Відео

Hi Dee, Really enjoyed your Podcast.The information you supplied was really informative.I'm a CKD Stage five.I reside in London and I'm treated at the Tottenham Hake Kidney Centre.I have an an interesting journey over 7 years reaching the stage where I'm on the Transplant List .Recently had a graph in left arm in preparation for dialysis. Shall be seeeking a councellor and Kidney psycologist as one's mental health is paramount when going through this journey.Currently off on sick leave from work as my kidney percentile is at 9%. I have been told my heomoglobin level is at 100 and should be higher.For a 6ft tall individual who has been very active,its a blow to my ego.Experiecing a lot of tirednes and wake up covered in sweat.Also I suffer from shortness of breath after not much exertion.So your Podcast has been very heilpful,keep up the good work. I'm also a Christian and having the faith knowing you can put all your cares on him helps.Stay Blessed keep up the good work. bryan.collins@openreach.co.uk.

please!

It’s so great to see this topic covered! I’ve been recently diagnosed with LPHS and with it being so rare, it’s nice to know there are others out there who understand what we live through every day.

Congratulations Dee on your wonderful podcast. Thank you for all your work you have done within our diverse kidney community. You have brought a voice to many of the voiceless on their journey. your story and all the others inspire me every episode and thank you to you for letting me be a small part of your wonderful podcast 🎉 xx

This episode is EXCELLENT. For all sorts of reasons. CONGRATULATIONS! I don't want to sound patronising. I sincerely appreciate the nuggets of truth that relate to life generally. I've learnt a lot. God Bless you both!

Thank you for sharing your PD experience. My husband just started PD, and I am hoping and praying to God that it works well for him. He still has his hemodialyis vein catheter, and it would not be removed until the PD Team determine is working as it should. God you and keep you strong and positive!

Congratulations

Thank you! Very interesting and helpful information.

Fight on Kidney Warrior ❤️ 💪 ❤️ You are always in my Prayers 🙏

Thank yiu

😢 My God

Great collaboration!! I’m literally at UWHospital and am now scheduled for several appointments for LPHS to receive an auto transplant. 🤗 🤗 to those whose experience a chronic condition and who pain. Not a lot of videos that have this information, so thank you so much! Bless 😊you for sharing your story, you are a WARRIOR 👏

New here glad I found your channel 💜💜

Thank you so much for sharing your story. I'm new to pd and suffering horrific pain during the drain cycles. I have been told it's constipation. I dread hooking up to the machine every night. I have my pet test in a couple of days time so hopefully I will be able to get it sorted x

Hey Dee, thank you for this episode. I'm also on the transplant list and it's hard living with the uncertainty. X

I did well

Thanks for your encouragement.

Bless you Dee! I hear your message loud and clear. Thank you.🙏

Thank you for sharing. ‘Hope’ - that is what we must have when facing a journey like this. Talking about everything you’ve gone through and experienced is very helpful for those facing similar situations, whether recovering from septic shock or living with CKD. Well done for being so brave to talk about it and thank you again for this podcast.

Ive had 10 months of persistent kidney Stone pain & blood in my urine. This is excruciating! My nephrologist has concluded LPHS just today! Mrs Gray

Great Podcast, learn more about kidney disease every day 😢🙏

Can you not do haemodialysis at home? ❤️👍❤️🙏❤️

Thank you so much for sharing your story! It is very scary, what happenned to you. My understanding you were on PD only 4 months? When did you notice, that your body, knees were swollen - it was from beginning? did your doctors were aware of that?

Thank you for sharing ❤️

Keep up the amazing work my beautiful sista 💯❤️💪🏿👀Im a kidney patient as well..your videos are helpful

Very informative Dee.🤩🤩🤩🤩🤩🤩

CanPrev brand Fibre Feel . Acasia fiber ( gum arabic) to flush kidney from toxins. Look it up .

Wow...this 2-part episode with Darren was POWERFUL! Like Dee, I too was speechless (& moved to tears) several times while listening to his story. Clearly, Darren is a fierce & determined kidney warrior. Dee is a soldier warrior too for managing her own kidney journey while finding the time & energy to share other's kidney stories with us. Thank you both for this moving 2-part episode!!! ❤🙏🏽💪🏽

❤️🙏❤️🙏

In soviet union health care was free , doctor's salary was the same, as salary of an engineer - a bit higher, than salary of truck drivers. For that reason doctors helped as little as possible. In the USA is opposite situation - doctors suggest hundreds unnessesary tests, procedures and surgeries, as it makes them rich. I do not know, if there exist any perfect health system in the world.

Whoever is reading this, know Jesus loves you. He died so we may live. He lived a perfect life that we could not. We deserve eternal death, but because of His grace and forgiveness we can experience eternal life with Him. This is the truth. Humble yourself and accept God’s forgiveness. His love will make you whole. It will change your life forever.

😢

You have put my mind at ease thank u

I like that

How long does every pd session takes?

Great podcast..

Thank you for showing this, trying to work out where and how we are going to store and work with all the "bits" as we are in a one bed flat with very little storage.

Be strong and you will make it. God bless you

Your more than welcome it was definitely some difficult times in my life but managed to make it through 🙏🏾 both my Grandfather and father are doing well thanks

It is possible to look after 8 months baby and get PD? Could PD patient lift a 12-pounds baby from crib ?

Thank you so much for such guest! He went through so much pain. I wish him the best! How is his grandfather and father now?

My Mom is on dialysis. She has lupus, rheumatoid arthritis, diabetes, scleroderma, Sjögren’s syndrome, she’s blind and she can’t walk anymore due to a stroke. She’s had issues with being non compliant with her dialysis due to depression, her lupus and arthritis causing her so much pain that she couldn’t get out of bed, and we live in the US where it rains and snows quite often in the winter and temperatures can be as low as several degrees below 0°F. She is currently in the hospital and the new kidney doctor she got suggested PD so she can have dialysis at home. She had surgery today to install her new dialysis port and since I’m her 24/7 caregiver, I’ll be learning how to administer her PD. All of these health issues have happened within the last 6 years. So as her daughter, I’m also learning how to live with these diseases, since I have seen them destroy her body in such a short time. I’ve had to grieve someone who is still alive. I grieved for the life I wanted her to have and the person I knew she could be. Now since she lost her eyesight 3 months ago due to having strokes in her eyes, she and I are navigating through learning how to be blind and how to care for a blind person together. No matter where this journey takes us, we will always be together and I will always take care of her. This isn’t just her journey. It’s ours.

UA-cam recommended me your video! love your content. By the way, are you currently interested in expanding your channel's reach and gaining more views? Let me know if you're interested?

UA-cam recommended me your video! love your content. By the way, are you currently interested in expanding your channel's reach and gaining more views? Let me know if you're interested?

Thanks for the reminder and by the way you look great❤

I am so sorry for you❤❤

Recipe please!!😋

HalleluYah