About

I’d be perfect if not for two missing kidneys.

GregHi, I’m Greg Collette and I write the BigDandMe blog, about living with dialysis from the recipients’ viewpoint -  yours and mine. I have been on BigD for 17 years, off and on, and I’ve learned that regardless of changes in technologies or practices there are some fundamental actions that anyone can take to live well on the BigD.

I started this BigDandMe blog on Easter Monday, 2009, to help other normal people whose kidneys have let them down (“kidney failure” is so judgmental!) deal with the daunting prospect of dialysis and transplant.

If you have just joined the BigD club, there’s much you’ll want to know: what to expect, how to stay healthy, actions to take to win back your life, what’s happening in the world of dialysis and kidney transplants, and much more.

So checkout BigDandMe: there’s a new post every fortnight.

In the other part of my life I’ve had my own business for 23 years, working first as a technical writer, then as a knowledge and business process management consultant.  I’ve had two transplants, and I returned to the BigD when my last transplant failed in November 2008.

I dialyse at Diaverum at Diamond Valley in Melbourne, Australia.

To contact me, please email greg.collette at gmail dot com.

80 thoughts on “About

  1. Greg, Like you I have I also have Renal failure and have been on Dialysis for almost 4 years. You website is a very helpful reminder about how important a positive attitude is when on dialysis.

    I now go to a gym 2-3 times a week and lead a “normal” life. I spend 3 hours a day (on dialysis) looking after my health and the rest of the day I can do what ever I like.

    Thank you for sharing your experience with the rest of us.

  2. Greg,
    You are an inspiration to all on Dialysis, keep up that great attitude, so nice you are sharing it, I will pass this on to the Big D person in my family too!
    Truly amazing…

  3. Hi Greg

    I love your site. I started on dialysis about four months ago and I am doing it at home. I still have fairly good residual function so I am only doing three hours every second day. I get up at 3.00am in the morning and I am done and dusted by 7.30am and on with my day.

    I think I make the dialysis fit in with my lifestyle rather than the other way around. It is great doing it at home. I am really well right now and for that I am grateful.

    Thank you for sharing. It is really terrific you have gone to that trouble to support people like me. xx

    • Thanks for your comments Cindy. It’s great to hear that you are doing so well so quickly. Keep well, keep going and keep in touch!

  4. Hi Greg,
    Im a nurse at the new North Melb Diaverum, LOVE your blog, will be recommending it to all our clients and nurses. Great information, you are doing a fabulous service to the ‘renal community’.
    Jen

  5. I went on hemo march 07 following open heart surgery.Went on manual home after short hemo.I finally had too many infections (the catheter becomes infected and has to be replaced). Iam back on hemo. I have had 2caths installed and removed from my abdomen. I had a fistula which was ruined by a pacemaker which created scar tissue in the wrong place. I have also had 2 shoulder caths installed and removed. I now have an implant which is working great. It has allowed me to go from 4 hrs to 3hrs and 15 mn. I am fortunate not to have diabetes. I eat eggs almost every morning to help keep my protein level up. I eliminate orange juice,bananas, tomatoes and potatoes. Sometimes I splurge a little on these as long as my figures stay within bounds. I keep my phosphate in bounds most of the time by watching milk products, chocolate, nuts and dried beans. I take two binders after each meal and three if eat say dried beans. Extra binder for snacks. I know high phos can cause itching and I may be into that a little now. I need to know if phos itch is accompanied by a rash.
    Thanks Jim joyner
    Peoria Ill

    • Wow Jim, what a ride you’ve had. A tough mix of heart and kidney problems. Thank goodness you and your team persisted, and your implant is working for you now. Do you know what kind it is or what it is called?
      Your diet sounds a lot like mine, a mix of being good and enjoying yourself! Whatever works eh? Yes the itching can be a real trial, but strangely enough, I have never had a rash where it itches. If you have a rash, it may be something else.
      Great to hear from you Jim, keep in touch.
      Greg

  6. Greg,
    I feel I had one of the best surgeons for open heart here in Peoria. And perhaps the best renal surgeon around. No problems at all.
    I don’t have rash with the itching I now have. So it might be Phos. Jus trying to distinguish it from a rash that I had for nearly a year. The dermo doc did pathology on that and never came to any definite conclusion. A note on the pleasant side: I played my harmonica at dialysis yesterday.
    I get dialysis at Fresenius on Main Street East Peoria, IL. If you are wondering I am 84.

