has anyone had reli bad agony sharp shooting pain... - LUPUS UK

LUPUS UK

32,241 members28,596 posts

has anyone had reli bad agony sharp shooting pains in back n had all reflexes go froms arms n legs all down on one side

shakylove profile image
6 Replies

well I found out I had lupus after my first child in 2009 I was 16 young mum had lots of joint pains n feeling ill all time I had low in iron it took 9 months to find out wat was wrong lots test all time n one blood test came back I had lupus sumthing was positive in my blood anyways I was feeling reli tired all time had gd days n bad days then I had lots stress going n when I tried for a bby I got pregnant n kept losing bby they did more tests n after 4 bby I lost they found out it was my lupus n everytime I had miscarriage I experienced small flare ups til this one time I end up at hospital wiv my husband coz he was ill n then I was walking decided to sit down n I cudnt feel n move one side of my body my arms n legs reflexes had gone they did lots test but cudnt find out wat it was n doctors was arguing wiv each other on wat it was then after few weeks I got everything back then I found out iwas pregnant they put me on fragin injections n then had few small flare ups in pregnancy but then at 20 weeks pregnant this side thing happened agen n I bin put thro to neuologicalist to find out wats happening n I still cant walk this time n I am in pain wiv my back tht bad I sleeping on couch coz I cant lie down on my back I keep getting sharp shooting pains in my back n cant travel I am stuck at home I am crying n screaming a lot waiting for mri scan but they hav to put me out to hav it done n also fallen down stairs when I was pregnant wiv lupus headaches

Written by
shakylove profile image
shakylove
To view profiles and participate in discussions please or .
Read more about...
6 Replies
Purpletop profile image
Purpletop

I'm sorry, I haven't experienced what you described but it sounds really painful, try and call NHS direct or out of hours doctors in your area, maybe they can send a doctor or nurse to your home to at least apply some lidocaine patches for your pain. You poor thing!

shakylove profile image
shakylove

it is awful I hate being like this but I hav since my specialists n they sed I hav to wait til mri scan so they know wat they treating just hope sumthing does come up so they can sort it out n I hav since doctors they give me the pain relief but it don't work no pain relief works they maxi it to wat they can give me now so I just in agony n very lil sleep n got two kids to look after its gd job my husband is fantastic n looks after us all

Purpletop profile image
Purpletop in reply toshakylove

I understand about the painkillers but you could ask for an injectable form that has an immediate effect. When are you seeing your doctor again? I get that you're waiting for the MRI but meanwhile your GP needs to do something about your pain, you can't stay like this!

shakylove profile image
shakylove

I end back up in hospital wiv flare up n watering infection n this attack down one side went a lot worse so they now trying me on morphine n more tablets n ringing up Monday to find out more about mri scan n it took air n gas n morphine together to get me down traveling to hospital it was tht bad I still was screaming wiv pain n how I am feeling now I am acheing from head n toe everything feels bruised n just pain coming from everywhere n struggling to walk even more n my back keep shooting pains all time I just cant sleep but at least I hav comfy couch to sit up n sleep on

Purpletop profile image
Purpletop

Blimey, that sounds rough, where is the pain coming from, the water infection? Have you tried hot water bottle on that area of pain?

shakylove profile image
shakylove

i found out today after having all them symptoms tht i am lacking in vitamin b12 n tht cud b causing me all these problems but got to wait for results from specialist about mri scan tht i had done to make sure its not nothing else n tht they pick everything up but i do need now 6 injections then i am on injection every three months n they need to test me for pernicious anaemia to see if it tht too

Not what you're looking for?

You may also like...

how is everyone doing in this weather with lupus

hiya just wondering how everyone is doing I know I am keeping myself indoors to stay away from sun...
shakylove profile image

Hair loss and thinning help

Hi my hair is falling out fast I was wondering does ne one wiv lupus sle have the same problem and...
Jakki27 profile image

Do doctors understand Lupus?

This is a bit long winded, but here goes. About 6 months back I had random bloods (find&treat)....
Gail41 profile image

Feeling lonely and fobbed off! What are these symptoms??

Hello, this is my first time posting so please bear with me.I am a 40 year old female. I was...
Starshine83 profile image

recently diagnosed and confused?!

Im still trying to get my head around this condition, along with sjogrens (still can't pronounce...
Chris21 profile image

Moderation team

See all
Debbie_kinsey profile image
Debbie_kinseyAdministrator
chelseawong profile image
chelseawongAdministrator
michaellasmith profile image
michaellasmithAdministrator

Top community tags

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.