I would think your doctor would immediately prescribe Nabiximols for your spasticity. Since 30% of survivors that have it and there is absolutely nothing else for treating spasticity(botox does not cure spasticity).
This has been out there for years;
Nabiximols is an oromucosal spray formulated in a 1:1 ratio of
tetrahydrocannabinol and cannabidiol and approved in several countries
for treatment-resistant spasticity in patients with MS.(How fucking incompetent is your doctor in not using it?)
The Broad Concept of “Spasticity-Plus Syndrome” in Multiple Sclerosis: A Possible New Concept in the Management of Multiple Sclerosis Symptoms
- 1Biomedical Research Institute of Malaga, University of Málaga, Málaga, Spain
- 2Department of Neurology, Ramón y Cajal University Hospital, Madrid, Spain
- 3Department of Neurology, Gregorio Marañón Hospital, Madrid, Spain
- 4Servicio de Neurología, Hospital Clínico San Carlos, Madrid, Spain
- 5Servicio de Neurologia, Complejo Hospitalario Universitario de Santiago, Santiago de Compostela, Spain
- 6Servicio de Neurologia, Hospital Universitari de Girona Doctor Josep Trueta, Girona, Spain
Multiple sclerosis (MS) pathology progressively affects
multiple central nervous system (CNS) areas. Due to this fact, MS
produces a wide array of symptoms. Symptomatic therapy of one MS symptom
can cause or worsen other unwanted symptoms (anticholinergics used for
bladder dysfunction produce impairment of cognition, many MS drugs
produce erectile dysfunction, etc.). Appropriate symptomatic therapy is
an unmet need. Several important functions/symptoms (muscle tone, sleep,
bladder, pain) are mediated, in great part, in the brainstem.
Cannabinoid receptors are distributed throughout the CNS irregularly:
There is an accumulation of CB1 and CB2 receptors in the brainstem. Nabiximols (a combination of THC and CBD oromucosal spray) interact with both CB1 and CB2
receptors. In several clinical trials with Nabiximols for MS
spasticity, the investigators report improvement not only in spasticity
itself, but also in several functions/symptoms mentioned before (spasms,
cramps, pain, gait, sleep, bladder function, fatigue, and possibly
tremor). We can conceptualize and, therefore, hypothesize, through this
indirect information, that it could be considered the existence of a
broad “Spasticity-Plus Syndrome” that involves, a cluster of symptoms
apart from spasticity itself, the rest of the mentioned
functions/symptoms, probably because they are interlinked after the
increase of muscle tone and mediated, at least in part, in the same or
close areas of the brainstem. If this holds true, there exists the
possibility to treat several spasticity-related symptoms induced by MS
pathology with a single therapy, which would permit to avoid the
unnecessary adverse effects produced by polytherapy. This would result
in an important advance in the symptomatic management of MS.
In the last two decades, the availability of new
disease-modifying therapies has radically changed the management of
multiple sclerosis (MS) and relapsing–remitting MS in particular (1), resulting in a longer life expectancy for patients with the disease (2).
Nevertheless, MS currently remains incurable and, in most patients,
disability will eventually progress and they must live with the very
many symptoms associated with the disease. These symptoms can have a
major impact on patient's quality of life (3)
and their management is considered important, although traditionally,
this area has received far less attention than disease-modifying
therapies (4).
A wide range of treatments are available to manage each of the MS symptoms (5–7).
Given that different agents are used for different symptoms and a
patient may have several symptoms present at the same time, many MS
patients are multi-medicated, particularly as most patients will also be
receiving disease-modifying therapies. This article will assess the
current fragmented approaches to pharmacological management of
spasticity muscle tone increase-related symptoms and their shortcomings.
Given that the treatment of MS-associated muscle spasticity has been
associated in a good number of clinical trials and also observational
studies with the improvement of several other functions/symptoms present
in MS (8),
we will conceptualize, and subsequently hypothesize, about the clinical
interest of introducing the more broad concept of “Spasticity-Plus
Syndrome” to provide a unified framework for managing all these
seemingly related functions/symptoms. By applying such a concept, it
would be possible to simplify the management of symptoms associated with
MS and reduce importantly the interactions and adverse effects
associated with poly-medication.
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