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Forum topic by Dallas posted 05-14-2014 11:02 PM 2026 views 0 times favorited 62 replies Add to Favorites Watch
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Dallas

3047 posts in 1177 days


05-14-2014 11:02 PM

I told everyone about my little setback with being diagnosed with CHF, class III what ever that last part means.

About a week ago I gave my boss back the beautiful Craftsman tablesaw he gave me last winter. I added a Forrester blade, and a good fence, although I think the the original was much more accurate and repeatable.

It kind of brought home that I will probably never be ever do any wood working again in my life.

I still have2 guitar kits I need to do, one I just started. I want to build them for my sons, but right now I can’t even stay on task for 15 minutes.

The doctors won’t give me any information, although I probably won’t be here in 2017. That is gonna suck!

How in the world will I piss off all the people here and on face book?

Bottom line? I don’t feel sorry for myself. The wife is my best friend and takes good care of me. I have had a very good live and am looking forward to the next few years, and who knows, I may be here much longer to bother everyone here!

-- Improvise.... Adapt...... Overcome!


62 replies so far

View luv2learn's profile

luv2learn

1768 posts in 993 days


#1 posted 05-15-2014 12:01 AM

Live for today buddy, that is all you or any of us can do. Let tomorrow take care of itself, who knows it might hold some pleasant surprises for you and your family. Stay in touch!!

-- Lee - Northern idaho~"If the women don't find you handsome, at least they ought to find you handy"~ Red Green

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Monte Pittman

14599 posts in 1028 days


#2 posted 05-15-2014 12:08 AM

Sad to hear the diagnosis. The reality is however, none of us are guaranteed tomorrow. Make the best of today and then do the same tomorrow if it happens. Keep up the conversations sir. We’re here to talk.

-- Mother Nature created it, I just assemble it.

View distrbd's profile

distrbd

1203 posts in 1136 days


#3 posted 05-15-2014 12:24 AM

I had to search google for CHF,class III,and found out:
Patients with cardiac disease resulting in marked limitation of physical activity. They are comfortable at rest. Less than ordinary activity causes fatigue, palpitation, dyspnea or anginal pain

I’m lost for words,I just hope you keep on posting here and share your knowledge with the rest of us as always.

-- Ken from Ontario

View gfadvm's profile

gfadvm

11242 posts in 1380 days


#4 posted 05-15-2014 12:29 AM

Dallas, I am so sorry. My dad had CHF and it was no fun but he did find that oxygen supplementation allowed him to get out and take care of his pigeons which was a huge deal for him. We are here whenever you need to talk.

-- " I'll try to be nicer, if you'll try to be smarter" gfadvm

View Dallas's profile

Dallas

3047 posts in 1177 days


#5 posted 05-15-2014 01:04 AM

Thanks guys. It is all much appreciated.

Andy, Mom passed from CHF at 72. Her dad at 61, Her grand dad at 102? All from CHF. Great grampa smoked at least 2 packs of Camel straights a day. At 95 he would be out at round up with the branding iron.
I am still going to work on the guitar projects. It just feels like something I need to do.

Sitting here in my shop using my laptop I hear no noise, nothing productive going on.

This cannot be the future. Not creating or producing is so foreign to me I don’t think I can accept that.

Great Grampa ran a mill shop for many years. It was run with leather belts and tools you started and stopped by knocking the belts off the wooden pulleys.
Dad changed it to a Ford 330 Industrial engine. More power, less smell, and I didn’t have to go out every 15 minutes and feed the steam engine. (Small Fairbanks Morse).

I have to keep pushing and I need help to do that…... Force me, PM me, call me, anything. I just have no motivation now.

-- Improvise.... Adapt...... Overcome!

View Buckethead's profile

Buckethead

1932 posts in 559 days


#6 posted 05-15-2014 01:28 AM

I should say that I enjoy your contributions here. You have vast and unique experiences, and are willing to share. Even when the recipient displays obstenence, and stubbornness. I’m hoping you’ll keep posting, and who knows what tomorrow brings?

-- Bucket, any person that spends 10k on a bicycle is guaranteed to be a $@I almost started to like you. -bhog

View crank49's profile

crank49

3458 posts in 1661 days


#7 posted 05-15-2014 03:28 AM

In my understanding of CHF it is a situation where the valves do not close properly. The heart contracts and pushes blood through the valve like it is supposed to but then when the heart expands to pull new blood in for the next pump, the valve does not close and some of the old blood slips backward through the valve and reduces the efficiency of the pump. I thought this condition could be repaired by replacing the valves and with drugs that slow the speed of the contractions.
Well, at any rate there are some pretty miraculous things being done in medicine today. Hang in there and see what they come up with. My wife’s best friend was told she had 3 months to live; 8 years ago. We went out to eat dinner with her and her husband last Sunday.

