Chronic Illness and Medical Mystery

Advocating

Advocating for Better

It boggles my mind, that we still have only have two major clinics treating our kids (at least publically) for this neuroimmune issue we have termed PANS and PANDAS, which begs the question – why? What is it about our kids that says to doctors and medical professionals “hmm, best not dig too deep on this one, give them XYZ medications until the parents move on and then we can all move on”?

Are my kids not worth the trouble? Do my kids not deserve to get the same respect and reverence as a child with say diabetes?

Seriously, what is it about our children that makes them seem not worth going to bat for?

It’s an interesting conundrum really when you think about it. Parents bring in a child who is ramped up, distressed, OCD with intrusive thoughts, or TICS that are debilitating or complex, low tolerance to stress, learning abilities shot to bits, challenging behavior, depression, super high anxiety and very often suicidal at a really young age, and it is typical for the family to be told: “hmmm, could be ASD, could be bipolar, could be ADHD, we don’t really know but let’s move you into mental health, perhaps some OT and we will see you periodically to do errr yeah nothing all over again”.

Most doctors first, of course, run rudimentary blood work, a CBC, CMP, maybe thyroid, cholesterol, even an MRI and perhaps an EEG, but what about digging deeper for the reason for this chaos when nothing obvious shows up? Why is no one looking for the complex clues? I like to think it’s a mandated time thing, not a – not wanting to dig deeper thing. We are waiting for them to say, “why is this child off the charts? What happened to this kid, why are they acting out, hitting their siblings, cursing at their parents, running away from school??” but they rarely do.

I don’t believe the majority think this is just bad parenting or a “bad” child thing either. Although there are certainly some that wonder if our kids just came out this way. “Sorry chaps, terribly bad luck, you just got a badly behaved child” or they think this is a genetic predisposition that is exacerbated by who knows what… but why, for the most part, don’t they show a spark of curiosity for chasing down the trigger?

Maybe the conversation in their head goes “whoa, I have no idea what this is but it looks complicated and confusing, surely psychiatry has a drug to dampen that down?” Or is it “whoa, I think I know what this is, but I know it is confusing and drawn out to treat, I know no insurance wants to cover the medications that help and there are no clear markers for what I am looking at, probably best to let the family move on to someone better who can spend the time looking deeper?”

I don’t know really, but I am on a mission to at least try and make it easier to access medical treatment where we live. As many of you know I am in the South and we are very limited here in terms of treatment options. However, after a full year of campaigning with some very, very awesome and cool parents, I am proud to say things are really looking up. One of our representatives has taken an interest in this campaign and we are hoping for an Advisory Council bill sooner rather than later.

Calm down now, it isn’t as sexy as it sounds, it is simply a bill that would allow for 18 volunteer professionals in this state to come together four times a year to brainstorm how to get the latest and most up-to-date information on PANS/PANDAS into the hands of every doctor, ER, school nurse, educator, and ergo parents, in the state. Five states so far have some form of legislation in this manner, another is very close, and 31 states (ours included) are on a mission to do the same.

In addition, those same very, very, awesome and cool parents have given up their precious time to beg, cajole, email, mail, ask, and present on this subject to anyone who will listen. It is working, people are listening, and we feel like we are winning. It feels good most of the time but today, I had my most liked/highest retweet ever, it said:

“Hate to be a downer, but life with PANS is hard. It’s hard on the whole family. it’s.so.hard to see opportunities lost, kids & parents feeling so inadequate, feeling odd/different, feeling like a failure. All because egos got in the way of a medical dx ?#PANS”

Up to now, I was sure my biggest tweet would be down to my sparkling repartee or stinging wit, but no, it was this. I thought wow – I post and retweet studies and statistics and advocate for treatment and care, and I love to retweet those who do what they do to make stuff happen. I follow and retweet all my heroes and all my legislators, I @ and hashtag all day long, but this, this is what gives me my most positive reinforcement Twitter moment ever (I am like Pavlov’s Dogs).

