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you are so strong!❤

I just received a transplant 7 days ago I feel so unbelievably lucky

Hi just Wondering what is your creatinine level now?

How is the medicine for suppressant?

I'm two weeks into post transplant. Thankful to the donor :) thankful to God.

This hospital is where I was dialyzed & got my first kidney transplant during my childhood years. They were great! I'll never forget them. I am now 35 and going to be 36 with my 2nd kidney transplant because my first one was rejected after a while. California Medical Center in San Francisco did my second transplant they were great too! Thank you, God, for Doctors 🙏❤.

😮😮😊

I'm waiting on my time.

How are you feeling now can you do an update video I will be on dialysis soon hope to get a kidney transplant but I don’t react good prednisone

Well is insomnia a bad thing or a good thing. I guess it's all about perspective. I take dexamethasone (4mg a day) and it fights my fatigue like nothing in this world. It keeps me up and energized longer I can stay up until 12 pm and get up and still feel good and not extremely exhausted as with the fatigue. So, in my case, it's a blessing. Unless of course it's kicking your butt and you feel drained, exhausted or not very refreshed. Yeah that's a prob. But it has not done that in my case. Been taking it for about a month now. Doc did switch me over to prednisone. I hope to god it fights my fatigue the same. I'm dead without it! Good video and thanks for sharing! I have one question that I can't seem to get a solid answer. I believe you have to take it for the rest of your life for the kidney transplant. I was told that steroids will damage the liver and kidney and therefore I can not take it long term. Is this true or B.S.. I have an autoimmune disease and I know of people who have to take prednisone for life. But they seem okay. So I am a little confused. Anyone have a straight answer? I know dosage and long term use plays some role in the outcome. But if I were on a low dose long term. Consequences? Safe? Things to combat the risk? Thanks!

Thank you for this x

I had a transplant 8 years ago.My kidney koreaan won from point 9 to point 8 to point 7.How did this happen from god amen hallelujah

Fortunately, or unfortunately as the case may be, I had a cystoscopy ( male) twenty years before I had a stent placed. I did t even know I was getting a stent and didn’t find out until two days after a planned surgery. Anyway, knowing what I did about the excruciating, to me, experience in the past I had to find a urologist who would removed it under general anesthesia

I’m in the transplant list now and have been on there going on 6 years. I’m a little scared to get a kidney but I definitely want one. How long after getting your new kidney did u start peeing? Was it a weird feeling? Are u limited on thing you can drink or eat still? How long have u had your kidney? Did u name your kidney? I’ve picked out a name for my future kidney, it’s Tyrone 😂

Be aware of the antinutrients on the plant foods. Solanines are in Potatoes, Sulforaphane in Cruciferous. The list goes on and on. Sulforaphane is called an antioxidant, no it is not, not for humans. Its Oxadative forcing the body to defend itself so the body upregulates its own antioxdant production such as Glutathione! Sulphoraphane compound is claimed as anti-cancerous. Not it is not, it its however used to destroy Cells, it does not target cancer cells, it destroys All Cells. Thats why its effective.

th-cam.com/video/Y0e-6vZ7u9s/w-d-xo.htmlsi=jzr5znw4N93vyosk Which bloods does your renal specialist check? Is PTH checked? Also pure Taurine 1g at night is a good start. It has reactions with coffee so lighten up ob that and only drink during the morning if youre not a fast clearer of caffeine. Blood pressure meds might need lowering too because Taurine rqualise blood pressure by itself through osmosis. Another product to check out is Cerule Ultra StemEnhance promoted by Professor Bart Kay. This releases endogenous bone marrow daughter stem cells from your own bone marrow. Most important part is bioavailable nutrition because everything that needs maintanace IS fat or proteins. Something people have difficulty accepting when the medical doctrine is anti this. Biotin being protein. Collagen being protein and forming structure to bone.

Thanks for sharing this experiences ..

Everyone is different with their experience. I’m post transplant since February 2nd of this year and I had no pain during the surgery.

Thank you so much you made me cry I'm 14 and I've been doing dialysis for 2 years now and I'm on the transplant list waiting so thank you so much for your help ❤❤❤(here's a little update I got my transplant it's going on 3 weeks and I've been doing great with everything)Feb,29,24

I have transplanted I drink water and walking every day

Can you do an update now ? Is your hair better now ?

