My dad went on PD for about 20 years, he was a warrior! He passed away in 2013 and this video brought memories, I got trained when I was a kid and learned to manipulate and do all the process in case he needed any help, which eventually happened. We had more strict safety measures, for instance, we would wash our hands like the surgeons do, with the same liquid/soap (a brown one) amongst some other measures and tricks that we learned. I'm glad this technology allowed dad to be with us longer than expected! It never ceases to amaze me the ability we have as humans to create this kind of technology. Thank God for giving us that! God bless everyone.
Hi brother @Jonathan Velasco Could You Please Let Me Know Is there is Any Side Effects Of PD ??? because My Father Age 67 Is Under hemodialysis since One Month So I want To Shift Him To PD,,, Please Guide
@@syedzabeeh92 if your father is on Hemo dialysis keep him on there. My grandmother was on PD and switched to Hemo Being on PD can cause the fluid to form around your heart, the machine sometimes stops working and will need a new one, you will constantly have to check the fluids every 3 or 4 hours. and sometimes all of the fluid won’t drain from the body, it will stay inside which will cause the person legs, etc to start swelling and then they will have to go to the hospital to get the remaining fluid drained. Please don’t switch your father if you don’t want him to suffer. It puts a lot on the patient and the family members that are helping. It’s very tiring
I was om PD for about a month and I could not stand it. The nurse wanted me to stay connected to the machine 11 hours a day and do a manual in the afternoon for 3 hours. I could not work my part time job. One night I got filled up with 3000 cc and I could not breathe at all. Next day I went back to hemo.
I make the solution for use in PD.It’s easy to forget just how much of a difference this makes in peoples lives and so videos like this help to reinforce why we do what we do…stay healthy Kelsie ☺️
I really appreciate patients on PD who take time to explain how it works. After 25 years on Hemodialysis, I will be going on PD, because I ran out of space in my arms for Hemodialysis. I am nervous, but watching these videos, eases my fears a little. Thank you.
My pleasure! PD really is so nice when you have so much life to live! I really hope you enjoy it. Thank you for taking the time to watch and comment. I wreckage it! I’ll try to make more content regarding PD very soon!
@@antoniajones9379 really?? lol REALLY?? having a machine that's here to help your brother "devastates" you??? think about what you're saying.......man people are so ungrateful
fall back what are you talking about???!!!!! I was just saying that going through this situation is being hard on us. And of course we are thankful for all that it’s there to help this problem.
Jessica Garcia she probably got a kidney transplant already but a kidney transplant will only last up to 12 years to 15 maybe if you are really lucky up to 20 years. I had my first transplant in 2018 I was 22 and my doctor told me I will probably need another 4 kidney transplant in my lifetime.
Thank you for this video. My husband gets his dialysis through his AV fistula and is considering switching over to peritoneal. We are trying to absorb any information we can for this potential new journey and praying for wisdom as we go.
Thank you thank you thank you!!! I’ve been doing hemo in a clinic for years and finally decided to change to PD. I have my initial appointment next week and was looking to see someone actually doing PD and seeing how much space everything actually took up. I’m happy to see that you posted a video and am also equally grateful to see a younger person doing it, as I rarely am around younger people when it comes to dialysis. Again, thank you for the video... I’m definitely a new subbie
I's so weird to see other people deal with all those bags, tapes, and wipes that are so familiar to me everyday when I do my exchange. It certainly helps me feel less alone knowing others are dealing with PD as well.
Thank you for this video, I'm 24 years old and have kidney disease. In the near future, I need dialysis and I'm so scared, it was refreshing seeing someone on dialysis who is vibrant and happy, thank you!
I really applaud you for putting this video together. I am learning about dialysis and wanted to see how the peritoneal at home dialysis is set up . Your video really helped me understand better. I wish you all the best and good health. Love and prayers.
Great video! As a PD nurse myself one suggestion. You only used hand sanitizer after touching your toilet to place the drain line. Hand sanitizer does not kill e-coli , c-diff...etc . You should definitely wash your hands instead with warm water and soap then dry with a paper towel. Take care!
@Gingerly Sisters you are very courageous for making these videos. I'm sure loads of people appreciate them! It's always more relatable when patients hear from other patients. Well done
Great suggestion! I used to put it in the sink, but the dextrose dried up and clogged it quite often. I think that could happen with the bathtub as well. The toilet has water in it already, so it doesn’t gunk up. And it’s not in the water, so it’s clear of contaminants such as e.Coli l, etc.
Hi there Kelsie I’m glad you share this video it actually help me see exactly what my friend was and is going through because my friend Christopher Orum has been fighting kidney failure since 2016 but didn’t realize it until it was almost too late because this year beginning of March 2022 he was hospitalize for swelling feet and legs so that’s when the hospital doctor told him about his kidneys failing so he has been diagnose with CKD for the last going on 6 months from now, he found out he had kidney disease by of the beginning March of 2022 then he was hospitalize for over a month or so because he found out his kidneys was at 80% of kidney damage nothing they really could of done to help improve his kidney function so he was only functioning on 20% then a month or so later he fell down too 13% so his kidney doctor decided to put him on dialysis he started his first hemodialysis on April 8th after he got his first catheter which is call the CVC catheter in his chest then after a few months of going to the Davita Dialysis Center in Winchester he switch over to do the PD home dialysis on July 12th 2022 he had his surgery for his PD catheter in his stomach/ side and went to go do his two weeks training at the Home Dialysis Center so now he been doing home dialysis at home for about a week now, he goes on August 18th 2022 at 1pm to get his CVC Catheter remove from his chest so this was a very great video to share I loved it and it was very inspiring and I feel like my friend, he should share his story because he is one of the toughest people I know he been through so many deaths including losing his close relative his brother back 7 years ago November 22nd 2015 to 2 heart surgeries and 2 minor strokes and now today he faces Chronic Kidney Disease so he has been going about the Kidney Transplant List on July 28th, he has one other thing to do then he can be put on the kidney transplant list so IF THERE IS ANY DONORS OUT THERE PLEASE FEEL FREE TO CONTACT ME THRU MY EMAIL ADDRESS! Richardcrystal82@gmail.com Thank you!
