LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Clindamycin - I'm scared. Input, please :-(

 - UBBFriend: Email this page to someone!    
Author Topic: Clindamycin - I'm scared. Input, please :-(
Nula
LymeNet Contributor
Member # 38409

Icon 1 posted      Profile for Nula     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi everyone,

My LLMD wants to put me on Clindamycin (since I'm currently plateauing on Minocycline, Azithromycin and Rifampin).

He's not giving me many other options (which I find odd and frustrating, since I know there are tons of other antibiotic combos I haven't tried yet ...).

He tells me not to worry about C. diff since I'm on high-dose probiotics. I'm scared, though.

I'm currently dealing with abdominal pain(candida issues, which I'm treating), and I have soft stools (i.e. almost diarrhea). I think it would be a mistake to start Clindamycin at this point in the game. Got a very bad gut feeling (literally!).

Any input/your experiences with Clindamycinwould be appreciated.

[ 02-27-2013, 12:41 PM: Message edited by: Nula ]

--------------------
I appreciate all your replies. If it takes me a while to respond, it is either because I'm too sick or because I am unable to log in. From European servers, Lymenet is very frequently inaccessible for days at a time ...

Posts: 235 | From Europe | Registered: Jul 2012  |  IP: Logged | Report this post to a Moderator
baileypup
LymeNet Contributor
Member # 22824

Icon 1 posted      Profile for baileypup     Send New Private Message       Edit/Delete Post   Reply With Quote 
The best drug I've taken....love it, however I take it in IV form. It's helped the most with lyme, babesia and joint pain.

I tried oral Clindamycin and wasn't able to tolerate it, as I got the usual symptoms (not c-diff). The c-diff Clindamycin issue is overrated. You may get diarrhea, or you may not be able to tolerate the drug, but you won't get c-diff in a few days.

Posts: 964 | From san diego | Registered: Oct 2009  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
What is your dosage of probiotics?? Brand?

Are you taking s.boulardii?

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
faithful777
Moderator
Member # 22872

Icon 1 posted      Profile for faithful777     Send New Private Message       Edit/Delete Post   Reply With Quote 
Been on IV Clindamycin for 7 months with no c-Diff issues but I take lots of probiotics. AND I am getting better!!!

Hubby is on it too with no issues but we are both taking IV Clindy plus orals.

By the way, the zith caused so much diarrhea I had to stop it. That will go away when you start Clindy as they are in the same family.

--------------------
Faithful

Just sharing my experience, I am not a doctor.

Posts: 2682 | From Colorado | Registered: Oct 2009  |  IP: Logged | Report this post to a Moderator
Nula
LymeNet Contributor
Member # 38409

Icon 1 posted      Profile for Nula     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thank you all for your quick and helpful responses :-)

Lymetoo, I'm on "Ultimate Flora Critical Care" (50 billion), which was my own decision, since my LLMD suggested a much lower dosed German brand.

I'm actually thinking of upping the dosage since most ILADS doctors seem to lean toward 200 billion.

I'm NOT taking s. boulardii! I want to, but my LLMD tells me it's "not necessary at this point", says I'm protected using regular probiotics. It feels like a I've watched a million and one ILADS lectures online, yet my LLMD (who is an ILADS member!) seems to take the opposite approach.

He keeps telling me I shouldn't worry. Of course, I am worried.

Baileypup & faithful, seems like you're making great strides - congrats! Sounds exciting. May I ask which probiotics (brand/dosage) you are on?

I don't think I can go the IV route. Got very, very bad veins (too small). Drawing blood causes problems on a regular basis.

Baileypup, what were your side effects on oral Clindamycin?

--------------------
I appreciate all your replies. If it takes me a while to respond, it is either because I'm too sick or because I am unable to log in. From European servers, Lymenet is very frequently inaccessible for days at a time ...

Posts: 235 | From Europe | Registered: Jul 2012  |  IP: Logged | Report this post to a Moderator
faithful777
Moderator
Member # 22872

Icon 1 posted      Profile for faithful777     Send New Private Message       Edit/Delete Post   Reply With Quote 
I take theralac, vsl#3 which is a prescription probiotic and saccromyces bouliardi. I frequently toss in another one to the mix.

You can go IV by doing a central line in the chest, port, groshong or hickman. My veins would never support a picc line but I have had a port in for a year now without any problems. My husband has a port too.

--------------------
Faithful

Just sharing my experience, I am not a doctor.

Posts: 2682 | From Colorado | Registered: Oct 2009  |  IP: Logged | Report this post to a Moderator
baileypup
LymeNet Contributor
Member # 22824

Icon 1 posted      Profile for baileypup     Send New Private Message       Edit/Delete Post   Reply With Quote 
I take VSL#3 probiotics with 220 billion good bacteria. I've also taken Theralac. S. Boulardi doesn't sit well with me so I don't take it.

Oral Clindamycin side effects were cramps in stomach and diarrhea.

Posts: 964 | From san diego | Registered: Oct 2009  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes, I would take a minimum of 100 billion CFU's per day, Nula!

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
beths
Frequent Contributor (1K+ posts)
Member # 18864

Icon 1 posted      Profile for beths     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am on IV clindy- no problems so far. I had a lot of GI problems trying to take it orally.

I take theralac or Klaire probiotics with a swig of kefir

Clindy has really helped me

Posts: 1276 | From maryland | Registered: Jan 2009  |  IP: Logged | Report this post to a Moderator
Sammi
Frequent Contributor (1K+ posts)
Member # 110

Icon 8 posted      Profile for Sammi     Send New Private Message       Edit/Delete Post   Reply With Quote 
Nula, I agree with the other posters about taking more probiotics. I also use VSL#3 Double-Strength.

Clindamycin was one of the best meds I ever took, though I did herx pretty intensely initially. I never had any yeast issues from taking it.

Posts: 4681 | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
Robin123
Moderator
Member # 9197

Icon 1 posted      Profile for Robin123     Send New Private Message       Edit/Delete Post   Reply With Quote 
Each of us is totally different in how we respond to meds - our genetic make-up, which infections and which strains we have, etc.

For me, oral clindamycin was IT! It stopped all my fibro and joint pain within one week of my starting to take it around the clock, 150mg every 6 hours, simply because that's what I'd been asked to do more briefly for a prior finger infection.

I herxed in a month's time, then dropped back to 150mg 2x/day. It worked for 5 years, then stopped working, probably because the bacteria mutated, would be my guess.

I never got C diff, and I think that report is highly overrated. I did get C diff from taking erythromycin once for an ear infection. So go figure.

With anything, I say go very slowly, try a small amount to see how you tolerate it, and go up in dose if you're doing ok.

And of course, take probiotics.

Posts: 13116 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.