posted
my shoulders hurt badly, around the blades near the bottom and sides exp. Hurts so bad darvocet barely touches the pain. Ducks wont give me anything, as I look like a druggie. Any thoughts welcome.
IP: Logged |
posted
James what really helps me for joint pain is a TENS unit on the muscles around the joint. A doc can prescibe this. Antifungals may help. Heat helps me, especially those Thermacare heat wraps- now they have them for joints. I take Vicodin 7.5/750 and it's the only thing that keeps me going some days (wet/humid,cold). Also I think massage might help to get the blood to the joints by getting the muscles around the joint. Some chiropractors work on shoulders (mine ) doing deep tissue massage and some will put moist heat on or use STIM pad (giant TENS). Hope that helps. I have tons of joint pain.
-------------------- RV Posts: 249 | From Healing in USA | Registered: Mar 2005
| IP: Logged |
posted
James - I use a hand-held massager called an Equalizer. I "vacuum" my back with it - it vibrates and has a medium pressure and always takes down muscle pain, especially where muscles attach.
Drugwise, clindamycin knocked muscle pain to zero in one week. I did 150 mg 3-4x/day.
Posts: 13116 | From San Francisco | Registered: May 2006
| IP: Logged |
jamescase20
Unregistered
posted
Sounds like I am already doing those things you mention...thank you though. I just helped it with a super hot shower...killer buggies too. Wish I could get some vicodine...ducks always think I am just alittle drugie.
IP: Logged |
CD57
Frequent Contributor (1K+ posts)
Member # 11749
posted
Try Tigerbalm!
Posts: 3528 | From US | Registered: Apr 2007
| IP: Logged |
CaliforniaLyme
Frequent Contributor (5K+ posts)
Member # 7136
posted
Treating Babesiosis!!!!!!!!
-------------------- There is no wealth but life. -John Ruskin
All truth goes through 3 stages: first it is ridiculed: then it is violently opposed: finally it is accepted as self evident. - Schopenhauer Posts: 5639 | From Aptos CA USA | Registered: Apr 2005
| IP: Logged |
posted
James. Aren't you treating yourself? You might want to keep an eye on the cipro you have been taking. Could be tendon damage, but then again could be a herx.
I have had this same problem after taking levaquin. I had to stop. The pain was sometimes in the shoulder but mainly in the tip of the shoulder blade on my back. I think it is more tendon related.
Posts: 25 | From Ohio | Registered: Jan 2008
| IP: Logged |
treepatrol
Honored Contributor (10K+ posts)
Member # 4117
posted
Continued treatment minocin and tindamax now minocin rifampin BUT the biggest differnce was B-12 shots. Overall pain down to 1to2to3 was 8to9to10 scale.
-------------------- Do unto others as you would have them do unto you. Remember Iam not a Doctor Just someone struggling like you with Tick Borne Diseases.
Aniek
Frequent Contributor (1K+ posts)
Member # 5374
posted
Tizanidine (brand name zanaflex). It's an antispamodic used for MS.
I've got the same pain. I've had it for years, and the tizanidine has worked wonders. I take 4mg at bed, 2mg with breakfast and 1mg in the afternoon. I can't take more during the day or it causes fatigue.
I also did really well for a while on Flexeril, a muscle relaxer. But it is not meant to be on for longterm, and I could no longer wake up on it after a couple years.
-------------------- "When there is pain, there are no words." - Toni Morrison Posts: 4711 | From Washington, DC | Registered: Mar 2004
| IP: Logged |
Foggy
Frequent Contributor (1K+ posts)
Member # 1584
posted
Time, ice heat, abx, TENS PT.
Posts: 2451 | From Lyme Central | Registered: Aug 2001
| IP: Logged |
lymebytes
Frequent Contributor (1K+ posts)
Member # 11830
posted
This was where my LD pain began and still hits...and I can tell you 2 things that helped. Heat and ibuprofen. I mean long term heat like Thermacare heat wraps - they really if worn all day as recommended. Can be bought just about anywhere. Info/pictures http://www.thermacare.com/products.jsp
Aniek
Frequent Contributor (1K+ posts)
Member # 5374
posted
I want to add, high doses of magnesium can help too. It won't get rid of the pain, but it might help a little. 1000 mg or more. It's recomended you increase until you have bowel intolerance, and then back off.
My doctor recommends magnesium malate.
Have you actually tried going to pain specialists? I've had really good experience with both physiatrists I saw. Physiatry is a medical specialty that looks at the whole body, and many pain specialists are physiatrists.
They usually combine drug therapy with other modaliteis like physical therapy, acupuncture and even psychologists who specialize in teaching pain coping techniques.
You might also want to put together a written medical history of your pain, including where each pain is on a pain scale of 1-10.
And is there a family member you can bring with you to an appointment? Doctors may be more willing to believe your pain if somebody is there to back you up.
Tizanidine, which I recommended above, is not a narcotic. So it isn't something drug seekers would be seeking. You might have better luck with a doctor prescribing that.
Unfortunately, the DEA has really screwed up pain treatment in our country. But there are prescriptions besides narcotics that can help. In fact, the tizanidine is much better than vicodin for my shoulder pain, although I still use vicodin for breakthrough pain.
-------------------- "When there is pain, there are no words." - Toni Morrison Posts: 4711 | From Washington, DC | Registered: Mar 2004
| IP: Logged |
posted
I suffered for years with that pain you are describing. I had tried EVERYTHING! Someone w/ Lyme referred my to her person that does Rolfing. It is similar to massage, but it is myofascial release. They can do it light or deep.
It took him 2 mins to get the tension to release, and it has NEVER come back. I felt like an idiot to have suffered so long!
Hope this helps! Bunny
-------------------- 4 strong winds that blow lonely, 7 seas that run high.
All those things that don't change Come what may. Posts: 103 | From Dallas/ Fort Worth. TX | Registered: Dec 2007
| IP: Logged |
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,
NJ08534USA http://www.lymenet.org/