patience

PLIGHT

If you have made it this far, you are wondering what in the heck this subject heading is about. Sure, I made it obscure, but after the past half of a year of watching my husband and seeing what is going on with his health, I had to comment.

After six years of living with a limb salvage patient suffering with pancytopenia and a hot mess combo of more.., I have noticed a pattern of good days and bad. Like most people dealing with chronic pain, they can present better to friends and family for a few days and then after that, their resources are gone and boom! Mic drop.  Nothing left, just bed or couch-bound.

Six years of using a cane on his dominant arm to compensate for his bad leg when it collapses when he walks has taken a toll. It’s so sore it keeps him awake and uncomfortable past the pain relief he uses for his back and limb salvage in his leg.  The twisting way he has to walk when he doesn’t wear the uncomfortable brace lurches his hip in a way they aren’t meant to twist. Degeneration is happening.

He has tried cortisone in his shoulder joint and it was as if he got shot up with water. I have had them in the past for my own health issues and they provided help, but for some reason my shoulder has been resistant to any sort of change too.

On a positive note, I had RF Ablation on both of my hips over 5 months ago and the deep bone pain is gone. I wish I could get my husband to try it as I hardly have to use any sort of Tylenol or anything to help with the aches! To me, it is as if I had received a gift from God.

The past few years have made me very aware of my health and how much I need to take care of myself for the rest of my family. If you were suffering from anything, wouldn’t you get it taken care of or try to get yourself in as best of a way of feeling better as you could? Why would you want to make your family suffer in watching you endure constant suffering?? There are other things that can be done to help chronic pain such as RF Ablation. It has helped me so much. I see reports all of the time about HBOT (Hyperbaric Oxygen Therapy) and how much it helps physical and mental issues. Also, there is a new shot that goes in the Ganglion nerve in the neck that helps reduce the symptoms of PTSD right away.

When do you stop researching as a caregiver and when do you push and how do you know the difference? I recognize it as poking a literal bear. Make a recommendation and then gingerly tap dance back to my corner.

So what do you do?? Any of you veteran caregivers of veterans have any advice?

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When do you stop?

Back in January, I started a support group for fellow wives of wounded soldiers in the Austin, Texas area. When I first started it, I was unsure how it was going to work out and worried that I might not be ready for something like this. It is hard to take on projects when your soldier does not allow you to get your 7 or 8 hours of sleep in one straight block. At my old age, I am not so able to thrive without rest. Funny how I took that for granted. I used to go one whole day without sleep when I had my own business. Talk about drive. I am still driven, just in other ways now.

Back to the group- I have found it to be one of the best things I have ever done. It has helped me a lot and I have seen where it has been useful for some of the other ladies, too. There is room for growth and I have big plans for it. I am so happy that others in similar situations don’t feel as alone anymore. It is something I am very glad I did. I get to hear about successes first hand from others trying different methods on fixing their husbands.

So, here is a big question about drive, research, and pushing. For all of you with wounded soldiers at home suffering with TBI (Traumatic Brain Injury), PTSD (Post Traumatic Stress Disorder), and other debilitating health issues, when is enough enough? I can’t seem to stop researching the latest and newest methods to help restore cognitive function. I am always googleing TBI, PTSD to see if there are new strategies in helping to remedy the side effects. Through one of my friend’s blogs, I see there are injections that are being given to soldiers suffering with PTSD and that they do help a lot on reducing anxiety. However they have to be repeated every 3-4 months. To get the shot, you have to go to the clinic, which is far from here. So my hubby would have to endure the painful journey of getting there as well as receiving the injection, which would be another kind of pain. When I started talking to him about it as I got excited when I saw Kristle’s blog, he said he was not interested.

What? You are not interested? You like having PTSD? You like having the nightmares that make you literally sweat out a gallon of sweat each night and have the flashbacks? You like waking up sick to your stomach when you experience one of your many horrible wartime experiences? How can you not want to get rid of this? How can you not want to try something new to get it eliminated?

I got upset. I thought WTF- why am I doing all of this research to help him regain his short term memory issues and other cognitive deficits that really frustrate him if he does not even want to try something that has a documented success rate?

He won’t even try acupuncture and I have many wives tell me how much it has helped their soldiers with pain and also some of their anxiety. Anxiety is the huge feeding pool which fuels PTSD. This is not fair. I hear about all sorts of new treatments and things to try and he won’t even consider it.

What do you ladies do? I am frustrated. I don’t want things to be like this for the rest of our life. I want him to have fulfillment from what he does and to feel good about himself again. I want him to one day wake up without the chronic pain that knocks him down and makes him sick to his stomach.

Is that too much to ask for? Do I just stop and give up?

When I look at my husband, who is still young at age 41 and has a life left in front of him- I can’t imagine him not trying something to help him feel more like he used to. Would he want to spend the next 25-30 years suffering with chronic pain? Would he want to keep going and keep the blinders on to alternative treatments around him?

Can I just stop and let him control what he tries next? Can I let go of this?