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Author Topic: My First Youtube Appearance: I Share My Personal Journey  (Read 3538 times)
Cordelia
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« on: September 10, 2012, 05:05:47 AM »

My first appearance on Youtube speaking about my personal story/journey!      I spoke at the Gift Of Life Walk in my community yesterday.    I raised just over $1300!!!!            :bandance;

http://www.youtube.com/watch?v=PpiTsktPaow&feature=share



« Last Edit: September 10, 2012, 04:06:27 PM by Cordelia » Logged

Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
Sydnee
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« Reply #1 on: September 10, 2012, 01:51:14 PM »

It made me cry. ( I turn 38 next month)
I'm glad you doctors cared about the headache. My mother and her father both died of a brain aneurysm, I also have an aunt that almost died and had 6 repaired. Yet my dr told me it isn't important to have MRIs to check.

I wish they hadn't cut you off not sure how much I didn't get to see.  So is there a way for you to know whether you have dominant or recessive PKD. Not that it makes a difference to you but maybe your kids would benefit or their kids.

It's nice to see that there are people learning about this.   
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After a hard fight to not start I started dialysis 9/13
started on PD
hoping for home hemo starting to build a fistula 1/14
cause PKD diagnosed age 14

Wife to Ed (who started dialysis 1/12 and got his kidney 10/13)
Mother to Gehlan 18, Alison 16, Jonathan 12, and Evalynn 7. All still at home.
www.donate2benefit.webs.com
Cordelia
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« Reply #2 on: September 10, 2012, 04:03:29 PM »

It made me cry. ( I turn 38 next month)
I'm glad you doctors cared about the headache. My mother and her father both died of a brain aneurysm, I also have an aunt that almost died and had 6 repaired. Yet my dr told me it isn't important to have MRIs to check.

I wish they hadn't cut you off not sure how much I didn't get to see.  So is there a way for you to know whether you have dominant or recessive PKD. Not that it makes a difference to you but maybe your kids would benefit or their kids.

It's nice to see that there are people learning about this.   

Hi Syndee!          :grouphug;

I'm so sorry, I have the full version now. I'm not sure what happened, but I think it was cut short when it was uploaded. Anyways, it's all there now. I think almost half was originally cut out of it. 

Here's the link:

http://www.youtube.com/watch?v=PpiTsktPaow&feature=share


I have thought of possibly genetic counselling to find out which gene, but if anything, I'd be more curious to find out for my kids.

I'm so very sorry to hear about your parents and your Aunt.  I'd be seeking another opinion if I were you with regards to checking, since  you have so many family members who have died from that.   Can you ask another doctor and see what he/she says?

Thanks so much for watching my vid and        :thx;     for all your awesome compliments!      :thx;      I hope you can watch the rest.   :thumbup;      So sorry for any confusion         :cuddle;
« Last Edit: September 10, 2012, 04:05:52 PM by Cordelia » Logged

Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
Sydnee
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« Reply #3 on: September 10, 2012, 05:52:10 PM »

Lori,
I watched the whole thing. you are so much more positive than I am. Maybe some day I will be too.
In my earlier post I should have written my mother and grandfather (her father) spooky part they both died at 53 years old. I did convince my dr to order the MRI after months of talking.  Seeing a different Dr would require me to go to a different state and travel and additional 1 1/2 hours. So I was glad that I convinced him. Thou he couldn't have chosen a worse time to retire. Ed and I met the new dr went the decided to start Ed on dialysis and admit him to the hospital.
How old are your kids now 12 or 13 and how old is your son?
Sydnee
Logged

After a hard fight to not start I started dialysis 9/13
started on PD
hoping for home hemo starting to build a fistula 1/14
cause PKD diagnosed age 14

Wife to Ed (who started dialysis 1/12 and got his kidney 10/13)
Mother to Gehlan 18, Alison 16, Jonathan 12, and Evalynn 7. All still at home.
www.donate2benefit.webs.com
Cordelia
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Posts: 2012