I guess today wasn’t tough just for us (#schoolrefusal, another day school seemed too daunting to even go). As PANS/PANDAS parents we ALL try so hard. We are ALL fighting for better but sometimes I know there are moments that we all just long for normal (not even going to say “whatever that is”, because truly in our hearts of hearts, we know what it could look like and we know that’s not what we have). Anyway, tonight as I sip my wine, I revel in the glow of my 10 likes and 8 retweets (hahaha move over Ellen DeGeneres (Verified account) @TheEllenShow with your 77 million followers – I got 10 LIKES – beat that baby). Tonight, I am a Twitter rock star … (#itsthelittlethings)

Life after treating Lyme

What’s life like after treating Lyme?

January marks month 7 on Laser Lyme protocol.

Where are we now? It’s been an interesting few months, new moons, full moons, Christmas, Halloween, New Years, quite the plethora of reasons to expect hyperactivity, tiredness, and general backsliding. To keep that in check, we still remain true to our NELL protocol, but with the kids back in school, hubs back to work and my commitment to campaigning for legislative changes here in the state, it could easily slip away from us.

That aside, where are we now? Are there regrets over that long summer in the camper in NE? Have we seen any further progress? How are we maintaining?

Well in true and typical fashion nothing is very easy or predictable but we are still sitting around 80 & 85% – we haven’t made any real progress forward in the last few months really but the good news is – we haven’t gone backward. That alone is worth celebrating. We have continued to follow NE Lyme Laser protocol because it is working for us (although we don’t do the exercise and oxygen every day, or the footbath every week, and we have also not been to a chiropractor since we got back), but we do take the drops religiously every day, 3 times a day to keep the Lyme at bay. We have also chosen to work with a nutritionist (Real Food Rebel) to try to address some other areas we know we have challenges in. We completed hair testing and in light of that Brenda at Real Food Rebel has determined a targeted supplement regimen for us. Now we follow a program for healing their digestion challenges. My kids continue to do “ok-ish” on both of these programs combined. The rashes are going or gone, skin is becoming clearer and overall the kids are functioning at home and at school, which is helpful for us all. One little bump in the road is that we are having to remove the amantadine that proved so beneficial in the beginning. If you read back through old posts, after much trial and error (actually 15 different trial and errors) our doctor had prescribed amantadine – just to try and affect some positive change in impulse control. Starting amantadine is what we now refer to as a turning point for our family. Initially, we didn’t see much progress on just 100 mg once a day but once we went to the twice-daily dosing schedule, we started to see big changes. Later a tonsillectomy and adenoidectomy proved equally as beneficial and finally, we got to a point of stability which then enabled a return to school – so life changed drastically from those two interventions for sure. Anyway, around October or November last year an intermittent arm/hand tremor started to became an everyday occurrence and it was decided the time had come to remove this NMDA antagonist/antiviral/ dopamine agonist drug. Tremors can be a side effect of this medication. Never the less, it is bittersweet (it helped so much but no one wants their kiddos on long-term pharmaceuticals) to let it go because we had seen that huge progress using the Amantadine (rationale for use).  It can also be tough to take this particular medication away so we are titrating down very slowly. We know that irritability, depression and suicidal ideation can be an issue with amantadine (both on it and coming off), so we are being cognizant that we might see positives and negatives in those areas before we are completely done.

As a parent, navigating all this information is overwhelming sometimes, I had heard the terms “NMDA antagonist” and “dopamine agonist” before all this started but it wasn’t my go-to in any conversation and I probably couldn’t have used either in a sentence. It was never anything I thought I would need to know, but now these terms and definitions are added to the ever-growing medical vocabulary tucked inside my memory banks. I feel like these definitions must be firmly solidified in my head because, during conversations with medical providers, we need to be semi-knowledgeable enough to agree with treatment plans which sometimes have to happen on the fly.

So what’s next?

MOLD

It turns out that life after (or with) LYME often centers around mold, and this is now the new rabbit hole we have decided to chase down. I am exhausted and would really prefer to snuggle under my duvet and ignore any more LYME, PANS, Mold or infectious disease processes, seriously I really don’t know whether to laugh or cry at the thought of starting a new project all over again. My house has been tested 3 times in the past year, and we have high levels of Aspergillus penicillioides amongst other fun stuff. We only found this out after much convincing to test from friends who all agreed more had to be going on. I really didn’t believe there was mold in my house because A: We have no active leaks and B: We had completely renovated the house 5 years ago when we moved in. I was positive there was no mold, but to stop the questions, I ordered an ERMI test from Mycometrics . No one was more shocked when the results came back really high and Aspergillus was the worst.

