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 » How do I get my doc to help me ??

 - UBBFriend: Email this page to someone!    
Author Topic: How do I get my doc to help me ??
coley77
Member
Member # 28924

Icon 1 posted      Profile for coley77     Send New Private Message       Edit/Delete Post   Reply With Quote 
Now that the oral antibiotic failed I am on Rosephin 1xday, a blood thinner, probiotics, vitamin D and mylanta. Its only been 6 days and already I am sick as a dog. I'm in SEVERE pain and my doctor doesnt seem to want to help me with it.

In the middle of all this I ended up with 2nd degree burns and the emergency room gave me 15 mg oxicodone and it worked great for the 2 days worth that they gave me. I ran out 2 days ago and have been really hurting ever since. When I took that I could eat, no bathroom 8 x's a day, I was able to hang out with my son and actually make a real dinner. I could function. I told my visiting nurse this when she came the past two days and she said to call my doctor and that its normal for cronic lymes patience ti be treated for chronic pain. When I called he said "it would pass but to come in on wednesday at 11am if it persisted".


I'm real upset about this. I dont know where to go to get the help I need and the pain is so bad that I constantly shake and have sweat running down my back. My legs and arms hurt so bad I just wanted to dig my fingers in to them if that makes any sence.. I guess just to change the sensation of the chronis aching. It's been so long like this .. I just want some relief. Where do I go ?

** edited to remove dosage **

[ 11-15-2010, 02:59 PM: Message edited by: sixgoofykids ]

Posts: 20 | From harwich ma 02645 | Registered: Oct 2010  |  IP: Logged | Report this post to a Moderator
sixgoofykids
Moderator
Member # 11141

Icon 1 posted      Profile for sixgoofykids   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I had trouble getting pain killers, too.

Epsom salt baths helped.

You might also go to a pain specialist. I know many here see them. I think the LLMD's are very careful about prescribing pain meds, they already get into trouble for prescribing the abx to treat us.

--------------------
sixgoofykids.blogspot.com

Posts: 13449 | From Ohio | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
Rumigirl
Frequent Contributor (1K+ posts)
Member # 15091

Icon 1 posted      Profile for Rumigirl     Send New Private Message       Edit/Delete Post   Reply With Quote 
If you were having diarrhea due to the antibiotics, make SURE that your LLMD knows that! You don't want to get C Difficile. Take some saccharomyces boulardi to make sure you don't get it (it's a specific probiotic). And lots of other top notch probiotics, too.

If you're feeling nauseous (the sick as a dog feeling?), you need lots of detox to help with the toxicity of the disease and the die-off. Search here for info on detox: coffee enemas, lemon or lime water, psyllium seeds, clay, etc. This can help with pain, too, esp the coffee enemas.

And lots of magnesium to relax the muscles. Magnesium oil is great. It's not really an oil, just feels like it. Swanson's is cheap and good.

And, yes, if your LLMD can't rx pain meds that do the job, see a pain management doc. Being in that much pain is NOT good (as you know all too well). Hang in there, and get the help you need.

Posts: 3771 | From around | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
momlyme
Frequent Contributor (1K+ posts)
Member # 27775

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

I am sorry you are dealing with this much pain and I wish I could tell you that something has helped my son. Not yet. I am going to try the Mag Oil that Rumi suggested. Another natural thing I have heard helps with pain is Tumeric aka. Curcuma - I plan to ask my LLMD about these.

Sometimes the pain killers are the only way to function. It took my 5 months of asking to get one script for a pain killer. My son got so bad on day 6 of rocephin... I begged for something. ANYTHING to give him relief.

Do you have a pain clinic?

I just pulled up my research file on pain... it's quite long and I don't want to paste the whole thing below. PM me if you want me to send it privately... there are references to the authors of the posts if I remembered to include them so you can follow up and research how people are doing with what they suggest.

Mainly, the issue and the reason there are so many things to choose from is... everybody is different! The same thing does not relieve pain for everyone. You need to experiment until you find what works.

I am still looking for soemthing for my son... never quit. You will find what works for your body!

You are in our prayers.

--------------------
May health be with you!

Toxic mold was suppressing our immune systems, causing extreme pain, brain fog and magnifying symptoms. Four days after moving out, the healing began.

Posts: 2007 | From NY/VT Border | Registered: Aug 2010  |  IP: Logged | Report this post to a Moderator
littlebit27
Frequent Contributor (1K+ posts)
Member # 24477

Icon 1 posted      Profile for littlebit27   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've been there. Many LLMDs won't prescribe pain meds and refer you to a pain clinic or tell you to ask your primary care doc.

Well I'm in a place where the ticks are friendly and they don't transmit Lyme Disease so no pain clinic would believe me and my primary care doc thinks it's all in my head and I need a shrink for that and thinks I'm a drug addict.

I have sense been able to get a script for pain killers and it saves my life. without it I woudln't be treating because I wouldn't be able to function and I have no choice BUT to function.

I hope your doc will help you out.

On a side note-herbs- Sasaprilla works wonders if it doesn't upset your stomach-it did mine. cat's clas the NON TOA free in capsules has been amazing for me for inflammation-prior to cats claw I would wake up in the morning unable to move my hands because they are so swollen. The still swell but not nearly as bad.

Also Curamin, I'm told works wonders, I bought it and it didn't help me but I have heard many people say it was a life saver for them. Everyone is different it might work for you. Good Luck to you, I know exactly how you are feeling.

--------------------
*Brittany Lyme Aware on FB*
http://littlebithaslyme.wordpress.com/

Posts: 2310 | From Southeast | Registered: Feb 2010  |  IP: Logged | Report this post to a Moderator
Tammy N.
Frequent Contributor (1K+ posts)
Member # 26835

Icon 1 posted      Profile for Tammy N.     Send New Private Message       Edit/Delete Post   Reply With Quote 
I think I would try to exhaust all natural remedies first -- epsom salts baths, turmeric, magnesium, etc. (and ask doc for more recommendations.)

Pain pills are so toxic to our bodies and especially our liver. Your body is going through so much all ready with antibiotics and die-off from the bugs.

Also, as hard as it can be, on my really rough days I try to go outside for a vigorous walk (30+ minutes). Even when I don't think I can, I just psych myself up and just do it. Usually half-way through my legs start itching like CRAZY. But it really helps!!! Followed by a bath, and it's an amazing turnaround. Truly. (Plus there is something victorious about accomplishing it. Very gratifying.)

Best to you,
Tammy

Posts: 2238 | From East Coast | Registered: Jul 2010  |  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 
Curamin is not very strong. That is for sure.

Maybe straight curcumin would be better.

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

Posts: 96222 | From Texas | Registered: Feb 2001  |  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.