  7. Hi Greg
    I am living in Hong Kong, to be closer to my grandchildren. My son-in-law was diagnosed with CKD -iga nephropathy in Dec 2008. Unfortunately the disease progressed quickly and he is at the end stage of CKD and due to have dialysis etc. He would really appreciate to speak with another guy who is positive like you and to share some of his feelings, and ask questions. Can he contact you by phone and have a chat with you from HK? He is a New Zealander, and we are from Melbourne. Thank you
    Judy

  8. Greg,

    I am living in Singapore. 8 years ago I donated one of my kidneys to my wife, Wendy. She recently had a lung infection which affected adversely the functioning of the one kidney she had from me. In the hospital she had to go through dialysis. The doctor has told us that she might have to go through it for the rest of her life. We are actually giving to go for her first one post hospitalization, and hope and pray that after 2 weeks her kidney will resume normal function. I found your blog when I was searching for a dialysis centre in Gold Coast QLD that we might have to visit in the unfortunate event that the kidney failure does not reverse. My questions here are do you know of a decent dialysis center we should check out at Gold Coast, and what are the considerations we should address for a second transplant ?

    You are truly an inspiration. Take care.

    • Hi Teck Soon, thanks for your post. The hassle with anti rejection drugs is exactly what happened to Wendy: you catch anything that is passing. I am very sorry to hear it and I hope it works out ok. Sometimes transplant kidneys can be quite resilient.

      About the Gold Coast BigD Unit. The one most people here go to (and think is pretty good) is the John Flynn Dialysis Unit (part of the John Flynn Private Hospital). The details are:
      The John Flynn Hospital Dialysis Unit
      42 Inland Drive
      TUGUN, Queensland 4224
      (or PO Box 1 at the same address).

      Email: dialysis.jfp@ramsayhealth.com.au
      Phone: +61 7 5598 9174
      Fax: +61 7 5598 9195
      Regards and have a good time, Greg

  9. Kia ora Greg,

    Awesome blog! I joined the Big D Club four months ago…..it’s good to learn about your journey.

    Being a newbie to the Club, your information & research have been very helpful to me.

    Naku noa,
    Shaun
    NZ.

  10. What a great discovery to run across this blog while researching dialysis. I’m not a member of the “club” yet, but both my heart and kidney doctors have warned me it’s coming. Considering I have diabetes and congestive heart failure, I’m apprehensive, but will do what I need to to keep on plugging away. Your insightful and humorous, but information posts help sooth some of my anxieties. Thanks!
    gary

    • Thanks for your post Gary. Everyone is anxious when dialysis becomes a reality. But it doesn’t take long to settle in, and to realise that it a treatment this gives you the rest of your life back. Good luck and keep plugging away. Greg

  11. I have been on dialysis 3 years plus-2 of those three years was on manual CAPD I was doing so well and so happy about it that I slipped up and had to go back to hemo. I want to warn those on capd about the neccesity of using sanitary conditions Please know what and how you have to do it. You have to be diligent about this at all times and if you forget something please contact your nurse at the first possible chance. When it comes to peritonitis three strikes and you are out.

    • Thanks for this timely warning James. Infection is the biggest drawback with CAPD. Most people only use it as an interim treatment (1 to 3 years) , maybe waiting for a living donor transplant, while the donor does the workup. Haemo is a little more intrusive, but statistically, much safer. Greg

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  13. Remember that a good positive attitude is really helpful. While you go thru hours of various stages of discomfort just remind yourself of the fact that you are still alive is a god given process.

    I had a friend who went on CAPD from the start and was on it 11 years, dying at the age of 85..
    Another success story is a man I met who was on hemo and had been for 25 years. 3 or more years seems excessive you may be just getting started.

    I haven’t updated my blog in a long time but but welcome those who might like to visit.

    http://picksandpicks.blogspot.com/

  14. I am reading everything in preparing for my husbands need for dialysis. He’s in his mid 50s, diabetic, works full time***, feel good but the creatinine gets high. Do people still work regular jobs? I don’t see much questions about this. We will need to prepare … Emotionally and financially I fear.

