but luckily had a GP who referred me anyway as she knew people could be sero-negative and still have RA. MTX (methotrexate) has been great for me, along with other DMARDS, and has given me my life back. So hope it does the same for you. Polly

Tillytop profile image
Tillytop

Hello Sophie and welcome from me too.

I am so sorry it took so long for you to be diagnosed but I hope very much that the mtx helps you.

Tillyx

Sophie123 profile image
Sophie123

Thankyou so much everyone for great support x

Treesha profile image
Treesha

Hi there and welcome to the RA family. This is a fab site and everyone is so supportive and helpful. I'm glad youi have finally been diagnosed and no longer feel like you're losing your mind. The MTX is great once it kicks in (if you can tolerate it ) lots of good luck and i look forward to reading how you get on. Take care xxxxxx

Josie2 profile image
Josie2

Hi Sophie

I too am a newbie both to RA and this site but this really is a wonderful site to find.

Everyone is so kind, patient and understanding and always helping with questions.

Since finding this place i no longer feel alone and isolated with Ra.

Xxxx

Not what you're looking for?

You may also like...

Just thought I would say 'Hi!'

Hello everyone, I thought i would stop by to just say hi! I have now had two lots of my...
PJ68 profile image

Newbie - Just wanted to say hello and introduce myself. Flare Up at the moment so not feeling great.

Hi All I have been on this sight for a few weeks now, reading all the lovely posts and seeing the...
lilolil profile image

Hi Everyone, havent forgotten any of you-thought i would say hello! xx

Hi all, how are we all doing? Haven't forgotten any of you-hugs to all of you. What have i been...
Jetblack profile image

Hiya, I'm new to this site, Just thought I would interduce myself.

I'm Shirley, I'm Married and have two daughters one is 30 and the other is 14, I'm 49 and was...
shirlthegirl profile image

Hi! I am brand new to this site. Just found you today. I have RA, fibro, and polymy. rhuematica.

The RA was newly diagnosed one month ago and my RA dr. Has me on plaquenel for that.I have also...
mgbella profile image

Moderation team

See all
Nicola-NRAS profile image
Nicola-NRASAdministrator
KateL-NRAS profile image
KateL-NRASAdministrator
Plankten profile image
PlanktenAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.