Please or to access all these features

Autoimmune disease

Mumsnet doesn't verify the qualifications of users. If you have medical concerns, please consult a healthcare professional.

Doctors, nurses, patients - if ANYBODY can help me, you’ll literally save my soul.

40 replies

26goingon90 · 13/10/2022 21:14

Before I start, this is definitely going to be a long winded one but stay with me here if you can 😂

I’m absolutely desperate for some kind of answers, advice, similar experiences - literally anything to make me feel like I’m not going completely insane. I’ve just turned 27 last month, I have 4 children. During lockdown in 2020 with loads of spare time on my hands (as much spare time as you do with 3 children at the time) I decided use that time to lose some weight & get healthier and fitter. I managed to lose 2 stone, and felt amazing for it. I was so much more energetic, and for the next 2 years I would walk miles every day, always out and about with my kids and just enjoying life. Always been healthy. Only health problem was postpartum thyroiditis, resolved every time.

In April/May time this year I started to notice that my feet & legs were going really, really blue. When I was cold, when I was in the shower especially, or sometimes just randomly. This then spread to my hands. After about a month, I rang the GP (in England - NHS) feeling a bit stupid for even doing so as it seemed such a minor thing. The GP assured me it was NOT normal, and I was right to ring. He ran some blood tests. All fine.

But after this it was like it snowballed. It was like somebody had flicked a switch. I was suddenly struck down with this awful fatigue, and started to get joint pain & stiffness. Started in my knees (which have clicked & popped for years) but then kinda spread to my hips, lower back, shoulders. I started getting pins & needles and numbness in my hands and feet. I also felt just generally run down + crap. I couldn’t work it out but I knew I felt rough. I started to feel cold a lot, but had some increased sweating and was also very thirsty + hungry. My first thought was diabetes. Rang the GP again, he said they’d already tested for it. It had come back normal. But they were going to run some basic rheumatoid & inflammation tests. I started to look into this more. By this point, it all seemed to fit. I had worsening joint pains, tiredness, stiffness in the morning, and by this point also had some general weakness in my legs/arms. They were all clear. I was referred to rheumatology anyway.

I was given co-codamol and naproxen. This went on for a few months, gradually worsening until I ended up in urgent care twice because of pain so bad I couldn’t take a deep breath. Both times I was put on stronger painkillers & steroids temporarily. Back to the GP - a new one who thought I had ankylosing spondylitis. The gene test for that came back negative.

After another episode of horrific pain, I had another amazing doctor at my GP practice who ran every immunology test under the sun. All clear. In fact, everything perfect really except a borderline high ALT, borderline high but normal WBC count, and a low potassium. Thyroid antibodies to be expected.. At this point, I was okay as long as I was moving around. The less I moved, the worse I felt. I stiffened, I got sore, I was in pain. So I kept moving and it was awful, but bearable. I began sleeping on the sofa because night times were the worst. I tossed and turn in pain and discomfort.

Onward to my rheumatology appointment last month. He reviewed all my tests, and said they all looked fine. He said I had hyper-mobility, and would send me for a nuclear bone scan to see what was going on.

Now, during the last month or so the general stiffness/pain in joints has slightly improved. I still ache, and hurt but not unbearably. But the weakness has become horrific. My legs give way from under me and buckle, I have days where lifting a spoon can seem too much, I shake, and I have zero strength or grip whatsoever. I’ve also started to notice I feel less co-ordinated, more clumsy, just sometimes not on this planet at all. I’ve started to get weird dizzy spells where I just feel almost drunk. I don’t drink either by the way! I go light-heated, sweaty, shaky. My heart races and I feel dreadful. Last week I spent the whole night awake with the most horrific pain in my right shoulder that went all the way down my right leg. The pain was bad in my shoulder, but most worrying was the complete weakness in my leg. It kept giving way & buckling on me. I went my out of hours doctor, who gave me muscle relaxants for a ‘muscle spasm’ and sent me on my way.

The weakness in my leg got worse over the weak, and then for some reason I was struggling to go the toilet. I’ve always suffered from constipation mildly, however this was as if I’d lost the ability to go at all. I was sent from urgent care to A&E, who x-rayed my spine and ruled out cauda equina and sent me on my way. I disclosed to the doctor that I was worried it could be MS, so they put in a referral for a brain mri. Awaiting this. Amazing.. but I’m still poorly?! I’ve spent the last week feeling the worst I have ever felt in my life. Weak, shivery, poorly, just unable to function whatsoever.

I went to the pharmacy for laxatives, who redirected me to my doctor, who sent me BACK TO A&E.

Are you losing the will to live with my story yet? Cause this is my life at the moment. 😂😂 it’s a ball.

