What happened to my moms face Part 2

The idea that you have a lot of pain is heartbreaking… I hope the doctors are able to help you manage it!

It’s scary how our body can just betray us sometimes. She’s awesome for educating people and she has such a good vibe. Blessing

I have never heard of KT. Thank you so much for sharing your story. Knowledge is power!!! Keep educating others. It is important, thank you and God bless you.

she’s still beautiful. i hope she gets what she is working really hard for! ❤❤

The liveliest voice. The most beautiful soul. God bless you and your family. ❤

I had an AVM on my face that started growing immediately after I was born. I had it operated on in 1984 when I was 18 months old. They were concerned that it would grow and block the blood supply to my brain because of its rapidity. I'm very lucky that the surgery it took them a year to develop worked. Thank you for spreading awareness and being positive.

So sorry that you are in pain. You are beautiful! Sending you my love and prayers.

Such a sweet disposition. I'm sorry about her pain.❤❤❤

I JUST LOVE how you honor your mother...👏🏾🤩🥰

My daughter was diagnosed with KT Syndrome at birth. She was excepted to live a week because her case was considered extremely involved. Before she turned 16 years old, we found out it it is actually PIK3CA SPECTRUM DISORDER or C.L.O.V.E.S. In her case, she does have a positive test for PIK3CA gene involvement. She will be 23 this year and currently is in horrible pain in her back. We are praying for an answer in August when we see our favorite surgeon. ❤❤

Your one of the most beautiful people I've ever seen .... kudos for your gorgeous hair and beautiful eyes ...❤❤

Thank you brave lady. I see your beauty!

I was born with the same type of birthmark on my face, chin, and neck. I’ve been told by doctors that if I were to fall or have any trauma to that area that it could cause deformities and/or tumors. I’ve worn makeup my entire life to cover my birthmark due to bullying and people staring. Seeing you on social media talking about it, normalizing it, and informing people makes me so happy. It’s just nice knowing I’m not the only one with this type of birthmark because I’ve never met anyone with one like me. Keep flaunting your beauty girl ❤❤❤

It’s nice to have you being so honest and open about your KT. Having a disability, or being different opens up a chance for people to connect on a personal level. Ty for sharing, I look forward to part 3

Your gorgeous, God knew you could handle this trial and your doing it with class!!! I hope you find something out there that helps your pain

Education rocks, thank you. Beautiful soul!

Shouts out to you for speaking your TRUTH and your still Beautiful Queen☀️🫡💯💯💛💛🙏🏼

She is beautiful 😍.your mommy's transparency is a blessing..Bless you

Thank you for sharing and teaching/telling us about it. I'm so sorry you're in pain. Sending lots of love ❤

Thank You so much for sharing your illness with us and for being brave enough to help others understand! You’re absolutely Fabulous inside and out! You go Girl! Wishing You and Your Family a Blessed 2024♥️