#LupusSymptoms - Fatigue

Much of our research focuses on discoveries that can lead to treatments to better address the debilitating effects of lupus while our funded scientists drive toward a cure. Fatigue is often cited as one of the most hated symptoms that treatments often cannot relieve. In this video, nine lupus warriors lupus share their experiences with fatigue.

Lupus affects millions worldwide, and there is no cure. Please help the Lupus Research Alliance to raise awareness and funds for lupus research.

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[familybills]

Trying to explain to people what tired means for a person with Lupus is so difficult - our society has not invented words that accurately describe how you feel.

[TaraSmallss]

I sent this to my husband because he just doesn't understand. I think he thinks I'm just being lazy, but he has no clue what we go through.

[smithy]

I think I have been living with lupus 15 years at least. It’s felt like a living hell that’s in my mind because everyone else thinks I’m crazy and nothing wrong with me. I’ve only just stumbled across what Lupus is and I want to thank everyone for spreading awareness. Everyone should know how to diagnose this horrible disease

[purplepatch]

God the end hit me hard. i feel like im running around like a crazy person when i do have energy cause i know it won't last.

[a.h.s]

That's exactly how I feel I sleep alot

[rikodelacuesta]

My wife used to tell me i was bipolar
Having energy some days and others don't,
Not beign the men she knew, Many fights over that, it use to angers me, now its saddles me....

[lovelyfree]

I love this channel I just found out about. I've been diagnosed for over two years now but had symptoms for almost a year. So technically it felt like three years. I could of been had lupus but the symptoms started showing in 2017 and I was officially diagnosed by rheumatologist Jan 2018 but in 2017 I had been in and out the ER and even went to hospital and had three doctors to say I possible have it. I just feel happy to be a lupus diva and that I'm not the only one who experience these things. So nice to see others who understand. We may look fine on the outside but inside is hard to deal with.

[ad]

Exactly but I push myself it's very difficult

[ziuenzx]

Living in Florida the more sunlight my body is exposed to the more my lupus inflames, and destroys me