Fellow Nutmeggers
I know this is an old thread but figured I'd post in case there might be recent interest in a Connecticut support group. I am fairly new to bone marrow failures and live in central CT. Would love to be in touch with others who are dealing with, dealt with or a caregiver of someone with AA, MDS or PNH. Have been in touch with Beth I (and looking forward to a budding friendship). Beth's story gives me hope in my own story.
Let me know if there is interest. I do believe comfort does come in knowledge and support
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Kathie - 54 yr old mother of 4, pancytopenia since 11/2014, moderate AA 8/2016, small PNH clone (now increasing), monitor bloodwork every three months
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