Hello everyone, hope everyone on here is doing well and on the road to recovery.
Wish I could say the same for myself but I am hanging on and live in hope that my HF will get better and enable me to lead a more functional life.
Please try to understand that my brain does not work very well after I had a stroke (brain clot due to afib) April gone. Cannot recall appropriate words...struggle to put sentences together...unable to recognise friends let alone recall their names, hence hope you can understand what I have written.
Since June last year I have been in constant afib 24/7 and was so weak I could barely walk. I was only taking anti coagulant....not allowed any anti arrthymia or rate control meds due to severe reactions. Basically, I was house bound on my own. One day I decided to try and get a GP appointment because I suspected that I had Heart Failure. Was lucky enough to get one. At the consult GP asked what she could do for me and I replied "I want a blood test to see if I have HF.
Blood test result indicating HF was 3970 the previous year it was 670. Was not contacted for follow up consult with GP. Have not even seen a cardiologist. Hence, I went private and several tests have revealed that I have constant afib, severe Tricuspid valve damage along with mitral valve damage. I am booked into LHCH for three surgical procedures to treat/repair AFib, Tricuspid and mitral valve 20 Feb this year. I have 10% chance of not surviving the surgery which according to my doctor/surgeon is quite high. I choose to focus on the 90% chance of survival.
Here goes, I am getting to point of this post. I asked the surgeon if HF levels shown above would improve after surgery. He did not answer me. His reply was "Lets put it this way. You will feel a lot better after surgery"
In all honestly, I know there is no cure for HF. I suspect HF has occurred to the extreme due to lack of treatment for afib since 2020. Question is does anyone know if HF can improve whereby I will be able to trek in the great outdoors again like I used to do?
It's costing me about 80,000 or more for the surgery...had to sell my home to get the money. Do believe if I had to go on NHS waiting list I would get much worse waiting for surgery.
What do you lovely people think?