Hi AdrenalinChick97,
Things can get pretty tough in the beginning of treatment.
Everything just seems to get weird.
You feel like you're going backwards, but you're really not.
That initial bacterial die-off is not fun.
You may have already researched this thoroughly, but if it's new information for you, I hope it will help make sense about some of your symptoms.
(Sorry if this is a repeat.)
Your meds Rocephin & Flagyl both affect the brain. They penetrate the blood brain barrier (BBB). The BBB usually keeps bacteria & other bad things from reaching the brain.
That's why symptoms feel 100 times more exaggerated. The meds hit those nerves & ouch. You feel everything intensify.
When you add Flagyl to the mix, it's especially hard on the nerves & liver too.
It affects the central nevous system so some folks get really achey on it.
Yes, it's a cyst buster, but it's also anti-fungal and anti-parasitic, so it alone packs a punch.
Rocephin penetrates the brain readily & Doxycycline penetrates the BBB in large enough doses.
Also, you mentioned difficulty swallowing...,
This is strictly my amateur opinion, but sounds like the meds are affecting your cranial nerves & making it diffult to swallow.
You'd have to verify that with your physician.
But from what I just read, difficulty swallowing can be affected by the 10th Cranial nerve (vagus nerve).
I hate to throw things at you to read when you feel bad, but you can print this article out & read it on a good day.
The article talks about how Lyme affects the cranial nerves in detail -----quite fascinating.
When to Suspect Lyme by John D. Bleiweiss,MD
http://cassia.org/essay.htm
I have neuro problems so this article was especially intriguing to me.
Another article-----really a symptom chart shows how Lyme affects every organ system of the body. It also lists citations.
I refer to this time & again.
It's in pdf file form so it's easiest to print out & have on hand to refer to later.
Click on the link. You'll need to scroll down the page to SYMPTOMS & click.
Lyme Disease Symptoms & Characteristics
http://www.lymeinfo.net/lymefiles.html
The last printout below was sent to all local support group members. Sorry, it doesn't show an author------I just hate that.
Disregard the title----it's for anyone with Lyme.
What it looks like to me is a handbook for new Lyme patients just starting treatment.
Be assured I do not agree with everything in the article.
Especially the part about pain.....heck, if I'm in pain, then I takek something for pain.
Anway, it's just some background reading; kind of encouragement for new patients & to let them know what to expect with treatment.
Also, disregard the medical advice, because that's simply between you & your physician.
I thought a lot of it was helpful------doesn't mean it's all technically correct though!
Patient Information
http://www.angelfire.com/me2/StarShar/Herx1.html
These 3 articles are not to overwhelm you while you're feeling horrible.
We just want to show in a tangible way that we are concerned for you & will try to help provide information, as you wish.
If you're having a tough day today-----just print it out on another day.
I think they're all good reference materials.
Hope you have a good day today.
Tell us how we can help.
Take Care,
Mama Jan from Texas
[This message has been edited by RECIPEGIRL (edited 22 September 2004).]
[This message has been edited by RECIPEGIRL (edited 22 September 2004).]