Kelsie thank you so much my wife just started her peritoneal dialysis 2021 and we were so nervous not knowing how this was going to work but your videos has giving us some tips for our own but must of all hope for a new kidney! I’m glad you have yours now 🙏🏽
I’m on pd! I was on pd for 18 months until I struggled with my fluid restriction so went on haemo dialysis instead, just recently I started pd again and this will be my 3rd year with dialysis 🙂
Ive been on PD for 6 yrs now ,I started out on hemo for a yr and a half but I had complication so I switch over to PD and fond it to be much better ,Im trying to get my weight down and Im very close but I still will have to go threw a few more hoops before I can sign up for transplant Thanks for your video I you the best thanks for your video
@@ehad972 Ive been on PD about 6 yrs now I hope in few months to get on the transplant list soon ,Ive meant the weight requirements ,The PD program works for me in my 2nd yr I had one infection and been good since the supply's takes up some room in the home but I don't mind when ever Im going to be away from home on an all day trip I take change with me to do in the car ,Its hard for certain family or friends to understand ur need for time to do changes when it needs done. just follow Dr and nurses training and you'll be fine. hope this helps you feel free to contact me here I'll do my best to answer any question
@@ehad972 I understand where ur coming from that was my main problem as well ,my main vein has nerve running along it and man the pain is indescribable I have nerve damage in my right hand cause by it ,thats why I went over to PD 6 yrs ago ,I say thank God there was alternative way Good luck hope u do well what choice u decide on
Medical student here watching PD machines on youtube to learn how they function and your amazing hair caught my eye in the thumbnail. Wonderful video. Hope all is well!
I have stage 3a ckd, and have watched your videos over and over. My egfr recently dropped about 9 points in 2 months, and I've been having some pretty erratic bloodwork lately. I have been told my NFK (nonfunctioning kidney) has probably shriveled up and not contributing at all. The "good kidney" is only doing like 74%. This past week I've been on a roller coaster of stuff, fluid retention went up, borderline anemia, dehydration, 30-pound weight gain in 3 months......So I think my time to go on dialysis, is speeding up and I might be there around Christmas. Your video inspired me to want to do Automated Peritoneal Dialysis first, so I can continue with my job, etc....... But from what I understand, you kinda have to be approved to do APD, have your home inspected, etc, suitable veins, etc. Fortunately, I do have another patient at work who has done hemo & APD, and says one form may work VERY well for you, and not at all, for me......or vice versa! Your videos and your optimism makes me look at all this in a "good light". I know it's something I "have to do", cuz the other option is "death"; poisoned by my own body.........You make it look so easy! And your smiles make me think I CAN do APD too, and do it well. Thank you for making this information availible for us newbies! lol
Hello John! Thanks for your comment. I’m so sorry to hear of your health. Our bodies experience so much, but they’re so strong. Have faith in your bodies capabilities and love it at this time. It’s worked so hard for you- but sometimes it struggles to stay strong. Give it grace. I hope you find the forest for mom of dialysis for your body. You’ve got this! Be there for yourself and don’t forget to advocate for yourself! Good luck on your journey! Don’t hesitate to reach out.
I'm on hemo dialysis, first time and it's been 9 depressing Horrible months, getting research done and information from Nurse, and will speak with My Doctor about switching to PD, I HATE All of it!! We need a cure for kidney disease/failure and a better way of cleansing than Huge 14-17 gauge needles and tubes out our stomachs 😠😠🥺🥴
I agree! I hope the bionic kidney will be approved soon! It would be such a massive blessing for so many. God bless you on this journey, it’s hard, but truly helps you realize the importance of LIFE!
Kelsie, thanks for the demonstration of automatic PD. I think you meant to say one of the PD Dialysis Bags contain 6 liters (1.6 gal). 60 Liters is 15 Gallons of liquid
Just got diagnosed with iga nephropathy and probably going to need dialysis in the near future. Don't know what kind of dialysis I will get yet, but videos like this certainly helps.
If transplant is an option for you if it gets to there, I suggest this kind. However, only 1/4 people diagnosed with iga nephropathy end up getting to end stage renal failure so there is that.
Appreciate you explaining all of this! I do Hemo and I'm thinking of doing PD instead. I definitely feel you about wanting to drink more. I think about water way too much now that my fluid intake is restricted. Total side note: your hair is pretty.🙂
Thank you for making this video. I am brand new to PD dialysis and this helped a lot . I will be getting my catheter in 3 weeks I am kinda nervous but your video helped.
My husband is going on on Thursday, April 11th to get his catheter put in to start this same PD. Thank you so much for this informational video. I understand it a bit more now. Lots of love to you and God bless.
@@kelsiethekidneykid8118 I had my catheter put in March 27th. Your video helped explain many things. I think of you whenever I load my set, "squishy side in". I watched your video when I was in the clinic learning how to do manual PE dialysis. Keep up the great work.
My dad has been on a renal diet for a while and his kidneys were better for a while, but now he’s lost most of his kidney function (almost 90% I believe). He has an upcoming appointment to plan the next step in his treatment. 😢
Something that may help you is a trash compactor. You wouldn’t have to go through as many trash can liners. Just a suggestion. Your video was very informative. Thank you for posting. I subscribed.
So are you loading the bags and tubes on the machine earlier in the day and leaving it all to sit a few hours until bedtime? Is that allowed? Or are all these steps performed each night at bedtime?
I am going soon to dialysis I really don’t know what to do, if PD is better or not, I am keeping active doing exercise, diet, work full time and hopefully starting part time university, and I wonder if hemo is better than PD because I want to keep doing gym … I really don’t know …
Hello guys! I'm also doing hemo dialysis. Always remember, you are strong and you are loved. Thank you foe sharing your vidoe. Hugs and kisses to everyone. Stay safe.
Thank you for that. I just started helping my mother with her PD. Even with the instructions I got, it still felt like I wasn't doing it right. I see you had a cord left-over too...I was like...shouldn't this go somewhere? Thanks again!
Allison Madsen hahahahahah! I was Post Malone for Halloween, and I had posted this just after the holiday so I still had the tattoos on my hands. 😂 Freckles definitely aren’t woes of kidney probs- just the perks of being a redhead! 🤗
My mom is about to change her cateter. So we are figuring out if PD dyalisis is a good choice. Ty for be so brave and share this video. Greetings from Peru
Hi! Hope you're doing well and hopefully have a kidney now! This came up on my feed, so bizarre as I instantly recognised everything. I've been doing this for about 2 weeks, getting a good routine down but it was interesting to see your setup and the little differences. Your machine must be much less noisy further away from the bed but canceling alarms must be a pain 😁
Thanks for this video. Soooooo helpful to see the whole production. I am curious about how you afford all those boxes of the solution. Does insurance cover all that?
