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Pregabalin Side Effects
A MyFibroTeam Member asked a question 💭

My gp started me on pregabalin about a week ago after I cried through an appointment because none of my painkillers are working. I haven't noticed much difference in the pain but I have noticed I've been developing really bad headaches and have little appetite. I often get tension headaches but these are ten times worse then the normal ones and last for hours. Is this usual? Will they go away? What have other people's experiences been?
Love to you all ❤️

posted January 14, 2018
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A MyFibroTeam Member

@A MyFibroTeam Member my gp refuses to prescribe anything stronger then cocodamol. If I say that I'm in pain and the cocodamols not working he just gives me more cocodamol. It's ridiculous. Hoping that once I go back to my rheumatologist she might be able to help.

posted January 15, 2018
A MyFibroTeam Member

Motrin 600 mg and Vick’s around my forehead help for the headache .

posted January 14, 2018
A MyFibroTeam Member

@A MyFibroTeam Member I changed doctors and now have a really understating one but as my doctor said to me she is not an expert in this field. It has taken me years to be on the right meds. Tramadol, pregabalin is the main one given for fibro and amitriptyline for sleep at night with pain. You should get these from a pain specialist. Unfortunately due to the Tories we have to wait more than double the time for an appointment!!! I used to try and cope with the pain with heat pads that go in the microwave and can also go in the freezer. The other God send I have is a recliner but I no is very expensive. I have been on p.i.p (disability benefit) just over a year so I was able to buy one and received a car due to lack of mobility. I only got all this due to having a support worker through my doctor as I was struggling to cope with depression. I needed someone to hold my hand and help with from right people ect... I hope this helps. Take care Lisa x

posted January 17, 2018
A MyFibroTeam Member

Unfortunately I can't change doctors I have to put up with whoever the NHS give me unless I want to go private which I just can't afford. My rheumatologist is lovely but I can't see her until I've had an MRI and a nerve test. It's just my gp I can't stand. Every time I told him about my pain he would downplay it as "aches and soreness" no matter what I said.

posted January 16, 2018
A MyFibroTeam Member

UPDATE: the headaches have been better and pain a little bit More manageable but I'm still needing to take the full doses of painkillers everyday. Maybe it just needs a while to fully work?

posted January 15, 2018

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