Mighty Milo’s Adventure with HIDEA Syndrome

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Mighty Milo’s Adventure with HIDEA Syndrome

Milo was diagnosed with a rare genetic disorder called HIDEA syndrome. I will use this page to keep

31/07/2024

👼🤍

Share Memories of Milo & Support the Alligood Family

28/07/2024

Absolutely anything helps, even just spreading the word! 🤍🦓

With a heavy heart, I share the devastating loss of Mighty Milo, who lived… Hannah Brazeau needs your support for Support for Mighty Milo's Family in Grief

20/12/2023

Snuggles and cheesecake before surgery in the morning! Everyone keep Milo in your thoughts and send positive vibes our way! He is having surgery in the morning to have tubes put in his ears💙🫶🙏

13/12/2023

To most of you this isn’t much, but to me this video is EVERYTHING. These moments are few and far between and I can not believe I was able to capture a video, I will cherish this forever 💙

11/12/2023

Milo is getting in the Christmas spirit 🎄❄️⛄️🧑‍🎄

hb_vivid_photography

01/12/2023

In honor of Milo’s birthday this coming Sunday 🎉 I can’t believe our baby is going to be three 🥺💙🙏

05/11/2023

To everyone that keeps asking, this year we have decided not to have a birthday party for Milo. RSV and covid are already making there way around and we don’t want to risk Milo getting sick! Instead, if you’d like to do something for Milo we ask that you make donations to NORD, which helps support research for rare diseases.
We also have an Amazon list of things that help us with the daily care of Milo. I can’t believe our boy is going to be three 🥺💙

https://www.amazon.com/hz/wishlist/ls/FKNP2FE1T25H?ref_=wl_share

25/09/2023

We haven’t posted on this page in awhile so here is a little photo dump of Milo enjoying life 🥰🍁☀️

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