Kelsie the Kidney Kid , kelsie hi , your video are very helpful, I wish you the best , I do have questions for you, can you tell me how I can get the machine, and how much it cost please?
insted of the toilet use a bucket (previously santitized) less risk of infection or contamination...keep your faith up, god make miracles, hope your illnes is transitory...you are very brave, god bless you and your family
can you drain that fluid out of your belly into the tub and why aren't you wearing gloves do you need them throughout the whole process do you wipe your machine down before and after your treatments how do you keep the area clean thank you again in advance
Hi my name is Amin and my mother 78 is doing PD Dialysis but we do the manual dialysis twice a day during the daytime. So we have been thinking to shift to a dialysis PD machine during the night but have some concerns/questions hope you can guide me. thx 1. Can one pause during night dialysis and go to the bathroom and then reconnect or the code/lead is long enough that u don't have to disconnect at all?? 2. I am assuming once you get on to the night machine you will not have to do any dialysis during the day, is that correct??
Hi! Yes you can pause the machine but only if it’s done doing a transfer. If your bathroom isn’t in your room, there are extension tubes that will be available for draining. I had to do machine and manual during the day. But I had zero kidney function. It sounds like your mom still has some function? I’m not her doctor, but I assume she’d just need nighttime transfers only.
I am new to your channel as well as a new PD patient whom have not yet started treatment … you explained everything so well, but it seems like so much and I am terribly scared imma do something wrong… or forget something.
Honestly, it depends on what stage ESRD you’re in and what your doctor recommends. Also, your diet and how much fluid you consume a day. I was stage 5 ESRD, and did PD 24/7. 9 hours on the machine at night, and then 1 manual exchange during the day. But, I didn’t have to sit in a chair for 4 hours 3x’s/week, and being a mom, that was important to me. So my doctors and I decided PD would be the best option. It’s not for everyone, but as far as freedom when your life depends on machines, PD gave me the ability to still live life and not be a slave to a machine during the day time.
@@kelsiethekidneykid8118 Thanks for the info. My mother recently started hemodialysis but I'm looking into switching her over to PD. She has stage 5 ckd.
@@Zo6LS7427 it’s worth looking into! She also has to be a candidate for it as well. Not everyone’s body can tolerate it. And it requires a very clean home. Talk to her doctor and discuss it!
Excellent. All the information about the procedure I needed to know. Question, I'm very active, play golf, fish etc...what activity restrictions do you face with your catheter?
I didn’t see you wash your hands at all or clean your machine (im assuming that the teachings are different we were told to have a bottle with water and bleach in it mixed and to use that spray to wipe down machine and table that you’ll be using before getting started) for those who are watching and has to do this be very careful wash your hand please any time you leave the bathroom or if you are continuously touching things stay as clean as possible with your hands that’s very important not just sanitizer when you leave the bathroom wash please the up to date machines has a reminder on the machine when to wash and one of those times you wash your hands is right after you put the drain In The toilet this is a great video but what she didn’t mention and what she should have mentioned is how extremely important it is that your hands are very clean and to be very careful to not touch things while you are getting this setup together I’ve been helping my fiancé through this journey and we have learned that the most important steps are to follow the machine step by step his machine is a more updated one and the other is to be extremely clean and wash your hands repeatedly and sanitize.
Thanks for doing this video Kelsie! My mom is considering switching to PD. What happens if you need to go to the bathroom in the middle of the night? Do you have to disconnect from the machine and how long does it take? Thank you!
Hi! Thanks for your comment. :) I hope she’s able to switch to PD, and if she does, I hope she enjoys it (considering). The freedom was important to me, being a young mother. As far as disconnecting goes, yes you can. You have to wait until you’re in a dwell to disconnect- it takes about 3-5 minutes to do so. And you have to use all sanitation measures. For me, I had my bathroom very close to me, so I very rarely unhooked, but I never had to pee either (lost that function of my kidney early on. ) but usually to throw up due to the RLS medications. You trade one negative for another, continuously with dialysis. You just have to decide which will give you some sort of normalcy in your life. Best of luck to the both of you. I hope she’s able to transplant.
Thank you, thank you, thank you!!!! After watching you I’m not afraid anymore! I will start soon with PD. I went today to my first interview with the dyalisis center. Thank god I don’t eat salt. I’m not swollen yet. My clearance is 10. 😘😘😘😘😘
Hello when you shower do you use a wash cloth or a sponge? I did hemo dialysis in 2005-2006 before my transplant I just had surgery for the PD this looks way better than Hemo do you get leg cramps or feel dizzy while on the machine?
I only get cramps if I stretch my legs. And I don’t notice any dizziness, but I also sleep through the night during my treatments. 🤷🏼♀️ I wash with my hand and antibacterial soap. As for my site, I use Except to keep it clean.
Jessica Garcia yes, you’re right! It’s hard when the spotlight is on you to remember everything (when there’s so much to remember!)- but this is just an informative video for my friends and family, or people who may be considering PD. I in no way condone this as “how YOU should do it” that could make me liable. You should be doing only as your clinic suggests, and that way only. Thanks for watching and making an important observation. ❤️
So the home have to be inspected before starting Dialysis at home.. the reason why I'm asking this is because my sister is supposed to be starting a her home soon
How do you know when your kidneys aren't functioning properly...I always had issues with bladder and kidney stones.. but since February I've had issues with not being able to urinate... I'll have the feeling like I need to pee constantly for a few days and then I can almost time it a few days later it will feel like I need to go but barely anything comes out...I get migraine headaches with it..high blood sugar readings and just feel like utter crap.. just when I think I have it nailed down it throws me for a loop
I have kidney failure and I am getting Peritoneal Dialysis around 21, 20 or 19th of May and I'm 11 years old. I am a bit scared because it's so close! :(
sorry can i kindly ask if you ever had experience of any infection? over-drain or over-fill? seemed like no one speaks much of an over-drain experience that's quite common. do kindly advise. thank you.
LeimertDreamer it all depends on your kidney function. I didn’t urinate at all. But PD is much better at fluid removal than hemo cause you do it every night.
LeimertDreamer same as hemo. Low phosphorus, low potassium, and low protein. Although, on PD you’re allowed more potassium and protein than Hemo cause it pulls off a lot.
Hey Kelsie, question, do you still experience draining cramps? I just finish my PD training, soon gonna start PD at home. Is it normal for me as a beginner to feel those draining cramps?
Hi! The cramps lasted a few months. You get used to them, and then they don’t happen anymore. I missed getting them though, cause they were a great indicator that your drained. Otherwise you sit and wonder (and hope) that all your fluid is out. God bless and good luck!
Thank you for your performent. You beautiful. And too young to dialysist.but what can we do? every body have a nice house.soon I daily hemodialysist home.
