3rd times a Charm: Just diagnosed with RA. 1st... - NRAS

NRAS

37,273 members46,139 posts

3rd times a Charm

Sharrelson profile image
6 Replies

Just diagnosed with RA. 1st appointment couple weeks ago. Doing extra blood work to see if Lupus. Gave a shot of depo. Not alot of relief. Next appointment they will start meds what have you. Been reading so much getting a little anxious about the road ahead. This is the 3rd time I have tried to post so we shall see. Just curious if RX pill, injection or iv therapy give quicker results?

Written by
Sharrelson profile image
Sharrelson
To view profiles and participate in discussions please or .
6 Replies
AgedCrone profile image
AgedCrone

Go with the flow Sharrelson...don't bother reading & trying to understand all you read until you've been diagnosed at least 6/12 months. Give your rheumatologist a chance to get on top of things.....then start the reading & comparing.

Don't even contemplate future meds ...that is the rheumies job....& he is restricted by NHS regulations as to what & when he can prescribe.

I was diagnosed 18 years ago....had some ups & downs,but didn't try to outguess the professionals...makes for a calmer stress free journey .

Good Luck....the Depomedrone may still kick in...I found it could last for 10/12 weeks& was my favourite " Go to" when it all got a bit much!

Sharrelson profile image
Sharrelson in reply toAgedCrone

Yea I agree. I need to stop looking into all of it. My rheumatologist seems really great so waiting for Jan 9

Appreciate your response. Thanks

AgedCrone profile image
AgedCrone in reply toSharrelson

You're very welcome.

I find overthinking RA from day one drags you down.

Hope your rheumy turns out to be a "star" as mine is.

Happy Healthy 2018!

Kai-- profile image
Kai--

.

If interested in a bit about newbie RA diagnosis ( healthunlocked.com/cure-art... ) & "speed of results" and/ or potential for addition of Lupus diagnosis ( healthunlocked.com/cure-art... ), there’s lots of realistic hope for an improved future, Sharrelson. ☺️ 🙏

Please, take gentle 😌 , loving 💓 care of yourself. Wishing you the very best. 🙏 🍀 🌺 🌞

.

🎄 🔖 🎁 🎅 ❄️ ☃️ 🌨

.

nomoreheels profile image
nomoreheels

Hiya Sharrelson, welcome to us here at the NRAS forum. I'm sorry to hear you've received a diagnosis but do hope your further tests don't reveal you also have Lupus. If it does turn out to be the case though there is also a Healthunlocked Lupus site you could also join if you wish.

Try not to bog yourself down with too much info just now, your Rheumy is the one who will answer any specific questions & arrange your med protocol. Unfortunately, if you're in the UK, he has to follow NICE guidelines so researching meds & their delivery will be somewhat fruitless. You'll likely start on tablets, they will be DMARDs (Disease Modifying Anti-Rheumatic Drugs), either monotherapy (one DMARD)... methotrexate, hydroxychloroquine, sulfasalazine or maybe leflunomide or a combination double or even triple therapy depending on your needs but your Rheumy will explain which & why. Maybe if you'd like to do some reading up it would be best to keep to reputable sites such as NRAS nras.org.uk or Arthritis Reasearch UK arthritisresearchuk.org, less chance of frightening the life out of you with those!

You've enough to think of at the mo, coming to terms with not only one diagnosis but the possibility of two so I wouldn't concern yourself with any more than your Rheumy recommends. There's time look at exercise, diet & such further down the line, just concentrate on your meds working in the early weeks & months. Unfortunately none of the DMARDs are fast acting, they can take 12 weeks or more to be effective although you may notice subtle differences before then. You'll be prescribed as needed, this may include a short course of steroids or a general steroid injection (which you've had & will hopefully kick in soon) & an NSAID, each work on current inflammation & in turn pain until your DMARD(s) start working.

If there's anything specific you're wanting answers to we'll be happy to help but just so you know we're not medically qualified so can't answer anything med related unless it's through experience & everyone's differs so you may receive varying answers. 😊

Sharrelson profile image
Sharrelson in reply tonomoreheels

Thanks for replying. I am in the USA North Carolina. Yeah reading post and alot in the UK seems to be a different type of health care there. I work for one of the biggest health insurance companies here, so I have read alot but going to try to 🛑 and wait for my next appointment. I know with my insurance some thing have to be tried before they will pay for others.

Not what you're looking for?

You may also like...

Only been on a few times.

Hi all I just wanted to let people knowi have been on methotrexate, lethunomide,and sulfasalazine...
Ruffles13 profile image

3rd dose

Had an appointment 2 weeks ago, went to said appointment, where is your letter, I do not have a...
Bootoo profile image

3rd covid jab dose Recieved

Update from my last post and after some confusions I have finally had my 3rd dose of covid...
Chrissycl profile image

Bad Times - A Cathartic Post

I'm usually very positive. I get upset and have a rant and moan sure, we are all human after all,...
ShellyWelly profile image

How frequently do people still trying to find a suitable treatment see their Consultant?

Is a 9 month wait to see your consultant usual practice because most consultants have a very heavy...
sash1985 profile image

Moderation team

See all
KateL-NRAS profile image
KateL-NRASAdministrator
Donagh-NRAS profile image
Donagh-NRASAdministrator
Nicola-NRAS profile image
Nicola-NRASAdministrator

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.