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These medicines are what I recommend my patients - Mutrakrichantak Churna, Chandanadi Vati, Phyllanthus niruri, Curcumin Capsules. These medicines by Planet Ayurveda have won over my trust and will surely win you over too.

C3G really changes your life, it changed me, it changed the people around me and how they treated me, it changed everything. I have a routine appointment at the GN clinic at Toronto General hospital in Just 4 days. After the age of 16 i developed severe anxiety and depression, started getting addicted to self harm and tried to attempt suicide but thats something most people fail at. Im ok now but i know patients like me just need to hang in there and try to keep a healthy lifestyle. I hope you are in a better place now than the one you might have been in when you were diagnosed. I wish you good health and good luck.

I try my best to take part in research and help raise awareness about this disease and similar conditions. I also use social media to the best of my ability. I thank you for sharing your story with the public, ive shared my story too when i was still being treated in Canada at SickKids but now im being treated at Toronto General Hospital after turning 18.

Im still trying to learn more about my condition and longterm health concerns. My doctors say im stable but if i was to have kidney failure, it would be 10 years down the road. I think what scares me is that i will get sick at a point in my life where i will have less help from family, more responsibilities and more lifestyle related issues. Have your doctors discussed renal failure concerns with you over the years.

I was diagnosed at age 9 and my symptoms also started at age 8. My diagnoses was for C3GN and have been through so many treatments. Im currently only 19 and have had 3 renal biopsies, had high bp issues, been in a coma, had a seizure and PRES.

I was diagnosed with C3GN at age 9, am 19 now, have had 3 biopsies since my diagnosis back in 2014 and am stable but disease progression is something that just continues longterm slowly

I am 19 and was diagnosed with C3GN at age 9. Had 3 renal biopsies since then.

I have C3GN and was diagnosed at the age of 9 in Jan 2014. Since then I've been put through a lot of treatments, renal biopsies, clinical trials and routine hospital visits. It has now in 2024 been 10 years since I was diagnosed and still I have not reached ESRD, but my nephrologist says if i was to experience renal failure, it would be 10 more years down the road based on my current health.

My mom goes to her primary care doctor frequently bc she is diabetic and hypertensive Not sure how it was missed but now she’s at the hospital w 20% function 😓

Me who had grade 5 hydronephrosis as a toddler growing up and now has stage 4 CKD Hahaha I’m in danger Note: I’ve never been diagnosed with s4 ckd but given the symptoms I’ve had and having hypertensive crisis it’s pretty likely I have it unfortunately

My mom is in her 60s and a year into dialysis. She is weak and deteriorated , and we are hesitant for transplant and do not have family donor. Home Dialysis is new to me and never addressed .

My mother is a CKD patient and on dialysis for a year now. It becomes hard both on patient and family. We are pulling on.....is what we are with

My father's kidney point is 12.Which stage is this? Please tell me as soon as possible

Don't send me this stupid add anymore. You suck!

nice information

Watched video at 4pm est. Thank you Dr Racgel for these very useful information on caring for the kidneys. I'm a PKD patient and any info I can get is very helpful. Thank you so much. 😊

This is something creepy to watch at a sleepover

Bip

Rachel, Yah.... Yah..... Yah... EVERY damn question. Further irritation.... noisy clearing your excess saliva.... VERY very often.... and noisy, distracting... I do appreciate your video.... Thanks

first time I've seen a 40 minute ad

My father is at stage 3 i hope he doesn't go up

20 Year old with Castleman disease with kidney failure here. I was scared for the treatment. I saw this video before i started my dialysis and it helped me calm down. When i started the treatment it went somewhat wrong and i was feeling sick and vomiting every time they started the machine within 10 minutes. So i was hooked up to an ICU dialysis machine which took over double the time 8-10 hours. But eventually it got better and i managed the normal machine. Now a year later, my kidnes started to work again and my values are almost back to normal. Free healthcare in my country aswell was fantastic. Thank you for producing this video for me and for everyone.

Do your government do this before start to use vaccine's COVID?

nice

Uhhhhhhhhhhhhhhhhhhh

I needed to hear this !!!!

Thank you great recipe❤

nice information

I had it at age 3 and again at age 46 in May 2023.

Woww great

Gracias excelente explicación la Dra está muy bien preparada y sabe muy bien la materia de la anemia y toda la función del riñón La felicito

Q

I keep hearing that home dialysis is not for everyone. Please elaborate

This was impressive. 💃

Excellent explanation. Much thanks.

good stuff.

nice video

I have stage 3 gfr of 59

They don,t even tell you nothing until stage 3🤦🏽

I have just found out by viewing my medical notes but not been told by my doctor that I have stage 3 kidney disease, why would they not have told me

If you feel the need to have on hand some prepackaged foods, look at the "organic" brands. Majority do not have phosphates added. You still have to be careful of the sodium content though. While some have a lower sodium level, several have as much or more than other regular brands.

At 66yo, I added CrossFit to my 6k/day run, I also started supplementing with creatine and my eGFR/cre dropped from 86 to 48 (in 4 weeks) . EGFR/cys stable at 89.

Good evening everyone

🙏🙏🙏🙏🙏🙏

Dialysis patients and their families need to know that if they are on dialysis for more than 7 years they have a risk of getting kidney cancer. Drs. knowing this, don’t inform patients about it & don’t screen yearly their patient for kidney cancer. It's inhumane & despicable for the whole health system to act this way. These are human lives not a piece of paper that you can throw on a trash can & start all over. They took the live of my husband who was an incredible human being, best partner, outstanding husband. Despite of his condition he made the best everyday. He was on dialysis for 30 years. He tried all treatments of dialysis. He spoke in several conference for dialysis. First in the Baltimore area to be on home dialisys. But health system failed him tremendously. He complained about being out of breath, coughing and his nephrologist didn't bother to send him for tests to find out what was going on. So, for all kidney patients, you need to be your advocate. The health system is horrible. It's so sad to take advantage of patients. They are here to make money. He is the strongest man that I've ever met. I miss him tremendously.

These all potassium phosphorus calcium are imp for our body if we quit all how our body wil get them?? Energy levels get low

I had around 2 years of headache where doctors ignored and sent me home every time I visited. But the new doctor looked at my blood pressure it was high. After a month, they say that I have shrinking kidneys and hypertension. Kidney doctor scolded me that I had been ignoring my headache in years, and it caused me that, but he seemed to doubt when I said the truth that doctors send me home every time I visit. After years, they say that I have chronic kidney disease at stage 3, and it lasted years. Now I get feeling pain in my back every day in weeks.

Love your energy thank you for sharing your story.

This is very helpful to kidney patients. Thank you very much for your efforts!

How are there over 300,000 views and no comments?