Great question! For me, I stopped peeing so it wasn’t an issue. But, I would have to throw up a lot, and in that case, I’d have to keep a bowl by my bed, but most of the time you’re in “dwell” mode. That’s where you’ve drained and filled again, and then it dwells for an hour or so. During a dwell, you can unhook from your machine. But you have to make sure your hooked back up in time for your exchange to start again. I hope that answered your question! Don’t hesitate to ask more if you have them.
Sweet girl, god bless you and gives you health and happiness, I am going to have my first dialysis soon! i hope it does not hurt. would you please PM me so i know more details about that machine and the process? thank you. AMIR
Very useful, thanks. Could I please ask if the machine is quiet and you are able to sleep OK or is it forever beeping and demanding attention in the night? Also do you have to lay on your back or will the machine allow you to lay on either side ? Many thanks.
In general, I suppose so. Fluid consumption is crucial. Following the fluid restrictions set in place by your dr is going to be your best bet at retention on the body. But, PD has red bags that pull of tons of fluid. But they’re also very bad for your peritoneum.
Thumbs up and a sub for you. Great video. I have the same machine and do the same process basically! I've been wanting to do one of these videos but never thought to have someone else record it for me. haha. Hope you are doing well and stay healthy.
Jessie Belano please reach out to her doctor. No one with no medical education should be offering advice on that. Please do what’s right and reach out to the right person.
Hi kelsie thank you for sharing ... may i know if there if you encounter any pain when the exchange is done? I Will be choosing PD as my treatment option and would be great to hear from you thanks!
No pain! There is some discomfort when you drain, some cramping. But you get used to it very quickly. That’s the only con to this treatment that I can think of.
Kelsie the Kidney Kid , thank you kelsie for responding to my message, but we don’t have this machine in my country, I did find one on ebay, do you advice me to buy it , it’s used but it’s in a good condition.
Absolutely not. You’d need all the solution and tubing, plus, caps, gauze, etc... do not purchase. Please. Stick with what you’re doing, it expect it’s hemodialysis? Stay put with that, please.
Hello! Yes, I received my transplant 2 years ago, on the 15th of this month! I’m 31, and had my first transplant when I was 14. Good luck with this journey!!! Feel free to reach out anytime.
‼️To everyone that’s fighting kidney failure keep on fighting and never give up...for every dark night there’s always a brighter day after that‼️
My dad went on PD for about 20 years, he was a warrior! He passed away in 2013 and this video brought memories, I got trained when I was a kid and learned to manipulate and do all the process in case he needed any help, which eventually happened. We had more strict safety measures, for instance, we would wash our hands like the surgeons do, with the same liquid/soap (a brown one) amongst some other measures and tricks that we learned. I'm glad this technology allowed dad to be with us longer than expected! It never ceases to amaze me the ability we have as humans to create this kind of technology. Thank God for giving us that! God bless everyone.
Hi brother @Jonathan Velasco Could You Please Let Me Know Is there is Any Side Effects Of PD ??? because My Father Age 67 Is Under hemodialysis since One Month So I want To Shift Him To PD,,, Please Guide
@@syedzabeeh92 if your father is on Hemo dialysis keep him on there. My grandmother was on PD and switched to Hemo Being on PD can cause the fluid to form around your heart, the machine sometimes stops working and will need a new one, you will constantly have to check the fluids every 3 or 4 hours. and sometimes all of the fluid won’t drain from the body, it will stay inside which will cause the person legs, etc to start swelling and then they will have to go to the hospital to get the remaining fluid drained. Please don’t switch your father if you don’t want him to suffer. It puts a lot on the patient and the family members that are helping. It’s very tiring
I was om PD for about a month and I could not stand it. The nurse wanted me to stay connected to the machine 11 hours a day and do a manual in the afternoon for 3 hours. I could not work my part time job. One night I got filled up with 3000 cc and I could not breathe at all. Next day I went back to hemo.
I make the solution for use in PD.It’s easy to forget just how much of a difference this makes in peoples lives and so videos like this help to reinforce why we do what we do…stay healthy Kelsie ☺️
Thank you for what you do!!! Without you, so many thousands would suffer more than they already are.
Thank you! ❤️
I really appreciate patients on PD who take time to explain how it works. After 25 years on Hemodialysis, I will be going on PD, because I ran out of space in my arms for Hemodialysis. I am nervous, but watching these videos, eases my fears a little. Thank you.
My pleasure! PD really is so nice when you have so much life to live! I really hope you enjoy it. Thank you for taking the time to watch and comment. I wreckage it! I’ll try to make more content regarding PD very soon!
Hi, why haven't you get a kidney yet??? It's been more than 25 years???
@@antoniajones9379 really?? lol REALLY?? having a machine that's here to help your brother "devastates" you??? think about what you're saying.......man people are so ungrateful
fall back what are you talking about???!!!!! I was just saying that going through this situation is being hard on us. And of course we are thankful for all that it’s there to help this problem.
Jessica Garcia she probably got a kidney transplant already but a kidney transplant will only last up to 12 years to 15 maybe if you are really lucky up to 20 years. I had my first transplant in 2018 I was 22 and my doctor told me I will probably need another 4 kidney transplant in my lifetime.
Thank you for this video. My husband gets his dialysis through his AV fistula and is considering switching over to peritoneal. We are trying to absorb any information we can for this potential new journey and praying for wisdom as we go.
Thank you thank you thank you!!! I’ve been doing hemo in a clinic for years and finally decided to change to PD. I have my initial appointment next week and was looking to see someone actually doing PD and seeing how much space everything actually took up. I’m happy to see that you posted a video and am also equally grateful to see a younger person doing it, as I rarely am around younger people when it comes to dialysis. Again, thank you for the video... I’m definitely a new subbie
I's so weird to see other people deal with all those bags, tapes, and wipes that are so familiar to me everyday when I do my exchange. It certainly helps me feel less alone knowing others are dealing with PD as well.
Thank you for this video, I'm 24 years old and have kidney disease. In the near future, I need dialysis and I'm so scared, it was refreshing seeing someone on dialysis who is vibrant and happy, thank you!
@Cynthia Nadine Hope everything is well and turns out for the best ❤
@Cynthia Nadine Thank you ❤
Thank you for sharing this information!! It was very helpful. and encouraging! I wish you well.
I really applaud you for putting this video together. I am learning about dialysis and wanted to see how the peritoneal at home dialysis is set up . Your video really helped me understand better. I wish you all the best and good health. Love and prayers.
