Howdy!

[JLHSmith]

Hey all. I'm excited to have this new C3G platform to connect with others through! My name is Jenna Smith. I'm 32 years old and have been living with C3G since I was 6. Been on PD then Hemo about....23 years?? lol - something like that. Had a transplant at 14 which failed due to DDD disease recurrence. Now I'm in the works for another transplant! So excited...and nervous...but so READY for it Hoping only for the best and excited about the trials underway in case the new kidney will need it.

[ANDYL_DDD Ambassador]

Hi Jenna, excellent news that you have joined this site. Hope you are keeping well x

[linfuller Ambassador]

Hi Jenna! It's great to have you here! I'm so excited for you that a new transplant is on the horizon - best of luck!

[DavidF_NKF Partner]

Hi Jenna! It's wonderful to have you in the community- I'm looking forward to your posts & the benefits of your experience with C3G. And it's great that you're going for the Tx- fingers crossed!

[Vik95]

You have a great attitude with all you have been through! Praying for meds for you and everyone 😊

[Vik95]

Hi Jenna,

Happy to connect with you. Do you experience any digestive issues because of C3g? My daughter was diagnosed at 14 and is going to turn 24 next week. The past 3 years she has had a lot of problems with her gi system. She’s developed many food intolerances and has difficulty with constipation/motility. Just reaching out to see if anyone else is experiencing anything similar.

Look forward to hearing from you,

Vikki