I Hate Dialysis Message Board
Introduction => Introduce Yourself => Topic started by: carson on September 12, 2008, 01:10:13 PM
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It's been almost a year since I've been on here. Lots has happened and I'm sure many new people have joined, so I thought I might re-introduce myself. I'm Lisa. When I was 14 I was a very sick girl. After many, many tests I was diagnosed with GN2 and almost immediately placed on PD. I did well on it until my transplant 9 months later. I lived a very good life for 15 yrs while my transplant worked it's wonders but eventually it slowed down to the point where I needed dialysis again. I felt as though I had lost a best friend. I cried and cried but I knew I had no choice. I started PD again in 1997. It went well for the first 9 yrs but eventually the changes in my membrane rendered PD useless and my doc convinced me Hemo would be my best option. Sooo, last Oct I had a central line put in and began hemo on my 41st birthday. I was so scared but once the blood started flowing and I realized it was painless I settled in. Now, it's been almost a year later. I have my Formula Hemodialysis machine at home and I dialyse 8 hours each night, 7 days a week. I have lost 15 kgs of water, I look and feel like a million bucks, and I am happy my previous neph. talked me into Home Hemo. So far I've still been using my central line without incident. I suspect one day they'll tell me I must change to a fistula. THAT I am REALLY afraid of as I'm sooooooooooooooooooooooooo scared of needles. In the meantime I'll just do my bes with the line and hope it all goes well!!
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Welcome Carson, good to have you aboard (again)
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:welcomesign; again Carson. You have been through a lot. Could you tell us more about your Formula Hemodialysis machine or better yet, post a picture. We hope to hear more from you. :cuddle;
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Hi again Carson, I have missed your posts and wondered what happened to you... I am glad you are back, my doctor mentioned just today about me doing dialysis at home (hemo) he wanted me to think about doing 2 hours everyday.... it would be with needles tho,we will have to talk about it
:flower;
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Welcome back Lisa. Sounds like things have been rough but not too bad for now. Don't worry about the needles, you'll cross that bridge when you get to it. :cuddle; :flower; :cuddle;
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Welcome back Carson it has been awhile. I hope your central line continues to serve you well until the next transplant.
Sluff/Admin
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Welcome back! Sounds like you have had a very interesting year. It is always good to hear how well home hemo works for someone. It gives hope to many. Thanks for sharing. :grouphug;
Paris,moderator
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:welcomesign;
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:waving;
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Hi Carson, good to hear from you again. So glad your home hemo is working out good for you.
You say you have a central line, is that the same as a neck cath? My fistula never worked, so I
will have to decide to have a neck cath or a graft. Glad to see you back and hope you keep on
posting.
Love, Mimi
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:welcomesign; back carson
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Welcome back, Carson. I just happen to live in the city of Carson in California! Come back and post often.
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Welcome back! So good to have you with us again. I like the sound of that home hemo. Well, now that you are back with us, I expect to hear more from you. Welcome back! :grouphug;
Bajanne, Moderator
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Thanks everyone for your warm welcomes! It's been an interesting year to say the least but I feel so much better now that I'm on hemo. There are a few posts asking me questions about the program and machine I'm on. I'll briefly explain:
I am on the Formula Hemodialysis machine made in Italy. It's about the size of most hemo machines but much bigger and more efficient than the Nxstage. I dialyze 7 days a week for 8 hours while I sleep on a very slow flow (300). I usually remove 1-2 kgs of fluid. When I wake up in the morning I am not washed out but I am very hungr! My BP is normal. My temp is normal. I can eat and drink anything I want. I had severe Hyperparathyroid issues before starting hemo. I took Sensipar for 3 months and now I am below normal in that dept. I am ENCOURAGED to eat more phos and calcium as they are too low. I still take Aranesp every couple of weeks and some iron too but not too much. The only meds I take are: 5mg Prednisone (from last transplant), Rocaltrol .25 mcg 3 times/wk, 2 Replivite and 1000mg of Glucosamine (I used to do heavy weights when I was well and now my joints hurt!!)
The line I have is inserted just below my collar bone and goes up into my neck, then down into my heart via the pulmonary artery. It is USUALLY a temp thing while the patient learns to use the needles, but I am SOOO very afraid of needles my doc has agreed to let me stay with the line until it's just not the best option. I'm hoping that day never comes!!
If I can get a pic of the Formula, I will put it on here for all to see.
Thanks for your interest.
KimCanada, we should talk!!!!