Ehlers Danlos Syndrome
EDS sounds awful, it is said to be an inherited disease that effects connective tissue.
There are said to be 13 types, but basically, you are looking at issues with hypermobility, dislocations, joint pain, fatigue, and bruising. Not pleasant at all.
The NHS state there is no cure, you just have to manage the situation and make the best of it with physiotherapy, support, counselling, and regular medicals.
I don’t know much about EDS, so I don’t want to waffle on too much about it.
But I do have one carnivore diet success story regarding EDS, from Dawn which is an absolute doozy and is very inspirational. I would encourage everyone to read it.
If anyone knows anyone else that has helped their EDS on Carnivore, please put them in touch with me. Cheers.
I will be releasing a “Meat Up” follow up post with Dawn in February… spoiler she is doing great.
Photo by Larm Rmah on Unsplash
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