Welcome the Logan Strong Blog

Announcing the Logan Strong Foundation Jennifer, Kevin and Logan Fogg are thrilled to share with you the establishment of the Logan Strong Foundation*. The Foundations’ purpose is to help raise childhood cancer awareness, and to provide items of comfort and support...

2107 Reflection As I look back on this past year, I am filled with mixed emotions.   It has been by far the WORST year of my life but also, the BEST year of my life.  I have learned so much, especially in these past 10 months.  I am not the same person I was this time...

Sorry for the delay in updating you all. It's been a whirlwind of a day. We are exhausted to say the least. Mentally and emotionally drained. Scanxiety is no joke!!   Thank you everyone for your positive thoughts, good vibes and prayers....THEY WORKED!!! His scan...

9/20/17 - WOW!  I can’t believe we are done with the better part of being inpatient for 6 months and aggressive chemotherapy.   It feels like the past 6 months have flown by but trust me, they didn’t!  It was rough and still continues to be at times.  Living in the...

  As many of our close family and friends know, I have worked for Aflac for over 5 years and yes, I am also a policyholder.  When Logan was born, I added him to my Aflac policies because he was in NICU for five days and I figured I might as well add him to all of...

As I sit here on the eve of Logan’s fifth round of inpatient chemo, also my birthday, I am overcome with conflicting emotions. Part of me is excited to go back to the hospital and finish inpatient chemo once and for all but there is another part of me that just wants...

I have literally sat down at least a dozen times over the past few weeks trying to write a blog post.  I actually have had a few different topics running around in my head that I have been trying to get on paper (computer) but time just gets away from me.  I...

As I sit here thinking about the past few months, I can’t believe all that our family has been through and has overcome already.  I am so excited that we finally get to go home tomorrow for nine days, it feels so surreal!!!!  I am beyond ecstatic and cried tears of...

Please click the link below to help support the Childhood Cancer Survivorship, Treatment, Access, and Research (STAR) Act of 2017 https://www.votervoice.net/Shares/BHvsWACsAClSMAeew3Q7FAA

This post comes with a disclaimer that there will be no filter.  I have been feeling so many different emotions lately that I just need to get it out.  So I will apologize in advance if I offend or upset anyone. Three months ago today our lives were turned upside...

We are coming off a week of absolutely amazing news.   In a matter of seven days Logan underwent two extensive brain surgeries where the doctors were able to resect 95% of his tumor!   This is everything we, and all of you out there, have been praying for (and boy do...

I don’t even know where to begin. These past couple of weeks have been another crazy rollercoaster ride. On Tuesday night April 25, around 11pm, Logan stopped tracking (following) and was just in a trance like state. I knew for a few days prior that there was...

To everyone who has taken the time out of their day to be here, to show us love and support, and to help us in this most difficult time…thank you.  It doesn’t seem enough for us just to say “thank you” when so many of you have gone so far above and beyond anything we...

Logan started chemo on Monday, March 20. They are able to treat his tumor very aggressively due to his age.  Children, especially babies are able to receive a higher dose due to their resiliency.   Unfortunately the tumor is too big for his little head to be removed...

When Jennifer and Kevin got married in June 2015, they knew the next step in their life was to start a family. They struggled with fertility and sought treatment. They were able to get pregnant after one round of treatment. When they found out it was a boy, they were...