Wildly fluctuating O2 levels
I’m experiencing wildly fluctuating o2 levels on finger oximeter. This morning already I’ve been everywhere from 71 to 99, especially while standing still.
I went to the ER June 3 with this and they couldn’t find anything. My pft of June 3 indicated restrictive lung disease. May or may not be due to Amiodarone.
I’m going to Mayo July 27 to see a pulmonologist.
Very scary and depressing.
I know if I go back to the ER they probably won’t find anything, and I read in my medical records that my pcp has diagnosed hypochondriasis(not the case, this is really happening).
Anyone else have this?
Interested in more discussions like this? Go to the Lung Health Support Group.
I have this too! Only recently diagnosed with a PFO. Surgeon doesn’t believe that is the reason .
Someone mentioned these are our people! I agree! I have the same issues. I requested o2 to protect my other organs at least while I sleep. That helps for nocturnal hypoxia. My daytime drops are Willy nilly like others in these posts. I purchased the O2 ring to prove it! The pulmonologist doesn’t believe the walk of shame with me and all is fine! I do have reynauds but my galaxy watch says the O2 is even worse. I’m getting older so even though I might have had this all my life it’s getting worse. I was tested and they found that I have a PFO . That’s a right to left heart shunt. I was referred to a heart surgeon who the then told me he didn’t think that was the reason. Chech in with him in 6 months. They usually don’t fix this unless you have had a stroke or heart attack. Really!!!!?????
Please read my previous posts. I also don’t have sleep apnea. I can’t wait for AI to read all these posts and come up with potential solutions. Although everyone is different, how can we all experience the same thing without something in common? Has everyone on this thread had the bubble test ? That showed my PFO. Local drs suggested Long Covid symptoms. I never tested positive for Covid., but apparently that doesn’t mean that I didn’t have it.
I wonder if the Covid vaccine has anything to do with this!
These posts are truly an autobiography. I agree Drs see a snapshot in time. The O2 ring shows all of the time you wear it.
I had all my tests done in Colorado aka high altitude. We went to Key West Florida and I had the same results. Altitude was not the reason for me. I suggest taking a vacation to the beach and see if you have the same symptoms and results.
I have the O2 ring. Tried wearing it the other night without supplemental oxygen hoping to see different results and was woken up every hour with readings below 88. I still wear it,but with supplemental oxygen to show the drs the difference.
Sounds similar! I have a PFO, and to their knowledge nocturnal hypoxia, so I qualify for nocturnal oxygen but not traveling oxygen! We travel! I’m blessed with my mother in laws innogen, but will need that dr letter to be able to take it on the plane! I suggest getting the O2 ring to see your daytime O2 and take it from there. These readings will be in my arsenal when I see the pulmonologist and cardiologist.
I have mitochondrial myopathy and mitochondrial dysfunction. After 2 years I had a repeat Pulmonary test and now show signs of restrictive lung disease. I have a repeat ecocardiogram tomorrow. I'm STILL trying to get to the bottom of this but things are leaning towards possible nervous system disorder, or not being able to oxygenate my blood properly. Getting closer.
Thank you for sharing. I’m making a list now of possibilities.