We set to cleaning every room with a combination of water and Everclear, we also threw away hundreds and hundreds of items that might have been contaminated by mold. We painted rooms with low VOC, mold resistant paint, and we even purchased an HI TECH machine along with 2 very large unattractive Dri Eaz air scrubbers, but the mold still remains somewhere in this house. Sure, our ERMI scores have gone down significantly but not yet low enough to be considered “acceptable” to live in for someone with a Chronic Inflammatory Response Syndrome (CIRS), which we seemingly have. So – as exhausting as it is – we plan on using a different company (Conflict Free Mold), to take new samples. This will mean I can afford to do every room individually. Prior testing was one sample from multiple rooms combined on the same cloth, we did it this way simply due to cost. Unfortunately, this means that while I know I have mold and what type, I have no idea at all where the mold is concentrated or where it has spread in the house. So, pith helmet on, flashlight in hand, crawlspace here we come… not really, I will purchase a kit, and send off 10 samples (one from each room) and see if we can finally pinpoint where our problem area or areas are.

This journey was never going to come down to just one thing I suppose. It’s been caused by many things stacking against us for a long time. Lyme may be one of our triggers but the post-infectious autoimmune encephalopathy we are struggling with now, is the end result of many, many, many things, or at least it is for our family. This may help explain further – Moleculara.  The longer this goes on, the more we find out, the harder we must work to resolve it. We want what everyone else wants – our kids to be as healthy and happy as possible in this life. Mold is toxic, gene SNPS create issues, bacteria, viruses, unhealthy diets, allergens and environmental toxins aggravate an already stressed immune system but we still want the best for them. So, for now, all we can say is:

“Mold!! – Challenge accepted.”

 

What about me!

What about me indeed…

It’s 6:18 pm and I had just woken up from a nap on the couch, woken by the sounds of my husband emptying the dishwasher and starting dinner. I fell asleep about 5, saying “kids need their meds, I am just taking 5 minutes and then I will get them ready.” Yet, here I was, 2 hours later, off schedule and sleeping once again. I hate napping, it makes me feel like crap. This time was no different. Whenever I wake up, I have to open and close my fists to get my hands working, because lately the little fingers on each hand have a pulsing and prickling feeling to them. It’s a weird sensation because they are not really numb, I can move them, so it’s more like that feeling you get from sleeping on your arm. Anyway, I woke up feeling crappy and guilty about sleeping instead of parenting, guilt aside napping isn’t unusual for me, I nap most days and feel bad every single time but honestly, I am usually just too tired to resist 5 minutes here and 20 minutes there. Anyway, tonight after I unfroze my feet (because they also seize up when I sleep) I wandered into the kitchen to finish dinner. I try for my own sanity to just crock pot, slow roast or Instant Pot everything and today was no different. I was grateful I had put a large joint of beef in the oven before we left today, so at least that part was taken care of.  The kids are getting tired of eating “stew” and soups but my energy is so depleted by dinnertime (and we follow a Paleo diet meaning everything has to be made from scratch), gourmet meals are just not realistic. I do know they are going to get fed. It will be edible and organic and nutritious but other than that, I don’t really know what to do about it all. I just seem to be a slower, less energetic, less motivated version of myself lately. I have mentioned before that I have my own battle with Lyme, even though the official diagnosis is fibromyalgia, yet what to do with this information, I don’t know. I don’t have the energy to even think about it. However, the day may be coming soon when I do

IEP meetings that don’t scare me

Friday was our yearly IEP update meeting for B. Not going to lie, had very few demands or expectations. Was just hoping to keep slipping by and doing what we are doing. Life has become easier and I like it. Again, remember that energy level I mentioned before? It applies to being able to wake up every day and manage emails and phone calls from anyone, never mind school. I just can’t do it anymore. Call me before 9 am and chances are real good I am not answering that call, call me after and I am not making it out the door quickly even if you want me to. There was a time in the past that I would send B off to school, get ready and wait, just wait for the phone call to tell me to come back and pick him up. Years of this, years and years of school management under my belt that I no longer have to be ready for. Imagine that? Just as well anyway, because as I already mentioned, not moving fast in the mornings anymore. If I had to come and pickup early now, I would have to actually shower and change out my PJs first, so fair warning please don’t call me in a panic before 11am, it is just not going to happen.

