I had some trouble registering a few weeks ago but i'm good now.
I'm Miguel. I'm doing dialysis right now while I post. Well, anyways...
I was diagnosed with Alports syndrome when i was 19 yo. My kidneys were @ 8 or 9% at that time so basically they were almost gone. Alports is a genetic disorder that kicks in at late teens. Its usually accompanied with hearing loss! Talk about kicking me while I'm down , huh? Its like winning the lotto twice.
I had a short stay in the hemo centers because I received a kidney from my father within 4 months. So, that was really nice of him. I especially know now because I'm back here doing this again after 14 1/2 years. I was aiming for 20 years. I felt that 15 years was good too so no complaints on my part. I know I'm lucky so i wont procrastinate and offend you guys who have had it harder.
BUT MAN I REALLY DO HATE DIALYSIS.
I'm grateful but.....lets just say its not something u cant get used to.
I started a blog at blogger to hopefully show some of the difficulties and the things we experience as esrd patients. My goal is to show that if i can do it maybe others who are afraid or are hesitant can overcome that fear. Also, it would show that were not just #'s. Our problem affects us more than just having toxins in our blood. I want empathy! Not sympathy.
I would walk away totally fulfilled if i knew that somehow i helped a young boy/girl overcome their fear and for him/her know that they are not alone.
Can i post the link or will that be spamming?
If i cant thats alright. I could find another method.
I do have a bunch of questions so I'll jump to the forums now.
Thanks!
mig