  15. I was retired when my kidneys failed so I can’t answer your question about working full time. I can tell you this: I’m almost certain you can find out about if you call your local dialysis center and contact the social worker there. I would probably be right if I said all the centers have these. They also have a kidney doc that not only watches my dialysis but also attends to anything else I have wrong and also a nurse practitioner.

    In one of my last replies someone asked about my implant. No name as far as I know..It is actually a piece of tubing in the form of a loop (about 4in.) that is connected to an artery on one and a vein on the other. It worked real well and I got my on time shortened some. A needle goes into each side. That’s 6 needles a week 352×6 a year they used it more than a and then had clean it out. I was only on for 3 hopurs for a while and had to up it to 3/1/2.
    I’ve thought of home hemo and would like to learn more about it

  16. @Karen,

    I worked full-time while on dialysis, usually about three hours during, with a rest during the last hour. Had my laptop and a phone I could tether the laptop to in order to access the Internet (the clinic WIFI was terrible).
    When I started initially, I was on second shift (10:30-3:30); only a few people worked, either during dialysis or at an office. When I moved to mornings (5:30-8:30 am), nearly everyone worked, going into the office after dialysis.
    It’s a long day, but certainly possible, if your employer can be flexible with schedules and time off for doctor’s visits.

    Gary

  17. Hi Greg,

    I’m a writer and I got the idea for a book about living with dialysis and the wait for a transplant without realising quite how difficult it would be to write as a narrator who experiences dialysis and the effects of it every day.

    It’s one thing to know all the facts, but it’s a real struggle to sound convincing as a dialysis patient- obviously there are so many little things that you learn over the years, and I found it hard to find a website where I could learn this “inside knowledge”.

    Your blog has been so helpful in researching everything I need for my story to be (hopefully!) convincing, so thank you so much for sharing your experiences, they are very much appreciated here.

    All the best, Jess :)

  18. Hi Greg,
    My Mother, 62, a diabetic for the past 10 years, 6 years on insulin, suffered Hypoglycemia three weeks back. Her creatinine started to spike with potassium, at their peaks Creatinine went up to 5.1 and potassium to 6.5. Now after two days of fluids in a hospital, her creatinine levels dropped to 4.8 and potassium under normal range 4.5.
    Initially, doctors at her current hospital were advising Dialysis, three times a week, life long, but after talking to the head of Nephrology, they said she is responding well to medicines and tests, but sugar levels are fluctuating 100-300. And they will decide in 2-3 days for dialysis.
    However, when I talked to doctors at AIMS (All India Medical Sciences), they said they don’t advice Dialysis for patients with constant creatinine at under 5, and suggest decreasing it by food control , diet and medication. Even if Dialysis is done, it will be maintenance one, not thrice a week/lifelong.

    These are the questions I have:
    1) Dialysis is needed at all? If Creatinine keeps on dropping slowly, even then Dialysis would be required?
    2) If Dialysis is needed, then it will be periodical, lets say monthly or twice a month, once in two months OR thrice weekly/lifelong.
    3) Kidney replacement for her is an option? She has diabetes.

    Greg, I need your advice ASAP, as my mother and my family would not like to opt for dialysis and would prefer to keep her Creatinine levels down with strict diet, and medication, Yoga and meditation.

    • Hi Vivek. I have spoken with two very experienced renal nurses, and they think as follows. If your mother was in Australia the doctors here would probably agree with the doctors at her current hospital and recommend that she start dialysis.

      The research shows starting early is better than later, especially if she has kidney failure symptoms, where she feels unwell. If she has only minimal symptoms she may be able to be monitored for a little longer, but they recommend an earlier start. What are her Urea and E-GFR numbers? They are usually a good indicator of how immediate the need is.

      If it is available and she has few symptoms, perhaps she could begin by dialysing 2 days per week. As her kidneys fail completely, the number of days will need to be increased (typically to three days per week). Periodical dialysis is not an option.

      A kidney replacement is an option, but its availability depends on the cut off age for transplants in India. If you mean a transplant from a live donor, the preparation in Australia can take 2 to 6 months. Diabetes is not a barrier to kidney transplantation.

      I hope this helps. Of course these are opinions based on experience. You should be guided by her Nephrologist or ask for a second opinion.