Anyway, Friday, IEP meeting. Raced to school for 9 am!!! Late (what’s new?), needed to make up time so husband was driving like a boss and we made it there dead on the nose, signed in and immediately, (adrenaline pumping) … have to leave school for a fire drill! I actually wasn’t upset, I went back to the car, spent time catching up on my breathing and finished my coffee. Went back in feeling a little more ready for what was to come.

Meeting went great. B is doing so well we were able to discuss removing some modifications meaning he is going to be more ready for high school classes beginning next year. Yes, B is actually heading to High School. I never imagined I would see the day, I always hoped but truthfully, after so many years of school refusal and school trauma, it was hard to imagine B functioning, happy and actually working toward independence in any classes let alone all of them. He has even managed to go from 4th-grade math to 6th-grade math in less than one year. If he can close the gap that fast again this year, he will enter 9th-grade math classes WITH his peers. Phenomenal and truly an achievement for a kid who was unable to manage life for many years especially after 3rd-grade. Interesting side note: Modifications in an IEP are different than accommodations and in high school that may potentially cause an issue.

So, more progress, more good things, more to look forward to. Treatment wise, both are now holding steady. Currently one (B) 85% recovery (just so many good things happening but still, he finds it challenging to manage stress and I wonder if this is ever going to change just by treating the Lyme). I cannot really say with A, if pushed perhaps about 80% better than when we started, but that nausea really took a toll and caused more stalling and backsliding. Removing the orthodontics (braces) from A’s teeth actually seems to have worked. Nausea no more. Or at least barely ever. She still gets occasional moments when she has to sit down and take a minute but the non-stop never-ending nausea has gone. No Zofran needed for the last two weeks at least. I now believe it may have been a migraine thing, she has/had also been complaining of intermittent pain over her eyes. The nausea was fairly chronic, and migraine makes more sense to me than allergy to the metal in the braces or other reasons why the braces would be the culprit. Maybe it was just the act of moving the teeth or jaw. I don’t know. I don’t but three weeks after taking off the braces, the nausea is slowly becoming a memory so, yeah that’s weird, but everything with us seems to be weird. I personally have learned to stop questioning why and just move on to the next problem.  I think she is still mildly flaring from having the braces on and then off, she is having moments here and there of goofiness, talking nonstop, following me around incessantly and some other PANS-ish symptoms. Again, not super sure why. Could be the cough-cold season, flu season, being back in school or just more of a sawtooth recovery than B. Thankfully, now the nausea has stopped the supplements and herbals are back on board and that’s helping tremendously. I think we will start improving again. So that’s it. I don’t know what day we are even at anymore, I know we have been home for 6.5 weeks and things have been great and not so great, and great again. Little things throw us through a loop but overall we keep improving. I am no longer trying to figure out how to pay for IVIG, no longer looking at rituximab, no longer praying for relief and best of all no more frantic doctor shopping. Good start to October, at this rate we might actually be able to afford Christmas!

How Many Times…

How many times …

I had reason tonight to go back over a series of blog posts about a program we had completed in 2011. As I was reading through the Brain Balance blog roll I realized we had actually finished that program with hope in our heart and a skip in our step. Okay perhaps we were not quite that enamored but certainly, we felt like we were in a really good place. When I wrote any of those earlier blog posts, I had no idea that those brief periods of respite (that we celebrated so much) would last a few months and then cycle right back around again. In reality, by the end of 2013, we had cycled into a far worse place than we had ever been before. If you have read this blog from the beginning you will know that that was quite an achievement.

By September 2013, a truly awful milestone had been reached. So even though we had enjoyed slightly better behavior, slightly less stress, slightly calmer days and nights, and definitely more cognitive ability during those 12-18 months after the BB program, it didn’t last, because in our world recovery has never lasted.

