Post-Intensive Care Syndrome (PICS) - Let's talk

Have you heard of Post-Intensive Care Syndrome? Sometimes it's called post ICU syndrome or PICS. PICS is defined as new or worse health problems after critical illness. These problems can affect your mind, body, thoughts, and/or feelings.

On Connect we would like to bring together people who have been affected by critical illness, and hopefully lighten the burden you bear. Patients and family members welcome.

Grab a cup of tea, or beverage of your choice, and let's chat. Why not start by introducing yourself?

Interested in more discussions like this? Go to the Intensive Care (ICU) Support Group.

@rosemarya

When I spent 5 days in ICU with sepsis, dehydration, acute kidney failure, and endstage liver disease, I was in and out of awareness. I was sometimes halfway aware of my surroundings, or activities happening to me and around me (only if I was moved, or a sudden noise). I have a partial recollection of the people and of the procedures. But I had no context time.
I have a vague recollection of being flown to another hospital. And arriving there. Although not in ICU, I was on the transplant floor at Mayo Methodist, and for the first few days, I continued to be in and out of awareness.
Later on, when I asked my husband, who is my caregiver, to explain to me what had occurred, I was shocked. So much had occurred that I didn't even realize. And on top of that , my memory of it, was all jumbled. For a while this really bothered me. But now, as time has passed, (8 years) it is not a concern to me, anymore.
Rosemary

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@rosemarya --There is not much known about TTp/aHUS, I have had tests done and they want to do more because it could potentially affect a new kidney. I have spoken with Dr's in Oklahoma who specialize in TTP and at the U of M. I am currently waiting for more labs and possibly genetic counseling . Noone really knows yet. These tests they do are not very " conclusive ".

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@rosemarya

When I spent 5 days in ICU with sepsis, dehydration, acute kidney failure, and endstage liver disease, I was in and out of awareness. I was sometimes halfway aware of my surroundings, or activities happening to me and around me (only if I was moved, or a sudden noise). I have a partial recollection of the people and of the procedures. But I had no context time.
I have a vague recollection of being flown to another hospital. And arriving there. Although not in ICU, I was on the transplant floor at Mayo Methodist, and for the first few days, I continued to be in and out of awareness.
Later on, when I asked my husband, who is my caregiver, to explain to me what had occurred, I was shocked. So much had occurred that I didn't even realize. And on top of that , my memory of it, was all jumbled. For a while this really bothered me. But now, as time has passed, (8 years) it is not a concern to me, anymore.
Rosemary

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@user_cha272278 Hello Dr. Ron:

I agree with @rosemarya that "Hanging on to hope is like a life preserver" is a great word picture. As you may have guessed, I'm a visual learner and if you can give me a picture of a concept I can understand it.

From your previous posts, I can see that you have found many "life preservers" since your health crises. Your wife, your medical team, friends your writing and probably many more.

Keep posting about hope as a "life preservers" we all need to be reminded of that!

Teresa

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@rosemarya

When I spent 5 days in ICU with sepsis, dehydration, acute kidney failure, and endstage liver disease, I was in and out of awareness. I was sometimes halfway aware of my surroundings, or activities happening to me and around me (only if I was moved, or a sudden noise). I have a partial recollection of the people and of the procedures. But I had no context time.
I have a vague recollection of being flown to another hospital. And arriving there. Although not in ICU, I was on the transplant floor at Mayo Methodist, and for the first few days, I continued to be in and out of awareness.
Later on, when I asked my husband, who is my caregiver, to explain to me what had occurred, I was shocked. So much had occurred that I didn't even realize. And on top of that , my memory of it, was all jumbled. For a while this really bothered me. But now, as time has passed, (8 years) it is not a concern to me, anymore.
Rosemary

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@beitel, Becky, I don't think it is possible, or even healthy, to block it out. But you can try to to think of positive or happy (like the miracle that you are alive, that you have a new kayak and all you want to discover...) It will be difficult for your loved ones, because they, also. were going thru it with you.
When I got my transplant, someone told him that we should celebrate the anniversary every year - like a birthday, or anniversary. For us that is a nice dinner somewhere. And it is always emotional, but it is a celebration for us.
If you have read some of the other posts in this PIC forum, you will have read of others who share your feelings of depression and also tears that just show up. Becky, there is no magic time fir it to go away. But it will get better as you move forward.

My suggestion is to try not to focus on the approach of 'that' day. Share with your counselor, maybe he/she has some ideas.

When are you planning to try that new kayak?

