This is topic Bicillin injection experiences (positive success stories) in forum Medical Questions at LymeNet Flash.


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Posted by Kristyn (Member # 51857) on :
 
Hello, I've started my bicillin injections for almost a month now, 2x a week. How did you (or someone you know) do with them? Replies and PMs are greatly welcomed and appreciated. [Smile]

I get it, it's frustrating every lyme patient is different in regards to treatment protocols/time of recovery. One magic pill doesn't fix it. I just want some more input in how people did and how long they were on them/or started to see improvement, herxing etc.

I do look up past posts in the search link about it. Thanks everyone!
 
Posted by lindadanis (Member # 51204) on :
 
I am so sorry that you didn't get even one response here. Years ago, there would of been at least 10 people responding. Hope you are doing well and don't give up.
 
Posted by Kristyn (Member # 51857) on :
 
Hey Linda, I know. You're not the only one who has said this to me. I'm not gonna take it personally and I'm not surprised, I think with the Covid-19 crisis ppl's energy's are on other things at the moment, I get it.

I come on here frequently and check forum topics out that are about bicillin.

I have allergies big time kicking my *** like it's been for alot of ppl and the herxing too...it's not fun. [Frown] Been on the shots 4 weeks now.
 
Posted by marie (Member # 3980) on :
 
There isn't as much support as there was years ago when I first came on. There was a consistent large group working together on many levels and they stayed together. I cant reach the same person to see about their ongoing progress with a dr or treatment. They may respond a few times and that's it.
 
Posted by Kristyn (Member # 51857) on :
 
I'm thinking they recovered possibly, moved on with their lives and didnt need this site anymore? I called my LLMD yesterday for a Rx refill. She wants to see me next month for a f/u. With the Covid-19, most likely will be tele conference.
 
Posted by Bartenderbonnie (Member # 49177) on :
 
While Lymenet seems like a ghost town lately, there is NO other place for first-hand Lyme patients experiences on LYME and Company treatments. The 'search' function is a treasure trove that cannot be dismissed or denied. Many members may not post but they come here to search for answers.

Quick search for you on Bicillin;
http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=search_tng;d=results;record=2458950-092233-5JEN;result_start=20
 
Posted by Kristyn (Member # 51857) on :
 
Thank you Bonnie, I've been doing that too, yes.
 
Posted by Kristyn (Member # 51857) on :
 
If my LLMD gave me the ok to do them everyday hell I would. I actually get excited the days I get them ( I mean who gets excited about having a 1.5 inch needle in them? ME!)
 
Posted by lindadanis (Member # 51204) on :
 
I am surprised that Dr. H wants to see you in a month or do a phone call. You are just asking for a refill. Interesting. good luck.
 
Posted by Kristyn (Member # 51857) on :
 
No Linda it's for a follow up, nothing out of the ordinary. By then I will have been on the shots for over 2 months. I'm looking forward to it.
 
Posted by lindadanis (Member # 51204) on :
 
good luck with that follow up. I hope the shots will be helping by then.
 
Posted by Kristyn (Member # 51857) on :
 
Thank you Linda! If I don't talk to you have a good Easter.
 
Posted by LabRat (Member # 78) on :
 
Hello you all from sunny Texas. I'm bored and five mins. away from king crab, I just glanced in to see which slackers were still whining and sniveling. I decided I was finally cured, just old, 82 now.
Bicillin (la) and Flagel, spell check is not happy today, anyway these two drugs gave me my life back from not being able to find a po box I'd had for a number of years to flying commercially.
My dose was double or more what you would give anyone else, hence my handle of labrat. I was able to get the big shot because my md wife decided to treat it like syphilis It has been awhile and I,m rusty, if I ever knew anything! Good luck to you
labrat.
 
Posted by Kristyn (Member # 51857) on :
 
That's terrific to hear labrat! Thank you for your reply. Looking through many other posts about Bicillin (LA) it seems there have been more positive than not responses of others using Bicillin for their treatment protocol and fully recovering. Mine is 1,200,000 units per 2ml, twice a week. I'm glad you had a no BS doctor of a wife that helped you and didn't mess around. One request...can you please bring that warmth and sunshine to us up in New England? Haha [Smile]
 
Posted by LabRat (Member # 78) on :
 
Absolutely not! You guys deserve some form of punishment for being so close to the lobsters. I remember my single shot once a week was 2,400,000 of "long acting" Bicillin. I feel for you, sorry and good luck!
 
Posted by Bartenderbonnie (Member # 49177) on :
 
I take Tindamax (Tinidazole) pulsed on Saturday and Sunday only 3 x daily for the cyst form of Lyme.

"Advanced Topics in Lyme Disease" by Dr Joseph Burrascano"
http://www.lymenet.org/BurrGuide200810.pdf
(page 12 - 16)
 
Posted by LabRat (Member # 78) on :
 
I had some improvement with Tinidazole, don't remember the dose but the most improvement was massive shots of Bicillin LA and flagyl. Good luck all
 
Posted by swimmeredurp (Member # 34305) on :
 
Part of my treatment plan was with Bicillin shots

(also 2x a week) and I am now pretty much symptom

free. I did this back in 2010-2011 along with IV

nutrients 2x a week. These two things plus the

treatment of Babesia is what knocked out my Lyme.

I did the Bicillin after I took oral antibiotics

for about a year and did not see major

improvement.
 
Posted by swimmeredurp (Member # 34305) on :
 
Oh, but also I do think I might have gotten a lipoma

from the shots (lipomas are not anything serious

just fat deposits under the skin). I think massaging

the point of injection can help decrease the chances

of a lipoma. Again the lipoma was no big deal (had

it removed pretty easily) and I would definitely

take it in exchange for the Bicillin shots and

knocking out the Lyme. I don't come on here very

often...just noticed by bio says still

experiencing symptoms, but I'm not! Will change

that.
 


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