Hi, everyone!

It’s been a while since I last posted about my health condition and my doctors and I are still looking for more specific insight as to the source and treatment of my debilitating pain—maybe you can help?

SYMPTOMS

Constant, debilitating mid-, low-back, and upper abdominal pain and spasms.

HISTORY

I caught my family’s stomach flu and threw up violently in NOVEMBER 2017. While throwing up, I felt a sudden, excruciating pain in my upper left abdomen (just below the ribs) that was painful enough to put me in bed for 3 days.

I was initially treated for an abdominal strain/tear with modified movements, opioid painkillers, and muscle relaxants—none of which alleviated the pain (but I felt all the nauseating, drowsy effects from the meds).

In MARCH 2018, I reached with my left arm and instantly the pain in my upper left abdomen doubled in intensity and over months, gradually spread across my abdomen and toward my kidneys. Sitting up, driving, standing, walking, bending, showering, and getting dressed became incredibly painful and sometimes impossible.

In JUNE 2018, the pain subsided enough that I could walk and stand for longer periods, and even enjoy a water park with my family (though still with great difficulty).

In JULY 2018, the pain spread to my back and nearly incapacitated me. I pushed through as best I could, using a cane to help me through each day, until SEPTEMBER 2018, when the pain became so unbearable that I became bed bound, where I’ve been for the last 2.5 years.

TREATMENT/CARE

As of MARCH 2021, I have:

-met with 53 medical professionals (including GPs, gastroenterologists, physical therapists, rehabilitation specialists, functional medicine practitioners, chiropractors, rheumatologists, naturopaths, neurologists, spine specialists, abdominal surgeons, pain management specialists, neurosurgeons, allergists, immunologists, and sleep specialists)

-undertaken multiple blood and urine tests

-undertaken extensive imaging (including x-rays, CTs, ultrasounds, endoscopies, colonoscopies, full-body MRIs, EKGs, and EEGs)

-been prescribed more than 30 medications (including NSAIDs, painkillers, muscle relaxants, dopamine promoters, anti inflammatories, antihistamines, tonic water, nonergot dopamine agonists, ACE inhibitors, anti-epileptics, phenothiazines, triptans, sedatives, antidepressants, corticosteroids, Lyrica, Bactrim, SSNRIs, chemotherapies, immunosuppressants, and medical cannabis)

-undertaken dozens of treatments and procedures (including multiple steroid injections, rf nerve ablations, and sympathetic blocks, celiac plexus blocks, physical therapy, rehabilitation therapy, chiropractic care, bodywork, body care, pool therapy, acupuncture, micro frequency therapy, diagnostic injections)

-undertaken home therapies and treatments (exercises/movements, ice/heat, TENS unit, body pillow, supplementation, icy hot, essential oils, meditation, massage, back brace, cbd oil, medical cannabis edibles/sprays/cartridges, breathing exercises, extended water fasts, intermittent fasting, autoimmune protocol diet, low carb/high fat diet, time-restricted eating, one meal a day)

-been denied acceptance by the Mayo Clinic, Undiagnosed Diseases Network, Johns Hopkins University, UCLA, and other facilities

DIAGNOSES

  • Rheumatoid Arthritis (later redacted by rheumatologist’s NP)
  • Mild sacroiliitis, spinal inflammation, transient synovitis, spondylosis, radiculitis, multiple broad-based disc bulges
  • “Atypical presentation of something rheumatological” (rheumatologist)
  • Possible fibromyalgia 
  • Possible AMPS (Amplified Musculoskeletal Pain Syndrome)
  • Possible Mixed Connective Tissue Disease
  • Mild, widespread, generalized nerve pain
  • Mild splenomegaly
  • Mild nonalcoholic Fatty Liver
  • 2.5 years of “bed head”

SUMMARY

I’m currently meeting regularly with a team of doctors, exploring dosing of new medications, eating a healthy diet, taking daily vitamins and supplements, engaged in weekly physical therapy, exploring the boundaries of my pain and range of motion, researching potential doctors/diagnoses/treatments, engaged in regular communication with online groups and individuals with or related to similar conditions, and continuing home treatments. 

