I am fine with the blood pressure’s I am a little overweight but not daft amounts
I thought it could be the AF but I don’t seem to find many with AF having the same issue
Just going upstairs or drying myself after a bath can leave me trying gasp for fresh air it’s like my body doesn’t have enough oxygen for basic tasks . I have also found being in a room with to much heat and no ventilation brings the feeling on
I have had the same issue now and again since I have had AF but can’t explain it. I think I have suggested before that you should try breathing out harder than breathing in, preferably through pursed lips. Once you start ‘overbreathing’ it forms a vicious circle.
Problems with thyroid is a major cause of AF. Then having undiagnosed thyroid cancer gave me AF which ultimately caused the left frontal lobe clot. I was not on any meds except B12 Solgar 1 x 3 days week sublingual nugget.
AF with the clotting risk sent a rogue clot.
The stroke happened at 2am when my H/R falls to 47 average.
Of course I was given an anti-co.agulation, I chose PRADAXA I was 70 and the main hospital gave me 110mg x twice. But I was transferred to my local hospital (only 4 beds in Stroke Ward Whangarei Northland) and went home with 150mg x twice.
When I put the 2 discharge papers together I rang and had my locum DR reduce my prescription to 110mg x twice.
It is always a worry about stopping PRADAXA 3 clear days prior to surgery (Just had Right Shoulder repaired) and there was an argument when to restart. I instigated 48 hours after surgery.
But a 83year old MS friend forgot to replenish her PRAXA 110mg x twice, missing 4 days and she had a little stroke. Got at her memory.
As I have little pain relief but on Avorastatin 10mg daily I think that it is helping by its anti-inflam properties. Also I put Tumeric in my soup with an egg which I have trouble cutting.
Latest is I should not have had an anti-co.agulant whilst I had cancer.
Honestly getting down to 60s H/R day was a break through.
I have to accept my lot and I used to be a 100 yard top runner.
Breathlessness was always one of my worst symptoms with AF. Prior to AF I had been very fit and within recommended BMI weight, healthy diet etc. and enjoyed walks of 8 - 10 miles. Suddenly I was breathless on the stairs and slow on hills. My GP explained it was the heart being less efficient at getting oxygen pumped around the system. Mine was persistent AF with HR in the 80 to90 range.
I hope you are able to find the right treatment to help.
My EP did put me on digoxin while I was awaiting ablation to help me cope with the symptoms. It doesn’t suit everyone but I found it very helpful as it strengthens the heartbeat as well as lowering HR, and doesn’t lower the blood pressure. So I was almost my old self on the hills. It’s an old tried and tested medication (foxglove derived) and I’ve heard some medics poopoo it but my EP is very up to date with all latest meds and it’s something we worked out together. I actually quite miss it now I’m back in NSR!
I’m very new to this Afib thing. Diagnosed with paroxysmal afib last year after being fitted with a Linq Reveal. Then Afib started on 13/10/23 and hasn’t gone away. My breathing has been awful, I’m gasping for air every time I move and it’s scary. Trouble is I don’t know if it’s Afib or something else. This week I’ve had chest X-ray and ecg, and I’m having breathing tests next Monday. I don’t like this new thing I’ve been saddled with, it’s the breathing problems especially.
Absolutely. BBs and Cacl Channel blockers make breathing mesds not as effective. Mine breathing is do bad thinking of going off AF mesds and taking my chances . Breathing is everything
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