I'm not a long covid sufferer myself (and thankfully my wife's LC didn't involved long term loss of smell or taste, though still has left other issues), but I a

I'm not a long covid sufferer myself (and thankfully my wife's LC didn't involved long term loss of smell or taste, though still has left other issues), but I am pleased that the issue is still being worked on, and that there continues to be more proof that this is a physical response to Covid, and not some just psychosomatic "all in your head". The amount of disbelief my wife faced in real life and online was frustrating - I hope this work helps others with ME and from the other post viral responses we are likely to see again with a novel virus.