by Jennifer Crystal
The end of the year can be a time for reflection. What have we achieved? What losses have we endured? How have we grown and changed for the better? We can examine these questions personally, professionally, and universally. We often see ups and downs over the course of twelve months. A lot can happen in 525,600 minutes, and this time of year allows us to pull back and see the proverbial forest despite the trees.
When you’re sick with Lyme or any of the tick-borne diseases, it can be hard to see that forest, both on a personal and broader level. If you’re sick every day, sometimes worse than the previous one, it can be hard to feel like you’re making progress. Over 52 weeks, though, most likely you have some gratitude for the long game. You might also wonder if any progress is being made towards better treatment or awareness generally.
The answer, it pleases me to report, is yes. While there’s still much work to be done, great strides have been made throughout the Lyme world in 2019. Here are a few highlights:
I’ve written about many of these advances individually, but seeing my roundup here shows just how much work has been done, across multiple arenas, in one year.
That said, work in these arenas is not yet complete. More research is needed on new drugs like Disulfiram to ensure patient well-being and safety. Now that the Kay Hagan TICK Act has passed, we don’t know how effectively or efficiently money will be allocated. Meanwhile, awareness efforts are greatly improving—more and more doctors and laypeople I speak with know the basics, and often the ins-and-outs, of tick-borne disease—though there is still a lot of misinformation out there. While Lyme and other tick-borne diseases have been in the news more with each passing year, some of the reporting from major news outlets this year showed gross inaccuracies that hurt the Lyme community. As with all news these days, it’s important for you to research further than a quick headline or article, and not take everything at face value.
There have been disappointments in the Lyme world this year, but they’re far outweighed by the upside, and that gives me hope. When I first got sick in 1997, Lyme disease wasn’t even on the radar of my health care practitioners—nor was it on mine. When I got diagnosed in 2005, there were fewer treatment options than today and much less Lyme literacy. Much has changed in the two decades since tick-borne disease has been part of my life, and I can only imagine the vantage point from which we will look back on advances twenty years from now. Compare how understanding and treatment of HIV has changed in less than forty years.
Here’s to more advances in 2020!