Sensitive Teeth & Gums Tip

This is a problem I face on a daily basis. Because the joints in my jaws are so tight and painful, visits to a dentist are all but impossible.

Lyme Inside - Living with Late Stage Lyme Disease


With Lyme disease we get very sensitive to all senses (sound, sight, touch..etc). But also our teeth and gums are very sensitive. It can be painful brushing our teeth and using mouth wash. Even cold or hot water can be painful. I eat sour candy to help with nausea and the acid will make my teeth extremely sensitive and I can feel nerves being hit when I brush near my gums.

Using my normal toothpaste was very painful and my whitening mouth wash made it worse. I could barely brush on some teeth without getting tears in my eyes. I found using Sensodyn Pronamel helps with this issue. Makes it a little easier to brush my teeth with less pain. After a week my teeth are less sensitive. I just can’t eat lemon juice or sour candy as often I need to. Hope this tip might help someone out there…

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You Have Value

From Facebook Post Dated February 3 ·

You have value If you have chronic illness, you know all about the guilt. It may be easier said than done but it is possible to find peace.

Lyme Carditis Can Cause Sudden Cardiac Death: Article from

Medscape: Multispecialty

Janis C. Kelly

October 31, 2014

 Lyme carditis associated with Borrelia burgdorferi infection was uncommon but was linked to two previously unsuspected cases of sudden cardiac death, Joseph D. Forrester, MD, from the Epidemic Intelligence Service, Centers for Disease Control and Prevention (CDC), and the Division of Vector-Borne Infectious Diseases, National Center for Emerging and Zoonotic Infectious Disease, CDC, Atlanta, Georgia, and colleagues report in the October 31 issue of the CDC’s Morbidity and Mortality Weekly Report.

“Health care providers should consider Lyme disease as a cause of cardiac symptoms in patients who live in or have visited a high-incidence Lyme disease region, especially during summer and fall months and regardless of whether the patient reports erythema migrans. Additionally, health care providers should investigate the potential for cardiac involvement in patients who have other signs or symptoms of Lyme disease, particularly if they report chest pain, palpitations, lightheadedness, shortness of breath, or syncope,” the authors write.

The follow-up investigation to a December 13, 2013, report of three cases of sudden cardiac death associated with Lyme carditis included examinations of Lyme disease in seven high-incidence states. Lyme carditis was defined as acute second-degree or third-degree atrioventricular conduction block accompanying a diagnosis of Lyme disease.

During 1995 to 2013, the 121,894 cases included 1696 cases of Lyme carditis. Age-adjusted all-cause mortality (0.6% within 1 year of Lyme disease diagnosis) was lower than expected based on national rates. “Two of these deaths (0.002% of the total) were classified as suspected cases of Lyme carditis–associated mortality after review of available clinical information,” the authors write.

The two new cases were men in their 40s and 50s, both had clinical evidence of disseminated Lyme infection, and both experienced cardiac arrest within 6 weeks of Lyme disease symptom onset.

Median age for Lyme carditis was 43 years, but carditis was more common among men aged 20 to 39 years, among women aged 25 to 29 years, and among those older than 75 years than in patients aged 55 to 59 years. Most carditis (69%) was diagnosed during June through August. Patients presented with “fatigue, malaise, muscle and joint pain, shortness of breath, chest pain, and syncope,” the authors note.

“In reported cases, sudden cardiac death remains infrequent when Lyme carditis is recognized and treated with appropriate antibiotic therapy. However, two additional suspected sudden cardiac deaths associated with Lyme carditis were discovered, bringing the total number of cases identified during this investigation to five (three confirmed and two suspected). These cases highlight the public health and clinical challenge that Lyme carditis poses and the need for better primary prevention strategies,” the authors conclude.

The authors have disclosed no relevant financial relationships.

Morb Mortal Wkly Rep. 2014;63:982-983. Full text

Why Do Those With Lyme Disease Become Estranged? – Tired of Lyme l Lyme Disease Support & Consolation

Why Do Those With Lyme Disease Become Estranged? – Tired of Lyme l Lyme Disease Support & Consolation.

⇑⇑⇑ Link to original article page ⇑⇑⇑


Health first.  Social Life second.


It’s a process that has a natural tendency to occur when a person undertakes Lyme Disease; they may become estranged from friends, family, or a lover.  While not everyone battling Lyme Disease becomes disconnected from the people that they love so dearly, nearly everyone battling Lyme Disease has a difficult time maintaining these relationships.  But why?

Lyme Disease, after a conscious understanding of its requirements  becomes the main focus and priority in a person’s life.  If it doesn’t, a person’s health may continue to decline and may even result in death.  This small bit of logic provides the foundation that those battling Lyme Disease use to justify their willingness to engage in a contentious manner with Lyme Disease, which then may naturally lead to estrangement.  It’s a justification that has every reason to exist.  So why does it become so difficult for a person to maintain an active social life while battling chronic Lyme Disease?

1. Mental and physical symptoms

Just being a biological organism requires the use of both physical and mental attributes in order to survive.  If any of these attributes become compromised or hijacked, being a human being can become very difficult very fast.  The symptoms those with chronic Lyme Disease experience are highly likely to be unprecedented.  Severe fatigue, pain, inflammation, the biological hijacking of the systems of the body, and mental and cognitive degeneration; all just don’t allow for a person to be a social butterfly.  They may attempt to continue to be social, but doing so is no longer the walk in the park that is was before Lyme Disease.  From a simple conversation, to skydiving, the body of a person with Lyme Disease simply just does not allow for, or easily welcome, social activities.

