Showing posts with label VA Medical Center. Show all posts
Showing posts with label VA Medical Center. Show all posts

Tuesday, March 24, 2020

NIAID - National Institutes of Allergy Infectious Disease




The NIAID - National Institutes of Allergy Infectious Disease is the institute that has been helping my husband (Colin Benson) with DRESS Syndrome.  We are so blessed to have a strong team of dedicated health professionals in his life and caring for him.

In May of 2018 the NIAID (after much research and analysis of Colin's specific condition) offered to take Colin into their full time care and hospitalize him with a trial drug, Tofacitinib.  They were also going to try anti-viral therapy for his HHV-6 reactivation.

Tofacitinib is also known as xeljanz. https://www.xeljanz.com/  Xeljanz is primarily used for Rheumatoid Arthritis.  It is a strong and powerful drug, one that comes with a black box warning label.

Our family was made aware of this drug around the time he was hospitalized at Walter Reed Medical Military Center (WRNMMC) in December 2017.  The medical team at WRNMMC had tried various other drugs and these medicines just weren't strong enough or able to hold back his break through skin eruptions, rashes and his relapses.  Not only was his skin shedding in great volume, but his labs were showing more damage to his kidneys and liver. Additionally labs showed reactivation of the HHV-6 Virus.  It was clear that there was a lot more going on than just DRESS Syndrome.  DRESS Syndrome should go away after removing the offending drug and after several weeks of mediciations.  Unfortunately, Colin complex condition was much more severe and longer lasting.

Because his condition was so unique and the medicine that NIH was interested in using was so powerful, we took Colin to Mayo Clinic for a second opinion.  A new set of brilliant doctors were looking over his entire body, labs and medical history only to concur that his case was unique.  His doctors were all in uncharted waters and no medical treatment plan existed for his condition, nor was there a diagnosis that really explained everything happening with him.  Even still, every doctor was still trying to determine just exactly what was his medical condition.  Since DRESS Syndrome is a diagnosis of exclusion all of doctors could only do one thing, keep testing.

Some of the suggestions provided by doctors at Mayo Clinic were to continue with IVIG (Intravenous Immunoglobulin Treatment).  He previously used IVIG three days in a row while hospitalized at the Burn Unit in Washington Hospital Center, Washington DC. Additionally, Mayo Clinic doctors were able to determine that Colin's CYP2D6 Gene metabolized drugs slowly in his liver.

After visiting the Mayo Clinic in Minnesota twice, it was now April 2018 and we were ready to move forward with Tofacitinib and the Anti-Viral with NIH in Bethesda, MD.  The process took a few weeks and he was moved into their hospital for observation in May of 2018.

He stayed in-patient at the NIH (NIAID) for over 6+ weeks.  (Thankfully it was across the street from WRNMMC, so I was able to see him every day.  I was also permitted to spend the night with him several times.)



Monday, October 7, 2019

Colin's Condition - October 7, 2019

October 7,2019

My husband has a very unusual, prolonged undiagnosed medical condition that is chronic.

They have temporarily labeled his condition as immune dysregulation and chronic "DRESS Syndrome" with a reactivation of HHV-6 virus.  
There is a HHV-6 Foundation website that contains "some" information that is helpful to us, but again there has been no one found in the world that has what my husband has.  

So this entire process has been scary, stressful, confusing and challenging.  Which is why we continue to pray for God to watch over Colin and to heal him.


Today's Update:
Colin had an appointment with National Institutes of Health (NIH) to review the immune protocol and the results so far of this experimental medication that he is taking.
He has had testing twice on his adrenal function to see if it is safe to take him completely off Prednisone and switch to Hydrocortisone. 
At that time, he was not yet ready.

So at a later visit (August 6, 2019) he took the test again.  
He "barely" showed within range (at the very bottom line).
We were instructed to continue with his Prednisone (steroids) and then switch over to Hydrocortisone when he has plenty of down time to rest and work through it.

He is a also a patient at our local VA (Lake Nona).  However, he is being followed closely by NIH.  


Today he is on: (Listing immune suppression medicine only)
ZERO mg of Prednisone!!
25 mg of Hydrocortisone
10 mg of Tofacitinib

No more Prenisone!  
Predisone has caused so many problems for my husband.
He has Cushings
He has Glaucoma & Cataracts - Steroid-induced posterior subcapsular cataracts (PSCs) 
https://www.ncbi.nlm.nih.gov/pubmed/17900234
(He had the surgery, they also placed a stint into each eye)

We don't know how he will react with this change in medicine.  
At the onset of his illness Colin was initially taking 125 mg of steroids!  That is a very high (dangerously high) amount of steroids.  He began taking this high dose back in April 2017. 


Colin currently has many red spots all over his back and legs. He is completely exhausted, constant head aches and lots of pain in his joints all over. 

I made the mistake of bringing him along with me to a business networking event last Tuesday. That totally wiped him out for the rest of the week. He barely got out of bed.

He was able to attend one of my doctor appointments with me, which was very comforting.

On Saturday he was able to walk, just a little, through a community event. We only stayed for about thirty minutes though.


He has not gotten out of bed now from the pain and exhaustion.
My heart goes out to him, every day and forever.  This situation has been really hard on me as well.  Hard on my body - I have a lot of doctors and procedures and care now that we have left Walter Reed.  I miss my husband.  Colin has no energy, he has no strength.  We don't get to do many things together expect attend doctor appointments.