Welcome to this week’s Editor’s Choice!
Dysautonomia is misunderstood and neglected. This week we have two posts that could help you deal with this condition.
We also have a heartwarming story on an adorable toddler with cystic fibrosis. Lastly, those of us with rare disease know what it’s like to hold in our thoughts. So we have a post on what those with MG are thinking, but never say, something all of us can relate to!
We hope you enjoy this week’s Editor’s Choice!
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How to Make a Dysautonomia Connection Count
When you have a neglected condition, it sometimes feels isolating and lonely. That’s why it’s important to connect with those who are in your community.
Check out this article on feeling united in the dysautonomia community.
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9 Things People With MG Want to Say But Won’t
It can be more than frustrating to have a rare disease that makes your health unreliable.
And sometimes, without proper understanding, we can come off as lazy since nobody can see our pain. That’s why we wrote up what some sufferers of MG might be thinking but never say out loud.
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Toddler Talia is Taking on Cystic Fibrosis with a Smile
In a Press Release provided by PW partner Breath With Me, Strawfie Challenge, details of an adorable little girl and her journey with cystic fibrosis emerge.
Check out how she and her family are tackling this disease head-on.
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How to Make Salt Your Dysautonomia’s BFF
As a sufferer of dysautonomia myself, I can’t say salt helps my symptoms. But it has been known to help a lot of dysautonomia patients, so it’s worth a shot!
Check out how you can make it an integral part of your diet.
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