Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
AusSue
I rang the local GP clinic at about 11am Wednesday as wasn't feeling well at all. I had gone to stand up & my left arm just fell by my side & my left leg would not move & speech was crappy. They said to go there & be triaged. Got a taxi there & was seen by the nurse fairly soon. She took bp 184/125 & then my Dr came in. They didn't like any of symptoms so called an ambulance.
When the ambulance originally came they said they were taking me to Dandenong hospital & that was ok. Then they wanted me to smile & then decided that was really off & face droopy so needed to go to Monash, I let drop the "F" word & everyone cracked up laughing, the 2 ambulance people, the nurse & Dr all thought it was hilarious. They didn't expect me to drop the "bomb" word. The 2 ambulance people said that a lot of people think that about Monash hospital but dont say it & Nurse & Dr said that is so unlike me to drop that word so clear. (lot of history on why I hate that hospital)
They agreed on Dandenong till I got neck pain, back pain & couldn't talk then changed to Monash. I didn't realise they had lights on till got there & I asked how come so quick & they said lights always speed it up. We got straight in at Monash into a cubicle. They had put morphine in through vein & can't remember much more.
As usual emergency stuffed me around, saw dr quickly then neurologist then had ct & xray but not allowed to eat/drink till after saw neurologist other than pain killers they gave me often.
Had bad night with left side not working, bp & temp taken often, lights on,
opposite main nurse desk & curtain open as they wouldn't close it, etc.
Thursday I was tfr to day theatre while waiting for bed. Neuro wanted me to go on steroids & I still refused even though he said I had optic neuritis long with all weak on left side. Physio & ot came & assessed me & both said that I was ok to go home if neurologist ok'd it so long as I took it easy for few days. Then registrar/neuro said wanted me to see consultant but when I said not going to change my mind, not going on steroids, he decided that I could go home so long as take it easy. Refusal of treatment
David has Friday off so will help me for next 2 or 3 days.
Still struggling & left hand doesnt reach mouth (fun eating) & left leg doesnt move far at all. Doesn't even meet back of right foot at moment.
Today/friday slept in which was nice & needed & then been feeling crap all day.
Still not walking good so in chair in lounge mainly & right eye is closed &
blurred & burning so not happy.
This has taken me ages to write & several rests imbetween so if disjointed or repeated - thats me & why. tv munchkin today mainly.
Anyway thats my excitement for last couple of days. Now still feeling crap to put it mildly & not happy that this has happened. I have been tryong as we all do to avoid it too.
Spoke to social worker at ms society & she offered more help but I don't know what I need so will wait & see after a few days. She is really good like that.
Sue
When the ambulance originally came they said they were taking me to Dandenong hospital & that was ok. Then they wanted me to smile & then decided that was really off & face droopy so needed to go to Monash, I let drop the "F" word & everyone cracked up laughing, the 2 ambulance people, the nurse & Dr all thought it was hilarious. They didn't expect me to drop the "bomb" word. The 2 ambulance people said that a lot of people think that about Monash hospital but dont say it & Nurse & Dr said that is so unlike me to drop that word so clear. (lot of history on why I hate that hospital)
They agreed on Dandenong till I got neck pain, back pain & couldn't talk then changed to Monash. I didn't realise they had lights on till got there & I asked how come so quick & they said lights always speed it up. We got straight in at Monash into a cubicle. They had put morphine in through vein & can't remember much more.
As usual emergency stuffed me around, saw dr quickly then neurologist then had ct & xray but not allowed to eat/drink till after saw neurologist other than pain killers they gave me often.
Had bad night with left side not working, bp & temp taken often, lights on,
opposite main nurse desk & curtain open as they wouldn't close it, etc.
Thursday I was tfr to day theatre while waiting for bed. Neuro wanted me to go on steroids & I still refused even though he said I had optic neuritis long with all weak on left side. Physio & ot came & assessed me & both said that I was ok to go home if neurologist ok'd it so long as I took it easy for few days. Then registrar/neuro said wanted me to see consultant but when I said not going to change my mind, not going on steroids, he decided that I could go home so long as take it easy. Refusal of treatment
David has Friday off so will help me for next 2 or 3 days.
Still struggling & left hand doesnt reach mouth (fun eating) & left leg doesnt move far at all. Doesn't even meet back of right foot at moment.
Today/friday slept in which was nice & needed & then been feeling crap all day.
Still not walking good so in chair in lounge mainly & right eye is closed &
blurred & burning so not happy.
This has taken me ages to write & several rests imbetween so if disjointed or repeated - thats me & why. tv munchkin today mainly.
Anyway thats my excitement for last couple of days. Now still feeling crap to put it mildly & not happy that this has happened. I have been tryong as we all do to avoid it too.
Spoke to social worker at ms society & she offered more help but I don't know what I need so will wait & see after a few days. She is really good like that.
Sue
Wishing you better health SOON!
Jill
Ps to everyone who follows Sue. She was featured in a recent MS magazine here - with NOT A WORD about her problems.
She is AMAZING!!!!!
The ms society approached me to that & it wasn't about my problems but other experiences - the help in workplace.
Now waiting on Plastic surgeon appt for basal cell carcenoma on nose & the sore is noticeable now. Also still waiting on foot surgeon appt for major surgery so still got boot on.
Just about had enough of this ms & other crap & vision out of one eye only sucks.
I will keep you in my thoughts and prayers daily. I hope you feel better real soon. I hope you allow the social worker at the MS society help you. Keep us posted. Lynne
Glad you are able to post and keep us updated and that you are home.
When you refused steroids,,,did Dr offer a different alternative?
I'm cautious with them because of side effects, and since I met you,,more, because you've mentioned that's the reason for some problems today. That's why I love DS , we tell each other what drs won't.
Hope you recover and surgery goes well. Let us know when you go for it.
Love, Alma
I am using pain killers & still on Gilenya but refused steroids at all. Have had lot of them b4 & they have cave caused/contribute to oste-arthritis & avascular necresis/kohlers disease which is basically break down of bones & only fix is surgery & thats why waiting for surgery for right foot.
sorry for typos will try to type more tomorow if vision is bettr. it is late at night so off to bed. just wanted to give bit of idea why refuse steroids incase not on line tomorow.
been getting more sore eye, red around eye & white face with lot of pain regardles of tablets so who knows what tomorow bring. Will prob just rest & watch tv.
again not reading thu, now there is typos but using right hand as left cramped & rotten vision so sorry & hope u get point.
eep well
sue
Congratulations on the magazine article. I wish I could read it. Is there anyway to get it online?
You will remain in my prayers.
Sorry your not feeling well, you've been through a lot. Congrats on the magazine and hope you feel better soon
Take Cre
Dave
http://www.mssociety.org.au/documents/intouch/2012/Intouch_Winter2012.pdf
I have put on weight thanks to steroids & have the puffy face - cushens disease so don't want any more.
Today is a crappy day with difficulty in vision & left leg is still slow etc so just resting. Hope I start improving soon but guess got to expect it to take time I just dont like it.
Glad the link worked ichoppell. The magazines are always good. We get 4 a year.
Being able to see Sue for real was very exciting!
Here is a link to the MS Australia page with all the publications available.
http://www.msaustralia.org.au/publications.asp
Perhaps someone not in Australia could try the link and tell us if it works.
Cathy