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383d
How do I successfully get my doctor to listen to me when I say I think my fatigue is more than a symptom of depression and should be classified as chronic fatigue? Every time I've ever brought it up they've just said yeah it's because you're depressed, but this fatigue has progressed to levels where I almost can't function and the doctors don't seem phased by it.
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Depression
Acute lethargy
Myalgic Encephalomyelitis
Lethargy
Chronic Pain
Migraine
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49d
@kunama oops at the end it should have read... Get in to see a physician that will be open to ways that you can treat the CFS!
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202d
My current GP has a similar attitude. Even though I have been diagnosed by a specialist and put on the disability pension for ME. But I decided to go along with him putting me on citalopram. He sold it to me as a drug that helps chronic fatigue by stimulating my adrenal glands. But it is technically an antidepressant.
369d
When I had COVID I got extreme fatigue that I believe was similar to chronic fatigue (although thankfully it passed after a month). It felt really physically and emotionally different to the type of fatigue that comes with my depression.
377d
Chronic pain, various medications, cause fatigue as well as many other things, I don't know how often you get migraines but when I get mine I often have days worth of worse fatigue after them. Definitely get another opinion as it sounds like it's been getting worse over time which isn't normal no matter what is causing it.
My anti anxiety/depression meds make me sleepy. So do my otc allergy meds. Look for a different doctor. Maybe a neurologist? Nutrition can be a factor, same with hydration. There us no one solution for most people. I hope you can find someone to help
Have you done a PHQ-9 screening recently? Any mental health office should do them at every clinical visit and every so often from your therapist. It's a screening tool for depression and is really really easy to fill out. Explain to them explicitly (but nicely too, etc.) that you feel that you are not being heard and that you feel your medical needs are not being met. Write down a list of specific questions you want the answers to and DO NOT let them blow you or your questions off with a single flippant remark.
I second that 👆🏻. Get a second opinion. Or third. Or fourth. You should never have to put up with a doctor that dismisses you instead of listening to your concerns
I solved this by changing doctors 🤷♀️ if the person you're seeing doesn't believe in CFS or isn't listening to you, unfortunately there isn't a way to magically change their mind. It's hard work to find a sympathetic doctor who's willing to listen to your perspective on your own symptoms and experience but once I finally found that person a diagnosis came relatively quickly. I feel for you and I really hope you can make progress on a diagnosis soon.
@kunama yes, switching MD's is a plus! I had to switch my doctor because she was so overwhelmed with all of her patient load that she didn't have time to think about my CFS. So now I see an internist that is so open to check in all different avenues. He can only go with what I give to him. There are days that I really don't want to even talk about CFS mainly because my family don't believe it even exists. The bad thing with CFS is that even when you look it up to get a result it says that no one seems to know how to take care of CFS. I know it has been around for a long time and I know that I'm not the first person that has felt these awful moments but get in a position that will be open to what you need is the first thing to do! 👍
☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision
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To get your doctor to listen, consider asking for a different doctor and request blood tests for autoimmune and vitamin levels. You can also ask for sleep tests or see a sleep specialist. If they refuse, tell them to mark it as a refusal in your charts, which usually shows you're serious about the issue.
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