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@rosemarya

When I spent 5 days in ICU with sepsis, dehydration, acute kidney failure, and endstage liver disease, I was in and out of awareness. I was sometimes halfway aware of my surroundings, or activities happening to me and around me (only if I was moved, or a sudden noise). I have a partial recollection of the people and of the procedures. But I had no context time.
I have a vague recollection of being flown to another hospital. And arriving there. Although not in ICU, I was on the transplant floor at Mayo Methodist, and for the first few days, I continued to be in and out of awareness.
Later on, when I asked my husband, who is my caregiver, to explain to me what had occurred, I was shocked. So much had occurred that I didn't even realize. And on top of that , my memory of it, was all jumbled. For a while this really bothered me. But now, as time has passed, (8 years) it is not a concern to me, anymore.
Rosemary

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Thank you for the insight. I tried my Kayak last week and it was amazing. I have been so busy dwelling on the anniversary of such a tragic thing instead of focusing on the celebration of life and healing. You really made a great point. Maybe it is something to discuss with my family also.

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@rosemarya

When I spent 5 days in ICU with sepsis, dehydration, acute kidney failure, and endstage liver disease, I was in and out of awareness. I was sometimes halfway aware of my surroundings, or activities happening to me and around me (only if I was moved, or a sudden noise). I have a partial recollection of the people and of the procedures. But I had no context time.
I have a vague recollection of being flown to another hospital. And arriving there. Although not in ICU, I was on the transplant floor at Mayo Methodist, and for the first few days, I continued to be in and out of awareness.
Later on, when I asked my husband, who is my caregiver, to explain to me what had occurred, I was shocked. So much had occurred that I didn't even realize. And on top of that , my memory of it, was all jumbled. For a while this really bothered me. But now, as time has passed, (8 years) it is not a concern to me, anymore.
Rosemary

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I went down Rouge River with. A kayak. Of course we had our rapids coach with us. Three day trip. Good food every night. They stop at lodges every night. You can choose a caping trip. I love rafting. My husband in his ,80s rafted. He went home happy.

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@rosemarya

When I spent 5 days in ICU with sepsis, dehydration, acute kidney failure, and endstage liver disease, I was in and out of awareness. I was sometimes halfway aware of my surroundings, or activities happening to me and around me (only if I was moved, or a sudden noise). I have a partial recollection of the people and of the procedures. But I had no context time.
I have a vague recollection of being flown to another hospital. And arriving there. Although not in ICU, I was on the transplant floor at Mayo Methodist, and for the first few days, I continued to be in and out of awareness.
Later on, when I asked my husband, who is my caregiver, to explain to me what had occurred, I was shocked. So much had occurred that I didn't even realize. And on top of that , my memory of it, was all jumbled. For a while this really bothered me. But now, as time has passed, (8 years) it is not a concern to me, anymore.
Rosemary

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@rosemarya , @beitel My transplant anniversary, my birthday and our wedding anniversary are all within three days of each other; so we were already celebrating two things, adding a third was no problem. To be honest, though, there was no celebrating the first few years because my health was so bad. Once I got my health under better control we could celebrate again.

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@rosemarya

When I spent 5 days in ICU with sepsis, dehydration, acute kidney failure, and endstage liver disease, I was in and out of awareness. I was sometimes halfway aware of my surroundings, or activities happening to me and around me (only if I was moved, or a sudden noise). I have a partial recollection of the people and of the procedures. But I had no context time.
I have a vague recollection of being flown to another hospital. And arriving there. Although not in ICU, I was on the transplant floor at Mayo Methodist, and for the first few days, I continued to be in and out of awareness.
Later on, when I asked my husband, who is my caregiver, to explain to me what had occurred, I was shocked. So much had occurred that I didn't even realize. And on top of that , my memory of it, was all jumbled. For a while this really bothered me. But now, as time has passed, (8 years) it is not a concern to me, anymore.
Rosemary

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Thank you so much. I have constructed a heartfelt message to help folks before during and after severe medical challenges that are life changing. Peacefully accepting a “new normal” can test one’s resiliency. The small message (attached) hopefully helps others.

After almost seven years of recovery (from a broken neck, 5 week coma, sepsis, MCI) the “lights in my mind” are turning on. I had acquired ADHD from the closed head TBI, which finally is clearing up.

I know there are many folks, less fortunate than I, and I have gained far more than I have given in terms of trying to “maintain “status quo” and let IT go. (“It” being non-life-supporting attitudes, behaviors and even toxic people. ).

I was in the brain and spinal cord ward, and met a veterinarian who was incredibly positive in spite of (or maybe because of) a spinal cord injury. I learned that physical disability does not have to diminish the human spirit of “doing unto others.”

