We are so excited and thankful to be able to share that Meredith has been given an opportunity to participate in the Dupixent trial. She has to go through a 3 hour visit with the study physician, have blood work and other tests completed, and we have to sign the Informed Consent for her to participate. As long as everything goes well, she will begin the trial after the initial visit. There will be a good bit of travel involved because the clinical study site is in Norfolk, Virginia. We are blessed to have a great aunt in Chesapeake, Virginia and she is going to let us stay with her when we have to visit the study site. Her home is just 25 minutes away from the study site, so we will be able to get a good night's rest before attending her appointments. We plan to drive back home after each appointment.
We are all very excited, but also nervous. Meredith has a 1 in 3 change of getting a placebo instead of the Dupixent injection. We are praying that she actually gets the medication and that it works. This study has already been completed on adults and adolescents. They had amazing results, so we have great hope that this will be the answer for Meredith.
Please keep us in your prayers as we continue through this journey.
Wednesday, October 31, 2018
Thursday, October 25, 2018
Eczema Stinks
Seriously, eczema is a tough disease and Meredith continues to fight against it. We have tried everything! She has had different allergy tests throughout the years to figure out if she was allergic to something. We have kept a food diary and tried to determine if a certain food was affecting her. She has used every topical steroid available, even the black label ointments. She has used oral steroids. She has tried oral medications, including Cell Cept, an immunosuppressant typically used for transplant patients. We have tried all natural alternatives. We have tried any and everything that friends, family, and acquaintances have encouraged us to try. We have prayed!
The #1 thing Meredith struggles with is confidence. As she has gotten older, her appearance has become much more important to her. She is beautiful inside and out, but this disease often affects very visible areas. She has been called names at school, had many people ask her "what is wrong with your face?", and even had kids and adults avoid her because they were afraid she was contagious. I have watched this disease affect every single aspect of Meredith's life; emotionally, physically, and mentally, yet, she amazes me with her strength.
On October 2nd, we made a trip to see Dr. McShane, Meredith's dermatology specialist at UNC Chapel Hill. These are just a couple of pictures of what Meredith was struggling with when we went to this visit.
As I've mentioned before, Meredith has been going to Chapel Hill and seeing Dr. McShane since she was four years old. At this visit, Dr. McShane told us that there was a new drug called Dupixent that had been first trialed with kids and adults with asthma. They are just starting a trial for those with severe eczema/atopic dermatitis. This is an injectable drug that would become a once a month injection. According to Dr. McShane, the use of this drug allows patients to not only have reduction in symptoms, but they don't have to continue use of topical steroids. Meredith was excited. We were excited. So, Dr. McShane submitted a request and preauthorization paperwork for this. Yesterday, we received a letter from the insurance company letting us know that the request was denied for the final time. We can appeal, but they will not allow Meredith to have the drug because she is not 18. So, after speaking with Dr. McShane, we have contacted the clinical trial administrator to see if Meredith can be a part of that trial. If she cannot, our next step is Cyclosporine, which is another immunosuppressant. Dr. McShane says this drug will affect her immune system, we will have to watch her kidneys, and there are other risks. Creig, Meredith and I will have a big decision to make this weekend as I will be taking Meredith back to Chapel Hill on Tuesday.
In my last post, I shared facts about atopic dermatitis. I want to share some questions that we often get related to Meredith's condition.
1. Is it contagious?
No, it is not contagious! You can't "catch it" from another person. The exact cause of eczema is not know, but researchers have found that individuals who develop eczema typically do because of a combination of genes and some environmental triggers. When an irritant "switches on" the immune system, the skin cells just don't behave like they should. This causes an eczema flare-up. These flare-ups can be minor or severe.
2. Isn't there something you can take or do to make it go away?
We wish it worked that way! It's not like having a sinus infection, where you can take antibiotics and it clears up. Unfortunately, there is no cure. There are treatments, but those treatments depend on the age and severity of the case. Meredith has been diagnosed with severe atopic dermatitis, which has allowed her a few more options when it comes to trying different medications. Treatment options can be over the counter remedies, topical medications, phototherapy, immunosuppressants, and biologic drugs. Some people find success with natural and alternative treatments.
3. Are there triggers?
Yes, there can be. Chemicals, soap, clothing, sweat, and scents can exacerbate the condition. Just touching a surface that had a chemical on it can cause a flare-up. Another trigger can be illness. If Meredith gets a cold, sinus infection, etc. it also affects her condition and can cause a severe flare-up.
