Muscle twitching!?: Hi all, I was... - LUpus Patients Un...

LUpus Patients Understanding and Support

3,447 members1,274 posts

Muscle twitching!?

Leah2014 profile image
4 Replies

Hi all, I was wondering if any of you have muscle twitching with their lupus? I know it's not a common symptom so obviously starting to worry its something else so if anyone could get back to me I'd really appreciate it! X

Written by
Leah2014 profile image
Leah2014
To view profiles and participate in discussions please or .
4 Replies
Bellaflowe profile image
BellafloweVolunteer

Hi Leah,

Which muscles are worse or is it all over? I get it in my legs. I don't think you should be worried but definitely let your doctor know. If any symptoms change for me I always let

my doctor know, so even if it's nothing to worry about it's written on my notes.

Sending hugs to you. Suzy x

lupus-support1 profile image
lupus-support1Administrator in reply to Bellaflowe

Your quite right Suzy!

lupus-support1 profile image
lupus-support1Administrator

It is important to tell your doctor every symptom and let him/her decide whether this is related to lupus. You may find it helpful to write down and record, with dates, your symptoms so when you have an appointment, you can go through everything you need to talk about.

Can you say a bit more about this muscle twitching. For example, does this occur when you are resting? Are there any other symptoms with your muscles?

Be well!

Ros

Bellaflowe profile image
BellafloweVolunteer in reply to lupus-support1

Completely agree with you, Ros. Leah, I keep a symptom diary. Because my memory is so bad, I write down anything that seems to have changed with my body, when it started and how long for. I was having horrendous nightmares for months and I thought nothing of it until my consultant asked me if I ever get nightmares. I didn't even know that vivid nightmares are a little known symptom of CNS Lupus. So now I write everything down. Even if you're short on time with young kids, keep a notepad and pen in your handbag to jot things down quickly.

I'm here if you ever need to talk. I've had lupus since 2002. Suzy x

Not what you're looking for?

You may also like...

Could this be my lupus or something else

Not posted on here for a while now but hoping to get a bit of advice if anyone can help.for a few...

Stroke or Autoimmune

Hi all, Has anyone else had stroke like symptoms with all normal bloods besides high Calcium?...

CNS Lupus & Noise Sensitivity

Hi everyone :) I haven't posted in ages, so I hope you're all well, or at least coping! I've been...

My lupus skin V the sun

Hi I've been suffering with lupus for 5 years but only got a definite diagnosis a few weeks ago. I...

GPs

I don't know if anyone else has a problem with their gp. On my last rheumatology letter (had to ask...