Log In or Register to Join The Conversation!

This topic is empty.

  • Author
    Posts
    • #26664
      Alyssa Silva
      Keymaster

      Morning! Wanted to share my latest column with you all. In it, I reflect on my diagnosis day (well, from what my parents have told me) and reflect on how my family must have felt receiving a diagnosis like SMA type I. Back then, very little was known about SMA and there wasn’t much hope in terms of treatments and life expectancy. I’m sure many of you can relate. What have you been told about your diagnosis story?

Viewing 0 reply threads
  • You must be logged in to reply to this topic.

©2021 KLEO Template a premium and multipurpose theme from Seventh Queen

CONTACT US

We're not around right now. But you can send us an email and we'll get back to you, asap.

Sending
or

Log in with your credentials

or    

Forgot your details?

or

Create Account

Copyright © 2017-2021 All rights reserved.