Inclusion Body Myositis: I'd like to talk with others
This is a form of muscular dystrophy that has no known cure.....I would enjoy someone to share the conversation about...there are several gene therapy trials going on at a slower than necessary rate.....thanks...Ted
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<p>I have iinclusion body Myositis after my last Covid vaccine. Iam 80 and have always gotten the yearly flu shot, but read that the Flu Vaccine can also be a trigger for Myositis, is that correct?</p>
Welcome, @karingroom. It must have been a blow to be diagnosed with inclusion body myositis (IBM) is an inflammatory and degenerative muscle disease. To help you connect with other members who are living with IBM like @jerziegerl @mklam @nmenonk2022 @marilynredder2367 and more, I moved your post to this existing discussion:
- Inclusion Body Myositis: I'd like to talk with others https://connect.mayoclinic.org/discussion/inclusion-body-myositis/
There are many symptoms with inclusion body myositis. What symptoms are you dealing with at the moment? Do you work with a physical therapist?
Hello Gail!How did they test you to get your diagnosis?Was it just a muscle biopsy?I had an iron infusion/possibly covid which set of a reaction a few days later.I lost all of the strength in my trunk of the body that I lost the ability to walk.After being bed bound for months.I am able to walk again,but it is not normal since I still don't have the midstrength.The doctors only found a couple things with the spine and neck,but nothing needing surgery.No doctor knows what it is.
Hi Dexter!I have a feeling I might have myositis or polymyositis.I have not been diagnosed yet,but have alot of the symptoms.What is the other medication that you are using to treat this besides predisone?
A muscle biopsy confirmed IBM after many years of symptoms.
Abuela4
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I was diagnosis with IBM in March of this year with a muscle biospy snd blood tests. z just went to a Rheumatologist and he says he is not sure it is IBM so how can that be ? He say Blood work is conclusive but not the muscle biospy, so what do I do now? Iam still on predizone, 5 mg a day now, down from 50mg,
I was diagnosed with IBM and doctors suggested 2 infusions of inmmonoglobulin treatments a month , my insurance covers only 80% , the 20% deductible is around $800 per infusion , is there any foundation or financial institution that helps because I am on social social security income only and I cant afford the treatments