The pain is constant and severe and is exacerbated by movement. Additionally, it can be difficult to think, work, and concentrate through the pain. I’m doing all I can to improve my health for myself and for my family. I’m anxious to be a more-involved husband, father, friend, and member of the community. I want to get outside and walk, hike, bike, swim, and travel. My faith, family, and friends sustain me, and I’m hopeful of improving my health. 

I don’t expect anyone to have the answers I’m seeking, but I think it’s worth asking about.

Thanks for any and all help you can offer!


13 responses to “2.5 Years in Bed—Looking for Help”

  1.  Avatar
    Anonymous

    My husband works with a man who was in extreme pain and ended up with an internal implanted TENS like unit that sends a constant stimulation to the affected area.

    1. Jess Smart Smiley Avatar

      I wonder if it’s a percutaneous spinal cord stimulator. The studies I’ve seen show a 50-80% efficacy, which is pretty good (and the reason I’ve brought it up with my spine specialists), but I haven’t responded well enough to other nerve-related interventions to be approved for the implant. Has it seemed to help your husband’s coworker?

  2. talyakholodkova Avatar
    talyakholodkova

    Hello!
    I am really sorry you are going through this. Just stopped by searching useful things about comics and saw this post. I hope this may help.

    I don’t know if you believe in energy fields, chakras etc. But ancient practices sometimes help in incredible ways.
    I’ve met this guy couple of years ago when he visited Ukraine. He knows different techniques of yoga and massage, he studied from different people while he was traveling around the world. I don’t know where he lives at the moment but maybe he knows how to help you or knows who can help. So feel free to write him, I’m sure he’s a kind person and should respond.

    https://www.facebook.com/mackadelic.maker

    Sorry for my bad English 🙂
    Take care and get well!

    1. Jess Smart Smiley Avatar

      Hello! Thank you so much for your thoughtful reply (and sorry for the sudden departure from comics talk :P). I reached out to William and am curious to know what he thinks about my situation and what might be done. Thanks again for your help!

      P.S. Your English is fantastic! I wish I knew even a little Ukrainian.

  3.  Avatar
    Anonymous

    Hi,
    Maybe you’ve already tried this, but have you reached out to Dr Lisa Sanders team? She has an incredible column for The NY Times called Diagnosis. I know they probably get many, many calls/emails but it’s worth a shot! https://medicine.yale.edu/profile/lisa_sanders/

    1. Jess Smart Smiley Avatar

      Thank you so much! Yes—I reached out to Dr Sanders (the tv show character House from “House” is based on her!) and I also reached out to the Center for Undiagnosed Diseases, which she has worked with. Unfortunately, I was turned away by both, but I’m continuing to look for great potential resources like these. I really appreciate your help!

  4. M. Cordero Avatar
    M. Cordero

    Im in a similar battle. Was diagnosed with SRS, but still without the proper care. According to one of the most famous Drs in the Island, he believe That I’m the only patient. We don’t have the surgeon. My insurance coverage won’t pay outside. When I read your pass thru the treatments and studies. Is like reading mine. The difference is that I can’t take pills. The blocks aren’t working. I believe that I can’t hold it anymore. If you find some physician please, can you share info with me. Until now, I have read a lot about surgeons profiles and techniques. Trying to have an appointment with ADAM Shiroff. I know about the other technique but I feel better when I read his patients reviews. Hope you can find the end of suffering. I’ve a video in YouTube but is in spanish. Mari Cordero Síndrome de costilla

    1. Jess Smart Smiley Avatar

      I’m so glad you reached out and shared Dr. Shiroff’s information. I am hopeful that we can both find ways to move forward in health.

  5. jasgardner Avatar

    Hey Jess I sent you a message in fb messenger… I’m not sure if you got it. If you did, awesome. If not, it’s there 🙂

    1. Jess Smart Smiley Avatar

      Thank you! I checked and didn’t see a message. I checked my message requests and spam folder and didn’t see it. Am I doing something wrong?

    2. Jess Smart Smiley Avatar

      Never mind—I found it!

  6. […] out this video I made (just days before my crazy health adventure began) to learn how to print, cut, and fold any or all of my Halloween zines—or learn how to make […]

  7. […] the meantime, I created this post, in the hopes of reaching someone who might be able to offer any help or insight into my […]

Leave a Reply

Your email address will not be published. Required fields are marked *