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Author Topic: No, Not ME, doc!  (Read 1317 times)
UkrainianTracksuit
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« Reply #25 on: March 09, 2020, 12:43:59 PM »

Does this make PT now Pea T? (Bad joke, I know, but peas are awesome. Peas on toast, but let's make sure this Pea T does not become toast!)
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PrimeTimer
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« Reply #26 on: March 09, 2020, 09:07:34 PM »

How are you doing today, PT?

I'm doing a little better, MM. Thanks for asking. Not much sleep last night tho because hubby was struggling with his own breathing. He's winded. A new tech infiltrated him twice so his Hemoglobin is down to 9  -lots of Epo now! And I am sure that having his wife on a ventilator was stressful. Was probably harder on him than it was on me (they had me on Fentanyl). He's having to do most all the chores at home, working and then dialysis. I feel terribly guilty that he is having to carry this load right now. So far, he's doing spectacular. I warned him about the increase in my Prednisone, very moody and of course, bloated. I don't care what I look like but I want to get better so I can do things and not be so much of a beached whale. Ooh yes...here comes the jokes about "Pea-T the Whale"....doh! 

Does this make PT now Pea T? (Bad joke, I know, but peas are awesome. Peas on toast, but let's make sure this Pea T does not become toast!)

Okay UT, but at least I am Pea-ing!
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Husband has ESRD with Type I Diabetes -Insulin Dependent.
I was his carepartner for home hemodialysis using Nxstage December 2013-July 2016.
He went back to doing in-center July 2016.
MooseMom
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« Reply #27 on: March 10, 2020, 07:46:19 AM »

I'm gllad to hear you're doing a bit better.  I know prednisone at higher doses can weird you out, but if it will help you get better in the long run, it will be worth it.

I like "Pea-T"!  Last night I was thinking "Prime Pea" because you're awesome, so I think we may be seeing both monikers used here on IHD!
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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."
cassandra
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When all else fails run in circles, shout loudly

« Reply #28 on: March 10, 2020, 11:06:46 AM »

I agree with MM  :cuddle;  keep improving girl  :flower;


Love to the both of you, 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
       still on waitinglist, still ok I think
PrimeTimer
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« Reply #29 on: May 20, 2020, 12:14:03 AM »

One moment we are okay, the next we are super-stressed. Having Sarcoidosis sucks but stressing over rent payments is almost worse. I have significant scarring on one lung and 2 calcified pulmonary lymph glands. Doctor mentioned sending me to be assessed for a lung transplant. I don't want one. Still on oxygen 24/7 but I'm breathing (no more ventilators in the picture). They added Methotrexate to my treatment. Still on high dose of Prednisone so we're having a lot of fun now. Pft...I'm dealing with the side effects. No biggie. Yeah, right. 

Meanwhile, hubby suddenly needed an artery in his leg scraped to clear a blockage. Whew! At least that went well! Was frightening but he really did okay. Unbelievable what he is going thru. His Hemoglobin is finally up to 11 but he's still winded. That and purple toes have to be dealt with next. The vascular doc wasn't concerned about his toes other than saying "no gangrene". OookayÖ.but purple toes on a diabetic is still scary and has to be dealt with. But oh, the rent! Up until last week and thanks to Covid-19 Stay-at-home orders hubby hasn't worked. His employer never officially laid him off so he didn't qualify for unemployment. He's back at work but like so many others, the piggy bank is running dry. Time to ask for help...from family? Sure, but not without very mean and nasty phone messages. In one message I was told to "get off my butt" and in another, this same family member said helping us made them feel like they were being raped. Wow. I don't know what to say to that. That one stung. So between both of us having medical conditions and stressed out over finances we get to deal with smart asses for "family".

Well, that's how these past couple months have gone. Just when you think it couldn't get any tougher...but we are both (still) determined to rise above all this and rebuild. Have to.
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Husband has ESRD with Type I Diabetes -Insulin Dependent.
I was his carepartner for home hemodialysis using Nxstage December 2013-July 2016.
He went back to doing in-center July 2016.
cassandra
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When all else fails run in circles, shout loudly

« Reply #30 on: May 20, 2020, 02:33:03 AM »

Jeeez PT what an awful situation. I wish I could help you, donít even know what to say. Just sending more coping-vibes to the both of you, and as always, lots of love, Cas


 :grouphug; :grouphug; :cuddle; :flower;
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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
       still on waitinglist, still ok I think
PrimeTimer
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« Reply #31 on: May 20, 2020, 09:35:04 PM »

Thanks for the coping vibes and love, Cas. I suppose I am venting but truthfully, I am also very exhausted from PROBLEMS. There are millions of people going thru their own stress and so I know we are no different. We really are in the same boat. Doesn't make it any easier tho. Every nite before bed I reflect on my day and try to find one good thing to be thankful for and surprisingly, there is always at least ONE good thing to be thankful for. Sometimes two. Sometimes three good things. Embracing hardship is not an easy thing nor attractive. I look and feel like hell but I am alive and fighting. I try to be strong. My husband tries to be strong. Together we are stronger. That is actually two good things!

