@R-F-J 

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R-F-J

Oxygen Therapy - Thoughts

Sorry not been around for a while, been busy moving from a house to a bungalow. Now we have moved my wife made contact with the MS therapy centre which is about 30 mins away. We went and visited yesterday and was really impressed, and they really believe that Oxygen therapy is a vital component is helping with fatigue, inflammation and mobility, so looking at giving a go, will be hard as is 20 x 1 hour sessions over 4 weeks Mon- Fri. Just asking what peoples thoughts and experiences are? Thanks
@sprout

I had Oxygen Therapy for years. Haven't had it since covid. My psoriasis misses it, not the MS.

@Clary

Hi, I was offered O2 therapy. It was explained to me that when there was a lesion in the brain, that having increased O2 would help new blood vessels grow around the lesion and make new pathways to help transmission of brain signals. I decided it wasn’t for me because I am a bit claustrophobic. I am pretty sure the brain does this anyway. Perhaps it is speeded up by the O2🤔. Not sure about the science. I think the jury is still out. I tend to try things, if it is non harmful. Good luck. It would be great to hear your experience if you do it.