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Please diagnose me - my life is falling apart due to this mystery illness.

72 replies

Painengrained · 29/08/2015 14:03

Please help me figure out what is wrong. I am stuck in the system of best guesses and waiting lists and in the meantime, my relationship is suffering, I have become depressed and have enquired (with horror and disbelief) about putting my disabled child into care as I am struggling to care for her. I desperately want to feel better. I will make this as concise as I can though its been a long four months Sad

At the beginning of May I started having shortness of breath. I was newly diagnosed as Hypothyroid (autoimmune) and as a result, had been putting all symptoms down to that (had felt fatigued, had hair loss, aches and pains, loss of drive etc for months) GP checked me over, Levothyroxine dose tweaked, bloods good, was put down to anxiety. The year had been extremely stressful up to this point so I was inclined to agree. GP also gave me an antibiotic for a rash around my mouth.

The shortness of breath progressed to chest pains and very bad reflux-type-pain. I took gaviscon and made another appointment. I had been taking Tetracycline antibiotic for peri-oral dermatitis so thought it must be that. The day before my appointment, whilst still on the antibiotic, I felt quite ill. the right side of my body felt weak and I just wanted to lie down. Had to cancel all my plans for the day, family had to care for DD. GP checked me over, said it must have been a reaction to Tetracycline and I would start to feel better in a few days.

A few days later, the chest discomfort and weakness progressed to right sided rib pain. Back to the GP, convinced that something more must be going on. GP examined my abdomen, thought it was muscular but could be gallstones. Told me to try relaxation techniques as I could have been holding my body in a 'stress' position and referred me for a gallbladder scan.

Toward the end of May, I had what felt like a gallbladder attack. Extreme pain just below my ribs on the right side, pain going around and through to my back, right shoulder, neck and shoulder blade pain. DH took me to A&E. Bloods were normal, I was advised to wait for scan as surgeons were busy, told to go back if it happened again. It happened again, I went back, a different Dr examined me, thought gallstones as my right abdomen was 'guarding' and the pain was spasming/burning. A scan was set up for the following day, he offered to admit me but as my bloods were, again, normal, said I could go home.

Went for the scan, pain had subsided but was still smouldering. Gallbladder clear apparently, all abdominal organs looked ok. The only thing the scan picked up was that my common bile duct was measuring at the top end of normal (7mm). I was sent to surgical ward for a chat wit the 'experts' who said it was possible I had passed a stone, hence the CBD dilation. Following an examination, they diagnosed a probable ulcer an prescribed 4 weeks of Omeperazole (at a huge dose) followed by an Endoscopy if symptoms hadn't improved.

During the following 4 weeks, I had constant pain. It would peak and trough but was always there. It felt as if it were emanating from my right ribs, into my back, up through my shoulder blade, into my neck, into my armpit, down the inside of my arm, in my chest, even down through my hip and down my thigh. The whole right side of my body was suffering. I had severe constipation and nausea. I would wake at 3-4am in severe pain. Codeine made things worse, Tramadol made me feel very strange so had to discontinue, Buscopan helped a little, paracetamol was pointless and I couldn't take any NSAIDs as everyone was telling me I had an ulcer.

Through June I suffered, I have visited the GP almost weekly. I became increasingly desperate so they contacted the surgeons to set up an endoscopy. The surgeons refued and said I needed a stool test for H.Pylori bacteria. I had to come off the Omeperazole for two weeks prior to the stool test. It made no difference. The pain was the same, never letting up, I was becoming less able to handle it, weak from exhaustion and too scared to eat. I was devastated at the surgeons U-turn, I felt as if everyone thought I was exaggerating.

The stool test came and went, negative. Here I hit a low point, weeks of non stop, fluctuating pain, home life suffering, relationship suffering, exasperated and frustrated. GP referred me for urgent endoscopy which took another few weeks... in the meantime, I found a swollen lymph node above my right collarbone. I made the foolish mistake of googling, lymph nodes here are bad news. GP took bloods to check for inflammation and a full blood count to try and abate my fears as by this point I am extremely worried that something malignant is causing my prolonged pain.

I was also sent for an MRI on my spine as one of the GP's thinks I could have a trapped nerve/disc problem due to the - sometimes extreme - right hip pain i've been experiencing. I am waiting on the results of this. The hip pain seems to have come after the rib pain. if I stand for too long or walk for more than a few minutes, I get a searing pain in my right hip and down the inside, or front, of my thigh. I made the mistake of going for walk a couple of weeks ago and spent the night in agony with a leg that felt swollen and boiling hot but looked normal. I dont know if it is linked or as a result of my right side pain.

