A recent article explored Chronic Pain and myotonic dystrophy. (click on link for full study). this is something that many of our patients experience. Heat was being used by 26% of patients. The only treatment that was relatively highly effective and was still being used by a substantial number of patients (26%) was heat. Perhaps this is because heat is an extremely accessible treatment (most people own a hot water bottle or heating pad) that has few, if any, negative side effects.
The most effective (rated as providing at least 5/10 relief)were ibuprofen and aspirin, opioids, massage, chiropractic manipulation, nerve blocks, heat,and marijuana. However, it should also be noted that many of these treatments also have significant drawbacks. For example, opioids, which were rated as the most effective (6.49/10)in this sample, had been tried by 33% of the sample but were only currently being used by 8% clearly, there must be a substantial downside to opioids for so many patients to stop using them, despite their reported effectiveness. Our clinical experience suggests that this downside is primarily related to the side effects, especially feelings of grogginess and constipation,associated with opioids that are taken at the doses required to provide substantial relief.
Results—More subjects with FSHD (82%) than with MMD (64%) reported pain. The most
frequently reported pain sites for both diagnostic groups were lower back (66% MMD, 74% FSHD)and legs (60% MMD, 72% FSHD). Significant differences in pain intensity were found between thediagnostic groups in the hands, legs, knees, ankles, and feet, with patients with MMD reporting greater pain intensity at these sites than patients with FSHD. Age was related to the onset of pain (participants reporting pain were younger than those not reporting pain in the FSHD sample), but pain severity was not significantly associated with age in those reporting pain. Respondents with both diagnoses that reported mobility limitations and used assistive devices (eg, wheelchair, cane)reported more pain severity than those with mobility limitations who did not use assistive devices,
who, in turn, reported more pain severity than respondents who reported no mobility limitations atall. The treatments that were reported to provide the greatest pain relief were not necessarily those that were the most frequently tried or still used.
I have myotonic dystrophy but I’m suffering with a lot of pain between my shoulders and neck my gp has prescribed naproxen but it isn’t touching the pain is there anything else I can do to help ease the pain it keeps me up most nights I will try anything
I’m in pain, I’m still mobile, I have a finger that crules and locks up hurts to straighten it, could this be part of my md. What if any new ideas as to help with the pain. Thank you
I have myotonic dystrophy type 2. I use medical cannabis for pain. While it does have drawbacks, it does allow me to function, especially socially. It is tough to be sociable when I feel horrible.
Heat followed by ice or a cold soak however brief the soak will provide immediate though temporary relief. This process should be repeated until inflammation subsides.
Resistance training ( low resistance ) of the iliacus and psoas followed by proper aligned stretching of the hamstrings is very helpful. Training should be followed by a cold soak.
Medical Cannabis, especially the higher CBD strains, in conjunction with ibuprofen has been very effective for a DM1 Myotonic Muscular Dystrophy Type 1 patient that I am very familiar with. This is the Myotonic Dystrophy marked by repeats of CTG on DMPK sequence of Chromosome 19, to be clear.
Has anyone else had a similar good finding ?
Time has passed since this article was firts written and:
1) MDA USA has done nothing to study medical cannabis and MD (boooo!)
2) Over half of the 50 states of the US will have Medical Cannabis access in 2015
3) The US Government will very likely reschedule Cannabis as soon as January 2015 to a pre-Richard Nixon level, and identify it as a medicine again
Hi my wife has had dm2 for some considerable time now she is age 63 the pain seems to be getting worse over time. Nothing seems to work any more she still keeps mobile really dont have any idea what to do.We do get visits from the OT but not much help there Regards Frederick B.