It made me cry. ( I turn 38 next month) I'm glad you doctors cared about the headache. My mother and her father both died of a brain aneurysm, I also have an aunt that almost died and had 6 repaired. Yet my dr told me it isn't important to have MRIs to check. I wish they hadn't cut you off not sure how much I didn't get to see. So is there a way for you to know whether you have dominant or recessive PKD. Not that it makes a difference to you but maybe your kids would benefit or their kids. It's nice to see that there are people learning about this.
Lori, I watched the whole thing. you are so much more positive than I am. Maybe some day I will be too. In my earlier post I should have written my mother and grandfather (her father) spooky part they both died at 53 years old. I did convince my dr to order the MRI after months of talking. Seeing a different Dr would require me to go to a different state and travel and additional 1 1/2 hours. So I was glad that I convinced him. Thou he couldn't have chosen a worse time to retire. Ed and I met the new dr went the decided to start Ed on dialysis and admit him to the hospital. How old are your kids now 12 or 13 and how old is your son?Sydnee
You touched on many issues I dealt with :- getting used to a 'new' you. Before any dialysis you can do what you want, whenever you want, on dialysis your life is scheduled around dialysis.- fairness. I don't drink, smoke, (not going to go as far as eating right ), so I thought it was unfair that dialysis was part of my life as well. - renal diet, that took some getting used to, after indulging on items like big macs, kfc, switching to something that is low sodium and watching phosphorous was a real change.Wow, 2 hours to death, that is way too close to comfort. I'm glad that you're up and walking now, and prey that Oct. will bring good news.
Very, very poignant. Made me cry, too. Thank you for sharing this with the world. It's important.