I had the endoscopy almost two weeks ago. Traumatic. And also negative. No ulcer, no gastritis, no cancer, no reason for this pain. The only thing it showed was some mild inflammation of my oesophagus. The Dr doing the exam said that would not be causing the pain that i'm suffering. The nurse looking after me said all my symptoms sound like my gallbladder. My bloods came back normal apart from a low Fibrinogen level which wouldn't be causing my pain (dr wants to investigate further but apparently it was low in 2013 too so isn't a new issue)

Last week I went back to the GP, with DH, to tell him that im struggling with life. I can barely look after DD, she requires constant care and I can barely function. Everything is an effort. I am in constant pain, couldn't sleep, hadn't slept in three months. He was very understanding, asked me to go over my symptoms and prescribed Mebeverine to take before meals and Mirtazapine to help me sleep, increase my appetite and 'lift my mood'. It certainly does help me sleep, it knocks me unconscious. And im eating everything in sight so at least I might put some weight back on, I lost a stone during this nightmare. He thought it could be Sphincte of Oddi dysfunction, which I've read is untreatable.

I have been urgently referred to Gastroenterology, it will still take a couple of months. A couple more months for me to google, to try desperately to figure out what the problem is and to worry myself sick. My worst fear is that it isn't going to go away, that this is my new normal. I cant stand up for long, some mornings I feel as if my pelvic bones have fused it hurts so much. The rib/abdo pain is constant but flares, the flares last days, it feels like there is something in there that shouldn't be or that something is inflamed. I am constantly bloated, sometimes painfully distended. Eating vegetables and meat seems to make things worse. My skin feels sore on my torso, possibly as a result of constant pain?

I do have Endometriosis but it has never felt like this. My gyne has agreed to do a laparoscopy to see if any has re-grown that could be exacerbating my pain, that op should be toward the end of the year. I am desperate for some relief, desperate to be a proper Mum and carer again. DH and I are arguing, we are both very frustrated. I am obviously depressed, I see no light at the end of the tunnel, whatever this is it has stolen our summer, it has stolen my ability to live my life. We have had to ask our disability social worker for a carer to help a few hours a week but DH is having to do the rest of DD's cares whilst working (from home, thanks to a very understanding boss) until she goes back to school. The holidays have been hellish.

I did book a private appointment with a gastroenterologist but realised we woudn't be able to afford any tests they requested so i'm having to rely on he NHS.

If anyone has made it to the end of this post, do you have any idea what is wrong with me? My life is falling apart, I am desperate.

OP posts:
Painengrained · 31/08/2015 12:06

peggy that sounds spookily similar. I've no history of bowel cancer or any digestive cancer. The only thing is my nan had acute pancreatitis but my bloods have always been normal, I'm not in nearly enough pain for it to be that. I can't do this for years! Gosh, the thought terrifies me.

Currently taking Lansoprazole for my reflux which does nothing for the right side feelings.

OP posts:
barleysugar · 31/08/2015 12:14

Have you had a CT scan of your abdomen?

Has anyone looked carefully at the pancreas? Some of your symptoms sound suggestive of a pancreas problem. This can cause biliary duct dilation, abdomen/back pain, weight loss, jaundice.

slugseatlettuce · 31/08/2015 12:22

This reply has been deleted

Message withdrawn at poster's request.

PurpleHairAndPearls · 31/08/2015 12:27

The problem with people suggesting stuff on the internet is that you can try and fit your symptoms to the diagnosis, rather than putting a name to your list of symptoms - if that makes sense.

It's worth asking your GP if you fit the referral criteria for rheumatology as there are a lot of auto immune stuff which has numerous symptoms. Be prepared though for a long wait...it's took me over a year with regular rheum appointments and blood monitoring to get a "tentative" diagnosis and then it was changed as more info became available!

Sadly a lot of time some conditions aren't easily diagnosable, the main thing in the meantime is to treat the symptoms you have, whilst all the work goes on in the background to "rule stuff out". It's very easy to fixate on trying to get a formal name for whatever you have, but I genuinely believe it can be counter productive. My rheum consultant said to me at the beginning, something along the lines of "you fit so many criteria and so much stuff is poorly understood at the moment, I may not be able to say to you, you have xxxx but I may be able to say you have "a xxxx type disorder" and at least having part of a named thing really helped me. It sounds like they are at least doing tests to rule stuff out and this may be the only way you get anywhere near a named diagnosis.