Thanks for the video, Kelsie! Very helpful to see the routine of home dialysis.
Christine Nichols thank you for your comment!
Great video! As a PD nurse myself one suggestion. You only used hand sanitizer after touching your toilet to place the drain line. Hand sanitizer does not kill e-coli , c-diff...etc . You should definitely wash your hands instead with warm water and soap then dry with a paper towel. Take care!
@Gingerly Sisters you are very courageous for making these videos. I'm sure loads of people appreciate them! It's always more relatable when patients hear from other patients. Well done
You’re definitely right, I should have! Video jitters, I was so worried about getting everything right with good information, I slipped up!
Y not put the drain line in bath tub instead?
Great suggestion! I used to put it in the sink, but the dextrose dried up and clogged it quite often. I think that could happen with the bathtub as well. The toilet has water in it already, so it doesn’t gunk up. And it’s not in the water, so it’s clear of contaminants such as e.Coli l, etc.
Hi there Kelsie I’m glad you share this video it actually help me see exactly what my friend was and is going through because my friend Christopher Orum has been fighting kidney failure since 2016 but didn’t realize it until it was almost too late because this year beginning of March 2022 he was hospitalize for swelling feet and legs so that’s when the hospital doctor told him about his kidneys failing so he has been diagnose with CKD for the last going on 6 months from now, he found out he had kidney disease by of the beginning March of 2022 then he was hospitalize for over a month or so because he found out his kidneys was at 80% of kidney damage nothing they really could of done to help improve his kidney function so he was only functioning on 20% then a month or so later he fell down too 13% so his kidney doctor decided to put him on dialysis he started his first hemodialysis on April 8th after he got his first catheter which is call the CVC catheter in his chest then after a few months of going to the Davita Dialysis Center in Winchester he switch over to do the PD home dialysis on July 12th 2022 he had his surgery for his PD catheter in his stomach/ side and went to go do his two weeks training at the Home Dialysis Center so now he been doing home dialysis at home for about a week now, he goes on August 18th 2022 at 1pm to get his CVC Catheter remove from his chest so this was a very great video to share I loved it and it was very inspiring and I feel like my friend, he should share his story because he is one of the toughest people I know he been through so many deaths including losing his close relative his brother back 7 years ago November 22nd 2015 to 2 heart surgeries and 2 minor strokes and now today he faces Chronic Kidney Disease so he has been going about the Kidney Transplant List on July 28th, he has one other thing to do then he can be put on the kidney transplant list so IF THERE IS ANY DONORS OUT THERE PLEASE FEEL FREE TO CONTACT ME THRU MY EMAIL ADDRESS! Richardcrystal82@gmail.com Thank you!
Kelsie thank you so much my wife just started her peritoneal dialysis 2021 and we were so nervous not knowing how this was going to work but your videos has giving us some tips for our own but must of all hope for a new kidney! I’m glad you have yours now 🙏🏽
My hubby is about to start PD and it's difficult finding vids. Thank you for this!!
I hope it helped!
Same here! My husband just got diagnosed this year in February 2024.
Great video! I did hemodialysis in center then transitioned to home hemodialysis.
I’m on pd! I was on pd for 18 months until I struggled with my fluid restriction so went on haemo dialysis instead, just recently I started pd again and this will be my 3rd year with dialysis 🙂
I love it! I notice I can drink more on PD and it takes it off. 🤷🏼♀️
@@kelsiethekidneykid8118 How much water can you drink on peritonal dialysis ?
dialysis isn't so bad it gets a bad rap imagine if it didn't exist the same people bad mouthing it would be clamoring for it
Ive been on PD for 6 yrs now ,I started out on hemo for a yr and a half but I had complication so I switch over to PD and fond it to be much better ,Im trying to get my weight down and Im very close but I still will have to go threw a few more hoops before I can sign up for transplant Thanks for your video I you the best thanks for your video
I'm going through complications and thinking about PD. What are you experiencing with PD?
@@ehad972 Ive been on PD about 6 yrs now I hope in few months to get on the transplant list soon ,Ive meant the weight requirements ,The PD program works for me in my 2nd yr I had one infection and been good since the supply's takes up some room in the home but I don't mind when ever Im going to be away from home on an all day trip I take change with me to do in the car ,Its hard for certain family or friends to understand ur need for time to do changes when it needs done. just follow Dr and nurses training and you'll be fine. hope this helps you feel free to contact me here I'll do my best to answer any question
@@BanthaPooDoo64 thank you, I'm strongly considering PD. At the facility, I go to the tech and nurses are having difficulty sticking me.
@@ehad972 I understand where ur coming from that was my main problem as well ,my main vein has nerve running along it and man the pain is indescribable I have nerve damage in my right hand cause by it ,thats why I went over to PD 6 yrs ago ,I say thank God there was alternative way Good luck hope u do well what choice u decide on
Medical student here watching PD machines on youtube to learn how they function and your amazing hair caught my eye in the thumbnail. Wonderful video. Hope all is well!
Paul Garrido thank you! I transplanted 1.5 months ago, doing great! Good luck on your schooling, thanks for your interest in PD!
I have stage 3a ckd, and have watched your videos over and over. My egfr recently dropped about 9 points in 2 months, and I've been having some pretty erratic bloodwork lately. I have been told my NFK (nonfunctioning kidney) has probably shriveled up and not contributing at all. The "good kidney" is only doing like 74%. This past week I've been on a roller coaster of stuff, fluid retention went up, borderline anemia, dehydration, 30-pound weight gain in 3 months......So I think my time to go on dialysis, is speeding up and I might be there around Christmas. Your video inspired me to want to do Automated Peritoneal Dialysis first, so I can continue with my job, etc....... But from what I understand, you kinda have to be approved to do APD, have your home inspected, etc, suitable veins, etc. Fortunately, I do have another patient at work who has done hemo & APD, and says one form may work VERY well for you, and not at all, for me......or vice versa! Your videos and your optimism makes me look at all this in a "good light". I know it's something I "have to do", cuz the other option is "death"; poisoned by my own body.........You make it look so easy! And your smiles make me think I CAN do APD too, and do it well. Thank you for making this information availible for us newbies! lol
Hello John! Thanks for your comment. I’m so sorry to hear of your health. Our bodies experience so much, but they’re so strong. Have faith in your bodies capabilities and love it at this time. It’s worked so hard for you- but sometimes it struggles to stay strong. Give it grace. I hope you find the forest for mom of dialysis for your body. You’ve got this! Be there for yourself and don’t forget to advocate for yourself! Good luck on your journey! Don’t hesitate to reach out.
