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The Sullivan Story

Friday, December 30, 2016. Miraculous: 6 Months of Treatment. For the last 6 weeks or so we have been celebrating HARD! I’ve unintentionally / on purpose postponed writing about my scan results because I just haven’t been able to wrap my mind around it. I told you, I take a LONG time to process things! November 11 (my husband’s birthday! My scans revealed that my cancer is MASSIVELY SHRINKING! 6 months after starting the. Pembrolizumab Axitinib Clinical Trial. After only 6 months! This is easily the most...

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The Sullivan Story | johnandbrittanysullivan.blogspot.com Reviews
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Friday, December 30, 2016. Miraculous: 6 Months of Treatment. For the last 6 weeks or so we have been celebrating HARD! I’ve unintentionally / on purpose postponed writing about my scan results because I just haven’t been able to wrap my mind around it. I told you, I take a LONG time to process things! November 11 (my husband’s birthday! My scans revealed that my cancer is MASSIVELY SHRINKING! 6 months after starting the. Pembrolizumab Axitinib Clinical Trial. After only 6 months! This is easily the most...
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The Sullivan Story | johnandbrittanysullivan.blogspot.com Reviews

https://johnandbrittanysullivan.blogspot.com

Friday, December 30, 2016. Miraculous: 6 Months of Treatment. For the last 6 weeks or so we have been celebrating HARD! I’ve unintentionally / on purpose postponed writing about my scan results because I just haven’t been able to wrap my mind around it. I told you, I take a LONG time to process things! November 11 (my husband’s birthday! My scans revealed that my cancer is MASSIVELY SHRINKING! 6 months after starting the. Pembrolizumab Axitinib Clinical Trial. After only 6 months! This is easily the most...

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johnandbrittanysullivan.blogspot.com johnandbrittanysullivan.blogspot.com
1

The Sullivan Story: Heavy

http://johnandbrittanysullivan.blogspot.com/2016/07/heavy.html

Friday, July 8, 2016. Another easy day of treatment. Brain fog and fatigue are still hanging around, not to the extent that they were a couple weeks ago, but still mooore than I would like. My appetite has mostly come back (gained a pound this week! And my other side effects seem to be under control with the barrage of Walgreens meds I'm throwing at them. August 17-19 will be my next scans. These are the ONLY SCANS I have EVER been EXCITED about getting! July 20, 2016 at 8:33 AM. Here we are again, heari...

2

The Sullivan Story: July

http://johnandbrittanysullivan.blogspot.com/2016/07/july.html

Sunday, July 24, 2016. Seems like it's about time for an update on my treatment, what do you think? Quick recap: May 20 I started a clinical trial using immunotherapy combination treatment to allow my own immune system to start fighting my cancer. I fly from Nashville to Miami every Friday for check ups, and every 3rd Friday for my immunotherapy infusion. It seems like the tumors I can feel are shrinking, even after only 2 months of treatment! And there you have it! Super boring and easy! Most recently m...

3

The Sullivan Story: Whole Brain Radiation

http://johnandbrittanysullivan.blogspot.com/2016/04/whole-brain-radiation.html

Thursday, April 7, 2016. Here we are again, hearing the news we didn't want to hear. Seems like that's been happening a lot, huh? After 4 sarcoma occurrences throughout childhood and adolescence, finding another at age 24. In my heart. During my pregnancy. That cancer showing growth and spread during my third trimester. More growth a couple years later. MORE growth on treatment. Can't I catch a break? Aren't we deserving of a WIN! What did I do to deserve this? A novel treatment that wasn't around for an...

4

The Sullivan Story: October Update

http://johnandbrittanysullivan.blogspot.com/2016/10/october.html

Thursday, October 13, 2016. I'm long overdue for an update. And I suspect you're tired of reading everyone's thoughts on the presidential debate, so here's something less dramatic for you to read :). I've been on my clinical trial treatment for Alveolar Soft Part Sarcoma for 22 weeks now (about 5 months). I have an appointment in Miami every third Friday. To receive my immunotherapy drug (pembrolizumab), and then everyday. And now we have more. Gone, I can't feel the one in my neck at all. Smaller than t...

5

The Sullivan Story: Never Ever Ever Give Up

http://johnandbrittanysullivan.blogspot.com/2016/08/never-ever-ever-give-up.html

Thursday, August 4, 2016. Never Ever Ever Give Up. I've been in the pit. You may know the pit, you might have been there before. Its that dark place where your most pessimistic thoughts hold you captive and warp how you perceive your reality. It’s a place of isolation and fear, of worry and anxiety. It’s a bad place, the pit. Am I even contributing to the world at all? Will this ever end? I lost my hope. And you know what? It gave me hope. Never ever ever give up. 8221; She said it so frequently and with...

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Friday, December 30, 2016. Miraculous: 6 Months of Treatment. For the last 6 weeks or so we have been celebrating HARD! I’ve unintentionally / on purpose postponed writing about my scan results because I just haven’t been able to wrap my mind around it. I told you, I take a LONG time to process things! November 11 (my husband’s birthday! My scans revealed that my cancer is MASSIVELY SHRINKING! 6 months after starting the. Pembrolizumab Axitinib Clinical Trial. After only 6 months! This is easily the most...

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