Next battle is figuring out what the foot doctor can do for hubby. Vascular doc says it's not gangrene but it sure looks like it is. Scares the crap out of me. And his RLS is keeping us both up every nite. For some reason his meds aren't working. It's like sleeping in a combat zone, all the thrashing, tossing and turning and elbows flailing about. He usually ends up going out to the living room to sleep in his recliner so I can sleep. This routine is getting old. I miss him in our bed. And I feel terrible that he can't sleep. He's lost his appetite and 35 pounds these past few months. His Neph says he is malnourished. I haven't been able to cook like I use to so he's suffering. I know it's not my fault but I feel terrible. Sarcoidosis is sucking the life out of both me and my husband. It is affecting both of us. At first, it sounded like no big deal and that I would recover in due time. Now I am doing battle with it. Never imagined I'd be this sick. Never. I suppose that is how hubby felt when he had to start dialysis...Like it says in that old INXS song, "hard to believe we need a place called hell".
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Husband has ESRD with Type I Diabetes -Insulin Dependent.
I was his carepartner for home hemodialysis using Nxstage December 2013-July 2016.
He went back to doing in-center July 2016.
iolaire
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« Reply #32 on: May 21, 2020, 04:26:06 AM »

Sorry PrimeTimer.
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Transplant July 2017 from out of state deceased donor, waited three weeks the creatine to fall into expected range, dialysis December 2013 - July 2017.

Well on dialysis I traveled a lot and posted about international trips in the Dialysis: Traveling Tips and Stories section.
MooseMom
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« Reply #33 on: May 21, 2020, 02:50:04 PM »

Man, PT, I feel rather overwhelmed just READING about your predicament, so I can barely imagine what it must be like to LIVE it.  I am so sorry that there are so many stressors in your life right now. 

I can see why you'd be concerned about hubby's toes.  OK, so it's not gangrene, but it is still worrying. 

I have a feeling that even if you were to cook up a banquet, hubby would still be malnourished.  If he has lost his appetite, a banquet probably wouldn't be that appealing.

And you're right in that the fact that other people are having a rough time, but that doesn't make your own rough time any less rough.  I hope "venting" helps even just a little bit.

Perhaps you could post each morning which thing(s) your nighttime reverie revealed as something to be thankful for.

 :grouphug;
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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."
PrimeTimer
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« Reply #34 on: May 21, 2020, 06:02:44 PM »

Yes, MooseMom, venting does help. I think there are a lot of people that could be venting right now and they should. People should let it all out. Venting may not be a solution but bottling things up inside doesn't help and in fact, may actually hurt. My husband and I talk, talk, talk and we fight and then talk some more. But even then I still feel the need to vent and not just unload it all on him. These are hard times -for us all. But besides venting I want to see some good in each day. I want to hear myself acknowledge some goodness and to feel it. I want something to smile about. I need to bring my stress down a notch.

Thankfully, my husband was able to get an appt for tomorrow with the foot doctor. This was actually a nice surprise. Thought it would be a couple weeks but no, they will see him pretty much right away. So we are VERY thankful for THAT! And I am thankful for roof over our heads and food on the table. Made hubby take advantage of his appetite and talked him into eating a little more today. I am thankful for that, too. Who knows, maybe we will both sleep tonite. Or something close to it.

Thanks, MooseMom for being there! You just gave me even more to be thankful for!! 
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Husband has ESRD with Type I Diabetes -Insulin Dependent.
I was his carepartner for home hemodialysis using Nxstage December 2013-July 2016.
He went back to doing in-center July 2016.
MooseMom
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« Reply #35 on: May 23, 2020, 03:14:47 PM »

How was hubby's appointment with the foot doctor?  I'm glad to hear he was able to see him so quickly!

AND

Did the two of you sleep any better last night?  I know you're both exhausted.
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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."
PrimeTimer
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« Reply #36 on: May 23, 2020, 05:16:33 PM »

MooseMom: Slept better knowing he had an appt. for the next day but was not good news. The vascular doctor kept saying "no gangrene" but the foot doc says it is "dry" gangrene. Next week they are going to send him for an MRI to rule out osteomyelitis (bone infection). He was going to have an MRI yesterday but they sent the order to a place that is out of our network for the insurance. So now we start again on Monday. They do not think he will lose a leg but maybe one toe. I am so upset about this. I use to check his feet for him but at some point, he took over that duty. I cannot stress enough how important no, how "critical" it is for Diabetics to check their feet DAILY.
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Husband has ESRD with Type I Diabetes -Insulin Dependent.
I was his carepartner for home hemodialysis using Nxstage December 2013-July 2016.
He went back to doing in-center July 2016.
MooseMom
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« Reply #37 on: May 23, 2020, 08:15:34 PM »

I understand that many people with diabetes can suffer from poor circulation to the extremities and that it is therefore important to look after the feet.  I am sorry that the news was not better, and I am also very sorry that you are having to deal with healthcare providers who are "out of network".   Why would they send you someplace that was out of network?  Is it the only imaging place around, or do they have some machine that is super duper fantastic or something?

Keep us updated, OK?  You two are really going through the wars.   :cuddle;
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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."
PrimeTimer
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« Reply #38 on: May 23, 2020, 10:24:38 PM »

My husband told them that the imaging center they wanted to use was out of network but the nurse insisted they weren't. We should've made our own arrangements for them to fax the order to a center that is in-network. Because of covid-19 social distancing orders I wasn't allowed to go with hubby to the foot doctor but if I had...by the time I found out about them sending orders to the out-of-network center it was too late in the day to do anything about it. Really ticked me off. And of course hubby didn't have the list with him so had to wait til he got home. He's also not as assertive as I am. My god, man! Stand up and have a backbone, take charge!! Oh well...too late now. They're going to hear from me Monday morning. And they had better listen. I don't think they will want to further upset an already angry woman on Prednisone and Methotrexate. One rude nasty family member has already gotten a taste. I am not putting up with any crap these days.
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Husband has ESRD with Type I Diabetes -Insulin Dependent.
I was his carepartner for home hemodialysis using Nxstage December 2013-July 2016.
He went back to doing in-center July 2016.
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