Tracy, Please read the forum rules before posting. . No advertising or links to advertising or "Spam" is permitted (including signatures) . Advertising or Spam is defined as posting a link for the...
Yes, I did the 1.2 mu dosage. I did it for about 10 months all together, maybe after 6 months increased to two a week, then on my own the last month or so got some leftovers from friends and started...
I was on that dosage for a long time, and my new LLD feels it is totally inadequate, and states it is like taking "water." She gives 4-6 times that amount each week....
Recently I have read that Singulair, an asthma med, has been extremely helpful in reducing the symptoms of a herx. You can also try Bendadryl and Zyrtec as over the counter options....
We have groups for both Bartonella and Depression on www.lymefriends.com. The site crashed last week and we had to rebuild it from scratch, but it is back up and running. There are a lot of people in...
I got a blood clot 36 hours after I got my PICC. I had a lot of pain from the underam/shoulder area right into my heart. My upper arm was very swollen though I did not realize that. I was short of...
The best thing I have found for constipation is Fiber Force Plus from Puritans Pride. I think that's what it's called, or Fiber Force 6. It amazes me how well it works....
PS....and my husband can't stop complaining about my breath!!!...
Eric and Mountainbiker, Wondering whereabouts in CT you are? We are also in CT. We have been having Sat night get togethers for Lymies, we even had a New Year's Eve party. It was quite the bash. A...
WEll my hubby and I are both Lymies; independently of each other. We spend almost all our time in bed together, but the only sweating going on is from our Babs herxes. It's a sorry state of affairs,...
OK, again just to clarify many members have donated to pay for the site costs, it really is a collaborative effort. We really like to keep it that way, that is how it should be....
Just to clarify what may be a misunderstanding, I read Rule #4. I am NOT the website owner....
Listen, I have no "vested interest" at all. We have over 600 members and have no reason to obtain more....this is a group effort, created by a group of Lyme patients, and if anything my husband and I...
Yes, I've totally had them and I LOVE your name for them!!! Mind if I borrow it????...
I just started a week ago! We can be IV buddies. The key thing for me is that I am also on about 5 other antibiotics. My LLD is very aggressive and is adamant that if you don't hit Lyme and co's all...
No, it's not MY site. It was created by a group of us. My husband did actually set it up but we have several people as Administrators and we share the cost among us. My husband and I donate all of...
Peacesoul, Have you joined us yet on www.lymefriends.com? Very friendly place!...
There is an excellent new doctor at the Marino Center in Wellesley, MA. She trained under Dr. Horowtiz and already has people flying from all over the world to see her. She has only been there 3...
www.lymefriends.com www.lymenet.org...
My LLD has recommended I take Allicin. The smell and taste make me so sick though!!!...
Post edited: this is considered advertising for a website. Even if the website is not making money, it still breaks rule #4 because you have a personal interest in it. I left the link on the other...
Seriously, there is a dating spot for Lymies! On www.lymefriends.com there is a group called LymeEHarmony. Join the site and join the group. It's a new site, only up for two months, but has over 600...