Does this make any sense? Fwiw, I really sympathise and totally understand your frustration and fear, particularly having disabled DC. I was able to get PIP without a formal diagnosis of xxxx so don't let that put you off. I hope this rambling makes sense, it's a bit early for me Grin PM if you want.

peggyundercrackers · 31/08/2015 18:56

Painedengrained your symptoms in your last post also sound very similar to my friend, pain 2 or 3 inches to the right of their sternum, low level dull pain in the front going to the back and goes round side, pain from hip to shoulder blade on side, soreness when taking big full breaths like their diaphragm won't expand enough. They had suffered a little dizziness too. Before whatever it is my friend had never ever had trouble with their bowels either.

friend had camera up and down and also barium meal but they found nothing. When they had an Mri of gallbladder they said there was absolutely nothing wrong, gallbladder was normal size, pancreas was normal size -no thickening of either, all the little tubes were normal size and were smooth which normally means they are fine. Liver was absolutely normal with no sign of fatty disease.

ArendelleQueen · 31/08/2015 21:47

Is your thyroid still out of whack? I know it can cause joint pain, so could potentially account for some of your pain.

Sorry if you've already said but are you being supported to manage your pain, both with medication (e.g. codeine) and non-medication (e.g. TENS machine)? Obviously you need a diagnosis but in the mean time, is there anyone to help with pain management?

Painengrained · 07/09/2015 09:55

I may be getting somewhere diagnoses wise but things have taken a nosedive ability wise.

My MRI results show a cyst on my spine which the GP says is incidental (not sure of location) I also have cervical spondylisis with an area of narrowing where a bundle of nerves leave the spine. The results were given to me over the phone so I didn't get chance to ask many questions, the GP said the radiologist advised I was referred to a neurologist because "my brain may be interpreting pain signals differently". I asked if the cyst was benign, he said it looks that way as they want me to have a follow up scan in a year, as opposed to sooner if they thought it suspicious.

So it turns out the GP I saw about nerve pain in my leg was right, a spine issue can cause abdominal pain, rib pain and arm pain.

I think an 18 week wait to see a neurologist is ridiculous. I'm at a point where I can't stand up longer than 15 minutes before I am overcome by pain, laying flat on the floor is the only thing that helps. My right arm, shoulder blade, ribs, abdomen, hip and leg feel uncomfortably tight. My right hand is clumsy, my neck muscles feel stiff, it's affective my vocal chords I think as sometimes my voice sounds strange, as if it's struggling. It feels as if my brain isn't working properly. Apparently there is no evidence of MS on the MRI so im trying to relax about that.

I have booked an appointment with a private neurologist this week. We can't really afford it but I need to know if there's anything I can do to help myself. Any exercises or anything. We've had to ask for carer support to do DD's bathing on an evening, DH is having to do her morning cares, the house and the cooking as well as his full time job. It's a nightmare. I can't do anything, I feel utterly pathetic And incredibly frustrated.

It has taken 4 months to get to this point. When I first went to A&E, I told the doctor the right side of my body felt different. When she was pricking my skin to test for numbness, I kept repeating "it doesn't feel numb but it feels different " why did this no alert her to possible spinal involvement?
I could have wept this morning when i realised there was no way I could get DD ready for her first day back at school. It is soul destroying. The fear of not knowing if I'll ever get back to normal is sometimes overwhelming, I'm trying my best to be positive and think good thoughts but I'm scared.

At least I get some temporary relief from laying on the floor. I don't understand how the entire right side of my body is being affected by a nerve problem in the top of my spine though. Am I overcompensating/guarding? Could that explain whey it feels as if someone reached into my ribs and pulled all my ligaments tight?

OP posts:
Painengrained · 07/09/2015 10:00

arandelle no pain management in place at the moment. Analgesics do nothing, opiates seem to make everything worse and naproxen isn't touching it, I get no relief from drugs. I'm hoping I'll be able to book myself in to a physio or an osteopath to help but I need to see the neurologist first, I'm terrified of making things worse.

I feel like my walking is being affected but I don't know how much of it is psychosomatic.

OP posts:
5608Carrie · 07/09/2015 10:05

I think you need to ask for H Pylori breath test. As far as I know the stool one is unreliable.

5608Carrie · 07/09/2015 10:07

Sorry didn't see your last post. Flowers

I really hope you get some relief soon.

Painengrained · 07/09/2015 10:20

Carrie I am still waiting to see the gastroenterologist so I will mention it. I'm still uncomfortably bloated, something isn't right with my digestive system.

OP posts:
PowerPantsRule · 07/09/2015 20:07

Costochondritis? I have prob mis spelled that, sorry.

