Can people with Behcet Syndrome work? What kind of work can they perform?
See how people with experience in Behcet Syndrome give their opinion about whether people with Behcet Syndrome can work and what kind of jobs are more appropriated for people with Behcet Syndrome
Yes, I think they could work in any field, but the place of work needs to be accommodating to you. Working part time would be best, choosing your own hours would be great too. I had to quit working as a special education teacher. The stress of the job had me constantly flaring and in pain.
It really depends on their symptoms. If they have serious joint pain, lifting and climbing can be a problem. Vaginal or rectal ulcers can make sitting uncomfortable. Fatigue can be a real problem for some patients. I'd guess that 50% can work in any field, 30% in specific fields and 20% are disabled/unable to work.
Yes. They can work in any capacity or any field in which their symptoms do not interfere in their work. I have worked full time as a social worker (a generally pretty stressful job) since being diagnosed; however, it is possible that my Behcets symptoms are less severe and/or better managed, as someone with more severe sx's may be unable to work full time or at all.
I currently cant work due to the disease and complications/side effects from the medication I take related to the disease. But i have worked before with the condition, i wouldn't recommend jobs that involve to much interaction with the outside population due to contamination risks! Not the bed immune systems!
BD is a highly individualized disease and effects each individual differently. BD patients would work best within the medical community spreading the word of advocacy towards a cure and recognition of this disease. I think it is highly misdiagnosed. For example, I was misdiagnosed with MS over ten years ago when it really was neuro BD. I do not think a BD patient with epileptic seizures should be working on ladders.
If one's health allows him, it's possible to get a full time job. Everything depends on person's condition, abilities and preferences. If BD is in remission the patient can choose any feield he feels suitable in. It's good to get the advice of doctor if a person is not sure if the job he wants to do is risky.
I worked for ten years before the symptoms got to the point I was no longer able to function at my career to a level that made me a valuable player in my field. The fatigue was the most troubling because I couldn't always be there when I was mostly needed. I truly believe that if you can find a job with flexible hours, flexible boss, and low impact you could be able to work. I can't say what percentage of Behcet's patience work full time but I know some are able to work successfully.
I cannot say that people with Behcet's cannot work but in my situation it's been a problem. Working from home at my own pace would be ideal. I live in a rural area where reception as well as transportation would be an issue. I know we need more rest than normal and pushing ourselves can result in a flare that takes us down and diminishes why we were pushing through in the first place.
ABSOLUTELY! Most people that have Behcet's go undiagnosed because it is so minor. I would approximate only about 3% to 5% are either on disability or choose not to work due to symptoms. I wouldn't suggest anything with large repetitive motion. For example, typing is okay; however, I would not work on an assembly line. There are some people that elect to be proactive and use a wheelchair to continue to work so they can conserve their energy and reduce pain, but that's a small demographic.
hi
im not gonna go on and on as I could like many or most of us!
as a child I always had suffered severe migraines with sickness, I suffered some sort of blackout for a while where I kept falling and cutting my face open and the school advised my m...
When I was 13 years old I spent at least one week in the hospital every month from February all the way to January of the next year. Every time, I was transferred to a pediatric hospital and then to a Women's hospital, and then pack to pediatrics. Th...
Hi all I'm new here, wanted to share my story and ask for your help....I was diagnosed with Neuro behcet's disease a little over a year ago and sadly I'm losing the battle. I'm a mother of 4 and am fighting the fight everyday. I am going blind, I'm n...
Well I got my first symptoms 8 years ago, a few months after my last child was born and a week after a traumatic tooth extraction, I once found a site which linked dental work with the onset of Behcets, but have never been able to find it again or an...
Those were my first words, after being diagnosed !!!!
I had never ever, even heard of the word ! I was scared , very scared, once I read what in fact I was diagnosed with, no one - not even my pharmacist had heard of Behcets !!!
Should I fall d...