Today Emma had her 7th oxygen treatment. The results are quite noticeable.
The thing is, having had CCSVI treatment and now oxygen treatement it's difficult to pin point what is making the improvements, but the important thing is there are improvements.
Fatigue is the big one, Emma has had to have a 4pm nap every day for as long as I can remember, that's now down to 1 or 2 days a week from 7 days a week.
Energy levels are increased, but when she is tired she sleeps soundly. Noticeably she also slept right through the night for a couple of nights this week.
I have to say I think a large amount of this is the oxygen therapy. But I have no doubt that unblocking certain viens have made it all the more effective.
Interestingly today we met a fellow CCSVIer who had treatment in Edinburgh two weeks before Emma, she was treoprting the same increases in energy and drop in fatigue.
It was nice to find someone else so local having been through the same thing reporting similar improvements.
I've now learnt enough how to operate the machinery and we start our first evening therapy on Thursday evenings this week, this saves me losing two days a week out of work getting Emma to Brighton and back.
Based on Emma's results I'd recommend the oxygen treatement, it seems to accelerate healing.