I know Kegels cause flares for most of us with IC and/or PFD. Kegels have the same effect on me but my question is one I haven't seen here, or anywhere:
Has anyone like us tried Kegel exercises for 6 to 8 weeks, three times a day, in spite of the constant flare agony?
Admins, I've asked my docs this question and they don't have a clue due to the nebulous nature of IC/PFD. They would like me to try this if I
can handle the pain and are curious to see what happens. They hope getting this muscle into shape will help with retention, spasms, pain, etc.
I mention two months because my PT, docs and all available literature say it takes at least that amount of time to get that muscle into shape.
It sort of makes sense to me as PT generally causes pain of various sorts until our muscles adapt and strenghten. However, I'd love someone here to give me an excuse not to put myself through this
My background in a nutshell: I've had very complex case of IC & PFD (even on SSDI due to severity) for over six years, am finally getting better, but progress has stopped.
Thank you in advance for your thoughts, opinions, answers and help!
CJane
Current Meds: Avinza, Hydrocodone, Valium, Neurontin - I've tried them all. Stopped using my Estrogen patch a few months ago - now trying homeopathic supplements instead.
Medical History: Too long to list here
Spinal surgeries, endometriosis, ovarian cysts, hysterectomy, pelvic nerve surgery, over 30 sedated procedures to block various nerves and more. Seen every type of specialist and had every test known to mankind.
Has anyone like us tried Kegel exercises for 6 to 8 weeks, three times a day, in spite of the constant flare agony?
Admins, I've asked my docs this question and they don't have a clue due to the nebulous nature of IC/PFD. They would like me to try this if I
can handle the pain and are curious to see what happens. They hope getting this muscle into shape will help with retention, spasms, pain, etc.
I mention two months because my PT, docs and all available literature say it takes at least that amount of time to get that muscle into shape.
It sort of makes sense to me as PT generally causes pain of various sorts until our muscles adapt and strenghten. However, I'd love someone here to give me an excuse not to put myself through this

My background in a nutshell: I've had very complex case of IC & PFD (even on SSDI due to severity) for over six years, am finally getting better, but progress has stopped.
Thank you in advance for your thoughts, opinions, answers and help!
CJane
Current Meds: Avinza, Hydrocodone, Valium, Neurontin - I've tried them all. Stopped using my Estrogen patch a few months ago - now trying homeopathic supplements instead.
Medical History: Too long to list here

Comment