4. Why doesn't she just stop scratching?
Itching usually causes scratching, which can lead to the vicious itch-scratch cycle. At times, the urge to scratch can be so intense. Scratching is definitely counterproductive to healing, but sometimes it is done unconsciously. Meredith often scratches in her sleep, which is why she takes certain oral medications to help her rest better and hopefully avoid scratching as much.
It is very important to me that others are educated on this condition. Meredith is so much more than this disease and that's what I want others to see. She is so smart, funny, friendly, compassionate, kind, and loving.
Please pray for us as we discuss our options this weekend and make decisions on our next steps.
The #1 thing Meredith struggles with is confidence. As she has gotten older, her appearance has become much more important to her. She is beautiful inside and out, but this disease often affects very visible areas. She has been called names at school, had many people ask her "what is wrong with your face?", and even had kids and adults avoid her because they were afraid she was contagious. I have watched this disease affect every single aspect of Meredith's life; emotionally, physically, and mentally, yet, she amazes me with her strength.
On October 2nd, we made a trip to see Dr. McShane, Meredith's dermatology specialist at UNC Chapel Hill. These are just a couple of pictures of what Meredith was struggling with when we went to this visit.
As I've mentioned before, Meredith has been going to Chapel Hill and seeing Dr. McShane since she was four years old. At this visit, Dr. McShane told us that there was a new drug called Dupixent that had been first trialed with kids and adults with asthma. They are just starting a trial for those with severe eczema/atopic dermatitis. This is an injectable drug that would become a once a month injection. According to Dr. McShane, the use of this drug allows patients to not only have reduction in symptoms, but they don't have to continue use of topical steroids. Meredith was excited. We were excited. So, Dr. McShane submitted a request and preauthorization paperwork for this. Yesterday, we received a letter from the insurance company letting us know that the request was denied for the final time. We can appeal, but they will not allow Meredith to have the drug because she is not 18. So, after speaking with Dr. McShane, we have contacted the clinical trial administrator to see if Meredith can be a part of that trial. If she cannot, our next step is Cyclosporine, which is another immunosuppressant. Dr. McShane says this drug will affect her immune system, we will have to watch her kidneys, and there are other risks. Creig, Meredith and I will have a big decision to make this weekend as I will be taking Meredith back to Chapel Hill on Tuesday.
In my last post, I shared facts about atopic dermatitis. I want to share some questions that we often get related to Meredith's condition.
1. Is it contagious?
No, it is not contagious! You can't "catch it" from another person. The exact cause of eczema is not know, but researchers have found that individuals who develop eczema typically do because of a combination of genes and some environmental triggers. When an irritant "switches on" the immune system, the skin cells just don't behave like they should. This causes an eczema flare-up. These flare-ups can be minor or severe.
2. Isn't there something you can take or do to make it go away?
We wish it worked that way! It's not like having a sinus infection, where you can take antibiotics and it clears up. Unfortunately, there is no cure. There are treatments, but those treatments depend on the age and severity of the case. Meredith has been diagnosed with severe atopic dermatitis, which has allowed her a few more options when it comes to trying different medications. Treatment options can be over the counter remedies, topical medications, phototherapy, immunosuppressants, and biologic drugs. Some people find success with natural and alternative treatments.
3. Are there triggers?
Yes, there can be. Chemicals, soap, clothing, sweat, and scents can exacerbate the condition. Just touching a surface that had a chemical on it can cause a flare-up. Another trigger can be illness. If Meredith gets a cold, sinus infection, etc. it also affects her condition and can cause a severe flare-up.
4. Why doesn't she just stop scratching?
Itching usually causes scratching, which can lead to the vicious itch-scratch cycle. At times, the urge to scratch can be so intense. Scratching is definitely counterproductive to healing, but sometimes it is done unconsciously. Meredith often scratches in her sleep, which is why she takes certain oral medications to help her rest better and hopefully avoid scratching as much.
It is very important to me that others are educated on this condition. Meredith is so much more than this disease and that's what I want others to see. She is so smart, funny, friendly, compassionate, kind, and loving.
Please pray for us as we discuss our options this weekend and make decisions on our next steps.
Monday, October 1, 2018
We Love Someone with Eczema!
October is Eczema Awareness Month, so I am going to try to share a little each week about this condition that our Meredith suffers from. I say suffer, because she really does struggle each and every day with this condition. Meredith was diagnosed with atopic dermatitis, an autoimmune condition, when she was just three months old. As Meredith has gotten older, some aspects of the condition have gotten a little better, while others have worsened. When Meredith was four years old, she was hospitalized due to an infection related to her condition. You can read more about that here: Meredith's Hospital Adventure
After Meredith's hospitalization, we were referred to UNC Dermatology in Chapel Hill. This began our journey with Dr. McShane who has been following Meredith's case since. Dr. McShane has tried many things over the years with Meredith. There was a trial that started last year and we were so hopeful that Meredith would get to be a part of the trial. Unfortunately, they decided the children included in the trial had to be over the age of 12. Meredith was so disappointed. Dr. McShane has stuck with us through so much. She has really been an encouragement for Meredith.