-- Michael :-{| “If you tell a big enough lie and tell it frequently enough, it will be believed.” ― A H

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CFrye

3371 posts in 530 days


#8 posted 05-15-2014 03:49 AM

Dallas, you will continue to be in my prayers. Miracles do happen. Can be very frustrating when you ”are comfortable at rest.” and ”Less than ordinary activity causes fatigue, palpitation, dyspnea or anginal pain”
Please keep posting and sharing.

-- God bless, Candy

View Dallas's profile

Dallas

3047 posts in 1177 days


#9 posted 05-15-2014 01:53 PM

Thanks all! I ain’t gonna let it get me down, but it does get annoying. I have always been active and done a lot of work outdoors. I have loved our postion here at the park because I had the whole place that I could play with and keep up.

Michael, the congestive part of the CHF is that fluid builds up in the lungs and some of the other organs. The fluid in the lungs has a tendency to screw up the ability to transfer oxygen to the blood.
This means that even simple tasks become monumental. I like to go to town on Sunday every week but I haven’t been able to get to the city since I was in the hospital.
I cannot ride in a car for more than 30 minutes without an hour long break afterward. Just sitting in the same place for too long can make you feel as if you are drowning in the fluid.
The Dr’s. have me on beta blockers, ace inhibitors and diuretics, LOL, lots of diuretics. They make me get rid of the fluid but also I get dehydrated and get severe cramps. I feel like it’s a catch 22…. I drink water to stay hydrated and then pee out twice as much, so I drink more water, and pee more.

-- Improvise.... Adapt...... Overcome!

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hairy

2068 posts in 2222 days


#10 posted 05-15-2014 02:03 PM

I hope to be as strong as you when I get my bad news. Hang in there.

-- the last of Barret's Privateers...

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mrjinx007

1710 posts in 457 days


#11 posted 05-15-2014 02:13 PM

I am not sure if this is some thing you can fight rather than live with. At first it devastating because it screws up the whole routine you have been used to. Eventually, you will have a new routine and this condition will be a part of that routine. A little less activity, a little more time and some disruptions. I am so sorry that you have to go through this and bid you much, much peace.

-- earthartandfoods.com

View ohtimberwolf's profile

ohtimberwolf

283 posts in 1042 days


#12 posted 05-15-2014 03:00 PM

“This cannot be the future. Not creating or producing is so foreign to me I don’t think I can accept that.” It isn’t!!

We move from journey to journey and a change in how we affect the rest of the world is sort of expected.

I know of people in a rest home that have been very active all their life in various ways and then must accept that their role has changed. That role now is to be a support and encourager to those who are not as strong in their ability to hang in there and to help them be able to enjoy some peace of mind that they may not be experiencing.

We all can do something to help ourselves by helping others who are worse off than we are to ease them in their situation even if it is just kind words. It does something to the soul that nothing else can.

Pause for a moment and contemplate Mica 6:8 and Psalm 4:8.
John 14:27 is not an empty statement.

I was diagnosed with cancer several years ago. I don’t let cancer block my mind from the good thoughts. Still here !!! AND, so are you! larry

-- Used to be a barn cat, now a lap cat...

View a1Jim's profile

a1Jim

112326 posts in 2267 days


#13 posted 05-15-2014 03:05 PM

Dallas
I’m very sad to here this news. I think you are taking the best approach available to you in making each day the best you can .Even though your diagnoses is not good, you have some one who loves and cares for you your best friend. Many folks who have similar challenges have no one. My thoughts and prayers are with you and your family ,you have been nothing but a positive influence here on Ljs as I’m sure you have all your life. We are all here second by second your only difference is that someone is saying when your time is up,they could be way off ,hang in there and enjoy what you can .
May peace and joy always be with you the rest of your days.

-- http://artisticwoodstudio.com Custom furniture

View moke's profile

moke

518 posts in 1466 days


#14 posted 05-15-2014 05:17 PM

Dallas,
While I do not know much about CHF, my wife is an advanced parctice nurse specialist at the hospital here in town. All she does is see CHF patients. If you have questions you can PM me and I’ll forward it to her. Include your real life email and I’ll have her respond. She is awesome, I truly married up…if there are things you have questions about Im know she could/would help.
Mike

View MrRon's profile

MrRon

2867 posts in 1933 days


#15 posted 05-15-2014 05:42 PM

Dallas, At 79, I’ve started to slow down. I try to keep active, but I realize I can no longer do the things I used to do. Dirty Harry (Clint Eastwood) once said; “A man has to know his limitations”. I have found out what my limitations are and have adjusted my activities accordingly. Others may try to “push” you to maintain their pace, but I just ignore them and stick to whatever it is I’m doing at my own pace. One has to be relaxed and “laid back”. Don’t let others aggravate you or place demands on you….. Ron

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