Thank you for sharing this process with us. I am going on this machine very soon so this video was a great help.
I'm on hemo dialysis, first time and it's been 9 depressing Horrible months, getting research done and information from Nurse, and will speak with My Doctor about switching to PD, I HATE All of it!! We need a cure for kidney disease/failure and a better way of cleansing than Huge 14-17 gauge needles and tubes out our stomachs 😠😠🥺🥴
I agree! I hope the bionic kidney will be approved soon! It would be such a massive blessing for so many. God bless you on this journey, it’s hard, but truly helps you realize the importance of LIFE!
Kelsie, thanks for the demonstration of automatic PD. I think you meant to say one of the PD Dialysis Bags contain 6 liters (1.6 gal). 60 Liters is 15 Gallons of liquid
Yes, correct!
Just got diagnosed with iga nephropathy and probably going to need dialysis in the near future. Don't know what kind of dialysis I will get yet, but videos like this certainly helps.
If transplant is an option for you if it gets to there, I suggest this kind. However, only 1/4 people diagnosed with iga nephropathy end up getting to end stage renal failure so there is that.
I have iga Nephropathy too!.
Appreciate you explaining all of this! I do Hemo and I'm thinking of doing PD instead. I definitely feel you about wanting to drink more. I think about water way too much now that my fluid intake is restricted. Total side note: your hair is pretty.🙂
Thank you for making this video. I am brand new to PD dialysis and this helped a lot . I will be getting my catheter in 3 weeks I am kinda nervous
but your video helped.
I hope your surgery went well and that you’re having as good as experience as you can on PD. May God bless you, and I pray you find a donor. 🤍
Hi Tony, how did your surgery go and how is PD going so far? My dad just had his surgery on the 8th
I hope you are ok,you are very brave girl,god bless you.
My husband is going on on Thursday, April 11th to get his catheter put in to start this same PD. Thank you so much for this informational video. I understand it a bit more now. Lots of love to you and God bless.
So happy this helped you gain some understanding! That’s what I wanted when I made this video! Good luck to him. PD is great!
@@kelsiethekidneykid8118 I had my catheter put in March 27th. Your video helped explain many things. I think of you whenever I load my set, "squishy side in". I watched your video when I was in the clinic learning how to do manual PE dialysis. Keep up the great work.
Kelsie the Kidney Kid . Much love to you.❤️🙏🏻 hope you are doing well.
My dad has been on a renal diet for a while and his kidneys were better for a while, but now he’s lost most of his kidney function (almost 90% I believe). He has an upcoming appointment to plan the next step in his treatment. 😢
My mum has 4% kidney function I don't know what to do please help
🙏🙏🙏🙏🙏
@@tariq1030🙏🙏🙏🙏🙏
Something that may help you is a trash compactor. You wouldn’t have to go through as many trash can liners. Just a suggestion. Your video was very informative. Thank you for posting. I subscribed.
So are you loading the bags and tubes on the machine earlier in the day and leaving it all to sit a few hours until bedtime? Is that allowed? Or are all these steps performed each night at bedtime?
As Dialysis patients, do guys think yes or no is better on prop 23. Specifically asking patients from California but all opinions are welcome.
Beautiful hair 😊
I would to see a video of ur pd machine running overnight to see how it really works god bless 🙏🏽
Thank you for this video & god bless you and your family!
I am going soon to dialysis I really don’t know what to do, if PD is better or not, I am keeping active doing exercise, diet, work full time and hopefully starting part time university, and I wonder if hemo is better than PD because I want to keep doing gym … I really don’t know …
Hello guys! I'm also doing hemo dialysis. Always remember, you are strong and you are loved. Thank you foe sharing your vidoe. Hugs and kisses to everyone. Stay safe.
Thank you for that. I just started helping my mother with her PD. Even with the instructions I got, it still felt like I wasn't doing it right. I see you had a cord left-over too...I was like...shouldn't this go somewhere? Thanks again!
No problem! Glad I could be a resource, that’s what I hoped I could be!!
I didn’t catch what you said about the marks on your knuckles.
Also are the freckles part of kidney woes?
Ps I love freckles 🥰🥰
Allison Madsen hahahahahah! I was Post Malone for Halloween, and I had posted this just after the holiday so I still had the tattoos on my hands. 😂 Freckles definitely aren’t woes of kidney probs- just the perks of being a redhead! 🤗
My mom is about to change her cateter. So we are figuring out if PD dyalisis is a good choice.
Ty for be so brave and share this video.
Greetings from Peru
Did she go with PD? I hope all is well. Thanks for the comment. :)
Hi! Hope you're doing well and hopefully have a kidney now! This came up on my feed, so bizarre as I instantly recognised everything. I've been doing this for about 2 weeks, getting a good routine down but it was interesting to see your setup and the little differences. Your machine must be much less noisy further away from the bed but canceling alarms must be a pain 😁
Merhaba ben PD baslayacam makinali olaninimi yoksa manuel olaninimi onerirsiniz tesekkurler
Tytyty your video is helpful to help me decide tnanks so much
Thank you! So happy to hear this! Hope it all went well.
Only got one question, did you give your Baxter a nickname?
I named mine succubus.
It was from Fresenious.
Thanks for this video. Soooooo helpful to see the whole production.
I am curious about how you afford all those boxes of the solution. Does insurance cover all that?
Yes, insurance. :)
Kelsie the Kidney Kid , kelsie hi , your video are very helpful, I wish you the best , I do have questions for you, can you tell me how I can get the machine, and how much it cost please?
What position do you sleep in for PD
insted of the toilet use a bucket (previously santitized) less risk of infection or contamination...keep your faith up, god make miracles, hope your illnes is transitory...you are very brave, god bless you and your family
Very personal, yet informative. Good work.
can you drain that fluid out of your belly into the tub and why aren't you wearing gloves do you need them throughout the whole process do you wipe your machine down before and after your treatments how do you keep the area clean thank you again in advance
Hi my name is Amin and my mother 78 is doing PD Dialysis but we do the manual dialysis twice a day during the daytime. So we have been thinking to shift to a dialysis PD machine during the night but have some concerns/questions hope you can guide me. thx
1. Can one pause during night dialysis and go to the bathroom and then reconnect or the code/lead is long enough that u don't have to disconnect at all??
2. I am assuming once you get on to the night machine you will not have to do any dialysis during the day, is that correct??
Hi! Yes you can pause the machine but only if it’s done doing a transfer. If your bathroom isn’t in your room, there are extension tubes that will be available for draining.
