Hey everyone gotta question for all of you.
My PKD has been on a rapid increase over the last couple of years. I have been seeing a pain clinic for about 6 months now. So far with 9 nerve blocks and pain meds its been tolerable.
Well the last month sleeping has been terrible.... Everytime my husband rolls over my kidneys scream at me.
Does anyone else with PKD feel this or could it be the nerve damage reacting with the movement? I think this question will be at the top of my list when I go in for my refill in 3 weeks.
I hope everyone is having a wonderful week. I'm off to work again
Kidney Diseases and Disorders
39 yr young female with,
Chronic Kidney Stones, PKD (Polycystic Kidney Disease), Chronic Kidney Failure, Severe Hypertension, Urological RSD
Also CHF (Congestive Heart Failure) and Sleep Apnea
Hopefully NO MORE........ I think I have it all