      Good luck and regards, Greg

  19. Thx a lot Greg,
    I just had a talk with Nephro, he said Dialysis is not required at the moment as Creatinine has dropped from 5.3 to 4.3 in 4 days and looks like improving further. Urea has dropped from above 200 to 150 and they said kidney has 15 pct function remaining.
    Doc said they are treating her for the infection in kidney, which was an CUTE infection when she was admitted to the hospital six days back. The reason why creatinine dropped 20 pct in 6 days, because she was severly dehydrated with infection, so after hydrating her and clearing infection, creatinine levels dropped.
    She may be discharged in a day or two, with even lower creatinine levels, or a constant number of under 4, I will write to you again with the discharge summary. Thanks for your help Greg, it means a lot to me, you are the guiding light for most of us.

  20. Hi Greg, Mom gt discharged with CKD of 3 from 5 :). Apparently, there is a term called “acute on chronic” where the acute impact can be reversed to the baseline which was before the creatinine gt spiked. Almost 30 pct of the people of CKD suffer from it, BUT if a doctor conducts a dialysis on these types of patients in a haste, then the damages could be permanent. My Nephro was quite knowledgeable on this front and which helped in not doing the dialysis, at least for now. She is on Ivanz injection for 10 days to remove infection plus insulin.

  21. Hi Greg, Im so glad I run into your blog and found so much info for dialysis especially travel dialysis. I started hemodialysis for almost two years now, when my age 30, now I’m 32. Doctor said my kidney getting worse because I had iGA NEPRITHIS or they call me iGA’ian. I can’t accept my dialysis life at first, especially when I need to bear the pain everytime they use the biggest Avf needles at my hand…but slowly I can build strength and be strong about it. But I still thought that travel is impossible till I read your blog. I’m thankfull to you for show me some lights in my darkers hour.

    I hope I can use your blog for my info to travel the world. Who knows if I got a chance to be in Melbourne. You might help me to which center I should go.

    Again thank you

    With lots of Love,
    rosdylia
    Kuala Lumpur, Malaysia.

    • Hi Rosdylia, lovely to hear from you! Coming to terms with dialysis is not easy or pleasant and I am very pleased that you are doing so well. You sound very positive and strong!
      Yes, travel is next. Take it slowly, try travelling locally first, to get the feel of being away from your home unit. Every unit is a little different and it helps to have an open mind. Preparation is the key to successful travel with each unit exchanging information about you just before you leave. It would be very nice to meet you one day at my unit in Greensborough, we often have visitors from Malaysia. Warm regards, Greg

  22. Hi Greg!
    My name is Brielle and I have been on dialysis for 22 yrs. I started dialysis when I was just 13 years old. I came across your site while I was doing research on the artificial transplanted kidney. I love that you have a blog about dialysis and living your life to the fullest:) I strive to do the same and not let dialysis hold me back. I hope one day in the near future that the artificial kidney will be an option for Big D patients:)
    To Your Health,
    Brielle:)

    • Hi Brielle, great to hear from you. I’m with you: the artificial kidney can’t come soon enough! There are several research programs on the go, some using small artificial filters driven 24/7 by small batteries, others are based on stem cell technology. I would prefer the stem cell version – less artificial and less subject to breakdown – I hope! Let me know if you hear anything. Keep in touch! Best regards, Greg

  23. Hi Greg

    Thanks for blog!!!
    We are looking at going to China for 8 weeks, I read your unfortunate experience and wondered if you had had the opportunity to eventually get to Peking Union Medical College Hospital in Beijing? We would really like to know if this is possible.

    Thanks Kylie

    • Hi Kylie. We have decided not to go to the Peking Union Medical College Hospital. Some Chinese friends of ours prefer another hospital, and we are talking with them now. All seems OK and I will let you know more are time goes on (our travel date is 1 May!).
      Regards, Greg

  24. Greg that would be great and much appreciated. Our 8 year old daughter has been offered the opportunity (for 2 weeks) to go to China as she has been learning Mandarin for 2 years. We are considering going over and living there for 8-12 weeks, this would really boost her listening skills and be an amazing experience. So as like you if we can sort out our obstacles – we will be able to make it happen. Looking forward to hearing how you go. Thanks again.

