Posts - NRAS | HealthUnlocked

NRAS
27,570 members31,584 posts

All posts for January 2020

Tocilizumab & Travel

I need a cheap way to take about 7 away. Journey post 28hrs including an airline...

20 years old seeking advice on process of being diagnosed with RA

I'm 20 years old and currently in the process of being diagnosed with RA. It's b...

Finally got a diagnosis

Hi, I thought I would update you all with the latest news on my health. I went t...
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How I minimized the uncomfortable feeling after taking methotrexate - 31/01/2020

Recently a few RA patients messaged me to complain that they have gastric proble...

Humira! Hooray!

I don’t normally post anything but I felt I had to write this. I was taken off H...

Hair loss / thinning

Hi everyone, I’ve just joined this group, apologies if this has already been as...

In the book about chronic fatigue was this

Credit for this wonderful list goes to my patient, Sylvia Waites) Thou shalt n...

Thought for the day

Should we think about campaigning to get Rheumatoid included in The NHS list of ...

Steroids

Hi. Can anyone help me with this problem. I have had RA for 25 years I'm on meth...

Gastro-resistant Sulfasalazine shortage?

Hi, I've just signed up to the forum. Nice to meet you all. I was diagnosed with...

Sleep

Got hit by the MTX sleep fairies 🧚‍♀️ last night bed at 945 and just woken up a...

& another pic

Maybe this angle gives you a better view of the dent.

DIPs

Following on from a post on here, I thought I’d ask you knowledgeable folk what ...

How come my Anti ccp became negative?

Hi all! For couple of years I have been dealing with joint pain. A year ago, I w...

Biochemical versus mental health

It's been a struggle for 14 months coping with RA and the aftermath of the diagn...

Persistent low level headache and dizziness since moving from oral MTX to injections . . . or just me being odd?

A little bit of background first. I'm relatively new to my RA diagnosis (althoug...

Afternoon chills

Hi, yes, I am glad that I googled this now. For the past 5 years or so, I get s...

Help!!

After diagnosed for R.A. 4 years ago, having infusions of Actemera, then Orincia...

Breathlessness and Gallbladders

Not posted for a while but I’m in hospital with inflammation of the Gall Bladder...

Looking for other mums with RA

Hi everyone I'm new here and although I am 6 years along in.my RA journey, I'm o...

Thank you

Thank you to everyone who replied to my question about RA services in Northern I...

RA and fibromyalgia

Hello I have been to my monthly Rheumatology clinic yesterday and I have been d...

After my day

decided to post this

RA and RA Cachexia update

As promised I said I would drop off a note for those interested in the strength ...

COLD SORE

I have a cold sore and I don't know what triggered it. Would my RD or IBS-D have...

Relative of RA suffers and Consultant's

Hi al, Anyone on here that is a relative of an RA sufferer. If so do they get re...

I do wonder if there are any RA sufferers that are not taking RA meds on this forum?

I have been here for five years and have never found anyone🧐

Coronavirus

The numbers keep climbing. I hope you are all taking as many precautions as you ...

Services in Northern Ireland?

Does anyone know what the RA services are like in Northern Ireland? We’re cons...

A heartfelt thank you

Thank you, each and everyone of you who responded to my post. I genuinely apprec...