Why even write the blog? I don’t make money doing this. I lose sleep because I only find time to do this late, late, late at night. I don’t have a million subscribers or even a YouTube channel. I often ask myself what’s the point, why do I keep writing this? Living in the chaos that stretched into years, I knew I would forget the nuances, the little things, the truly chaotic nature of what was going on and when? Although it probably would be better for us all if I had just forgotten a lot of what happened and moved on. Initially, I truly hoped someone would read what I was writing and say “I wanted to contact you and let you know, I know what this is, I know how to help you” but as desperate as we were that sadly never happened. We spent years hoping for the cavalry and by the time I started writing this blog we were really heartbroken and lost about what was going on with our beautiful, cute, adorable son. It was only many years later it eventually occurred to us WE ARE THE CAVALRY. We have spent years on this hamster wheel, praying to get off never really knowing how but we never stopped trying. I, like millions of other parents, refused to give up. When we went from one doctor to another, from one mediocre treatment to another, we never gave up.

When I first learned that we had a spectrum disorder at 18 months, I thought to myself “well, we are not doing this, he’s going to be fine” and being who I am, I got on with the business of healing my child. I really thought, for sure by the time he was 3 we would have this thing resolved. I wasn’t worried. I had it in hand and was egotistical enough to believe that by the time he was eligible for early intervention, we wouldn’t even need it. Later, when the Easter Seals combed over paperwork the Arizona Early Intervention program had sent when we moved, I assured our caseworker that we would be done before his 3rd birthday and a place in the local school district was unnecessary. Just help us get settled I had said and we will take it from there. Yet when he started developmental pre-K on his 3rd birthday, screaming relentlessly as I left him at the school, I allowed them to placate me as they reassured he would be fine and I thought, “Okay, I am a little disappointed we didn’t get to where we needed to be already but by kindergarten, we WILL be sorted.” It turned out that kindergarten actually went pretty great. We figured we were making progress, we congratulated ourselves because what we were doing was working. A little later, when we again began having challenges, I really still had great hope. As part of that hope, we switched to a private school for 2nd grade, I thought, “HA! I had missed a part of our puzzle, I believed I had figured it out. It was the school that was the problem. I naively thought, “the new school will make it better for us all” and for a while it did. Around this same time, we had completed Brain Balance and then chose to re-enroll in another round of OT about 6 months later. It was actually going well in the small Christian school he was enrolled in.  However, we all know how this story goes and by the end of 3rd grade, we found ourselves right back to square one. It was a perfect storm of both a challenging teacher and what we now know was a defunct immune system.  These autoimmune triggers can wax and wane depending on environmental situations, bacterial exposures, viral loads and even just from the etiology of the disorder, we didn’t know this at the time. Those behaviors were actually a symptom, not a side effect of what was going on. Those behaviors controlled all of us because we never truly knew what we were really dealing with. Even though many, many, many times we allowed ourselves to believe we were on the winning side of all that was going on.

Anyway, nostalgia night, that’s really all this post is about. I have been reading back through my blog and I see how many times we truly believed we had cracked the code. Even now – as well as we are doing – I know to err on the side of caution. I know from past experience this recovery could just be a fake out, this could all be smoke and mirrors. What we have going on may just have hit a down cycle and that alone might be the reason for our calmer normality. Next week, next month, even next year we might very well be right back where we started, but until then we choose to believe the cavalry finally arrived. Ever the optimist, I am choosing to believe that this time, this is THE time we finally have it figured out.

Lyme Laser – Day 86

 Lyme Laser Treatment – Day 86

Maintaining at home

Ideally, we would have only just been returning home from NE. This is a 12-week program but as previously mentioned, we were forced to return home a full 1.5 weeks earlier than we should have. Initially, we figured missing those couple of weeks wasn’t a big deal but it has definitely interrupted the flow of diet and supplement schedules. So yes, now I am wishing we stayed for the duration but as that wasn’t possible, here we are.

A few things have happened since we got home, one kiddo is still battling chronic nausea that began around week 8 while in NE, the other still has an infection on the forehead that was there when we arrived. Both kids have returned to school and that’s where we knew we would either confirm true progress or we would crash and burn. So for ease, I will break this down into two parts: Physical and then social – because realistically we struggle with both but they are separate challenges for us.

Physically both are doing pretty great (not perfect, but pretty great). Joint pain is mostly gone, for sure neither kid has woken up with “growing pains” since we returned, no more random weird muscle pain in their upper arms and no more strange shooting pains up their legs or in their toes, and of course, the foot pain I have mentioned before – still has not returned.

