Is there any way to see a specialist without a referral?
Posted , 13 users are following.
Hi,
I've posted about being shrugged off by my GP before, so I hope you don't mind me ranting a little bit more.
I saw my GP today about my persistent feelings of fatigue - this is the third time I have been to see my GP about this, except this time I mentioned I had heard of CFS and could relate quite strongly to the symptoms. I was told he couldn't diagnose me with CFS because I haven't had a viral infection, and there was no point anyway, because "there isn't really any way to treat CFS". My GP then told me I just had to do more excercise and go out more; he insisted this is the only way things could get better, despite me mentioning that I had tried excercise and it always resulted in my headaches and dizziness getting a whole lot worse. Apparently I can't trust anything I hear about CFS on the internet because if the people on there spent half the time they do complaining "getting a life" (his words), they would feel a lot better.
As you can imagine, I'm kinda ticked off right now. I got "just excercise more" the last time I saw my GP too, so it's basically looking like I don't stand any chance of getting a diagnosis or referral from this practice.
Is there any way for me to see a specialist without a referral? Or should I register with a different GP?
I'm 16, if that makes any difference.
Thanks.
1 like, 16 replies
tina58520 Cae
Posted
All the best and good luck.
Txx
Cae tina58520
Posted
Thanks, hopefully I will be able to switch GPs as soon as possible. I don't think my parents would be too keen on the idea - do you know if it's possible for me to be registered with a different GP than the rest of my family?
I'll also take a look at ACTION FOR ME. c:
Fidd Cae
Posted
I actually think that your doctor's cynicism about the value of specialist CFS services is well founded, even if in other ways he seems ill-informed and prejudiced. Most people who end up with the symptoms of CFS as a teenager go on to recovery naturally anyway, without needing treatment. Hopefully this will happen for you, although it will still be a frustrating and difficult time while you are feeling ill.
It is also possible that something else is wrong which has been missed, or that you are one of the unlucky ones who does not go on to recover - in which case it's hard to know what to advise.
sharon777 Cae
Posted
I'm so sorry to hear that your GP is not taking you seriously. I say yes, register with another GP and I believe if you wanted to bypass your GP to get a referral then you would have to go private (and pay money). Please people out there correct me if I'm wrong.
I semi went down the private route. Firstly, I saw a private GP who said my symptoms sounded like CFS. He gave me a list of all the tests that I should ask my GP to do. I got those tests done via my GP (NHS) and then my GP referred me to a CFS clinic. BTW the first specialist I saw wasn't very good so I then got myself referred to another clinic. The second clinic is a lot better.
Good luck.
Cae sharon777
Posted
I'll try to register with another GP, and thanks for the info.
It's good to hear the clinic you're at now is helpful to you.
cheryl5535 Cae
Posted
Cae cheryl5535
Posted
Yeah, I'll try not to overexert myself. Kudos to you for being able to work full time with 2 kids while having CFS, and it's great that you've found support.
katharine81627 Cae
Posted
This is something I'm waiting on now. I've been back and forth from my doctor since January and he has signed me off work since then.
This subject is so difficult as you are constantly battling people thinking it is in your mind and that you are lazy, with feeling rubbish constantly
Cae katharine81627
Posted
Yeah, I feel you. I've been told I'm "just lazy" so many times while I'm spending ages in bed because of how awful everything is.
wknight Cae
Posted
With regard to seeing a CFS consultant I would research who in your area is actively involved in research activities or has written papers. I am lucky as my GP recognises the condition and has other patients and sent me to see one of the UK leading experts, albeit some 50 miles away but then its easy for me to travel.
If you are 16 what support are you getting from your parents?
Even if you get a diagnosis the problem is that there is no magical cure. After many years of sufferring I am now doing so much more, my brain fog has lifted and tomorrow I hope to ride 20 miles on my bicycle. How did I get there, by pacing. Its very,very hard to do because you have to get the balance just right between enough activity to get the body moving and not too much to set you back. Most fail because they do far too much and then write off pacing as never working. I did that until I found a pacing system that worked for me.
Best of luck
jackie00198 Cae
Posted
bronwyn97278 Cae
Posted
jinny23 Cae
Posted
I understand that you are 16.
My GP was so useless at the time I needed her, I made the decision to take the batter into my own hands !
I searched the Internet, found an ME clinic in my county and emailed them.
They gave me advice and I returned to my doctor but with an email, telling her what I expected of her.
The patient has a right to be a part of that process.
I am now on a 6 month support programme.
By the way, my cousin who had ME from 13 to 16 is now back in school doing A levels and he had major support, based in Gwent.
Good luck on your journey.
You will beat it
Best wishes
Jinny23
alison44235 Cae
Posted
ChrissyC Cae
Posted