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MCS and Oxygen Therapy

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I suffer with severe facial and to some degree part of my head hurts as well. I

recently recieved a prescription from my intergrative doc to try

oxygen therapy at night while sleeping. I used it for a month. Medicare

will not cover naturally.. grr.. Anyway, I feel the therapy may have

helped to some degree but I am sooo chemically sensitive. The tubing

caused me so much discomfort. Under my nose where the tubing layed was raw and

red. Inside my nose was sores and bloodied. I even tried a plastic type mask

that the company offered but just having the oxygen run through the tubing my

nose was so sensitive after this month long

experiment that it was painful as well.

Does anyone have any other idea`s? I will not be seeing my doc for another 3-4

weeks and I sent the oxygen back.

I hate to think it may have been helping but I can`t tolerate it because of the

MCS. So tired of all this...

nne~

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