Thought I would update on what I remember of what happened. I had been having having asthma since Friday afternoon & on Saturday it got a lot worse. I was trembling & had no control of body basically. Kept using nebuliser & ventolin imbetween.
When we had decided to have soup before tea (we eat in front of tv with stable tables) David gave me mine & I kept blanking out & not responding to him. Was wearing half the soup as with th trembles lost control. He kept yelling at me as I wasnt getting the soup to my mouth & took it from me & told me to go to bed since I couldnt stay awake/with it.
This was only 7pm. I got my walker in front of me with the tray on it & that has all my bits like hearing aids, glasses etc & got about 6 steps & just lost strength totally, knocked everything flying & me on the floor.
David had to help me get up & walk me to bed & put me in bed.
I was still coughing & wheezing so he got me to use ventolin.
I don't remember much till about 10pm David told me to get up & use nebuliser. I used it & still could barely talk, breathe & wasn't with it at all.
David pressed my button to the alarm company & told them what was happening & they called an ambulance. That arrived in about 10-15mins which seemed quick as I was not aware. I used their oxygygen & still no better so taken to hospital.

This time went to casey (local) hospital which was good. I was taken in to a cubicle & worked on me immediately. David said they had me on one one of those 100% oxygen, lots of tests etc again. Had a chest x-ray & this time it was very cloudy with pneumonia so that was compared with a clear one 2 weeks ago. Shows how quick it can hit. I was on drips, tablets oxygen etc.
The scary part is I didn't even know what was happening or that I was so bad & very close to be being put in a coma.
Poor hubby was obviously scared about it all. I know each time I asked for water he would lift my head & give me a sip at a time as that is all I could take without coughing bad which was continuous.

David eventually went home about 3am for some sleep & I think I was already in a private room by then. I have to be in a private room as I have a vre bug that means that all staff/Drs/nurses etc put the plastic gowns & gloves every time they come in. It is a hospital aquired bug.

Of course the ms symptoms kicked in with weak legs, arms, still had trembles a lot.
I was on the nasal oxygen when I was in the room & they gradually reduced it, that was as well as the ventolin regular & lots of pain tablets & additional ones.
I gradually was able to do more each day & as soon as I was on oral medications they said I could go home as I could walk with walker & do basics. Safer to go home as there are so many virus/infections in the hospital etc that it could be a danger to me. Also I am booked in at 7.30 for a 8.30 mri at monash so easier to do it as an outpatient.
Anyway, came home late yesterday. Still very croaky, coughing a lot & weak really. It will take time to get over the pneumnia & everything else.

As a different note I have got another appointment with my foot specialist for trying to go to cat 1 which is is what one of the other other Dr's wrote & requested. It is next Thursday morning.

Sorry for long post but it try to explain whats going on.