I had to do machine and manual during the day. But I had zero kidney function. It sounds like your mom still has some function? I’m not her doctor, but I assume she’d just need nighttime transfers only.
I am new to your channel as well as a new PD patient whom have not yet started treatment … you explained everything so well, but it seems like so much and I am terribly scared imma do something wrong… or forget something.
Thank you, God bless You!
Slm çalışma hayatına herhangibir zorlama oluyor mu
I thought pd only took an hour to do everyday. How long is the pd treatment everyday?
Honestly, it depends on what stage ESRD you’re in and what your doctor recommends. Also, your diet and how much fluid you consume a day.
I was stage 5 ESRD, and did PD 24/7. 9 hours on the machine at night, and then 1 manual exchange during the day. But, I didn’t have to sit in a chair for 4 hours 3x’s/week, and being a mom, that was important to me. So my doctors and I decided PD would be the best option.
It’s not for everyone, but as far as freedom when your life depends on machines, PD gave me the ability to still live life and not be a slave to a machine during the day time.
@@kelsiethekidneykid8118 Thanks for the info. My mother recently started hemodialysis but I'm looking into switching her over to PD. She has stage 5 ckd.
@@Zo6LS7427 it’s worth looking into! She also has to be a candidate for it as well. Not everyone’s body can tolerate it. And it requires a very clean home. Talk to her doctor and discuss it!
Excellent. All the information about the procedure I needed to know. Question, I'm very active, play golf, fish etc...what activity restrictions do you face with your catheter?
You’re able to do nearly all activity besides swimming, as long as you don’t have fluid in your peritoneal.
Is this machine available in india please tell me.
I didn’t see you wash your hands at all or clean your machine (im assuming that the teachings are different we were told to have a bottle with water and bleach in it mixed and to use that spray to wipe down machine and table that you’ll be using before getting started) for those who are watching and has to do this be very careful wash your hand please any time you leave the bathroom or if you are continuously touching things stay as clean as possible with your hands that’s very important not just sanitizer when you leave the bathroom wash please the up to date machines has a reminder on the machine when to wash and one of those times you wash your hands is right after you put the drain In The toilet this is a great video but what she didn’t mention and what she should have mentioned is how extremely important it is that your hands are very clean and to be very careful to not touch things while you are getting this setup together I’ve been helping my fiancé through this journey and we have learned that the most important steps are to follow the machine step by step his machine is a more updated one and the other is to be extremely clean and wash your hands repeatedly and sanitize.
Thanks for doing this video Kelsie! My mom is considering switching to PD. What happens if you need to go to the bathroom in the middle of the night? Do you have to disconnect from the machine and how long does it take?
Thank you!
Hi! Thanks for your comment. :) I hope she’s able to switch to PD, and if she does, I hope she enjoys it (considering). The freedom was important to me, being a young mother.
As far as disconnecting goes, yes you can. You have to wait until you’re in a dwell to disconnect- it takes about 3-5 minutes to do so. And you have to use all sanitation measures. For me, I had my bathroom very close to me, so I very rarely unhooked, but I never had to pee either (lost that function of my kidney early on. ) but usually to throw up due to the RLS medications. You trade one negative for another, continuously with dialysis. You just have to decide which will give you some sort of normalcy in your life. Best of luck to the both of you. I hope she’s able to transplant.
Thank you! Huge help!
Thank you, thank you, thank you!!!! After watching you I’m not afraid anymore! I will start soon with PD. I went today to my first interview with the dyalisis center. Thank god I don’t eat salt. I’m not swollen yet. My clearance is 10. 😘😘😘😘😘
I watched this with my mum before starting her PD, She passed away first few days in PD from a chest infection :(
I’m so so sorry for your loss! Kidney disease is cruel. I hope you’ve found peace with her passing.
How old is your mum? Is the infection caused by PD?
Hello when you shower do you use a wash cloth or a sponge? I did hemo dialysis in 2005-2006 before my transplant I just had surgery for the PD this looks way better than Hemo do you get leg cramps or feel dizzy while on the machine?
I only get cramps if I stretch my legs. And I don’t notice any dizziness, but I also sleep through the night during my treatments. 🤷🏼♀️ I wash with my hand and antibacterial soap. As for my site, I use Except to keep it clean.
Will I get my energy and mental sharpness back after I start PD?
I did not
@@dwaynewilson7847 I am very sorry
I'm on hemodiálisis right now and want to switch to PD the big question is how do you shower with catheter on stomach???
Hi is this a good price for the amia PD system?? www.ebay.ca/itm/373370443018
Nice, but you didn't wash your hands after touching the toilet. Just an observation!!
Jessica Garcia yes, you’re right! It’s hard when the spotlight is on you to remember everything (when there’s so much to remember!)- but this is just an informative video for my friends and family, or people who may be considering PD. I in no way condone this as “how YOU should do it” that could make me liable. You should be doing only as your clinic suggests, and that way only. Thanks for watching and making an important observation. ❤️
Does the home have to be sterile for the use of Dialysis at home and do the home have to be inspected before starting in you home..?
Yes
So the home have to be inspected before starting Dialysis at home.. the reason why I'm asking this is because my sister is supposed to be starting a her home soon
Norrese Powell yes, the nurse will come home and do an inspection and set up your machine.
Ok thank u so much.. this was so helpful..🙂
Is there any cramping I’m just curious I’m on hemo dialysis.
LIFE. OF NATURE at first you will experience some cramping when you drain, but your body acclimated pretty well.
How do you know when your kidneys aren't functioning properly...I always had issues with bladder and kidney stones.. but since February I've had issues with not being able to urinate... I'll have the feeling like I need to pee constantly for a few days and then I can almost time it a few days later it will feel like I need to go but barely anything comes out...I get migraine headaches with it..high blood sugar readings and just feel like utter crap.. just when I think I have it nailed down it throws me for a loop
You need to see a nephrologist.
Did you ever do hemo dialysis or start of with pd
I started with hemo for 3 months. And when I was pediatric, I did it for 9 months.
I have kidney failure and I am getting Peritoneal Dialysis around 21, 20 or 19th of May and I'm 11 years old. I am a bit scared because it's so close! :(
You’ll do great! I hope you’re liking it so far!
sorry can i kindly ask if you ever had experience of any infection? over-drain or over-fill? seemed like no one speaks much of an over-drain experience that's quite common. do kindly advise. thank you.
Never had either of those! The machine is very smart and only puts in what you tell it to.
Never had either of those! The machine is very smart and only puts in what you tell it to.
Never had either of those! The machine is very smart and only puts in what you tell it to.