  25. Hi Greg,
    Just came across your blog and love it. I have been on dialysis for about 16 years. I have Alports and 2 of my 4 brothers have it. I lost one of them when he was 24. My other brother has been on hemo for 26 years. I was on for about 5 years then had a transplant spent 2 months in the hospital rejecting but finally it ended up working, Had it for 5 years, then found out I was pregnant. The drs. told me to terminate but I couldn’t do that. They ended up taking my daughter at 29 weeks and I did lose the kidney but I got a beautiful baby girl out of it. Went back on for another 5 years and had another transplant but the antibody I have attacked it and it was 6 months of hell. So, have been back on since 2006. Lately, I’ve been having a hard time getting my fluid off. This seems to happen to me once or twice a year. Crazy thing, pressure drops so low I come off heavy. I was wondering about the foot detox pads you mentioned. Where do you get them?
    Keep up the blog it is fantastic!

    • Hi Beth, thanks for your comment and your story. Life can be very tough, but fortunately not all the time. Congratulations on having your daughter!
      Sometimes things are easier and more stable on dialysis than with a transplant, especially with the combination of rejection and all those damn drugs.
      I don’t remember writing about foot detox pads, but if you discover something, please let me know.
      One option to keep blood pressure up is the suck ice throughout the run. Not great chunks, but slow and steady. It worked for a couple of people in my unit.
      Regards, Greg

  26. Greg,
    This is Brielle Gazzara and I wrote to you several months ago. I love reading your blogs!!! I wanted to comment on Beth’s comment about low blood pressure and having fluid on. I take a whole food supplement that is low in potassium and phosphrous. It’s called Vasculin and it’s made by Standard Process. I have been taking it now and then when my bp gets low and it works great. It is made from food so it won’t react with any other medications:) you can read more about it on standardprocess.com , maybe this will help some patients out. It had helped me:))

  27. Hi Greg and Brielle,
    Thank you both for the info. One question, the Vasculin helps to keep your pressure up while on treatment? Do you take it before you go or when you are on? I will try that and the ice.
    Sorry Greg, I thought you wrote about the foot detox but it was someone else. I’m so glad you have this blog. Being on so long I’m usually the one with the answers but glad to know there’s more to learn.

    Thanks Beth

  28. Hi Out there. Since I don’t have high pressure they put me on a drug called Midodrine 5Mg. It helped a lot and how I don’t have to wait to go home.

  29. Hi Greg – I just found your blog tonight (restless legs keeping me up) and want to let you know I like your style and your positivity. Like you, I discovered I only had one kidney right at the time I needed a spare… renal cancer in my case.
    I just got the all clear on my cancer this week, so the BigD is all I have to worry about now. I’ve been dialysing for 15 months, and tbh I think so far I’ve been lucky. But these jiggly limbs drive me crazy.
    Love the blog, keep up the great work!

  30. Greg
    A good word for all those on dialysis After 5 yrs. on dialysis, I am now 87.Do as much as you can to stay busy.I play guitar and harmomica and also I’m learning more on the piano I hope I never have to stop learning..I’ve started Painting again though I’m not a pro. I’ve just finoshed a painting of the USA flag. it is large and neatly done. Just to have more to do and to see how it would turn out.

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  32. I am so glad i found your blog. I just told my mom all about it. She is getting ready to start dialysis shortly and i know she will get a lot out of reading your story.
    Thanks

  33. Hi Greg,
    I am studying Bio-medical Engineering and I have to do a report on Hemodialysis next week. Your blog is great and really gave me a good perspective on the lives of people who have to live with BigD, you nearly had me crying at times.

    I hope engineers(future me) can continue to development technology that can help people like you to live a more comfortable, normal life.

    Good luck and thanks for being such an inspiration.

    Regards,

    Hein

  34. Hi Greg,

    I am a Hemodialysis RN in an acute care setting in the US. I am doing research for a HD information presentation for new, critical care RN’s when I ran into your site. I think this is wonderful! I am sure your site has been a great source of information to many people who have found themselves confronting “the Big D”. Thanks for your effort!