Headaches: These really only affected one kid but they too seemingly are gone. We are still struggling with braces (orthodontics) pain in teeth and gums but the TMJ-type pain along with the headaches thankfully no longer seems to be an issue.

Nausea: As I mentioned, one is still struggling a lot with nausea first thing in the morning, sometimes it’s really bad but regardless it tends to pass about an hour after the alarm goes off. Truthfully it is a little disturbing and we have been addressing it with our PCP since returning home (adding in small carbohydrate bursts, little piece of fruit, no water on an empty stomach, adjusting supplement schedules, small snacks before bed, different probiotics, activated charcoal, famotidine, etc) but it remains the same and I am now leery that it has something to do with the braces situation. Have to research that some more.

Stamina: This is an ongoing issue, PACER testing at school keeps triggering asthma attacks. However, the change here is that there is a desire to be fitter, which is a massive change in attitude. Realistically it will take time to get into a routine that involves physical exercise over computer gaming but we have the desire, so that’s a step in the right direction. We did order an oscillator so we can add that to our routine at home.

Skin eruptions: Both have ongoing weird skin issues. One has an almost fungal looking patch on the head, which is being addressed by a dermatologist and the other has dark patches on the forearm that honestly I just thought was dirt when it showed up initially. The patches are not raised or painful but the skin has a dirty gray discoloration to it. It is more visible later in the day and encompasses a large-ish part of the forearm, we had seen something similar early on in treatment on the neck area but that section is completely gone now. I am just assuming that this is due to some weird detox reaction.

Bartonella Rash: Seems to have stayed status quo now for the duration, it is definitely less than when we started but at some point stopped fading and is still visible especially for one kiddo.

Social: School is going superbly well. Both were happy to get back to their friends. Luckily the last two years have been favorable for that. Friends were scarce in the beginning, especially for B because the behavior was so erratic and extreme, but last year that began to turn around. They both now have a couple of really good friends and having a group to hang with at school, always helps the day go better. They both also report that their memory is improving which makes classroom work much easier. Even as late as May this year, B could only follow the first one or two sentences his teacher would say, after that his auditory processing became an issue in addition to the memory challenges and he was lost pretty fast in every class he went into. Both seem to be having an easier time understanding what is being said by the teacher without having to follow up or get extra notes afterward, this is an exciting piece of our puzzle. Processing instructions given verbally for assignments and/or tasks have been a significant problem in the past and caused many upsetting returns home from school. This seems to be resolving little by little as we continue on. I am also ecstatic to report that behavior in school has been great and we are managing to get to school on time which is huge. We had many, many tardies last year and one of our big goals this year was just to get to school on time. Now that sleep is becoming a regular thing, getting up on time is of course much easier and thinking about it logically, this probably helps the memory challenges just as much as working to reduce inflammation and killing Lyme has done. Chicken or the egg…

Homework is still not being completed by B (I just keep saying “breathe, lady, breathe – Rome was not built in a day…”) this is a big struggle because mentioning anything remotely homework related can cause a meltdown of epic proportions. This is where we see the most sparks of prior behaviors. Conversely, A has consistently been an attentive student even in the worst of times, A would cry and struggle and try super hard to keep up even during our homeschool periods. Homework has always been important and completed on time so again status quo reported here, nothing has changed for either of them in this regard.

Diet – Both are now allowed a wide variety of fruits and veggies and even 1 or 2 carbon sugars (honey, maple syrup). Both are taking lunch every day and B is pretty rigid about sticking to the diet, he apparently likes feeling so much better although the “anorexia” part of his OCD has always been a little discouraging. Anyway, he really is eating, eating well and eating in front of us so we know it is not an issue, we tell ourselves his pride in how his body has changed is kinda normal but still, this is a little anxiety driving for us. We have struggled with body image, choking feelings and food refusal several times for both of them and we don’t want that to become a recurring issue. However, they have finally started to grasp the “calorie matching” principle we were told to stick to and so we are just going to proceed with caution on this part of the program. Truthfully, A is struggling a little harder in this area. The desire to eat pancakes instead of protein in the morning is overwhelming and probably relatable to the nausea feeling. We did find a respectable almond flour pancake mix which is also Paleo, no sugar or soy and relatively high in protein. That seems to be a decent starter for the day and is working out well so far. We also found KNOW Foods, which is a huge bonus for the times when I am just too exhausted to cook and be creative or they are craving something cakey.