After Meredith's hospitalization, we were referred to UNC Dermatology in Chapel Hill. This began our journey with Dr. McShane who has been following Meredith's case since. Dr. McShane has tried many things over the years with Meredith. There was a trial that started last year and we were so hopeful that Meredith would get to be a part of the trial. Unfortunately, they decided the children included in the trial had to be over the age of 12. Meredith was so disappointed. Dr. McShane has stuck with us through so much. She has really been an encouragement for Meredith.
We actually get to see Dr. McShane tomorrow. Meredith hasn't seen her in about 6 months and she has lately been struggling with major flares, so she cannot wait to see Dr. McShane.
What is Atopic Dermatitis?
Today, I'll share the difference between eczema and atopic dermatitis. Eczema is actually a general term for dermatitis. Dermatitis means inflammation of the skin. All of the types eczema cause redness and itching, but some will blister, weep, and even peel. There are several different types of eczema. Atopic dermatitis is considered a severe and chronic or long-lasting form of eczema. Each type of eczema has different triggers, symptoms, and treatments. It's important to know why type you have, in order to be able to manage it appropriately.
What are the Symptoms of Atopic Dermatitis?
Atopic dermatitis is chronic. It does not usually go away in a few days or weeks. For many, this is a lifelong condition. It is very itchy and can cause damage to the skin from repeated scratching or rubbing. It normally appears on the cheeks, legs, and arms, but can be found anywhere on the body.
Symptoms include:
* dry, scaly skin
* redness
* itching
* cracks behind the ears
* rash on the cheeks, arms, and/or legs
* open, crusted, or "weepy" sores (typically occurs during flares)
Because the skin can become open during flares, infections are common.
How can Atopic Dermatitis be treated?
Depending on the severity of symptoms, the condition can be treated with:
* topical medications (such as steroidal ointments)
* phototherapy (light treatment)
* immunosuppressant drugs (curb the immune system)
* biologic drugs (target specific areas of the immune system)
* systemic steroids by mouth or injection (used in extreme cases)
Unfortunately, Meredith has experienced all of the above symptoms, plus! She has also tried many different treatments. Some work better than others. Now that she is older, she is much more concerned with her appearance. She has been bullied and picked on at school many times. I am amazed at her strength and how resilient she is. This year alone, she has been called "diseased", "scab face", and more. She came home one day last week and told me that a boy in her grade had made an ugly comment about her face to her. Her reply to him was "thank you" and she kept walking. This girl has gone through more than I ever did as I was growing up, but she still manages to keep a positive attitude, smile on her face, and a kind heart.
Meredith, I know you will read this. I want you to know that I am so proud of you! You are beautiful inside and out. I only wish I was half as strong and brave as you are. Love you more than you will ever know!
Wednesday, May 30, 2018
Our Story- Foster Care
May is National Foster Care Month. I promised to not only
share information about foster care this month, but to also share our story. I
was trying to decide how I would begin and quickly realized that in order to
begin to tell our story, I have to start at the very beginning of our journey,
which began in 2006.
In March of 2006, Creig and I were so excited to find out
that we were pregnant. We couldn’t wait to tell all of our family and start
planning a nursery. Sadly, we went through the tremendous pain of losing that
precious baby. After working with my doctor and using fertility treatments, we
became pregnant again. I remember being terrified, but thankfully nine months
later our beautiful Meredith was born. My pregnancy with her was rough and my
delivery was very difficult.
Two years later, Creig and I decided that we wanted to try
to have another child. With the help of my doctor, we again used fertility
treatments for quite some time. We then decided that we would stop the treatments
and just put it all in God’s hands. Creig and I had discussed many times the
different options we had. We considered domestic or international adoption. We
considered adopting through foster care. We considered the fact that maybe we
were meant to be the parents of one child. When Meredith turned 9, we really
began researching adoption through foster care. We didn’t want to make the
decision without talking to Meredith, so we had multiple conversations with her
and explained everything. Our biggest concern was the fact that any child that
entered our home could be reunified with their birth family, which would mean
that Meredith would also experience that loss. Her response to that is what solidified
our decision. She said, “Well, I will be sad, but I will be happy to know that
we could love them and take care of them while their mom and dad couldn’t.”