Tumor surgery coming up on my left kidney. Your story very helpful🧑‍🎄

Having a transplant 12/27th sister is a donor, Thank God

So inspiring. I had my kidney transplant 5 days ago from my sister (who donated stem cells for a bone marrow transplant 6 years ago) So far, so good. I will be discharged tomorrow and looking forward to LIFE. Don't ever give up!!!!!

Hello dear first of all so much courage to you and your family 😢 it's a long story and a tremendous transition of life, but then also with will power strong people can achieve greatness in life at any situation.😇 I'm from India and my sister is suffering from ESKD and we have to plan a kidney transplant for her. I know she'll be in pain at such a young age, i.e. 17 and I just hope for her for a speedy recovery after that and a peaceful and happy life. She is so brave like you. I just hope she'll be fine one day. I love her so much.😢😔🫂🥺💜💙 Btw loved your video🥲🙂💛

Thanks for sharing

I loved your kidney transplant journey. It made me cry. I haven’t got my kidney transplant yet. But I know Gods got this!! You are very blessed to have your mum give you her kidney. I will be praying for you and your family. Ty for posting

I now I praper this way transplant 😢😢

I have completed 8 years journey tq u also enjoy the life

I HHHAAATTTEEE this script!!! I don't want to spend the rest of my life worrying about my bones breaking while I'm trying to live out the rest of the barrowed time I have left. I'm a year and a half post kidney transplant and I made it here without becoming diabetic. I was on the machine for 16 and a half years. After transplant, I don't like the mood swings that I mostly keep to myself and the constant hunger. How can we curb that?! Now I'm also dealing with my foot being broken and taking forever to heal.

I had my kidney transplant last Sunday and I’m soooooo happy 😆

I got my transplant at UCLA 2020 almost 2 years now and counting.I’m happy to have my life back please you all on dialysis don’t give up I waited 3 and half.While on dialysis I was still workin I do my PD at home.With the most caring staff specially my nephrologist and RNs .

😢😢😢😢 very painful

I donated on 7/12. Very painful but one month later I’m feeling 80% better. Those first steps are the hardest. It gets easier each hour, each day and each week as a donor.

My fiance will have a kidney transplant this year 2023. Our good friend decided to be a donor. God bless him and thank your mom always she saved your life. God bless both of you.

The setup is long tbh

I am on my second transplant going on 11 years!!

Thank you for a wonderful video. I have been on hemodialysis for eight months and it is the most depressing thing I’ve ever experienced. I have been researching PD and your video has reassured me that my decision to go with PD is the right choice for me. Again, thank you and God bless.

You look very happy after you received your mother’s kidney. How is she now?

God bless you

Are you ok now.

We need all types of blood group kidney, patient

God is great all the time

That's awesome that your mom gave you the gift of life. I hope and pray that you and your family are doing well. I have been on dialysis since 2019 and it's brutal waiting for a deceased donor match is exhausting but I keep trying to think Positive but again thanks for your story it was very inspiring

Your videos are great

Be mindful of every detail. Including the type of catheter for peritoneal dialysis. I had no fistula !!!!! A PRESTERNAL Catheter. Not that thing in your tummy , it’s called a BATH CATH or PRESTERNAL CATH. I CANT TELL YOU ENOUGH how much better it is for PD. I hated hemo I never could handle it well. I got sick 🤢 everyday. I knew all my dialysis buddies. I never got depressed I was there to try to cheer people up. I pretended it was my job. But I went to PD and researched everything. That PRESTERNAL cath saved me !!!! I just tucked it in my bra. Not the tummy rubbing , or taping n pain. Please look into this. I now have had my daughters kidney 9 years. We’re both great. It was so long ago , except for the pills I forget ….weak stomach muscles. Being cut for transplant. But I wouldn’t trade that gift for anything. For your own good choose a non steroidal hospital. The steroids are not needed. !!!!!!! Mayo , Johns Hopkins and others are non steroidal. I did and have some major effects. Also since I went to PD I wouldn’t let anyone put a fistula in me. I’d of never used it. Remember check out PRESTERNAL cath y’all 💚💚💚💚💚

God bless you sister.❤

My transplant done 8 years

I had mine 1/13/23

I hoping to get on a transplant list, but my weight is too low. It's so hard to gain weight while on dialysis. I have one final test tomorrow