    Tim Martin

  35. Hi Greg, I came across your blog after googling info about dialysis. My 69 y.o. Dad just started HD a few weeks ago and isn’t bouncing back as quickly as my mom has hoped. But I’m trying to explain to her that everyone is different and responds to treatment differently. I’m going to show her your blog to reassure her that there is “life after dialysis”! She and my dad are complete opposites (physically, health-wise and personality) so I think the way SHE would approach her treatment is completely the opposite of how my dad’s doing it!

    I was reading some comments and its a little more assuring to know that my dad’s not the only one going through this. And I think showing your blog to my mom will help manage her expectations a little as well. Thanks for sharing your HD experience and I’m looking forward to reading more!

    Cara, from NJ

  36. Hi Greg,
    Thank you for sparing me the huge effort of starting and doing just what you are doing here. Otherwise I was in the process of relating experiences with dialysis.
    Had to chuckle at some of the things written , as I’ve gone through many of the same experiences. Of course those experiences are laughable now, but at the time were a real pain in the ……
    Will be back to fill in some things I’ve been through.
    Again, splendid job of detailing as you term it, the big D
    Be Well

  37. For unknown reasons, my fistula vein, has decided to dance around to avoid getting the needle.
    HA.
    Exactly what I don’t want.
    Stop the dancing vein, and allow those two needles, that look much like night lamp posts that line the streets here in Chicago, Illinois. Nah, I know those needles are much smaller but they feel like lamposts going into the skin and vein.
    So online I go to add to my ‘given’ instructions about exercises for the fistula. If my veins had been in other than good shape, it would have been a ‘graft’ put in the forearm.
    More on that another time though.
    There is conflicting information on ‘when’ and ‘how’ to do fistuila exercises.
    After some confusing trial exercise periods, thought it best to use plain common-sense.
    (Oh, has been well over a year and thought all was well.)
    But the dancing vein has changed that picture.
    Sooo anyway what I”m doing now is:
    Tourniquet on the forearm just ahead of the elbow.
    (Instructions called for above the elbow.) My way give more pressure on the fistula vein.
    Squeezing a special exercise rectangular tube (it allows the finger tips to touch when squeezed)
    I do 20 squeezs-50 s-75 s- 50 s- 20 s with a brief pause between each number of squeezes.
    I them use a set of bands (from the dialysis center) looped and tied together to perform wrist lifts,
    much the same as the ‘squeezes’.
    Pause a longer time and repeat the process.
    Yes my fingers find it very hard to squeeze when the 75 s, is reached.
    This exercise would of course vary for each person.
    Some will be higher, some will be lower in squeeza.
    For me this seems to be the way to go as my forearm and fingers feel the rep exercise strain.

  38. Hi Greg,

    Thanks so much for your words of encouragement. I am 32 years old and recently diagnosed with the collapsing form of FSGS. The doctors have not found a cause. RIght now I am in the prednisone/cyclosporine treatment stage, however most information that I have read states that this is an aggressive form of FSGS which can quickly lead to dialysis. I am also a nurse, so you can imagine all of the horror stories I have seen as I rarely see dialysis as it goes well, only when it goes wrong. I have saved your site as a favorite to keep up to date and as a reminder that this is not the end of the world, although it sure feels like it right now with 2 small boys to chase after. Thanks again!

  39. Hello Readers,
    Been doing my exercise routine, and while I don’t see any dramatic improvement, the dialysis technician seems to see an improvement in what she is looking at.
    Missed, one day, putting on the ‘numbing’ cream on my fistula area. Almost was ‘not’ going to allow a hookup due to my apprehensions of ‘painful needle insertion’. Decided to try anyway. Ha, while it did sting badly, it was not as bad as I had perceived.
    Ha, funny how one’s mind alters reality.
    Due to having lost weight while in the hospital (year or so ago) and wanting to regain that lost weight, proved to be a challenge with what is called ‘dry’ weight at weigh-in time on dialysis days.
    Doctors just didn’t want to believe that ‘all’ weight gain was part muscle or whatever, and normal. Nope, to the doctors it was a’’ ‘water’ gain and has to be pulled out with dialysis.
    Needless to say I was completely’ wiped out’ .
    Ah, and this is important, ‘completely wiped out’ an hour ‘after’ dialysis. Mind you, an hour after I got home is when the low energy depletion hit. POW completely wiped out.
    When I complained to the doctors about this energy depletion they couldn’t understand it. Then I realized where the miscommunication was. Normally I was asked ‘how do you feel’ after dialysis was over. Feeling ok is what I would respond with. True at the time, but not true an hour later.
    So now entered true, weight gain, versus ‘water’ gain, for dialysis machine setup, for new ‘dry weight’.
    As I regained the lost weight, it was a constant battle to get the doctors to adjust the dialysis machine to the ‘new’ dry weight. Have a new doctor now and the new dry weight adjustments are more readily achieved.
    Pulling out wallet, keys,etc, and wearing much the same weight clothes for weighing in on dialysis day is a must. Otherwise too much is ‘pulled out of you, and one starts to feel ’not good’.
    Even while on the dialysis machine, any change in vision, or body sensation shoul / must be called to the technicians attention.

