A Midsummers Night Blog

This is just going to be kind of a random blog about Gabe’s progress and life in general.

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Lindt chocolate ball,  mmm

Gabe is now 5 months into topical steroid withdrawal.  I know I left off with sharing what rough shape he was in a couple weeks ago (with what may or may not have been measles…) without any real update.  He did get better.  Now he is back to his usual TSW self.

His skin looks much better than in the early days (or even two weeks ago with mystery illness!) but his energy levels are still very low.  I imagine long term topical steroid use caused major adrenal gland suppression and it is just taking a long time for them to “re-boot”.

At this point he is still sitting in his favorite spot, the recliner, for most of the day.  He doesn’t want to go anywhere.  I can’t blame him.  Minnesota summers are hot and very humid and it aggravates his condition horribly.  Just 5-10 minutes outside will lead to a 20 minutes “itchfest” where he’ll scratch till he is bleeding and in pain.

One of the hardest things is feeling guilty because so much of my time goes to taking care of Gabe.  My other two children just aren’t getting as much attention.  We could have picked a better time to start!  I feel like we are all missing out on summer fun, seeing as how we spend most of our time indoors.

I know next summer will be different, will be better.

In the mean time I can’t wait for school to start.  I know moms aren’t supposed to say that, but it’s true.  I am truly an introvert, and I need a good deal of peace and quiet every day for a sense of emotional well-being.  Being mostly stuck inside all day with three loud children is very draining!  That plus the fact that many nights Gabe is literally up till midnight and then up again at 7 am, needing care.

As someone who is naturally prone to depression, I feel like I have been handling this all really well.  My husband is my support system for sure.  Plus my sweet dog (the subject of my last blog post) he is always there with his comforting presence.  And of course, God (!!!).

There has been quite a lot of pain along the way.  In that this condition is very alienating and I haven’t gotten as much support from other people in my life as I would hope for.  I have felt judgement (real or imagined) at our decision to take Gabe off of his potent steroid creams.

I know that ultimately it really doesn’t matter what anyone else thinks.  My husband and I are 100% on the same page.  We feel like God led us to this point.  I know that Gabe will heal and that will be vindication in itself, along with being our greatest hope realized.

In closing I think that so often we feel like if God is with us, the journey would be easier.  We feel like if we are hurting and exhausted, God can’t possibly be involved.  But that just isn’t the case.  Just like how he met with the Patriarchs in the desert, he meets with us in our “desert”.

“I will make rivers flow on barren heights, and springs within the valleys. I will turn the desert into pools of water, and the parched ground into springs.” Isaiah 41:81

“Lord, help us to find your streams of life-giving waters in whatever barren wilderness we find ourselves in.  Help us to rise above our circumstances as we keep our eyes on you.  Do a work in our hearts as we submit the brokenness of our situations to you.  Help us to know that you are the prize we seek and that we have eternal value as your workmanship in Christ Jesus.  Amen”

 

 

 

 

 

 

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Update and TSW Treatment

Gabe started topical steroid withdrawal in mid-February of this year so he is 4 months in. 19113521_10158905728715074_8900016741876609406_n

The bright red skin of the first two months has faded and now it just looks like he has horrible eczema/was in a car crash.  The areas that still look really awful are where we applied steroids the most and longest- wrists, feet, ankles and legs.  His face is flaring though we never really applied steroids and he never had eczema there.

His energy levels are still maybe 35% of what they used to be.  He still spends a lot of time sitting in his favorite spot, the recliner.  He is able to be active and enjoy some quality of life thanks to some supplements we do everyday.

Right now what is really helping him is astaxanthin.  It’s a super potent antioxidant that is reportedly 6,000 times more powerful than vitamin C!!  I carry him out of bed in the morning and after breakfast he chomps up a 12 mg capsule of astaxanthin and within 10 minutes he is feeling 80% better and is able to get up and run around and be a normal kid.  His mouth is perpetually stained orange but it works!!  Astaxanthin is a naturally occurring antioxidant found in red algae (and sea food).  It’s what makes flamingoes pink!

We still give him CBD oil (yes, from marijuana) when his pain and anxiety levels are very high.  We give him 3-4 drops and he holds it in his mouth for 30 seconds before swallowing.  It really helps him and the benefits go behind pain relief.

We also give him detox baths every other day.  Epsom salts, dead sea salts, lavender oil and sometimes a bit of bentonite clay.  He likes the water very hot and even though it usually stings at first, he never wants to get out.  It’s the only place he doesn’t feel pain or itchiness.

Gabe also take probiotics and drinks a lot of kombucha.  He is constantly asking for fruit so we try to stay stocked up.

His sleep is still a nightly struggle.  So 1-2 times a week we give him 10 mg of hydroxinine to help him get some uninterrupted sleep.  We get a break and he gets to sleep through the night without shredding up his skin.

I just ordered liviaone topical probiotic spray and I am pretty excited to try it out.  I really think it will help Gabe heal because of so much of what he’s been through (similar to most people with eczema/TSW) destroy good bacteria on the skin- the steroids, the antibiotics, and bleach baths…. that I really feel he will be able to heal much more quickly with the introduction of healthy bacteria to his skin.

