Top Tweets for #CFMiniCon
I'm excited to be speaking on 2 panels at #CFminicon: Transplant on Nov 14!
Where you can find me:
SESSION 1 - 5:10pm PST
"Not Pursuing A Transplant"
SESSION 2 - 6:20pm PST
"Real Talk: My Transplant Experience"
Best part? It's free! Register now at https://t.co/tDbDbMlhVW
#Cysticfibrosis comes with many unique challenges, but it's just one part of your life. Register today to join other adults with CF online for CF Adults Connect, our last #CFMiniCon of the year, and meet with friends old and new! https://t.co/D0pE3WR2iP
What's the best way to celebrate the end of the year with other friends living with #cysticfibrosis? Register today for CF Adults Connect, our last online #CFMiniCon of 2018, to chat with friends, participate in fun activities, and more! https://t.co/Tv6JgG2diK
Managing life with #cysticfibrosis is a balancing act, and it's important to make time for fun! Register today to connect online with other adults with CF about your passions at our last #CFMiniCon of the year on 11/7. https://t.co/D0pE3WR2iP
Life with #cysticfibrosis is more than breathing treatments, clinic visits, and taking care of your GI system. It's important to find time for fun, too! Register for our last #CFMiniCon of the year, and connect online with other adults with CF. https://t.co/D0pE3WR2iP
I have such admiration for those who go through the #transplant process. #CFMiniCon was AHHHHMAZING. ๐๐๐
This #CFMiniCon is gut wrenching. I'm learning so much, mostly things I just needed reassurance on, but all of you are such amazing people. ๐๐
@CFF_DC A special thanks to our own Jackie Price and Danny and Jackie Bessette for all the time and effort they committed to todayโs Lung Transplant MiniCon. The program is incredible. You can still register! https://t.co/VNTFJyqfwx
#CFMiniCon #lungtransplant #CysticFribrosis
Incredible, over 400 people have registered. Register now. There is much to learn during this program. Congrats to Somer and Laima for their leadership, all involved and to the CF staff, who excelled again. #CFMiniCon #CF_Foundation #lungtransplant
๐ป Join me at
CF MiniCon: Transplant!
โ
You or a loved one have #cysticfibrosis
โ
are considering a lung transplant
โ
preparing for transplant
โ
post transplant
โ
August 15
โ
free virtual event ๐ฒ
@CF_Foundation
#CFminicon
Register now: https://t.co/nmvsQnTGEP
Learning about my reproductive health, y'all. ๐๐ป๐๐ป #CFMiniCon
Itโs on! #CFminicon
Talking to your partner about your #cysticfibrosis and sex may feel uncomfortable. Virtually chat with other adults with CF about how they handle these challenges in an open and honest forum at #CFMiniCon on 4/8. Register now: https://t.co/Du3kTB9Odf
Thinking about starting a family? Discuss with other adults with #cysticfibrosis the different ways to grow your family with CF at #CFMiniCon on 4/8! https://t.co/CCR9Ye8dBX
Join me at CF MiniCon: Sexual and Reproductive Health! Find out more at https://t.co/GFm5IYaTTa #CFminicon
#Cysticfibrosis affects more than just the lungs โ it can affect the male and female reproductive system, too. Register for our next #CFMiniCon on 4/8 to openly chat with other adults with CF about these experiences in small group video breakouts. https://t.co/i6l9VKAUGv
People with #cysticfibrosis are living longer, more fulfilling lives, and for many that includes sexual and romantic relationships and the possibility of starting a family. Chat with other adults w/CF about these experiences at #CFMiniCon on 4/8. https://t.co/Du3kTB9Odf
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