rheumatologist from hell

I recently visited the world's worst rheumatologist. He ignored all my symptoms and simply waisted my time. He actually said "as you merely don't want painkillers then you obviously have a low to no pain threshold for any pain " WHAT AN #@$/^^'$. I am deadly allergic to any painkillers. Then not only said I had simply cold knees and need to just rub them. I now have to use an electric wheelchair to get about as my joints just give way and I'm in permanent agony. Then topped himself by giving me a prescription for meds that clearly say not to be taken by a female let alone one with heart problems. That man was deadly dangerous let alone the fact I was in agony after the so called appointment and have photos of the hand marks and finger prints on my knees and hands/wrists. Bruised badly and was in agony for days. That man should be struck off.

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  • Welcome to LUpus Patients Understanding & Support (LUPUS) at HealthUnlocked.

    I am very sorry to read your post. Although you have every right to be upset, angry or any other emotion, I think you need to see your GP and explain what happened during this consultation.

    I don't know where you live, but I am assuming the UK.

    I recommend that you ask your GP for a referral to see Dr David D'Cruz, Director of the Lupus Clinic at St Thomas' Hospital, London. If you have private insurance, I would recommend, Professor Graham RV Hughes, who is at the London Bridge Hospital. Dr D'Cruz studied under Professor Hughes, as did most lupus specialists in the UK.

    We also have another website called the LuPUS Message Board where you can also post questions and talk to other people. Registration is FREE and we offer free information and free online psychological support.

    We specialise in psychological support with our own counsellor/psychotherapist available.

    By becoming a Member, you will have access to the private forums and because they are private, only Members have access and even bots and search engines are forbidden.

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    Finally, please go to: lupus-support.org/LuPUSMB and Sign Up.

    I look forward to talking with you more!

    Sometimes we need to talk to people who understand and who are not family or friends.

    With good wishes!

    Ros

    Disclaimer: No attempt is made to diagnose or to make any medical judgement. You are advised to seek the advice from your own physician. LUpus Patients Understanding & Support (LUPUS) is not a substitute for your own doctor.

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