thelymelight.blogspot.com

The Lyme Light

Tuesday, March 10, 2015. Now, I identify most with the Dysautonomia diagnosis. I still struggle with the same major symptoms as I did years ago:. Severe musculoskeletal pain (Severe Fibromyalgia), SI and hip joint pain being the most severe along with Sciatica. Severe, chronic Fatigue. POTS (low blood pressure and tachycardia). Brain fog (problems with cognition and memory). Anxiety, panic attacks and OCD. Nausea, no appetite. Hypoglycemia (low blood sugar). And these new or worsening symptoms:. And a fe...

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The Lyme Light | thelymelight.blogspot.com Reviews

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Tuesday, March 10, 2015. Now, I identify most with the Dysautonomia diagnosis. I still struggle with the same major symptoms as I did years ago:. Severe musculoskeletal pain (Severe Fibromyalgia), SI and hip joint pain being the most severe along with Sciatica. Severe, chronic Fatigue. POTS (low blood pressure and tachycardia). Brain fog (problems with cognition and memory). Anxiety, panic attacks and OCD. Nausea, no appetite. Hypoglycemia (low blood sugar). And these new or worsening symptoms:. And a fe...

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The Lyme Light | thelymelight.blogspot.com Reviews

https://thelymelight.blogspot.com

Tuesday, March 10, 2015. Now, I identify most with the Dysautonomia diagnosis. I still struggle with the same major symptoms as I did years ago:. Severe musculoskeletal pain (Severe Fibromyalgia), SI and hip joint pain being the most severe along with Sciatica. Severe, chronic Fatigue. POTS (low blood pressure and tachycardia). Brain fog (problems with cognition and memory). Anxiety, panic attacks and OCD. Nausea, no appetite. Hypoglycemia (low blood sugar). And these new or worsening symptoms:. And a fe...

INTERNAL PAGES

thelymelight.blogspot.com

1

The Lyme Light: May 2009

http://thelymelight.blogspot.com/2009_05_01_archive.html

Monday, May 25, 2009. Links to this post. Sunday, May 24, 2009. 1) Avoid sick people at all costs. 3) Continue all immune system support and preventive measures. This includes frequent hand washing for 15-20 seconds, sanitizing hands often and before taking any medications, temporarily taking high dose vitamins (ex. Airborne), wearing surgical masks at home since my mother is sick. 4) Fever reducers, as needed. . Links to this post. Saturday, May 23, 2009. Links to this post. Monday, May 18, 2009. I'm st...

2

The Lyme Light: I'm still here...

http://thelymelight.blogspot.com/2015/03/im-still-here.html

Tuesday, March 10, 2015. Now, I identify most with the Dysautonomia diagnosis. I still struggle with the same major symptoms as I did years ago:. Severe musculoskeletal pain (Severe Fibromyalgia), SI and hip joint pain being the most severe along with Sciatica. Severe, chronic Fatigue. POTS (low blood pressure and tachycardia). Brain fog (problems with cognition and memory). Anxiety, panic attacks and OCD. Nausea, no appetite. Hypoglycemia (low blood sugar). And these new or worsening symptoms:. And a fe...

3

The Lyme Light: Trips to the doctor or lab over the last 6 months...

http://thelymelight.blogspot.com/2009/12/trips-to-doctor-or-lab-over-last-6.html

Wednesday, December 2, 2009. Trips to the doctor or lab over the last 6 months. How many times have I been to the doctor, to a lab, or to a medical facility for a specialized procedure or test over the last 6 months you ask? Well, the answer is. That comes out to, what, once every 4 days? That sounds about right. To be honest, that feels like a conservative estimate. . I found this out when I pulled up my claims summary for the last 6 months on my health insurance website. . February 4, 2010 at 2:33 PM.

4

The Lyme Light: Lowering the Dose of Methylprednisolone

http://thelymelight.blogspot.com/2009/11/lowering-dose-of-methylprednisolone.html

Wednesday, November 25, 2009. Lowering the Dose of Methylprednisolone. However, since then I have been able to bring the dose from 4 tabs down to 2! Now here's the exciting part. Since the kidney infection has been treated and I've been stable on 2 tabs of Methylprednisolone a day for 5 days now, I'm thinking of trying only 1 tab today! So this morning, I only took 1 tab. I will see what happens and report back. . Subscribe to: Post Comments (Atom). The Absurd (The Lighter Side). View my complete profile.

5

The Lyme Light: October 2008

http://thelymelight.blogspot.com/2008_10_01_archive.html

Sunday, October 5, 2008. Links to this post. Subscribe to: Posts (Atom). The Absurd (The Lighter Side). I am 26 and have been living with chronic illnesses for over 10 years, including Late-Stage Lyme Disease, Dysautonomia and Epstein-Barr. In my case, these diseases have been been severe, stubborn and disabling. I have been actively participating in a variety of treatments for over 7 years and am attempting to record, organize, and present my experiences so far. View my complete profile.

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The Lyme Life

Friday, March 20, 2015. Time has passed so quickly since my last entry on this blog and I am still facing immense challenges. I'm twenty-eight years old and staring upward at the largest set of obstacles I've ever had to fight against. A ticking time-bomb that has been laying dormant has finally taken a daring step forward. My Lyme disease was previously treated improperly for eight months by the head physician before my amazing year with my original nurse practitioner. A weak medication better-suite...

thelymelight.blogspot.com

The Lyme Light

Tuesday, March 10, 2015. Now, I identify most with the Dysautonomia diagnosis. I still struggle with the same major symptoms as I did years ago:. Severe musculoskeletal pain (Severe Fibromyalgia), SI and hip joint pain being the most severe along with Sciatica. Severe, chronic Fatigue. POTS (low blood pressure and tachycardia). Brain fog (problems with cognition and memory). Anxiety, panic attacks and OCD. Nausea, no appetite. Hypoglycemia (low blood sugar). And these new or worsening symptoms:. And a fe...

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The Lyme Light Blog. The Lyme Light Blog. Faces of Lyme: Your Stories. Having fun INSPITE OF LYME! Daily Living with Chronic Lyme. Fun Things to do! Shedding Light on Chronic Lyme Disease. A place for Lyme Disease patients to come together.

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