Never had either of those! The machine is very smart and only puts in what you tell it to.
I have somany questions about it but I am from 8monts doing this and before that 4years in hd
I’m nearing end stage CKD and barring some sort of miracle this looks like it’s gonna be in my future....
Hi is this a good price for the amia PD system?? www.ebay.ca/itm/373370443018
I heard you mentioned fluid restriction
but I’ve always been told you can drink and eat what you want on PD versus hemo. Is that not true?
LeimertDreamer it all depends on your kidney function. I didn’t urinate at all. But PD is much better at fluid removal than hemo cause you do it every night.
Kelsie the Kidney Kid Thanks for the info! What about dietary restrictions on PD?
LeimertDreamer same as hemo. Low phosphorus, low potassium, and low protein. Although, on PD you’re allowed more potassium and protein than Hemo cause it pulls off a lot.
Kelsie the Kidney Kid Thanks for the info!
U're gorgeous and well educated girl , salute !
Thank you!! 🤍🤍🤍
They are recommended I start this , I am not on any dialysis , will I feel a bit better if I start this?
If your numbers are too high, then dialysis should make you feel better. Not amazing, but better. Best of luck to you!
one question about how much all of this cost for a week🤦🏻♀️🤦🏻♀️🤦🏻♀️
$$$$ a lot. But it’s all covered by insurance. :)
$$$$ a lot. But it’s all covered by insurance. :)
$$$$ a lot. But it’s all covered by insurance. :)
That was also my question. My dad doesn’t have insurance. 😢
@@RealMexFoodShouldntGiveUDrrhea im in Australia and it cost us nothing. all covered by our government
Hey Kelsie, question, do you still experience draining cramps? I just finish my PD training, soon gonna start PD at home. Is it normal for me as a beginner to feel those draining cramps?
Hi! The cramps lasted a few months. You get used to them, and then they don’t happen anymore. I missed getting them though, cause they were a great indicator that your drained. Otherwise you sit and wonder (and hope) that all your fluid is out. God bless and good luck!
Thank you for your performent. You beautiful. And too young to dialysist.but what can we do? every body have a nice house.soon I daily hemodialysist home.
I'm going to start soon. Thank you so much for sharing, you have given me hope, God bless. I just hope I can still work, children to support
I’m stage five doing three manual exchanges a day and I go to work everyday. Don’t even really feel any different to be honest
You are so pretty! I’m going dialysis soon!
Hi Kelsey does pd feel uncomfortable when it dwells in your stomach
LIFE. OF NATURE hi! At first it will feel very full. But you definitely get used to it!
Is there any cramping
How do you go pee if your hooked up to the machine? Can you detach easily ?
Great question! For me, I stopped peeing so it wasn’t an issue. But, I would have to throw up a lot, and in that case, I’d have to keep a bowl by my bed, but most of the time you’re in “dwell” mode. That’s where you’ve drained and filled again, and then it dwells for an hour or so. During a dwell, you can unhook from your machine. But you have to make sure your hooked back up in time for your exchange to start again. I hope that answered your question! Don’t hesitate to ask more if you have them.
Kelsie Sondrup yes thank you so much!
This is informative and you have a nice red hair.
Sweet girl, god bless you and gives you health and happiness, I am going to have my first dialysis soon! i hope it does not hurt. would you please PM me so i know more details about that machine and the process? thank you. AMIR
I don't know if you read these or not but I'm just starting in your video is very hopeful and I wish you well
Very useful, thanks. Could I please ask if the machine is quiet and you are able to sleep OK or is it forever beeping and demanding attention in the night? Also do you have to lay on your back or will the machine allow you to lay on either side ? Many thanks.
Hi is this a good price for the amia PD system?? www.ebay.ca/itm/373370443018
Is this better at getting extra fluid than hemo
In general, I suppose so. Fluid consumption is crucial. Following the fluid restrictions set in place by your dr is going to be your best bet at retention on the body. But, PD has red bags that pull of tons of fluid. But they’re also very bad for your peritoneum.
Hey Kelsey, thx for the video. I’m about to start this process. How are you currently doing? Still on PD?
Hey! Thanks for the comment! How are you doing so far? I’m still Doug great, probably even better than in this video!
What’s the dimensions and weight on the machine?
Raylene Rojas for Baxter, it’s about 2x1.5 feet and about 15-17lbs
Thumbs up and a sub for you. Great video. I have the same machine and do the same process basically! I've been wanting to do one of these videos but never thought to have someone else record it for me. haha. Hope you are doing well and stay healthy.
Wouldn’t the line from the toilet Be contaminated from feces and bacteria
Yes, but it’s a out put line, and is very long. Waste is pushed through and drained into the toilet. Just like urine.
hello, have you ever experience bloody dialisate/fluid. kindly explain the cause please
Jessie Belano hi! I never experienced that during my treatments. Also, I’m not a medical professional- please seek out advice from your doctor.
@@kelsiesondrup7795 i hope..one of you viewer could explain based on their experience...my wife has bloody fliud two days in a row..im kinda worried
Jessie Belano please reach out to her doctor. No one with no medical education should be offering advice on that. Please do what’s right and reach out to the right person.
How much water can you drink on peritonal dialysis ?
Eddie Salas it depends me only 32oz a day.
@@godson1of1 I like PD alot more than hemo its more freedom
Thankd for the tip 😊
Hi kelsie thank you for sharing ... may i know if there if you encounter any pain when the exchange is done? I Will be choosing PD as my treatment option and would be great to hear from you thanks!
No pain! There is some discomfort when you drain, some cramping. But you get used to it very quickly. That’s the only con to this treatment that I can think of.
Is anyone know from where can I buy the machine?
You cannot buy one. Your renal clinic provides you with one with you’re out on dialysis.
Kelsie the Kidney Kid , thank you kelsie for responding to my message, but we don’t have this machine in my country, I did find one on ebay, do you advice me to buy it , it’s used but it’s in a good condition.
Absolutely not. You’d need all the solution and tubing, plus, caps, gauze, etc... do not purchase. Please. Stick with what you’re doing, it expect it’s hemodialysis? Stay put with that, please.
How much price apd mechine
s. Bala we don’t pay for it. Medicare does
Have you gotten a kidney transplant yet? Thanks for the video I’m 37 and will be starting pd in a couple weeks
Hello! Yes, I received my transplant 2 years ago, on the 15th of this month! I’m 31, and had my first transplant when I was 14. Good luck with this journey!!! Feel free to reach out anytime.
Hi please rate this machine
Thank you for sharing.