Trying oxygen therapy

[Janeandme]

Hi I'm new to this so here goes with my first question I'm going for a course of oxygen therapy tomorrow at a ms centre near me my cfs is now affecting my quality of life I'm bedbound for weeks now at every flair up I'm hoping for some symptom relief has anyone tried this therapy and any advise?

[Shazzzy]

I wanted to try this but was not allowed as I have asthma. Good luck with the treatment and let us know how you get on

[Janeandme in reply to Shazzzy]

I will post regular up dates wish me luck 😊

[mmariaaaaaaaa in reply to Janeandme]

good luck

[Steve49]

Hi.

Your very welcome to our site.

Yes I had a 3mnt course off Hyperbaric Oxygen Therapy in 2006ish.

And wow the instant difference was truly amazing.

I had mine in Portsmouth which is a beautiful place.

I think I need a top up !!!!!

Please let me know how everthing goes !!!!!

Wow my feet have "become very itchy"

Steve.

[Janeandme in reply to Steve49]

Hi Steve yes I will post and let everyone know how I get on its expensive but I'm desparate hope I get some relief I'm doing a 3week course first so fingers crossed

[Isitme_ in reply to Steve49]

I've never heard of this treatment. Can you direct me to some information regarding the treatment, intended outcome, science behind it's efficacy. Also, have you heard or ketamine therapy for fibro & depression?

[Steve49]

Hi Jane.

Yes I'm in the same "Ship" as you.

Can you please let me know how much it will cost ???

Sorry but where will you be having your treatment ???

Sorry for all the questions.

Thanks.

Steve.

[Janeandme in reply to Steve49]

I'm having my sessions at the Leeds ms centre it's £15 per session they recommend 15 consecutive sessions then 1 to 2 sessions every week thereafter yes it's expensive but you pay as you go and I need to try this as my quality of life is affected greatly with cfs.

[Steve49 in reply to Janeandme]

Hi.

That's great thanks.

We have got a localish centre & I have made contact with them so fingers crossed.

The one that I went too thein Portsmouth has closed.

Can you please let me know how things go !!!

Steve.

[chocolatemuncher in reply to Janeandme]

Thanks for posting, I live in Leeds and had never heard of this place, or oxygen therapy for that matter! Would love to hear how you get on with your sessions. Do you know if they open in the evening at all? I work so wouldn't be able to get there in the day.

[BlueMermaid3]

Hello Janeandme

Welcome to the forum

You may like to have a look at our mother site for more information on Fibromyalgia fmauk.org

Our members are extremely kind, compassionate and caring.

I am sorry that I cannot help you with your question, but I do know that this topic has cropped up from time to time on the forum.

If you type "Oxygen Therapy" into the search bar at the top right of your screen you will be able to read up on past posts on this subject.

If you need any help navigating the forum, please give me a shout.

Wishing you less pain and more peace

Lu x

Administrator

[TheAuthor]

Hi my friend,

Welcoem to the forum and it is wonderful to make your acquaintance. I have asthma and COPD so I have never done this myself. I want to sincerely wish you all the best of luck with this.

All my hopes and dreams for you

Ken