Folks, I went to my GP & A&E recently as I've been getting a lot of mid chest pain and pain around the stomach and surrounding areas. These pains have also been accompanied by pins and needle on left hand and feet 
But the GP told me that if there was any ORGAN involvement in my lupus I would not feel the pain from it as it would be affecting the kidneys etc silently, and the only way to detect it would be via blood, scans and biopsy. He put it down to anxiety but I know that when all these pains started again I was not in the least bit anxious - in fact I was beginning to accept this illness.
Is what the GP told me about "no pain in organ involvement" true or a myth? Can anyone who has organ involvement offer any advice please?
I've done as was recommended by him and took pain killers but the pain is still there - sometimes bad sometimes not so bad.
But the GP told me that if there was any ORGAN involvement in my lupus I would not feel the pain from it as it would be affecting the kidneys etc silently, and the only way to detect it would be via blood, scans and biopsy. He put it down to anxiety but I know that when all these pains started again I was not in the least bit anxious - in fact I was beginning to accept this illness.
Is what the GP told me about "no pain in organ involvement" true or a myth? Can anyone who has organ involvement offer any advice please?
I've done as was recommended by him and took pain killers but the pain is still there - sometimes bad sometimes not so bad.