What I’ve tried that hasn’t been successful-

A high grade sodium bicarbonate (baking soda).  There is a lot of buzz about safe soda helping people heal very quickly on the TSW pages.  Problem is, this stuff is super expensive and hard to get.  I tried what seemed to be a similar alternative but without success.  I haven’t ruled out safe soda but it’d be painful to spend $60+ on a small contained of baking soda.

Essential oils.  I’m a huge user of them.  I’ve used them near daily for the past four years.  I just can’t put them on Gabe because his skin is so sensitive that they make him worse.  A couple drops in the tub is ok, applied topically just seems to be too much.

Homeopathy.  Granted we went right in the beginning and we were exhausted and overwhelmed.  We left with like 20 supplements all with complex directions.  Half of them were pills that he couldn’t even swallow.  It was basically a waste of $500.  It probably would have worked better later on in his treatment and if it was more simplistic and doable.

 

Spring, Sadness, Hope

I watched this video yesterday and broke down crying.  It pulled on my heart strings because I know exactly how each of the moms feel.  You struggle privately and have to put on a brave face for your kiddo.

Going through TSW is incredibly isolating because it isn’t a well known condition.  People have never heard of it.  Whenever I post updates or pictures I always get people saying things like, “OMG!  That’s an allergic reaction!”  or “coconut oil took care of my small patch of eczema!”  Insert head-slap here.

Also not particularly helpful is reaching out to the mother of a sick child….trying to sell them something as a MLM distributer.  We’ve tried every lotion on the planet at this point, I’m sure yours isn’t going to be the magic bullet that will end his suffering.  But….um thanks for offering??

Or posting progress pictures.  I always point out that’s he still has a long way to go.  But still people “be like” Hallelujah!  He’s finally healed!!  Um…slow down.  He’s still very much suffering and going through this.  I just like to post pictures when there is any progress to encourage myself and let everyone else know how he is doing.

Speaking of that, he has come a long way.  When you deal with something like this it is easy to fall into hopelessness because it just goes on….and on.  He’ll make major progress and then flare again.  Our hopes will rise, then get squelched.  But I know every single day we weather brings us one day closer to him being healed.

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This was about 1 1/2 months ago.  Yep, RSS is that horrific.
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That’s him now.  Not healed but making progress!

At the moment he is flaring on his face pretty badly.  He doesn’t want to leave the house, because he is so embarrassed.  He’s lost weight off of his already very skinny little body.  In spite of seemingly eating 24/7 he is very thin and his clothes hang off of him.

I also believe he is healing on the inside too.  His organs became steroid dependent as well.  Every morning he has a hard time getting going.  We need to carry him out of bed, get him breakfast, and then bathe him.  I still need to wash all his bedding every single day.  Because every night it gets bloody and crusty and covered in his dead skin.

We are hitting this thing from every possible angle.  Probiotics, vitamins, homeopathy, bone broth, garlic, sea salt….just every thing we can do to help him.

That’s been our focus and it’s really brought us all together.  I feel closer to my husband than ever.  I thank God for our solid marriage.  He has been my partner in this 100% and is so quick to sacrifice for his family.

Most days we are doing pretty good considering.  When you’re going through a long term crisis everything else get’s backburnered.  We barely celebrated Easter.  We haven’t really been able to go to church in ages because it takes so long to get Gabe going in the morning.  I was ok with that until I drove past a cross with ribbons billowing in the wind the Monday after Easter.  I felt an unexpected tidal wave of sadness at not being able to celebrate my favorite holiday the way I would have liked.  It threw me into a bit of a depression for the rest of the week.

But I know that next year will be totally different.  Next year we will go all out for Easter.  Next year we will properly celebrate our Anniversary.

We know that our faith has carried us through this and also all the many prayers offered up for Gabe.  Thank you everyone for your continued support and prayers!!

One Day at a Time

This has rapidly become a “TSW” (topical steroid withdrawal) blog.  I know, I know.  Just shy of three weeks ago we were thrust into this world we weren’t aware of.

Now I look back and I can see that at least 90% of Gabe’s “eczema” we’ve been treating for ages was, in fact, actually symptoms of damage and addiction from the creams we were using.  How horrible is that?

It is vindicating to me, in a way; as a more natural-minded type of person.  I never wanted to use steroids anyways.  I did when I felt like it was the only option.  Now I know there are so many natural ways to treat eczema.

It’s a difficult process to go through any sort of withdrawal.  Though topical steroid withdrawal is particularly brutal.  Many adults going through this have gotten to lows where they are suicidal.  Because the pain is that bad.  The itch is bone deep.  You can go days without more than a few hours of sleep. Your skin looks absolutely horrific to the point where you don’t want to leave your house.

