By jim yadlon my name is jim yadlon and i am recovered gbs patient. After being diagnosed with guillain barre syndrome, a serious disorder that occurs when the body's defense (immune) system mistakenly attacks part of the nervous system, debbie had a tracheotomy and would be on a respirator for two months and couldn't walk. But one never forgets the gist of time with gbs even though i have forgotten some of the smaller details.
Guillain Barré Syndrome Medcomic
One important detail that i will never forget is the love…
Gbs|cidp foundation international 375 east elm street, suite 101 conshohocken, pa 19428 phone:
There have been many ups and downs during this time. The roller coaster of diagnosis. December 8th, 2016 who we are. Wearemore is a chronic disease patient blog that focuses on providing to support, motivation and education for
The gbs|cidp foundation invites you to join patients of all ages, caregivers and heros who have contributed their experience and inspire others living with gbs, cidp, mmn and related conditions. Check out some tips below to help you share your story. Mar 5, 2025 patient stories last updated: An amusing story on the lighter side of being a gbs patient.
Bill cole (usa) bill developed motor symptoms that left his doctors at a loss.
Read steve's story about overcoming gbs, and his relapse. Asger lauridsen (denmark) retired physician. Admitted twice with gbs, treated with physiotherapy and discharged. We love sharing stories from our patients and their experiences with us.
The therapists are key to recovery, she said, they keep you motivated, and they celebrate small improvements. Small gains are good. (gbs) is a rare neurological condition, affecting approximately one in 100,000 Susan slovak was at her job as a customer service representative in january 2019 when her feet began to ache. Gbs is an autoimmune disorder in which the body's immune system attacks part of the peripheral nervous system.
Gbs is rare, affecting only about one
Gbs is a neurological disorder in which the body's immune system mistakenly attacks the nervous system. It's rare and is estimated to affect only about one in 100,000 each year, so there's The gbs|cidp foundation invites you to join patients of all ages, caregivers and heros who have contributed their experience and inspire others living with gbs, cidp, mmn and related conditions. Check out some tips below to help you share your story.
It can be a gift if you allow it. That does not mean it has been easy. We all know gbs/cidp is excruciatingly difficult for patients and their families. Gbs|cidp foundation international 375 east elm street, suite 101 conshohocken, pa 19428 phone:
/r/guillainbarre is a small, welcoming community for those who have survived or are currently battling guillain barre syndrome or chronic inflammatory demyelinating polyneuropathy, the family/friends of patients and survivors, and for those curious about the disease.
He's in the 20 percent of gbs patients who don't recover an earlier version of this story referred to nurses I spent 9 months in the hospital. They had no treatment at that time, no ivig. now, more than 50 years later, judy is the oldest known surviving gbs patient. I remember the physical and occupational therapy was very creative.
Patient stories / my wife, caregiver and gbs hero / my wife, caregiver and gbs hero. My name is jim yadlon and i am recovered gbs patient. But one never forgets the gist of time with gbs even though i have forgotten some of the smaller details. One important detail that i will
Gbs|cidp foundation international 375 east elm street, suite 101 conshohocken, pa 19428 phone:
Gbs|cidp foundation international 375 east elm street, suite 101 conshohocken, pa 19428 phone: Volunteers from the gbs|cidp foundation, visited my friend morgan in the hospital. I know that made all the difference in her recovery. She was very motivated and in very good spirits after the visit!
Gbs|cidp foundation international 375 east elm street, suite 101 conshohocken, pa 19428 phone:
