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Author Topic: Where is everyone?  (Read 14336 times)
jeannea
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« on: November 01, 2014, 09:23:34 AM »

So many of our regular commenters have gone missing. Did they get better and move on? Did they die? Did we bore them or were we mean to them?

I guess I've become so tired of the meanness on the Facebook version of this board. I worry we have driven members away.
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kristina
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« Reply #1 on: November 01, 2014, 11:48:00 AM »

That is very interesting jeannea. I was wondering about the same question...

There are quite a few IHD-members who had a transplant and now we hardly hear anything from them anymore...
I was wondering whether their transplant has made them independent again and they are very busy to continue with their careers?
... Or they continue after the transplant with their “old life”, as it was before kidney failure and dialysis
and they don’t want to be reminded of their dialysis days too often anymore?

I do hope they are doing well and I would love to hear from them sometimes...  :waving;
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Bach was no pioneer; his style was not influenced by any past or contemporary century.
  He was completion and fulfillment in itself, like a meteor which follows its own path.
                                        -   Robert Schumann  -

                                          ...  Oportet Vivere ...
obsidianom
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« Reply #2 on: November 01, 2014, 12:36:43 PM »

I have noticed a big drop off here over the past few months too.  There are a lot of people over on facebook. I dont like that as much. I prefer this .
I still think we have a lot to offer here. 
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My wife is the most important person in my life. Dialysis is an honor to do for her.
NxStage since June 2012 .
When not doing dialysis I am a physician ,for over 25 years now(not a nephrologist)

Any posting here should be used for informational purposes only . Talk to your own doctor about treatment decisions.
cassandra
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When all else fails run in circles, shout loudly

« Reply #3 on: November 01, 2014, 12:42:39 PM »

I'm actually getting worried. Like I miss Cariad, who was unlikely to go on FB, and has her transplant a long time.
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I started out with nothing and I still have most of it left

1983 high proteinloss in urine, chemo, stroke,coma, dialysis
1984 double nephrectomy
1985 transplant from dad
1998 lost dads kidney, start PD
2003 peritineum burst, back to hemo
2012 start Nxstage home hemo
2020 start Gambro AK96

       still on waitinglist, still ok I think
MooseMom
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« Reply #4 on: November 01, 2014, 03:31:37 PM »

For what it's worth, I'm still here but don't post unless I have something worthwhile to contribute to either pre-dialysis or transplant members of IHD.  So far my tx is doing well and I've had no problems, so I've not had any reason to post questions.

I've spent quite a while visiting friends and family in London so haven't been online very much.

I've never been to the IHD FB page.  Does it differ much from this site?
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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."
SooMK
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« Reply #5 on: November 01, 2014, 03:40:24 PM »

I've been missing the people I have come to think of as "regulars" too. So glad to see you here MooseMom. It also seems like there's just fewer postings in general lately. I briefly checked out the FB page but I don't care for the format.
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SooMK
Diagnosed with Uromodulin Kidney Disease (ADTKD/UMOD) 2009
Transplant from my wonderful friend, April 2014
Volunteering with Rare Kidney Disease Foundation 2022. rarekidney.org
Focused on treatment and cure for ADTKD/UMOD and MUC1 mutations.
Joe
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« Reply #6 on: November 01, 2014, 04:19:48 PM »

I'm kind of in the same space as MM, I'm cruising the boards regularly, but don't always respond unless I feel that i have something different to add. I will try to be better about contributing to the overall community. My transplant is doing very well, I have my 1 year clinic appointment on the 10th of November. My donor had hers 2 weeks ago and everything is going very well with her, thank heaven.
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Live simply. Love generously. Care deeply. Speak kindly.
Leave the rest to God...
Jean
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« Reply #7 on: November 01, 2014, 04:21:59 PM »

I agree, the FB website is not to my liking at all. I like IHD much better. I will always wonder what happened to Kickstart and YL Guy and others, too. Wish we did not have to have our chat room turned off, thanks to the people who cant control themselves. Oh well, this is still the best.
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One day at a time, thats all I can do.
PrimeTimer
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« Reply #8 on: November 01, 2014, 06:02:35 PM »

I'm kind of in the same space as MM, I'm cruising the boards regularly, but don't always respond unless I feel that i have something different to add. I will try to be better about contributing to the overall community. My transplant is doing very well, I have my 1 year clinic appointment on the 10th of November. My donor had hers 2 weeks ago and everything is going very well with her, thank heaven.
Congrats on your (very soon-to-be) first year anniversary of your transplant! Hope you post about it and that it is all good news.

