BarneyBear
New member
Hi all,
I’m new here and very moved by many of the stories that I’ve read. I don’t have much to contribute today as reading is much easier than typing at the moment. Wanted to express my thanks to all first of all for helping me to realise that there is hope after 7 months of illness (Borrelia, Bartonella, Babesia) that have rendered me housebound and hanging on a thread whilst the medical profession figures out what to do with me. Sometimes the days and nights seem to blur/ into an endless cycle of pain, exhaustion and frustration as I struggle to manage even the most basic tasks. I often feel helpless and vulnerable, despite a very understanding partner, friends and employer who do their best to help in whatever way they can despite my growing disability. I am very fortunate in this sense, but I still can’t help feeling like a burden on everyone. But this journey has taught me many valuable lessons about gratitude and humility - life is precious and I am grateful to be alive despite everything.
Moving forward, I want to get better and help fellow sufferers of this wretched illness much as I can. I’d also like to campaign to raise awareness and push for improved testing facilities/procedures here in the UK which are totally inadequate. I was labelled as delusional and sent to a Psychiatric Hospital for my “self harm” before a private testing facility confirmed that my skin lesions were caused by Bartonella. So, the battle goes on. Thanks for listening and best wishes to all.
I’m new here and very moved by many of the stories that I’ve read. I don’t have much to contribute today as reading is much easier than typing at the moment. Wanted to express my thanks to all first of all for helping me to realise that there is hope after 7 months of illness (Borrelia, Bartonella, Babesia) that have rendered me housebound and hanging on a thread whilst the medical profession figures out what to do with me. Sometimes the days and nights seem to blur/ into an endless cycle of pain, exhaustion and frustration as I struggle to manage even the most basic tasks. I often feel helpless and vulnerable, despite a very understanding partner, friends and employer who do their best to help in whatever way they can despite my growing disability. I am very fortunate in this sense, but I still can’t help feeling like a burden on everyone. But this journey has taught me many valuable lessons about gratitude and humility - life is precious and I am grateful to be alive despite everything.
Moving forward, I want to get better and help fellow sufferers of this wretched illness much as I can. I’d also like to campaign to raise awareness and push for improved testing facilities/procedures here in the UK which are totally inadequate. I was labelled as delusional and sent to a Psychiatric Hospital for my “self harm” before a private testing facility confirmed that my skin lesions were caused by Bartonella. So, the battle goes on. Thanks for listening and best wishes to all.