2. Fear of ridicule, embarrassment, or misunderstanding

It’s hard enough for a person with Lyme Disease to track down and attain all the answers for themselves regarding their own state of health, and then to be questioned about their battle with Lyme Disease from another person?  Forget about it!  Lyme Disease, in a nutshell, temporarily hinders and collapses the life a person knew.  They lose their ability to work, go to school, and even perform their once indulging hobbies.  It’s not easy for a 45 year old woman to tell her friends and family that she no longer works because of an bona fide illness that may appear delusionally to others as pure laziness.  It’s surely no self-esteem booster for a 14 year old boy to tell his friends that he can’t come out and play for the fourth week in a row because he’s too tired.  And of course it’s a crushing  blow for a 21 year old junior in college to unwillingly bring his college endeavors to a halt.  The raw nature of Lyme Disease is unusual and bizarre to a mind that has never embraced or experienced it, and surely will breed misunderstanding in conversions.  The misunderstanding or ignorance of Lyme can lead to ridicule about the person with Lyme Disease, giving them all the more reason to not only isolate themselves, but justify their disconnection from socializing.

3. medicine

Depending on their treatment protocol, a person battling Lyme Disease may be taking an extensive amount of medicine to help themselves heal.  Extensive is by no means an exaggeration as the amount of medicine that needs to be taken in a given day, the method for application, and the rate at which it must be taken, tend to dictate a person’s daily schedule.  While a person  may be able to turn their treatment protocol into a mobile protocol once in a while, doing so time and time again can be very frustrating, and be a burden.  It can be so frustrating at times that the social activity a person with Lyme intends to engage in doesn’t even become worth the effort.  The ease of taking medicine at home becomes more appealing, and further crushes the chances a person with Lyme may take to become socially active.

4. Herxing

While herxing could easily fall into reason number one, it is its own entity when it comes to battling Lyme Disease.  A person may have physical and mental symptoms deteriorate, but the cause is not always bacteria die off.  Herxing itself, which is the result of treatment (i.e., bacteria die off), can be generally agreed upon as being worse than having Lyme Disease without treatment.  This is why many people refuse to restart their treatment after starting and then stopping it – they felt better before its application.  Herxing is very unpredictable, can be lengthy, extremely debilitating, and even harder to bring under control.  While normal Lyme Disease symptoms cause severe physical and mental symptoms, herxing really allows symptoms to reach their maximum power and prominence on a person.  Symptom unprecedentedly manifest to the most unbearable levels.  And it’s not uncommon for a person to feel as if their IQ level had dropped 50 points.  The tools that allow the human body to become socially engaging become hijacking during a herx.  The prevailing desire is to simply avoid all human contact.

Without your health, you have nothing

Of course it’s not easy to disengage yourself from the people you’ve surrounded yourself with for nearly your whole life.  Being social is part of what makes us human, and to have that ability nearly entirely taken away, it hurts.  It really does.  It is important to remember that this process of becoming estranged from family and friends is normal.  Many people battling Lyme Disease encounter this sociological symptom of Lyme as it’s nearly inevitable.  But, as social as we human beings are, and as important as socializing is for our minds, you can get through the periods of isolation.  You’ll survive.  It won’t be easy to endure but it can be done.  Socializing may not even be on the list of objectives to complete in the beginning stages of Lyme Disease treatment, but as healing occurs, you’ll find not only the desire to want to be social becoming more prevalent, but as well as the ability to do so.

It’s a simple logic: Put your health first!  Friends, a lover, and family will likely be there when you’ve recovered.  And even if they aren’t, you will possess the ability to make new friends and even repair relationships.  It’s a reward that will return for the strenuous efforts you put forth to overcoming Lyme Disease

My Lyme Today

Most days I don’t complain about how I feel. It serves no real purpose and changes nothing in my circumstance. Some days though, I just need to vent. Today is that day.

You know, I wish I could say that each day is different lately, but that wouldn’t be true. For over a week now, my wrists have caused constant pain, and it shows no sign of stopping. In fact, there are new knots developing in the joints of my already disfigured wrists.

Some of my fingers are already showing disfigurement and sometimes get stuck in an extended position that causes physical pain to adjust. The sad thing is that, as bad as my fingers are already, my toes are much worse. Most of them are drawn and knotted making any attempt at walking very painful. That pain is made worse by the pain and swelling in my knees, especially the right one for some reason.

To those ailments, I can add joint pain in my right shoulder (sometimes it just pops and shoots pain up my neck and down my arm), my left jaw, and sometimes my neck. There is spinal damage in my lower back, I have migraines, there are knots on top of the bones in my legs that run from my knee to my ankle. My left foot is permanently drawn to the inside and I am so tired I feel like I could sleep for hours. My memory is terrible now, and sometimes I can’t think of the right word to the point that I get frustrated and angry.

I have been getting treatments since the end of 2009. I am better than I was but nowhere near better. I likely have some damage to my body that will never go away, so some days (like today) I have to indulge my “poor me” tendencies. I am only human.

2012 Lymewalks

2012 Lymewalks.

Please take a moment to read my Chronic Lyme story and the information about the Lyme Walk (I am a virtual walker).

If you know more about the personal battle each person you will understand more about this often invisable  disease. Please read, then help with research or providing help to those without money to get just a little help.

You do as you are led. God bless you.