My intent in all this is to payfoward, in some way, all the compassion and care showered upon me for weeks, months and years. At long last this Humpty Dumpy IS put together again, for a Happy Ending for Life. ( PS, don’t worry, the Attached “The seven year hope” message is only 500 words long). Dr Ron. .. Make Today Count. I look forward to your reflections of hope during troubled (but temporary) waters. THANKS for allowing me to share (and Learn) from Y’all.

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@rosemarya

When I spent 5 days in ICU with sepsis, dehydration, acute kidney failure, and endstage liver disease, I was in and out of awareness. I was sometimes halfway aware of my surroundings, or activities happening to me and around me (only if I was moved, or a sudden noise). I have a partial recollection of the people and of the procedures. But I had no context time.
I have a vague recollection of being flown to another hospital. And arriving there. Although not in ICU, I was on the transplant floor at Mayo Methodist, and for the first few days, I continued to be in and out of awareness.
Later on, when I asked my husband, who is my caregiver, to explain to me what had occurred, I was shocked. So much had occurred that I didn't even realize. And on top of that , my memory of it, was all jumbled. For a while this really bothered me. But now, as time has passed, (8 years) it is not a concern to me, anymore.
Rosemary

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@beitel I have a strong faith base and have practiced yoga and meditation for a long time. These things help me keep grounded and deal with whatever comes along in life. I also suffer from depression that cycles. My worst times are usually in the winter. I had so much trauma occur during the winter holidays that I feel ruined that time of year for me. I am confident that is what causes my depression to increase at that time of the year.
As for when your grief will change, only you will know. Every person has their own journey through grief and depression is usually part of grief. Some people bury it for years with business and a stoic demeanor. Other people cannot stop crying for months or years. I encourage you to: Schedule a "sad" time every day. Plan for at least 10 minutes where you just think about your grief. Journal during your "sad" time. It can be helpful to look back after a week, month or year to see how/if things have changed for you. And lastly, focus on meeting daily needs of food, clothing, personal hygiene, and making enough money to pay your monthly bills. Blessings for your future.

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@rosemarya

When I spent 5 days in ICU with sepsis, dehydration, acute kidney failure, and endstage liver disease, I was in and out of awareness. I was sometimes halfway aware of my surroundings, or activities happening to me and around me (only if I was moved, or a sudden noise). I have a partial recollection of the people and of the procedures. But I had no context time.
I have a vague recollection of being flown to another hospital. And arriving there. Although not in ICU, I was on the transplant floor at Mayo Methodist, and for the first few days, I continued to be in and out of awareness.
Later on, when I asked my husband, who is my caregiver, to explain to me what had occurred, I was shocked. So much had occurred that I didn't even realize. And on top of that , my memory of it, was all jumbled. For a while this really bothered me. But now, as time has passed, (8 years) it is not a concern to me, anymore.
Rosemary

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Thanks. I will try yoga. Down here in North Carolina they have goat yoga. Fortunately they are Pygmy goats. Where are you from. And don’t give up. Dr Ron

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@rosemarya

When I spent 5 days in ICU with sepsis, dehydration, acute kidney failure, and endstage liver disease, I was in and out of awareness. I was sometimes halfway aware of my surroundings, or activities happening to me and around me (only if I was moved, or a sudden noise). I have a partial recollection of the people and of the procedures. But I had no context time.
I have a vague recollection of being flown to another hospital. And arriving there. Although not in ICU, I was on the transplant floor at Mayo Methodist, and for the first few days, I continued to be in and out of awareness.
Later on, when I asked my husband, who is my caregiver, to explain to me what had occurred, I was shocked. So much had occurred that I didn't even realize. And on top of that , my memory of it, was all jumbled. For a while this really bothered me. But now, as time has passed, (8 years) it is not a concern to me, anymore.
Rosemary

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@2011panc I also have a strong faith which has grown tremendously in the last year. Little things hit me or remind me of my past and what led me here and my stomach sinks. Yesterday my youngest son,14 yrs old wanted to go for a walk. He took me to where my accident was, the tire marks and certain things are still there. I guess it is his way of trying to heal, he talked a lot about that day and his feelings since he was behind e on the 4-wheeler. It brought back a lot of different feelings. My other son , on the other hand, did not want to go but eventually did, for him he does not like to talk about any of it. I am still so confused about the events of that whole month. My depression also gets worse n the winter, especially Holidays. I pray a lot. I know I wonder off on my thoughts but I feel like my mind is 100 miles a minute. The more I try to relax the worse it gets. Is there a special kind of Yoga that you do? My counselor suggested reading a good book . Do you have any that you could suggest?

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