I went back to A&E who diagnosed me with faecal impaction and sent me on my way with laxatives. But not before they’d taken my bloods and put me in the waiting room as standard. 10 minutes later they are running in for me and putting me in a private room in emergency care, telling me I’m having a hypo and I need a glucose drip fast. My blood sugar was at 3. I’d an hour before eaten a bagel with Biscoff spread because I’d felt so weak & shaky.

So I’m now at a complete and utter loss. I’m stumped, seriously. I have some healthcare/medical experience, I work in science, I’ve worked in midwifery, nursing care. I’m not a doctor but I have some knowledge there. And I’m seriously just baffled by what is wrong with me. I know for a fact I don’t have fibromyalgia. That’s all I do know. But I’ve cycled between RA, lupus, axial spondyloarthritis, diabetes, MS, ehlers-danlos. I just don’t have a clue what is wrong with me and it is completely ruining my life.

I have days where I can’t function, I crawl through the day most days. Then I have days where I think - mind over matter, I WILL get better. And I’ll go to work, or take my kids out for the day, have an amazing day. Then the next day I feel like I’ve been hit by a bus. It’s impacting my relationship, my parenting, my job, my life. I don’t know if I need a rheumatologist, a neurologist, an endocrinologist. My GP don’t seem to want to help unless I beg or hound them. I understand the pressures GPs are under before anybody says otherwise, but mine really have fallen short with me quite a few times. But I also, I understand that they seem at a loss as to what to do anymore. If anybody could help me, it would mean the world & more ♥️

OP posts:
lordloveadog · 22/10/2022 09:52

Have they tested for Neuromyelitis optica? Or rather NMO spectrum disorder.

www.nhs.uk/conditions/neuromyelitis-optica/

The leg weakness, bladder/bowel problems and pain episodes make me think this should be checked.

lordloveadog · 22/10/2022 09:55

Also, I'm really sorry you're going through this! Sending strength to your doctor-hounding. It's such a shame one has to hound when symptoms clearly need investigating.

Backtobed13 · 22/10/2022 10:35

Wow OP, when I read your post it was like reading my own story. Years of tests, no answers, going from doctor to doctor and slowly losing the will to live. Questioning my sanity and wondering if I'm imagining all my symptoms and that somehow this is my fault and I deserve to suffer like this. My life literally destroyed, can no longer work as a nurse, only 36 but living the life of a recluse. Worst part being the not knowing, feeling in limbo and like your life is on hold.
I have muscle weakness, can't climb more than one flight of stairs before my legs won't move and buckle underneath me. Arms so weak can hardly dry my hair. Have had viral meningitis THREE times. The last episode being in 2020 where I had seizures and my legs were paralysed for one week. Worst part being the doctors labelled me as being hysterical and said I had conversion disorder, despite my lumbar puncture coming back as positive for meningitis. I have not been the same since. Been left with myoclonic jerks, severe muscle weakness, strange rashes and swellings, night sweats, low grade fevers, joint pain, hazy vision, dizziness, complete brain fog, completely spaced out and detached, just basically everything you describe. Not to mention ptsd from my hospital experience and a new phobia of doctors. Seen neurologists, rheumatologists, immunology,next is endocrinology! Most tests normal including ANA and gene for ankylosing spondylitis, MRI's normal. Only a few bloods off that may point to a problem with immune system, and positive anticardiolipin antibody which can be associated with some autoimmune diseases but when repeated it was negative. Also one positive antibody for a type of myositis called dermatomyositis which I have all the symptoms of but again, then negative. Waiting for that to be repeated. Doctors won't commit to a diagnosis because ANA negative, even though you can be seronegative and have an autoimmune disease. I am losing hope and the doctors are not listening ; I know they think I am crazy and just anxious. It's terrifying knowing that your body is literally breaking down and no one can tell you why. Oh I am also hypermobile and have attacks of tachycardia and dysautonomia but again, doctors keep dismissing possibility of ehlers danlos or POTS.
I'm so sorry, I'm rambling, but your post has resonated with me so much. I feel so isolated and friends starting to distance themselves because they think why am I still sick...shouldn't I be better by now? No one understands when you're undiagnosed and start thinking you must be a malingerer or something. So you withdraw and suffer in silence because it's easier that way. But please OP know you are not alone in this. I get it and I hear you, I feel your pain. Please DM me if you want to talk.
One thing, maybe ask for a myositis antibody panel to be done to check for autoimmune muscular diseases such as polymyositis or dermatomyositis. Don't give up. When doctors say oh we may never find an answer and you may have to accept this and try to live with it well, I'm sorry, but no one should have to resign themselves to living like this. Being undiagnosed and suffering daily literally destroys your life, from robbing you of your self esteem to wrecking relationships and work. Keep advocating for yourself if they are not listening, as exhausting as it is. Get in touch OP if you just want to talk.

