Hi, my name is mariel59! Anyone had a similar experience with CIDP?
mariel59
Online Community Member Posts: 1 Listener
Hi firstly my heart goes out to everyone dealing with CIDP. I was diagnosed in March and have since been having IVMP once a month. I was lucky enough to be referred to uclh and they are amazin.
My symptoms started after I had covid . 6 weeks after covid I had double pneumonia and a clot in my lung. Then 2 months after the cidp started.
Anyone else had similar?
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Comments
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Hello @mariel59, welcome to the community. Thanks for sharing your story, I'm glad UCLH are treating you well 😊
I haven't got the same condition myself, but I just wanted to pop in to say hello and welcome you to the community. I hope you'll find some friendship and support here. If you have any questions about anything please don't be afraid to ask.
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