« Reply #4 on: September 11, 2012, 12:37:26 PM »

Lori,
I watched the whole thing. you are so much more positive than I am. Maybe some day I will be too.
In my earlier post I should have written my mother and grandfather (her father) spooky part they both died at 53 years old. I did convince my dr to order the MRI after months of talking.  Seeing a different Dr would require me to go to a different state and travel and additional 1 1/2 hours. So I was glad that I convinced him. Thou he couldn't have chosen a worse time to retire. Ed and I met the new dr went the decided to start Ed on dialysis and admit him to the hospital.
How old are your kids now 12 or 13 and how old is your son?
Sydnee

 :cuddle;       :cuddle;     Sydnee.  Thanks for your sweet words!  I always figure there are people worse off than me.  I'm pretty lucky, I have no other health issues, well, other than Arthur! LOL
But, I don't have diabetes and I don't have cancer. I'm very lucky, and thankful.

I'm so glad you convinced your doctor!! Wow, I can't imagine driving all that distance. The longest I ever had to drive for treatment was about 40 mins. Now, my hospital is right behind my house---you can't get any closer than that!!

My twin daughters are 13 and my son is 11.

I'm so glad you were able to watch the whole video. Not sure what happened why it didn't all upload the first time.
Logged

Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
mcclane
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« Reply #5 on: September 11, 2012, 02:17:53 PM »

You touched on many issues I dealt with :

- getting used to a 'new' you.  Before any dialysis you can do what you want, whenever you want, on dialysis your life is scheduled around dialysis.
- fairness.  I don't drink, smoke, (not going to go as far as eating right  :rofl; ), so I thought it was unfair that dialysis was part of my life as well.
- renal diet, that took some getting used to, after indulging on items like big macs, kfc, switching to something that is low sodium and watching phosphorous was a real change.

Wow, 2 hours to death, that is way too close to comfort.  I'm glad that you're up and walking now, and prey that Oct. will bring good news.  :bow;
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MooseMom
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« Reply #6 on: September 11, 2012, 03:55:14 PM »

Very, very poignant.  Made me cry, too. :cuddle;  Thank you for sharing this with the world.  It's important.
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"Eggs are so inadequate, don't you think?  I mean, they ought to be able to become anything, but instead you always get a chicken.  Or a duck.  Or whatever they're programmed to be.  You never get anything interesting, like regret, or the middle of last week."
Cordelia
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« Reply #7 on: September 12, 2012, 04:09:44 AM »

You touched on many issues I dealt with :

- getting used to a 'new' you.  Before any dialysis you can do what you want, whenever you want, on dialysis your life is scheduled around dialysis.
- fairness.  I don't drink, smoke, (not going to go as far as eating right  :rofl; ), so I thought it was unfair that dialysis was part of my life as well.
- renal diet, that took some getting used to, after indulging on items like big macs, kfc, switching to something that is low sodium and watching phosphorous was a real change.

Wow, 2 hours to death, that is way too close to comfort.  I'm glad that you're up and walking now, and prey that Oct. will bring good news.  :bow;

 :thx;           :cuddle;      Mcclane

You are so right          :thumbup;   . Before, never having to give second thought with what I was eating, having to change, everything!  I hear you !!         Having to get used to it, took time! 

Thanks for your best wishes for next month.          :cuddle;     Fingers and toes crossed that they will find a match for me!         :thumbup;
Logged

Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
Cordelia
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Gender: Female
Posts: 2012


« Reply #8 on: September 12, 2012, 04:11:29 AM »

Very, very poignant.  Made me cry, too. :cuddle;  Thank you for sharing this with the world.  It's important.

 :thx;        :cuddle;       MM

Thank you so very much for your compliments!       :grouphug;           :thx;

I will keep on speaking, I'm finding I really enjoy it!     :thumbup;    Thanks so very much for watching and posting your thoughts        :cuddle;          :thx;
Logged

Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
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