Other thing I thought was auto immune which can do some very wacky stuff as someone else said up thread.

Scoobydoo8 · 08/09/2015 07:01

You sound horribly stressed, understandably, can you get some help with that. It might be exacerbating the problem, clouding the symptoms.

MusicIsMedicine · 02/02/2017 19:23

How are you getting on op?

mycavitiesareempty · 02/02/2017 19:51

Sounds absolutely terrible. You poor, poor thing. There must be a reason :(

furlinedsheepskinjacket · 02/02/2017 20:15

hi op

i have had all your exact symptoms and many many more

i have ME

re the hip/leg pain i had it one side for about 18 months - agony
then i got it the other side

i saw a physio privately who sorted it in ten minutes

OvariesBeforeBrovaries · 02/02/2017 20:29

This thread is from September 2015; I hope the OP has had a diagnosis and some treatment by now otherwise the NHS really is on its knees! Not sure why this zombie thread has been resurrected but just in case you're about, OP, hope you've got some relief Flowers

mylaptopismylapdog · 02/02/2017 20:56

I have ehlers danlos hypermobility and have fatigue and depression issues for many years and pain mainly on my right side, hip etc. also problems with digestion. Have spent many times on own as rest of family gone out and about so know how desperate that can make you feel. Getting a diagnosis has helped immeasurably to accept its limitations, this link gives details:- www.ehlers-danlos.org/about-eds/types-of-eds/hypermobility-ehlers-danlos-syndrome/. Just a thought but have you tried the carers associations to see if they can offer any support.

Painengrained1 · 26/06/2017 11:26

I'm the OP!

It won't let me use my old username?

An update is long overdue. Since posting:
I have been diagnosed with Sphincter of Oddi type 2, I avoid a lot of foods that trigger it and try to avoid stress (impossible)

I have been diagnosed with ME/CFS
I am functioning at about 50% of what I used to, if that. I have pain but the pains in my OP have calmed, it's more a widespread, simmering pain now. Manageable most days.

I was severely vit D deficient.

Hashimotos still swinging, now on 100mcgs Levo.

I'm trying to avoid dairy and gluten but eating any fruit or vegetables causes crashes and pain. Not many foods I can eat! Developed allergies left, right and centre.

Beta blockers helped calm my blood pressure and fluctuating heart rate.

I have more support for DD. Carers come in to help once a day.

My relationship fell apart. He wasn't supportive, I couldn't look after him and DD, I believe the stress he put me under contributed to me ending up in this mess. I have met someone else, I am happy.

I had a laparoscopy early last year, a patch of endometriosis was removed from my stomach wall, this resolves all the pain in that area. It is only now starting to come back, but I'm not anxious, because I know what it is.

I have cervical spondylosis, my neck does hurt a lot. I get a lot of nerve headaches. And I have fairly bad TMJ which I'm currently under a specialist for.

I was diagnosed with a blood clotting problem. Under investigation for that too.

Having changed things, got rid of as much stress as I can (life as a carer is stressful, I can't get rid of that) avoided people who cause me stress, educated myself on what is (theoretically) happening to my body, let standards slip with the house (begrudgingly) and said 'no' a lot more, my anxiety is minimal and I'm fairly stable. I'm forgetful, brain fog is almost constant. I miss the quick witted, articulate me. I think I'm still grieving for the life I lost, perhaps I always will.

I would be classed as disabled if my pride would allow me to be. But I'm ok. I try not to worry about the future. I'm enormously appreciative of the NHS, despite having to diagnose myself and take my evidence to them for confirmation. I've found two doctors who listen but I feel their patience wears thin, I realise I'm a 'heart-sink' patient.

I'm trying my best. Staying positive most days. Thank you for all your suggestions and help back then, I was in a mess. It kind of did ruin my life, but maybe it needed a shake up. I needed to sit still x

Minnie747 · 27/06/2017 00:08

I would highly recommend visiting a chiropractor for the musculoskeletal complaints. Perhaps even a functional health doctor also (have a google search. Someone like www.functional-health.co.uk). I do however appreciate that this is not available on the NHS.

At best a chiropractor's treatment may even have a positive effect on your overall health and function. At worst they may be able to give you pain relief from some of the pains you mention.

Really sorry to hear you are feeling so unwell Op.

Minnie747 · 27/06/2017 00:11

Just saw your update and still recommend my first response. Chiro and function health doctor to enhance function.

Inneedofadvice20172234 · 27/06/2017 21:24

Thank you so much for providing an update. I hope you continue to get the treatment you need and feel better. Well done on preserving for diagnosises

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