This is an example of why I like this site so much. It is BY FAR the MOST informative and the only reason why it is, is because people are willing to share their experiences. Thanks to everyone!
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Husband had ESRD with Type I Diabetes -Insulin Dependent.
I was his care-partner for home hemodialysis using Nxstage December 2013-July 2016.
He went back to doing in-center July 2016.
After more than 150 days of being hospitalized with complications from Diabetes, my beloved husband's heart stopped and he passed away 06-08-21. He was only 63.
del
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del and willowtreewren meet

« Reply #9 on: November 01, 2014, 07:02:56 PM »

I'm here too but don't post often!! :beer1;
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Don't take your organs to heaven.  Heaven knows we need them here.
okarol
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« Reply #10 on: November 01, 2014, 07:05:19 PM »

I sometimes send a PM to people I haven't seen post, I am sure they'd like to know they are being thought of.
I should update Jenna's status, will find my thread and add to it.
 :thx;  :waving;
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
kitkatz
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« Reply #11 on: November 01, 2014, 07:08:22 PM »

I find the facebeook IHD.com site to be full of people who are mean to one another, so not a whole lot of commenting over there. I think it may send the wrong ideas about the home site being supportive.  It worries me that people are not coming over the the main site.  I have always found this site to be very supportive when I needed it.  God knows I have had a busy two months so far so I have not been online too often to post.  With a 50th high school reunion for Victor and two weddings to get through, I have traveled to three states.  I want IHD.com to flourish and be as strong as Epoman wanted it to be.  It takes the entire community to make this site be successful. 
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lifenotonthelist.com

Ivanova: "Old Egyptian blessing: May God stand between you and harm in all the empty places you must walk." Babylon 5

Remember your present situation is not your final destination.

Take it one day, one hour, one minute, one second at a time.

"If we don't find a way out of this soon, I'm gonna lose it. Lose it... It means go crazy, nuts, insane, bonzo, no longer in possession of ones faculties, three fries short of a Happy Meal, wacko!" Jack O'Neill - SG-1
PrimeTimer
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« Reply #12 on: November 01, 2014, 07:25:58 PM »

I dunno. Maybe we should send Darthvader to "Alert all commands and calculate every possible destination along their last known trajectory..."  :P
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Husband had ESRD with Type I Diabetes -Insulin Dependent.
I was his care-partner for home hemodialysis using Nxstage December 2013-July 2016.
He went back to doing in-center July 2016.
After more than 150 days of being hospitalized with complications from Diabetes, my beloved husband's heart stopped and he passed away 06-08-21. He was only 63.
del
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del and willowtreewren meet

« Reply #13 on: November 02, 2014, 06:37:40 AM »

I don't like the facebook site much either!!  It does seem like more people are posting there though.  I am guilty of reading posts but not taking the time to respond on this site (don't post on the facebook site at all or even read it much). 
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Don't take your organs to heaven.  Heaven knows we need them here.
Rerun
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« Reply #14 on: November 02, 2014, 06:38:43 AM »

Because this site does not require Registration to lurk we have a LOT of "Guests" on all the time who get information.  Right now we have 60 guests and 4 members on the site.  If no one else EVER posted but this site remained up and running it would be a wealth of information to someone just starting dialysis or wondering about a transplant or interested in NxStage.  That is what Epoman wanted.  We also have members who have never posted.... shy I guess. 

This is still the best site ever!         :thumbup;  :grouphug;
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Razman
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« Reply #15 on: November 02, 2014, 08:47:50 AM »

I'm still around a look almost everyday but I don't log on ( I know I'm bad ).   Look on Facebook as well.  My kidney's are 'hanging in' and if I can keep the loss to be the same rate I could last a long time.  I must keep my protein , phosphorus and potassium and sodium very low and and I have to watch what I eat but it is worth it.  I don't know if I could ever handle dialysis.   Anyone who can is a hero.
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jeannea
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« Reply #16 on: November 02, 2014, 10:44:14 AM »

Good to hear from all of you. (I was wondering about you MooseMom.) I had tried to comment on the FB version but so many are mean and nasty. I worry it makes people think we're the same over here. Then one of the new moderators over there posted that it wasn't a support site. Weird.