We read everything we could about foster care, talked to
people who had been foster parents, and had multiple conversations with the
director of Agape of NC. In April of 2016 we began the foster care licensing
process. We completed our home study, fire inspections, background checks,
fingerprinting, extremely long- 35 page family self-study, CPR and First Aid
certifications, trainings, and so much more.
We received a phone call in May of 2017 letting us know that
we were officially licensed. We were also told that our agency preferred to
have new families provide respite at least one time before they have a child
placed in their home. This way they can see what it is like to have someone new
entering their home and the effects it can have on everyone in the family. On
May 23, 2017, we received our first call and were asked to provide respite for a
sibling group of three. A (female) was 6
years old, L (male) was 3 years old, and A (male) was 2 years old. We were told
that these siblings had been in foster care for almost a year and a half and
that their foster mother had to go out of town. She just needed someone to
provide respite for Memorial Day weekend. We agreed, but had absolutely no idea
how this three day experience was going to change our lives forever. We picked
them up on Friday and they had to go back home on Monday. We fell in love with
these three kids in just a matter of days and I was so sad to have to watch
them go.
It was just a week and a half later, on June 5, 2017 that
Creig and I were having lunch in my office and received another call from the
director of Agape. She informed us that she had received a call about an infant
that was currently in the hospital in Chapel Hill. She was just a month and a
half old and had been in the hospital since birth due to a heart defect
requiring open heart surgery. She told us that the agency and the area DSS had
been looking for a family to take her for days and had not had any luck. Creig
and I immediately said “yes, absolutely. We will take her”. She told me that at
least one of us would have to go to the hospital and stay overnight to be
educated on her needs and medical conditions. I was ready to go then, but we
were told to wait until we received a call. The following day, I received a
call from a physician at the hospital and she told me that they had been
informed that we were going to be the foster parents for baby S. She asked that
I come as soon as possible to meet her. I left within the hour and was so
thankful that my mom went with me. I will never forget walking into that
hospital room and seeing my precious little girl laying in that crib all alone.
The nurse picked her up and laid her in my arms and in an instant, she had my
heart. I think I slept about an hour that night. I spent so much time just staring at her,
holding her, and taking care of her. The next day, we were released to go home.
In just one week, we will celebrate one year since S joined our family.
Almost two weeks later, I received another call from Agape.
I was told that the three siblings we had provided respite for were in need of
a new home. I was also told that they were likely going to be separated for
various reasons and asked if we would consider taking one or two of them. I
knew exactly what Creig would say, but I told the director that I would need to
call and talk with him first. When I called the director back to tell her that
we would take any of them, I was told to sit tight. The next day, we were told
that all three had been moved to a home in their area together and that they
were hopeful that it would work out. Creig and I were thankful that they were
able to stay together and continued to pray for them. The following week, I
received another call from the director. She told me that the siblings were not
moved just once in that previous week, but a total of three times. She then
asked me again if we would consider taking any of them. I again told her yes,
and she asked if we would take the two boys. After double checking with Creig,
I called her back to find out when and where we would need to pick them
up. The following day, L and A were back
in our home, but this time long-term. Their sister was placed in another home,
but her foster parents were also clients of Agape. Thankfully, this meant that
we would be able to have contact with them and work together to help maintain
contact for A, L, and A.
Never in a million years, did we see our journey going in
this direction. I had assumed we would hopefully adopt one child through foster
care. It never crossed my mind that we would ever be considering adopting three
children. Here we were, June of 2017, a family of 6. We had two boys and two
girls, ages 10, 3, 2, and almost 2 months. In just two short weeks, our lives
were forever changed.
I would love to be able to say that from that day forward
everything has been sunshine and rainbows, but that would be a lie. We have
struggled, we have cried, we have hurt for our kids, and we have felt so
defeated at times that we questioned how in the world we could ever be enough
for them. But, we have also loved our kids more than we ever could have
imagined. We have fought for them, advocated for them, encouraged them,
supported them, and become their biggest fans. The traumatic and tragic
experiences that our kids have had will forever be a part of them, but we are
thankful to be able to hold them up in those difficult times and support them
through it all.
Today, as I look back over the past year, I am so thankful
and just so amazed at how far we have all come. I cannot even begin to express
how much I love all of my kids. I am grateful that God chose us to be their Mommy
and Daddy and can’t wait to watch them change the world.
Until today, we have only shared this with our family, but
we have recently signed adoption petitions for A and L that are currently being
filed with the Clerk of Court. We will soon be sending in our adoption petition
for S as well. It is our hope that all three adoptions will be completed by the
end of summer. We can’t thank all of our family and friends enough for all of
the love and support given to us throughout this journey. It’s certainly not
over yet, but we are so excited to soon begin a new chapter. Stay tuned!
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