Friday, May 19, 2017

So...I was in the hospital

Patients with multiple sclerosis often experience hospitalization over the course of their lives. Last month, I was hospitalized for a second time. I went to the ER with shortness of breath. I went through a myriad of tests in the ER until I had a CT scan of my chest. After my CT, I was immediately whisked off to the ICU. It turned out that I had bilateral pulmonary embolism (PE). A PE is a blockage of an artery in the lungs by a blood clot that has traveled from elsewhere in the body through the bloodstream. In my case the blockage were blood clots that came from my legs. In the ICU, I was given IV drugs to work on dissolving the clots in my lungs. I also had an IVC filter placed to prevent any further blood clots from traveling from my legs to my lungs. Once I was stable, I was transferred to the regular hospital. There I continued to improve. Unfortunately, this incident set off a flare of my MS. I had lost strength in my arms and hands. I knew I couldn’t go home in this condition. I needed rehab.

Once my insurance approved rehab, I was transferred to acute inpatient rehab. There I would work at three hours of therapy (PT and OT) a day. While the therapy was extremely helpful and I grew stronger every day, the experience with some of the rehab staff was surely lacking. The ICU and hospital nursing staff were impressive. Unfortunately, I can’t say the same about the rehab nursing staff. The rehab staff did not seem to be trained to treat patients with chronic illnesses. I cannot walk or move my legs so I needed help in nearly all aspects of my care. I often felt like a burden when I needed help getting dressed or transferring to my wheelchair, commode, or bed. At times, I felt that I didn’t receive the attention, understanding, or empathy I deserved.

I learned a few lessons in my experience. First, you need a good advocate. I learned that I needed to be my own advocate and had to direct details of my own care much of the time. Fortunately, while my husband and I are able to advocate effectively, I can imagine others in that situation that would not be able to. Having a family member or close friend that can be there regularly and help communicate with your care team is necessary. Second, don’t assume that nursing staff know what they are doing all of the time. It’s fine to ask questions or probe staff to get a better understanding of what actions they are taking and why. If the person resists your questions or doesn’t know why, this is a red flag, and should be raised with your doctor. 

Often, recovery is in your own hands.

5 comments:

  1. As an OT in acute, outpatient and home care​ I am saddened to hear this. Thank you for bringing attention to this! I hope you are home again and regaining your strength.

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    1. My rehab therapy was great. OTs and PTs are special. I am home and doing well.

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  2. Having the right care is always important to recovery & maintenance. A PT specialist that understands neurology is something I never knew existed. I am glad I have one now. This disease has made even recovering from the simple so complex....

    Happy to hear you are on the mend. Thank you for sharing your tales.

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  3. I am thrilled you are back to writing. Your strength amazes me and your spirit is refreshing. Welcome back!

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  4. Missed your blog and insight... I hope you share with the hospital when they send you one of their happy little how did we do letters. A friend of mine had a similar experience when transferred post surgery to a rehab facility. They had no nurses on staff or equipment to deal with her needs and improvised at best. As we continue to move from hospital to secondary care facility this problem will continue. Most of us are good advocates for ourselves.. But I this week I met with a PA with a little voice and didn't hear all of what she said.... Getting the most out of a health care visit depends somewhat on training staff appropriately to meet ALL the needs of patients. Keep on building your strength.... And keep writing... You are a force😊

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