My experience with oxygen therapy
Disclaimer: this is based on my personal experience. I am one person. What works for me may not work for others
I have been having oxygen therapy twice a week for about three months now. I was warned that it may make me more fatigued at first and it would take around 16 sessions before I felt any effect.
Exactly what I was told is what happened. After the first few sessions I slept for about a day after. And around 16 sessions in I began to notice an improvement in my symptoms.
I have moderate MECFS, triggered by a viral infection. I have had it for 12, nearly 13, years. I have spent years bedbound. I use a wheelchair when I leave the house. I had to drop out of education. I have never been able to attain a job. My life has been incredibly restricted.
I am starting to be able to walk more. I have been able to bake. I have been able to go out and meet friends. I have needed to sleep less, and my quality of sleep has been good. When I have flare ups they last for maybe a couple of days, instead of weeks to months. People in my life have noticed these changes and commented on them. I physically look more well.
For the first time in 12 years, I feel hopeful for my future. I feel that I may be able to return to education and start a family.
I definitely still have MECFS. There is no doubt about that. But my symptoms have become significantly less severe.
I feel the need to share my experiences because i truly did not believe it would help. But it did. And i hope that there are others it can help.