Lyme Time with Paula Jackson Jones

  Author:  Paula Jackson Jones Orig Published:  12/21/2017 As 2017 nears its end, many reflect over the past year, embracing the good times, thankful that the difficult ones have past and consider some necessary changes for 2018. I have been known to make a resolution or two, as I’m sure have many of you and most of those either never came to fruition or fizzled out. It wasn’t because my heart wasn’t in it. Maybe it was because I was more comfortable with the way things were that I couldn’t bring myself to commit to the idea of change. Change can be hard, even painful at times. Change requires a different mindset. You must stop thinking of things the way you always have and start thinking in the way you want to see come about. You must commit to something that hasn’t yet happened but that you have a great desire to bring to fruition. The definition of Resolution is as follows: 1) a firm decision to do or not do something; 2) The action of solving a probl

Author: Paula Jackson Jones Orig Published: 12/13/2017 There are times in our lives when our expectations are marred by the reality of the situation. Take the holidays for example. Children behave as best they can, sit on Santa’s lap and leave milk and cookies, in hopes of finding a new bike, Xbox, pony or puppy under the tree Christmas morning. For some, those expectations are met. For others, the expectation is marred by circumstances whether it be due to financial issues or some other issue beyond the comprehension of the youngster. Beyond comprehension is where Lyme patients reside. They don’t feel well so they go to their medical provider with the expectation that they will be treated and returned to good health in a quick fashion.    Back in 2009, I had the expectation at that initial visit with my medical provider that I would find answers and get better and when that didn’t happen, visit after visit, provider after provider, I began to lose hope of ever feeling be

Author: Paula Jackson Jones Orig Published:  12/7/2017 Something that I’ve noticed happens to chronically ill people is that they tend to over time lose their voice. Not literally but figuratively. As the duration of their illness goes on over time, they start to feel invisible and as they slowly lose hope of ever regaining their health back, they become quieter and quieter thus losing their voice. Sometimes this is caused by those entrusted to care for them. Patients are acutely aware of how friends and family react to their ongoing health issues and tend to not discuss them. Or how they are treated at a medical appointment when they raise a concern and it is met with disbelief or distain. After a while, the patient stops complaining or even talking about their illness and isolation sets in. As an advocate, I am constantly encouraging people to use their voice when they feel that their needs are not being met. I do not encourage anger and confrontation but emp

Author:  Paula Jackson Jones Orig Published: 11/29/2017  How do you explain to someone something that they have never personally experienced? We use analogies but sometimes even that is not enough. Sometimes, until someone experiences what you are going through, there is going to be a void in the fullness of understanding.  When I give a prevention talk or share my personal story with someone newly diagnosed, I use a lot of analogies to help make the connection to better understanding. Tick-borne disease is a very complicated disease and until someone experiences for themselves firsthand, there is going to remain a void. Such is the case with prevention. I can talk until I’m blue in face about the importance of using prevention products on your skin and clothing and pets to protect against a tick encounter. I can educate that ticks are still active in temps above 32 degrees. But all that goes by the way side until someone finds a tick embedded on them, their child or p