Thank you everyone for all the messages. I was so exhausted last night when i Got home I just crashed. I don't know if it was reaction to the weekend or the new tablets.
First my dog was fine. She'd only just had surgery with lost of instructions on painkillers, feeding and exercise so I was worried. Apart fron the exercise bit my husband coped ok and she has her check up today. She went razy crying and squeaking when i got home.
Around 4pm Friday my heart started racing and I kept feeling faint. Checked pulse and it would be as low as 42 then up to 102. At 10.45 it was pounding so hard I rang 111` which didn't answer so I did the online 111 which said to ring 999. The ambulance too 5 hours. A&E was more than packed. A nurse said they had 600 trolleys and wheelchairs lined up on corridors. My spine was excruciating in a hard wheelchair. Around me were 5 metal health patients; one self harming, on drugs, a man with bipolar and three ladies with dementia. I didn't get triage until 6am, ECG and bloods. Was sent to an "ambulatory emergency care ward at 9 am and finally saw a doctor at around 2pm. She admitted me, found me a bed to lie on in their dept until a ward bed became free which was at 7pm. Having been up all night I crashed until someone prodded me awake. I truly thought it was 7am next day.Sent to a medical ward and finally saw a cardiac doctor around 4pm Sunday. He diagnosed unstable angina and extrasystolic arrhythmia. Put me on clopidogrel which was later stopped and prescribed diltiazem and doubled my statin even though my cholesterol is low. They wouldn't discharge me until they'd found out whether I reacted badly to the diltiazem but I persuaded them to let me go in teh evening so I could get my dog to the vet check up today. Then of course the long wait for meds, discharge letter and transport. I was shaking with tiredness and pain by then. I don't know if it was the tablet or the situation because I shoudl have had it early morning but they didn't get it until after 4pm. So now I'm trying to find out from GP when t o take it today but they can't do anything until they get my discharge letter which hubby has just take to he surgery to be photocopied. Everything was also massively slowed down by a new patient record system that no one knows how to use yet.
Even the letter that was hand delivered here about a pre op appointment tomorrow had no phone number to contact them to cancel it.
The biggest problem has been never getting my painkiller on time and sometimes over an hour late. It's due every 3 hours but wears off half an hour before that so I was left 90 minutes without pain relief and then playing catch up with the extra pain. I will be complaining; not about teh staff but the hospital policy. As long as they are aware, they should let those with long standing chronic pain, control their own pain relief. It would help the patient and free up two nurses.