My Nonprofit Reviews

My twin boys are TTTS survivors born at 30 wks 5 days. I had laser surgery at 18 wks gestation at stage 4. Lawsyn & Landyce are my living miracles, & I'm so grateful to have them with me today. The TTTS Foundation is such a great cause, & the founder, Mary Slaman has been such a huge blessing to so many families such as mine. I didn't find the Foundation till after my ordeal, however, I have seen so many others get the help & support they needed from Mary & her Foundation. She gives hope & relief to all the TTTS families, & there isn't anything the Foundation won't do in order to help save your pregnancy, or to even help you grieve. Mary has been through it herself, & because of her graciousness, many others are able to have a chance. I like to give back to the Foundation whenever I can, & to help others just as her. The TTTS Foundation needs all the support it can get due to the rarity of the cause, but with the mortality rate as high as it is with this disease, it's just as important.