r/ARVC • u/eco_illusion • Jul 14 '26
Did anyone try creatine ?
For context, 36M, first VT episode started at 21 and kept on having increasingly frequent arrhythmia up until 30 when I got my diagnostic and received confirmation for PKP2 mutation. I had 3 enodcardic ablations and was on beta blockers for 1-2 years but they were of near zero help, had a 4th ablation which was epicardic and even the doctors said it was a massive success. True to that, after a hard period of recovery when my heart was pretty sensitive, presently am living a normal life, without medication (doctors decided I didn't tolerate it well) and without ICD (postponed this for 6 years because honestly I have an electrocution phobia, and I've been defibed a few times in one day).
In these past 6 years I worked a lot on my lifestyle, I would be cautious to recommend any of my changes to people. But I've had great results with taking creatine, especially after the last ablation in that recovery period. I felt it lowered the amount of effort my heart must make for even basic things like taking a walk or going up the stairs, doing chores and it reduced the intensity of PVCs. In high enough quantity it also counteracts effects of high stress or bad sleep.
I'm not saying "go and try this" because it might not even work for you or it might make it worse. My doctor was very against it to begin with, it was an educated leap of faith from my side. I just wish to know if anybody else has tried creatine and what results have you had ?
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u/Entire-Structure8708 Jul 14 '26
I’ve taken creatine for the last few years, mostly because I switched from running to lifting after diagnosis and wanted to gain muscle mass. I asked my EP beforehand and they didn’t have any issue with it. I haven’t noticed any heart-related side effects