My name is Kristin Shelley, I am 26 years old I was diagnosed with IGA Nephropathy in 2007. I didn't know that from the time of my diagnosis in December 2007 to May 2010 , I would be on dialysis.I am writing this in hopes of my experience helping others understand the situation completely.This is not an easy journey. It is though the journey life has taken me on, as well as one you may have to take; and with every day I am stronger mentally and emotionally.
Friday, September 9, 2011
Doing a lot of thinking
Sitting here tonight doing a lot of thinking. I am tired, a lot of people think you have your transplant and your back to normal right away. Your not your still tired and your stamina is low it takes time to get use to the pills and to get all the energy back. I have been getting migraines a lot and HOT FLASHES while everyone is cold I am sweating plus my kidney hurts and my old ones still hurt. I know I will get my energy back with time I just wish I had it now but I am not going to push it's not healthy. Don't get me wrong this transplant was the best thing that happened to me it's just hard still sitting back not being able to do everything I want to do I know in time I will be able to do a lot of them but some I won't (like eating sushi) :) As dumb as it sounds I still can't wrap my mind around the past 2 years it seems so unreal I don't know how to explain it it's just weird. But GREAT NEWS my Dad had his thyroid removed Tuesday and he is doing FANTASTIC! I am glad everything went well with him though I was really worried about him but now that everything is ok that is all that matters. Well thank you for letting me vent a little and tell you all the good news about my Dad.
Thursday, August 4, 2011
Thursday, July 28, 2011
Doctors Apt
Had a check up yesterday everything went great. But my doctor did say something to me and I can't get it out of my head...You know if it wasn't for your Uncle you wouldn't be here. It's weird apart of me always felt like I don't know how much time I have I was so tired and just drained, at points I just thought today is my last day I can't go on like this. I just never realized how mentally and emotionally this journey would be. At first I was like oh this will be over in no time no big deal and well then it started kicking my ass and with all the denials add more ass kicking. I am just so thankful for every day now it was such an amazing gift (it was really the gift of life) I just hope my blog helps everyone who reads it know that it will happen it just takes time but this disease does prove just how strong we all are.
Monday, June 27, 2011
Alison
Alison...You are going to get your turn. I think about you often I don't just do my blog for me but I also do it for you. I don't want you to ever think you are alone I am here if you need anything. Dialysis is hard waiting for the kidney with all of the ups and downs that come with it is even harder but know that there is a light at the end. I think that is great you want to volunteer I am actually going to do the same I have to wait 1 year after transplant but I am thinking of giving my social worker a call from the dialysis clinic and asking if they have any volunteering I can do. Right now I am looking at going back to school to do something in the renal field. Anyways, I just want you to know I am here and I will keep blogging about how this is all going but please let me know how things are going with you.
Friday, June 24, 2011
Been awhile
It's been awhile since I have been on I have been working and just trying to get through each day, I have been so tired. I am thinking of going back to school not sure though. I know for sure I want to do something with dialysis or transplant patients. I keep thinking that would be a great career for me since I know what people are going through because I went through it myself. I just can't actually go to a school since I am still working full time. The kidney is doing great creatine is 1.3 it still shocks me how I went in and my creatine was 10 then in a matter of 4 days it goes to normal lol. Just fascinates me...I can't wait to see what they come up with next. Well sorry to keep it short but I am tired and want to lay down. CAN'T WAIT TIL MY STAMINA IS BACK!
Monday, May 16, 2011
In and out
Since the transplant I have been running into some problems. Just last week they thought i was rejecting and did and kidney biopsy come to find out it was Procraf intoxication so they stopped that and now have me on Rapimune while I was in the hospital my WBC went up (but they are pretty sure it was caused by steroids and not an infection at the biopsy) then my RBC wen really low but they gave me 2 EPO injections and now I am making it on my own but good news my creatine is going down which is fantastic! Today though i had a little episode at clinic I went out to talk to Alvina and schedule my next apt and got really light headed cold sweat and almost pasted out they had me sit down and they checked my BP and is was 84/69 so I sat there for a bit and they gave me chicken broth then Alvina walked me to Grandpa and he just had me hold on while I walked to the car. It was really scary I did not like that feeling at all. They stopped my BP meds and now I am just taking it really slow today since I am alone I just don't want to pass out. Breathing is a little difficult but I am just taking it easy. I slept pretty much all day today and I could go back to sleep now.
Tuesday, April 19, 2011
I HAD MY TRANSPLANT
I had my transplant April 13th! It was to most amazing gift but it was the most painful thing I have gone through. No more dialysis!!!! Instead a hand full of pills but swallowing pills is better then dialysis. Uncle Jim is doing good he is in pain but it is expected the took his kidney. Let me tell you his kidney "Lefty" makes me pee like I have never peed in my life. I will check in again soon I am just not feeling very well and the pain is coming back which means the Vicodon is wearing off. Thank you for all the prayers Uncle Jim and I appreciate it all.
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