This site was amazingly helpful when I started dialysis. I'm really glad it's here. Rerun, you're right about the info being here to read even if people don't post.
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talker
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« Reply #17 on: November 02, 2014, 01:39:46 PM »

So many of our regular commenters have gone missing. Did they get better and move on? Did they die? Did we bore them or were we mean to them?

I guess I've become so tired of the meanness on the Facebook version of this board. I worry we have driven members away.
Along similar lines of (regards this new Topic here) thoughts, was:

http://ihatedialysis.com/forum/index.php?topic=18315.msg488079#msg488079

While I'm a relative newbie here, have really spent time reading the many posts here.

Now that the door to further thoughts has been opened, and the risk of being  pilloried for the saying, here goes:
Had noticed a number of trends taking place here.
While 'some' response comments here, are not intended to 'hurt', many do just that.
No, not just 'the thin' skinned, sensitive, folks.
Have detected sarcasms and what appears as downright cliquishness , in some instances.
I may be the only one with this perception.
Granted, it may not be by design that these things happen, yet over the long haul certain 'perceptions' did come to the fore.
Realized if I didn't like it, I should just move on.

Now, don't misconstrue what is being said here.
There are vast amounts of valuable dialysis and other experience's listed.

Great.

BUT...........

Yes, I've noticed, that I've throttled down my normal enthusiasm, and expectations doing any posts here.
Why!
Well, had to dig down deep, and as stated above, certain 'little' things, kept causing me to reword what was going to be posted. Spontaneity was gone.
So I went more toward the 'games', with very little responding to posed Topic questions.
Did read, way back in this forums time, that religious / spiritual type posts, caused some problems.
Did do a few posts here with my usual style, but soon dropped back to highly rewording the way my words came out.
The joy of responding with positive hopes, and posting my way was missing. 
Yes, do realize it was self imposed.

Bares repeating:
               Now, don't misconstrue what is being said here.
      There are vast amounts of valuable dialysis and other experience's listed.

So here I am.
Yes, is a fine line between fact, fiction, fantasy, myth, and engineered deception.
What might be part of the solution!
Well, I endeavor to NOT rain on anyone's parade by my choice of words.
One can be gentle, as opposed to harsh, when voicing an opposing view point.
Do like to toss in a higher Source at work, even in the face of not fully understanding the 'why' of it all.
Regardless, will not enter into any of the usual 'my pa can whip your pa', endless back and forth battles, that happen under these kind of forum circumstances.

What next! Not sure at this point.
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Be Well

"Wabi-sabi nurtures the authentic by acknowledging three simple realities: nothing lasts, nothing is finished, and nothing is perfect."

Don't ever give up hope, expect a miracle, pray as if you were going to die the next moment in time, but live life as if you were going to live forever."

A wise man once said, "Yesterday's the past, tomorrow's the future, but today is a gift. That's why it's called the present."
MooseMom
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« Reply #18 on: November 02, 2014, 01:56:18 PM »

I had tried to comment on the FB version but so many are mean and nasty. I worry it makes people think we're the same over here. Then one of the new moderators over there posted that it wasn't a support site. Weird.


There is something about FB that seems to bring out the worst in people.  I've withdrawn from all FB kidney support sites as a result.  IHD's website is the only social media site in which I participate with any regularity.

I don't tend to log in often, but I do read fairly often as there are certain people here I have "known" for quite a while or who may be in the same situation as I am in; I like to keep tabs on those particular members.

It doesn't help that the email notification of PMs function no longer works.  If I get a PM, I won't know about it for months!
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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."
monrein
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Might as well smile

« Reply #19 on: November 02, 2014, 03:35:04 PM »

I too check in here pretty regularly and feel somewhat guilty, although that is too strong a word for it, that I contribute way way less than I did before when I was on dialysis. Quite honestly it is because I don't spend as much time on the computer. I check in but then I go. I'm one of the very lucky ones for whom life is really good with a transplant and my energy gives me a whole new active life that I'm very aware could disappear, poof, just like it did before and I don't want to miss a moment of doing things. As for the Facebook version, I feel that one never really gets to know people there, kind of superficial and frankly often quite weird.
I do think of everyone here very often, care just as much as I always did and also know that when we are not feeling great it can be hard to hear about other people doing what we would like to be able to do. I wish I were a better typist so then I could whip off quick responses to some of the posters that I feel I could contribute something to be of help to them.
I do see a fair number of people on regular Facebook so know what's going on with them a bit there.
This site remains the best for in depth support and information.
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Pyelonephritis (began at 8 mos old)
Home haemo 1980-1985 (self-cannulated with 15 gauge sharps)
Cadaveric transplant 1985
New upper-arm fistula April 2008
Uldall-Cook catheter inserted May 2008
Haemo-dialysis, self care unit June 2008
(2 1/2 hours X 5 weekly)
Self-cannulated, 15 gauge blunts, buttonholes.
Living donor transplant (sister-in law Kathy) Feb. 2009
First failed kidney transplant removed Apr.  2009
Second trx doing great so far...all lab values in normal ranges
cassandra
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When all else fails run in circles, shout loudly

