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International MPS Awareness Day

User Profile: WellsFiction
WellsFiction May 15th, 2025

Today is international MPS awareness day. I have MPS disease type one. It's basically storage enzymes  that are suppose to recycle GAG aka complex sugar molecules in different cells. Since I don't have the correct enzymes this means different parts of my body such as my liver, lungs, or stomach can get damaged overtime.#notcool   

I receive enzyme replacement therapy. It helps my body to function, stay healthy and be well. Although having this disorder can be difficult, I'm thankful for all the amazing people it has brought into my life. There is so much research going on, seeking new, better treatments and ultimately a cure for my disease and many others.  Whether you have a rare disorder or not our health matters and it's important to seek medical help and also to remember we're not alone. Let's all shine a bright light together 😊💪💜🖤

https://mpssociety.org/ If you'd like more information please visit the MPS society website. Rock on!

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User Profile: AffyAvo
AffyAvo May 15th, 2025

@WellsFiction Thanks for sharing information about this with us!

3 replies
User Profile: WellsFiction
WellsFiction OP May 16th, 2025

@AffyAvo Absolutely! You're welcome, Affy :)

User Profile: MistyMagic
MistyMagic May 16th, 2025

@AffyAvo I agree and thanks for sharing this post with us.

1 reply
User Profile: WellsFiction
WellsFiction OP May 17th, 2025

@MistyMagic Thank you Misty. MPS is not a very well known disorder. I'm happy to spread awareness and share my story :)

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User Profile: MistyMagic
MistyMagic May 16th, 2025

@WellsFiction Hi, thanks for raising awareness of MPS. It would be interesting to hear more!

User Profile: Eman144
Eman144 May 17th, 2025

Thanks for sharing information to us .💛💛

1 reply
User Profile: WellsFiction
WellsFiction OP May 18th, 2025

@Eman144 Of course! You're welcome, Eman :)

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