I feel like we have been extremely fortunate in that Gabe is still sleeping relatively well.  He is doing very well emotionally.  He seemed ok to me but I wanted to make sure and I was asking him questions about how he was doing “on the inside” with all of this.  He didn’t know what I meant so I said, “does going through all of this make you feel sad?”  He looked at me like I had asked him an inane question, “of course not, why would it?”  He has had a good deal of pain and discomfort but he has taken it in a stride.  He is handling everything so well.

We’ve been doing everything we can to help his body heal.  He was on antibiotics because his skin had gotten “staphy” at one point early on.  He’s been drinking a lot of kombucha to help build up his good bacteria.  I’ve also made a couple pots of super healing soup.  The combo of bone broth, veggies, and spices is so good for him…and it tastes good too!

We did get great news from the dermatologist we saw last week.  She has swabbed Gabe to check for pathogenic bacteria.  I was actually shocked when it came back negative.  She said Gabe had normal skin flora and that the Doctor said she thought our regime is working well, and to keep it up.  That is huge because the main risk now would be from a serious secondary infection (from staph or step) until his skin is in better shape.

We were doing two baths a day when he was in really rough shape.  Now we just do one, at night, with warm water, sea salt, ACV, and lavender oil (we avoid soap cause it dries him out).  After his bath I put on coconut oil, Egyptian magic, clove oil (just two drops, heavily diluted) and silver gel as needed.  Our magic potion ingredients- 20170307_221256.jpg

I’ve read that there isn’t much you can do to speed up the process of withdrawal.  But I don’t think that’s true.  I’ve scoured so many blogs and articles and I really think that you can aid the process of healing along in many ways.

A huge way to hasten recovery is with positivity.  I’m a faith person so I believe 100% in the power of prayer.  I know Gabe has so many people praying for him and that has carried us through to this point.  I also believe that our faith has kept us positive and joyful, even during our worst moments.  We are looking for and celebrating every sign of improvement.  We are looking on the bright side.  We are practicing thankfulness.

He is showing improvement.  I don’t want to jump the gun, because I know that recovery is cyclical, but we are happy, nonetheless.

This was his back about ten days ago- 20170227_171250

This was him today- 20170307_134034.jpg

His neck and torso were initially the worst spots.  Now they are looking much less red and inflamed.  Though it seems to be working it’s way out, down to his legs and up to his face and his hands.  His legs are almost purplish as the blood vessels are very dilated.

“One day at a time” has been my mantra and that is how we will continue to handle this.  We will do everything we can but ultimately trust that we are doing the right thing and that God is sovereignly guiding this process.

The good that has come has been that we have drawn closer together as a family.  We now finally know the cause of Gabe’s ever-worsening “eczema” and more importantly, we know what to do.

Update on Gabe

I ended up deleting my past 4 posts for a couple reasons.  My husband didn’t like that I was putting Gabe’s suffering out there for the World to see and also that we want to be able to do what’s best for Gabe without fear of outside forces *ahem* meddling.

My husband and I process things very differently.  He is very stoic and private.  I’m an open book and sharing (with as many people as possible) makes me feel better.  But I respect his wishes and I see his point.  We will probably share more when Gabe is well along his healing journey.  We do want to raise awareness.

But still, there is good news and darn it, I want to share!  Gabe is doing a lot better than he was last week.  A lot of the more frightening symptoms have subsided.  His skin doesn’t look nearly as red.  He still has a lot of healing ahead of him, but we are so encouraged.

His actual eczema is almost non-existent.  I still believe God touched him and healed his eczema.  We saw enough of an improvement that we were prompted to get him off the steroids- the medicine that was poisoning his body.  Now we just need to go through the withdrawals.

Like so often, healing is a journey.  It’s a path.  There are good days and bad days, ups and downs.  But you discover so much along the way.  The journey itself becomes sacred in it’s own way.

We have also found an online community of people on this same journey.  There is a lot of encouragement and help to be found.

I do believe that God is blessing Gabe with a quick healing.  Some things I am doing to help are…

-twice daily soaks in the tub.  Sometimes up to an hour.  We toss in Epsom salt and essential oils or olive oil and fresh garlic.  After twenty minutes or so his pores really open up and I think he has been able to do a lot of detoxing that way.  The steroids cause the skin to constrict, and he was on them for so long his skin hasn’t properly detoxed in ages.  TMI alert- the bath water takes on the characteristic icky ooze smell so associated with TSW after awhile.  It gets pretty gross.  I theorize that it’s toxins and trapped sebum in the water.

We’ve also been using a zinc oxide (diaper rash cream) on his really bad spots.  For the rest of his body it is Egyptian magic, coconut oil, silver cream, and a drop or two of clove or lavender oil.

He is on antibiotics because he had gotten ‘staphy’ on his arms and torso last week.  That looks a lot better and we hope this is the only time he’ll need them.

We met with a new dermatologist today.  She was very understanding and admitted she thought Gabe did have a problem related to the steroids, though she stopped just shy of labeling it as “RSS”.  She was very supportive of us treating him without steroids.  She wrote us a couple perscriptions that may come in handy.

Gabe is handling this all really well.  He has been such a trooper.  We explained to him what was happening and why, and he has been so brave in handling a process that is very painful and difficult.