« Reply #20 on: November 02, 2014, 03:51:12 PM »

MM, Monrein, Del so nice to hear from you.

Love, Cas
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I started out with nothing and I still have most of it left

1983 high proteinloss in urine, chemo, stroke,coma, dialysis
1984 double nephrectomy
1985 transplant from dad
1998 lost dads kidney, start PD
2003 peritineum burst, back to hemo
2012 start Nxstage home hemo
2020 start Gambro AK96

       still on waitinglist, still ok I think
kristina
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« Reply #21 on: November 03, 2014, 01:01:01 PM »

I'm still around a look almost everyday but I don't log on ( I know I'm bad ).   Look on Facebook as well.  My kidney's are 'hanging in' and if I can keep the loss to be the same rate I could last a long time.  I must keep my protein , phosphorus and potassium and sodium very low and and I have to watch what I eat but it is worth it.  I don't know if I could ever handle dialysis.   Anyone who can is a hero.

Hello Razman, good to hear from you and I am glad that your kidneys still serve you well ...
I don't quite know, how I shall be able to handle dialysis when it comes to it and I do hope for the best...
I send you my best wishes and good luck from Kristina.
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Bach was no pioneer; his style was not influenced by any past or contemporary century.
  He was completion and fulfillment in itself, like a meteor which follows its own path.
                                        -   Robert Schumann  -

                                          ...  Oportet Vivere ...
kristina
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« Reply #22 on: November 03, 2014, 01:08:19 PM »

I am very glad to read that Joe, Del, MM and monrein are doing well.
It is good to hear from you,
best wishes from Kristina.
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Bach was no pioneer; his style was not influenced by any past or contemporary century.
  He was completion and fulfillment in itself, like a meteor which follows its own path.
                                        -   Robert Schumann  -

                                          ...  Oportet Vivere ...
MooseMom
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« Reply #23 on: November 03, 2014, 01:10:08 PM »

What monrein said...
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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."
KarenInWA
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« Reply #24 on: November 03, 2014, 07:24:13 PM »

Like some of the others on here, I visit here almost daily,  but don't respond often. Maybe I should change that. November 23rd marks 3 years for me and my kidney, Lynette. I go in this Wednesday for my 3-yr post-op visit. My kidney is still hanging in there after being permanently injured by a biopsy less than 4 months after transplant. My GFR is anywhere from 15-17, my creatinine is anywhere from 3.0 - 3.3. I work FT, live a normal life, and faithfully take my meds. I admit, I feel like I did in my "normal" days. I like to travel when I can, take advantage of opportunities when I can (like to go to a show or a concert). I have been back on the list since last July, but am doing very good otherwise.

KarenInWA
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1996 - Diagnosed with Proteinuria
2000 - Started seeing nephrologist on regular basis
Mar 2010 - Started Aranesp shots - well into CKD4
Dec 1, 2010 - Transplant Eval Appt - Listed on Feb 10, 2012
Apr 18, 2011 - Had fistula placed at GFR 8
April 20, 2011 - Had chest cath placed, GFR 6
April 22, 2011 - Started in-center HD. Continued to work FT and still went out and did things: live theater, concerts, spend time with friends, dine out, etc
May 2011 - My Wonderful Donor offered to get tested!
Oct 2011  - My Wonderful Donor was approved for surgery!
November 23, 2011 - Live-Donor Transplant (Lynette the Kidney gets a new home!)
April 3, 2012 - Routine Post-Tx Biopsy (creatinine went up just a little, from 1.4 to 1.7)
April 7, 2012 - ER admit to hospital, emergency surgery to remove large hematoma caused by biopsy
April 8, 2012 - In hospital dialysis with 2 units of blood
Now: On the mend, getting better! New Goal: No more in-patient hospital stays! More travel and life adventures!
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