Horrible gp

Posted , 5 users are following.

Sorry for this post but I just need to vent. Ive had symptoms for 10yrs, last couple of years I gave up on drs and haven’t been to gp very often, I’ve avoided medication for most of this 10yrs trying a few things which didn’t agree with me and never stuck with anything except diazepam when really bad. I’ve just tried to filter out the bad days by riding off the good days.

Well last month or 2 my pain levels have been ridiculous again, I went to private physio which made things worse and after spending days reading as many positive reviews about Amitriptyline as I possibly could I finally got to the point where I convinced myself to try it, I’ve avoided for years due to the side effects and the worry that I will be stuck on them forever. Got dr appointment on 23rd may (earliest they could do) but today I just couldn’t hack it so phoned again and asked for a dr to call, reception insisted I came in to see dr instead.

Went in to see dr and came out of there burst into tears, had to get to my car as quickly as possible and was sobbing hysterically on the phone to my partner who couldn’t understand me. I drove home sobbing and came in still sobbing.

She refused to give me amytriptlyn, my complaint was muscle pain and stiffness and excruciating headaches which have got worse. My joints hurt, my face feels like it’s being stretched like my muscles have turned to stone. I didn’t even get the chance to tell her this, she was so dismissive saying Ami or any of the other anticonvulsant causes rebound headaches and she also said that my pain wasnt nerve pain and that ami only treat nerve pain. She also told me that they had done enough medical tests over the years and that my symptoms were not able to be medically explained. Funny thing is she didn’t check my joints, she didn’t ask me what my pain felt like, she told me I don’t have migraines which I mentioned I think I might have but she hadn’t asked me any questions about it. She didn’t check my blood pressure which I would imagine is something to do with worsening headaches. She treated me with contempt, didn’t apologise that pain clinic or muskoskeletal clinic referrals had fallen by the wayside for years and months.

I have read enough over the last 10yrs as I’m sure all of you have and Ami is the first line of treatment for persistent or chronic pain. Then come the anticonvulsants and do on. The fact that my pain has ramped up I should have been offered inflammatory blood test, just to check or she should have prodded my joints to make sure they weren’t inflamed etc.

After not wanting to make a fuss I decided not to take it lying down and called drs back and asked to speak to a senior dr who has now called me back and told me to take the ami and see how it works as it’s a pain treatment for all types of pain.  I don’t know what the first drs problem was. It was a fairly young woman as well who I normally find the most helpful and proactive.

Thanks guys for listening, hope your all having a good day😁

1 like, 8 replies

8 Replies

  • Posted

    I am happy amytriptline works for you. It didnt work for me and i have a lot of pain in my face neck and shoulders. Nothing works for me
    • Posted

      I don’t know if it works yet, first pill taken tonight so we will see. Dont want to take them but desperate at the moment. Have they given you an answer to what the pain is or is it chalked down to Fibro? 
  • Posted

    I was diagnosed with FMS over 20 years ago.  At first Doctors thought FMS patients were all “crocks” that they were making up pain that travelled all over the body; that morning headaches with no known cause was a lazy persons excuse to go on disability so they didn’t have to get up early for work. . Now Drs for most part accept FMS as a real disease but the government is now over reacting with no plan for the innocent in their war on drugs and doctors are frightened with arrest and other severe punishment that doctors would rather dismiss a patient in pain than take the chance of a government audit of their prescription practices.   In the end we FMS patients feel as though we are worthless drug sucking no goods that the doctors our families and friends have written off. . AND Meanwhile our pain continues to get so  bad we wish we could find Dr Kaforcian in the yellow pages.  I believe there has to be a way to fight drug addiction for the poor souls that have lost the desire to fight for a good life while providing folks like us who don’t want to be high- we just want relief from REAL EXCURCIATING  pain just long enough to sleep at night OR play with our puppy. I want nothing more than to feel like God loves me and isn’t punishing me for something I’ve done by making me live “hell on earth”
  • Posted

    Charlotte, Have you tried massage therapy. It isn't a cure , but may give you some relief

    • Posted

      Yes I have an amazing very caring massage therapist but on good days I’m scared to go in case it sets it off and on bad days I can’t always go but I try to see her regularly and she is pretty good about fitting me in the same day when she can. 

      Im old hat at all this pain I just couldn’t believe that the gp behaved the way she did, I’ve been offered all sorts of drugs from specialists and pain clinics when I really didn’t want them and the one time I’ve finally convinced myself to try she refuses and then treats me like I’m mad and making it up, as if anyone would be still making stuff up after 10yrs of complaining about symptoms. 

      I was just flabbergasted, if I went in with simple ongoing back pain I would have been offered pain meds or muscle relaxers.

      I also thought her knowledge was atrocious, I’m sure everyone on this forum and all other chronic pain forums knows the actions of ami and what it treats, I research a lot and read about all meds and supplements. Her statements without even touching me were just stupid, she didn’t ask about the type of pain but told me I don’t have migraines and I don’t have nerve pain. Luckily her colleague was more knowledgeable and less of a stuck up expletive!!!

  • Posted

    Sorry about your experience  Charlotte with the doctor. Doctors don't seem to be intelligent caring people anymore . They are "bean counters". I wish you all the very best including a total healing!

  • Posted

    Good on you for ringing back. I've been there, done that and fallen out with a couple of very well educated Specialists many years ago over Fibro. I have muddled my own way along for 21 years finding my own pain relief in the form of 'heat bags', massage occasionally, Osteopath, and stretches, and a soft exercise ball to place under my most painful spots.....and Dr Google once a year to see if anything helpful has been discovered.

    ?There are 'people' you will meet along the way, who will never believe, or accept what they cannot see or experience themselves. They cannot ever see outside the circle. That is the wonderful thing about this site - you can vent - and most of us will totally understand what you are experiencing.

    Take care of yourself, do things you enjoy and keep your mind active. It does help.

    All the best.

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