Afraid of our GPs. : I'd noticed a few... - Fibromyalgia Acti...

Fibromyalgia Action UK

59,986 members67,154 posts

Afraid of our GPs.

Bennett1943 profile image
17 Replies

I'd noticed a few times how some FM sufferers want to ask their GP to refer them to a Rheumatologist or Pain Clinic so that they can discuss their pain more fully and to get the best treatment they can. I'm one such person and I wonder what it is that I'm afraid of. Isn't our GP there to help us ? Way do other FM sufferers think ?

Written by
Bennett1943 profile image
Bennett1943
To view profiles and participate in discussions please or .
17 Replies

Hi I seem to be afraid of every body I find myself buying things online rather than from the shop around the corner just to avoid the confrontation.

With my gp she is very nice and easy to talk to but I find I get anxious when I see her and forget half of what I was going to ask her. So in a nutshell I think with me it is anxiety.

In the end I took my wife with me and kind of pushed her a bit to refer me.

in reply to

I think you are right Rich- I don't go outdoors much now, don't go shopping because I cant carry it home, so yes I think many of us feel a little intimidated with the world outside..

I am fortunate enough to have a good rapour with 3 g.p,s in my practice and I usually get referred if I want to, I usually ask when g.p cannot go any further with treatments/meds, there is a limit to what a g.p can prescribe and a consultant can instruct to use something else.. in my case I am using hydrothrapy which I pay a small fee for and waiting to see rheumo nurses for some acupuncture.. I found my rheumo doc referred me to pain clinic for help. You have a right to ask for a referral and if one doc wont then go to another in the practice.

Bennett1943 profile image
Bennett1943 in reply to

A lot of what you say is true. The bottom line really is being made aware of what is available and then at least we would accept it and get on with our lives !

bluebell99 profile image
bluebell99

I find having my husband with me boosts my confidence to ask anything I need.

Bennett1943 profile image
Bennett1943 in reply tobluebell99

Can I ask what the doctors reaction was ? Did he become more defensive or do you feel it helped at all ?

Well, my Rheumatologist wrote to my G.P to refer me to the Pain Clinic. I went to see G.P about making this appointment and he said NO he would look after/manage my pain. I came away with Brutan patches and Lyrica tabs which turned me into a Zombie according to my hubby ! So after seeing Rheumy team I weaned myself off the Lyrica then started to reduce the batches until I was on none. I can think straight now thank goodness BUT I would have preferred to see what other non meds treatment would have been offered by pain clinic.

Bennett1943 profile image
Bennett1943 in reply to

The set up is just too hit and miss and I can sympathize with so many people on this website. I wonder sometimes if it is because a Medical Practice is trying to stay within its budget. I'm going to follow the advice I was given and change to another surgery altogether. It would be helpful if there was some kind of guideline available to the public as to what our rights are and what we can reasonably expect from our GPs.

TheAuthor profile image
TheAuthor

Hi Bennett1943

I think that you are spot on my friend! When you see a GP you simply never know which way they swing with Fibro and it can put you on edge? Then, when you ask for something like a referral or medication many of them go on the defensive? I walk into appointments expecting confrontation half the time! I want to sincerely wish you all the best of luck and please take care of yourself my friend.

All my hopes and dreams for you

Ken

Bennett1943 profile image
Bennett1943 in reply toTheAuthor

Thank you for your kind reply.

Jan810 profile image
Jan810

Hi, I think for me, it makes my anxiety bad. After going back and forth for 4 years and getting no answers, offered no advice, no medication I think I lost trust. I spent a year in bed where I could barely walk but yet never visited my g.p as they were no help before. I had never heard of a rheumatologist before. Until after 4 years I went to a different g.p again and he suggested I see one. It knocks your confidence and makes you feel like you are losing your mind. They always blamed it on my mental health. I'm so happy to finally have an official diagnosis but will still avoid my g.p at all costs. X

Bennett1943 profile image
Bennett1943 in reply toJan810

GPs lack of feeling

Jan810 profile image
Jan810 in reply toBennett1943

Definitely. I think the majority of them are overworked. It must be an extremely stressful job. There are still some lovely caring doctors out there who genuinely care though, finding them is a problem.

Superc4t profile image
Superc4t

I wonder if anyone can clarify where a rheumatologist fits it? I attend a pain clinic for fibromyalgia and see a pain psychologist and a pain consultant - all liaise with my GP but my pain never improves. I also have osteoarthritis and circulatory problems in my feet which cause me serious mobility problems which seems to be ignored when ever I bring it up. Could referral to a rheumatologist help with this?

Thanks

Jan810 profile image
Jan810 in reply toSuperc4t

Hi. I really don't know, but I don't see why it wouldn't be of help to you. It sounds like your g.p is disregarding your symptoms. I saw the rheumatologist to confirm whether I had fibro, he asked questions About other symptom so that they could rule out things like lupus. He referred me to a physiotherapist too. I hope that someone can help with your mobility problems, it must be a real struggle. X

Bennett1943 profile image
Bennett1943 in reply toJan810

Thank you

Bennett1943 profile image
Bennett1943

I've had that happen to me when GPs don't listen to me because of my having anxiety/depression. They don't or can't listen with an open mind because most times they don't expect a backlash. Depression is described as anger turned inward so maybe we have nothing to lose by giving them a broadside and getting our feelings off our chest !

Not what you're looking for?

You may also like...

Medication advice

I have chronic FM and am taking Co-Codamol and Amitryptiline but often they don't give me much...
Bennett1943 profile image

How many of you, use a wheelchair or walking aids to get around.

I ask this because my GP has refused to refer me to the NHS Wheelchair centre because he states "FM...
Belle67 profile image

Scientists prove Fibromyalgia really exists - it's not just in our heads. Take this to your non-believing GPs.

I found this today... A second scientific study has confirmed that the Fibromyalgia blood spot...
Sandy247 profile image

FM lets find out what we all have in common (apart from pain)

Is there nothing this site can put up that could start tracking what people post regarding when...
Seamus14 profile image

Medications

Hi allMy gp has informed that the medical council has decided the pain meds will be shortly be...
Ferndale profile image

Moderation team

See all
Hazel_Angelstar profile image
Hazel_AngelstarAdministrator
Lynda_FMA_UK profile image
Lynda_FMA_UKModerator
Sarah_fmauk profile image
Sarah_fmaukModerator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.