HelpMeGetThrough · 22/10/2022 11:29

CRP of 21 (previously 0.3 consistently)

This sticks out to me. That's bloody high. Some of the symptoms you have are exactly like I have. I have rheumatoid arthritis. At its worst, my CRP has been 50, but during a nasty flare, mine is around the 20+ mark. My knees do give way too. Not fun when you are carrying a mug of coffee upstairs.

Co-codomol and naproxen will bung you up. I'm a regular codeine taker for pain management and can get "backed up" if I don't take a softener.

Evamaisie · 09/11/2022 23:15

Sorry to hear the problems you are having 😟 it may not be relevant but I noticed you have high ALP and ALT - has anyone looked at your liver?

UnmentionedElephantDildo · 09/11/2022 23:23

Have you had covid and when?

Because the symptoms you describe are all associated with long covid (and the high CRP fits with it too). It affects cardiovascular system, and the blue fingers could mean microclots in your capillaries. Fatigue and muscle aches are also very common features

Mombie · 28/12/2022 00:54

Hi Op,
I know this is an old thread but did you get anywhere with diagnosis or treatment. You sound so much like me, I have been repeatedly going to the doctors since mid October with worsening muscle weakness. I was fobbed off with painkillers and vitamins and then finally a blood test to check my CK levels in early December showed that this was unusually high and I have been referred to rheumatology for suspected myositis, like Backtobed13.

I’m waiting on my appointment and getting worse every day now. Barely able to hold myself upright or walk unaided, I feel like I’m falling apart whilst I wait for someone to
do something. I hope that they can offer me some form of treatment because I can’t do anything at the moment and I really want to be me again. 😟

I hope you and Backtobed13 managed to get somewhere with your diagnosis and treatment.

JRAKR · 25/02/2023 22:39

sorry for short message but I really wanted to reply but don’t have a lot of time- feel free to DM too … but I would check

  • thyroid- full panel- what is TSH, T3 and T4? You need to look at all together to get a full picture of thyroid health. Also be aware that a ‘normal’ tsh varies between doctors. It’s absurd. And each person has their own personal limit. For example I feel exhausted if my TSH is above 1.0. Fortunately I have an amazing endo who responds to this but many doctors would dismiss anything around 1.0 as being completely normal. If you’re on FB I suggest joining as many thyroid groups as possible.
  • diet ! It sounds like you have severe inflammation at the moment. Strip everything back to an AIP diet. It’s so boring but try it for a month and see how you feel. You might also feel worse before you feel better while the body expels toxins. Then if you’re feeling better you can eventually introduce more foods (move up to a Keto diet for ex). lots written about this but Chris Kresser and Dr Josh Axe talk a lot about the relationship between food and chronic inflammation.
  • im always a big fan of natural remedies but when you’ve been in such a stressed state for so long your body is producing so much adrenaline and cortisol you need to reverse this… it might be worth looking at taking a low dose of diazepam or an anti-depressant, for a short while to begin with. I think there is quite a bit of evidence that it supports people with chronic pain and fatigue

i hope this helps. I know how scary it is to feel so unwell, don’t give up hope!

IndiganDop · 25/02/2023 23:00

Dumping syndrome?
My uncle had it. More often associated with bariatric surgery, but can occur spontaneously (as in his case).

ReallySeriouslyNope · 26/02/2023 08:29

@26goingon90
How are you doing? Hoping you've been diagnosed and are receiving treatment

Reddress2023 · 11/03/2023 21:55

Are you anaemic? Lots of symptoms could be caused by low ferritin.

Alargeoneplease89 · 11/03/2023 22:01

Myositis is another to research. Auro immune diseases aren't cut and paste though you could have an overlap etc.

Summer2424 · 11/03/2023 22:19

Hi @26goingon90 i just read your post x
I don't have any advice i'm so sorry but am sending you lots of strength and lots of positive vibes that you get better quickly x ❤

greenspaces4peace · 11/03/2023 22:35

CREST syndrome?

ThankYouVeryMuchGerry · 20/03/2023 20:53

I'm just about to see an endocrinologist and a rheumatologist as the GP suspects I might have scleroderma. I've had similar symptoms and also my arms legs and hips have gone practically solid int muscle and fat. My feet and ankles have also gone funny on the skin and my hands are like claws. I'm really scared.

Have you had a diagnosis yet? I'm hoping you're getting some help now x

New posts on this thread. Refresh page