  40. Hello Greg,
    hope you’re feeling well. I found your blog while searching for holiday dialyses around the world, especially Bali. I’m 46, have ill kidneys since I was a little boy. First dialysis at 16, first transplant at 17, second transplant at 19 and third (from my mom) at 37. Now I’m at dialysis again since a few weeks. 3 times a week for 3 hours, because I have still a little bit function (GFR 10). I do dialysing in the afternoon, because I still work full as a radigrapher at university hospital. Just ask me, if you have any questions, I’m sure I’ll follow your blog, its nice and informative.
    Greets from Munich/Germany!
    Thorsten

  41. Hello Greg,
    My mom is 66 and she supposed to start dialysis last Tuesday (she had her fistula surgery on March 4th) but they put the needles to start the treatment and it started to come a lot of blood (hemorrhage) so they suspended the dialysis until her arm is healed. I do not understand doctors said fistula was already established, why she had the hemorrhage? Now her arm is very bruised, like black, and she has pain. Now she just called me that she is worry because it hurts and she feels her arm a little hard.
    She is very tired, no energy these past weeks.
    I think I would be entering frequently to your web page to learn more about dialysis and to ask you some questions. Thank you. Rossana

    • Hi Rossana. From your description, it sounds like your mother’s fistula was “blown”. For normal dialysis, two needle are inserted into the fistula, one to draw the blood out and into the machine, the other to return the blood from the machine back to the fistula. Sometimes, especially when the fistula is new and quite soft, the person doing the needling accidentally pushes right through the fistula and out the other side. If this happens the returning blood, is pumped directly into the flesh of the arm rather than into the fistula. This is called blowing the fistula. It is painful and ugly, but not life threatening.

      Blows are more common with new fistulas, which is why most units have only their most experienced staff putting in the needles during the early stages of dialysis.

      Most people have a blown fistula at least once during the early stages, either because the person needling pushes the needle right through, or because the patient accidentally moves her arm in a way that forces the needle through he wall of the fistula. Your mother’s arm feels hard because it is full of blood. It is black because the blood loses oxygen and turns very dark. It takes 2 -3 weeks to gradually get back to normal (sometimes longer if the blow is a big one).

      She is probably very tired because she needs dialysis. The sooner she gets into a regular dialysis routine, the better.

      I am sure this is both frustrating and traumatic for you mom, but things will improve with time.
      Regards, Greg

      • Thank you Greg for your reply. Tomorrow doctor after see the results of a urine test is going to tell my mom if she needs now a cateter in her chest, I hope not.

  42. Hi Greg enjoy your blog, A lot of our UK clients now have iPads etc. and spend their D.time floating around the internet. In case they didnt already know of you I wondered if you would mind us puting a link on our website to your blog for our patients and travelers to read about your positive force and information resource! Regards Brian

  43. I’m a little late in asking about this! And I can’t find my info darn it……but whats worse…..PUMPKIN PIE or PECAN PIE….I realize its phosphate binders with either/or…..but in the grand scheme/scale…any advice?

    In other words, mom is going to have some….I cant seem to stop her….LOLOL. So advice is great:)

  44. Hi Greg, just want to say hello and greets from bigD staff at BIMC Bali! I said hello from you and they still remember you and shown me your card. Having a great time here at Ayodya resort although my blood pressure is down in the cellar and I passed out yesterday at Bali collection after dialysis..
    have never been nearer to Australia!
    Cordial greets!
    Thorsten

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