When we started on this journey a thousand years ago, we didn’t initially know when or how we would get our child (and later our children) back, we didn’t even know what was wrong or where to focus, but we knew we had to bring our kiddo(s) back someway, somehow. When the other one got sick, the panic became even more real. How does one envision supporting two adult children (who are struggling to function) long term, especially at our ages (less than 10 years to retirement) – it becomes very scary to think more than a few days ahead believe me and our conversations became more frantic as the years went by without real healing or relief. Yesterday, was our quarterly psychiatry follow-up appointment. This physician has been on the journey with us for over 4 years now. When we first started meeting with him, we all agreed, B struggled with memory, self-esteem, depression, struggled to stay on topic or focus on general conversations. Most conversations would jump randomly from topic to topic in no particular order. Everyone we had sought out told us B was very complicated and/or complex and many didn’t even know where to begin to try to help us resolve these challenges. Our psychiatrist has been an active participant of our long term support system, despite the fact that we either failed (and sometimes refused) many pharmaceutical or natural supplements, he has never given up making suggestions, talking us through and brainstorming different options. Yesterday, he was so happy to report to me at the end of the session that B’s mood is reportedly “great.” Yes, the kiddo who was been depressed for over 5 years is now reporting feeling “happy” and “ok about stuff.” He is coping well and actually using the strategies learned from years and years of CBT with both the psychiatrist and therapist. These people have been instrumental in helping him reframe the negative thoughts he has always had. However, prior to treating Lyme, rational thought processes or calming techniques were just not accessible to a child, in that moment, who had a brain on the boil.

So on that note, technically we are done, although of course we really aren’t, we are just done the core part of the program.

We will now stay on maintenance for however long it takes to get to 100%. As of today, nothing much changes until next week, then we take a few days break from one of our key supplements – not gonna lie, little terrified about that one but Dr. Wine has assured us it is a very valid next step in the program. So until the next update, wish us continued success and we will see where this takes us… If you are interested in learning from the clinic, contact them at Lyme Laser Centers of New England. However, I will say this, after many years of jumping down one rabbit hole to another (thanks mainly to information like this found on the internet at 2 am), I would caution you to do your own due diligence. Are we 100% well? No. We are only probably around 70-80% better than we were 6 months ago. Both kids still struggle emotionally, both still meltdown and rage randomly but certainly not the chaos it was before. Was this magic? No. There is no magic pill, not one that I have discovered anyway. Was this hard to pull off? Yes. We had to live away from home for nearly 3 months and commit to a program we had no idea would work. Is the diet part tough to maintain? Yes but as time goes on it becomes easier and easier. Does diet even help Lyme? I don’t know, I am not a doctor, it certainly helps us. Gut brain connections are being studied more and more, and so we felt it was an important part of any program, other people don’t. You have to choose. This has helped us get to probably about 80% healthy, this has helped us reduce rages (not eliminate, just reduce) and improve memory, this has helped them both feel mentally and physically better but conversely, there are a thousand different other things we tried that were amazing for others but didn’t help us at all, or it only helped a bit, or the gains didn’t stick, or the cost was prohibitive. So again I would caution you to do your own due diligence. I try really hard to not get caught up in the moment and I try to be realistic about where we are. I would never assume this is it for us, this is all we need because the reality is so many times recovery has been tenuous and treatments that have started successfully, ended up fizzling out. I would never suggest anyone do what we did because again, we are not where we need to be yet and even if we were, this may not be the answer for you anyway. We still also take additional supplements to those that were suggested a LLCNE. You have to read as much as you can (PubMed is a wealth of information), you have to talk to people, and only you can decide what’s next for you. But I can say, this is what’s working for us, right now, today and if I had to do it over again, I would. In fact, I am plotting and scheming how I can get myself through the program because the relief they got, I want for me too. 😀

Happy labor day everyone.

You can reach me at dancingbonfires@gmail.com if you have specific questions otherwise, until next week.

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