Hello everyone,
I am reaching out to the community for insights and personal experiences regarding the management of Polycythemia Vera (PV), particularly in relation to autophagy, intermittent fasting, and vegan diets.
Autophagy and PV: Has anyone with PV experimented with or has knowledge about the effects of autophagy on this condition? Any scientific research or clinical trials that explore this connection would be greatly appreciated.
Intermittent Fasting (16/8):I am curious to learn about the experiences of those who have PV and have tried intermittent fasting. How has it affected your symptoms or blood counts? Are there any specific fasting regimens that you found helpful or otherwise?
Vegan Diet (low iron): Lastly, I'm looking for information on how a vegan diet might influence PV. If you've followed a vegan diet, did you notice any changes in your health related to PV? Are there particular aspects of this diet that are beneficial or potentially concerning for someone with PV?
Additionally, if you have any relevant links to scientific papers, clinical trials, or other reliable sources that delve into these topics, I would be immensely grateful.
Thank you in advance for your time and for sharing your experiences and knowledge. Your insights could be incredibly valuable for those of us navigating PV and considering different lifestyle approaches.
Best regards,