FAQ/Help |
Calendar |
Search |
Today's Posts |
![]() |
|
Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS) |
Reply |
|
Thread Tools | Display Modes |
|
![]() |
#1 | ||
|
|||
Member
|
I've lost count over how many relationships I personally watched erode away as RSD ruins another life. From my view, I'll never accept that RSD is the cause of any decent relationship actually breaking up, but I do see that those who are already having additional problems long before the RSD hit in many situations can't take one more thing. In your case the RSD was just one more thing. Hopefully you two will stop looking at only one cause for your relationship breakdown, but will look at all the issues that have drawn the two of you apart and then figure out if you still have enough love and desire to fix the problems and put your lives back together or if there really are irreconcilable differences that can't be fixed now or ever. Personally speaking, I know well the additional burdens RSD can bring into a relationship, so we've just got to do anything and everything it takes so these additional problems don't tear apart both the person and the people anymore than it need to. Instead of throwing all our problems in one big pot and mixing it all together, I find it's always it bit more manageable if you keep each issue and concern separate and then deal with each to the best of your abilities. Then for the things you can't fix or change, accept that's just the new way things are going to be and go forth. Here's hoping that the two of you will figure out that the two of you can always handle any problem better as a unit than you can alone, because even though you've broken up, the problems are still there. Instead of allowing the problems to tear you apart, my hope is that your commitment to each other will be great enough that you'll work the problems together for a common goal and that your life will once again be whole. Bob. Quote:
|
||
![]() |
![]() |
![]() |
#2 | |||
|
||||
Member
|
Oh my! I think you misunderstood. It was a nightmare LOL. My husband is wonderful to me and is the best caregiver I could even imagine having!
Thank you for your response. I agree, if something like this tears a relationship apart, there were likely already other stressors in place. |
|||
![]() |
![]() |
![]() |
#3 | |||
|
||||
Senior Member
|
Quote:
Having been in this movie for almost 10 years, I've had some time to reflect on the problem. Unfortunately, a huge issue is the tendency of not just individuals with chronic pain (ICPs) to engage in "pain catastrophizing" (“an exaggerated, negative focus on pain and is related to psychological distress, pain severity, and other negative outcomes in pain samples” or - simply put - an unproductively aversive response to the pain combined with a grasping for how life used to be) but their spouses to do so either as well or on their own. And while an underlying predisposition may have been present all along, typically due to depression and/or anxiety, it may never have been a huge problem in the marriage until the chronic pain hit. I think we're probably in agreement on this point, but I'm not sure. In my case, I can't say that my wife’s catastrophizing was never an issue in the marriage (I was on notice when I lost a job early on), but where she had grown up entirely under the specter of her father's chronic illnesses, it completely took over when I got my CRPS. To the point that where I came to terms with this fairly quickly through a Mindfulness Based Stress Reduction (MBSR) class, she was unwilling to consider addressing the issue in any context. This may be instructive: The significant other version of the Pain Catastrophizing Scale (PCS-S): preliminary validation, Cano A, Leonard MT, Franz A, Pain 2005 Dec 15; 119(1-3):26-37, PubMed Central FULL TEXT @ http://www.ncbi.nlm.nih.gov/pmc/arti...ihms104448.pdf Abstracthttp://www.ncbi.nlm.nih.gov/pubmed/16298062 And at page 11 of PubMed version of the article: Spouse catastrophizing was also correlated with ICP depressive symptoms. Specifically, ICP catastrophizing was not related to their own depressive symptoms when their spouses reported low levels of catastrophizing but was positively related to their own depressive symptoms when their spouses also reported a high level of catastrophizing. This result was found when accounting for spouses’ perceptions of pain and interference and their own depressive symptoms, indicating a robust effect. It is possible that catastrophizing in both spouses results in specific behaviors that may exacerbate depressive symptoms in ICPs. For instance, the typical high catastrophizing couple may consist of a worried ICP and a healthy spouse who is over-involved in the ICP’s care and emotional wellbeing (i.e. solicitous). In these cases, ICPs may be concerned about the future of their pain and perceive themselves as a burden on their spouses. High catastrophizing couples may also be unable to meet each other’s need for intimacy because they are so focused on the pain problem. On the other hand, a catastrophizing ICP who has a partner low in catastrophizing might be better able to manage their thoughts and feelings. ICPs who express their concerns to their low catastrophizing spouses may be met with support, validation, and reassurance as suggested in the communal coping model of catastrophizing. Therefore, these ICPs may be protected from high levels of depressive symptoms. No such interaction was found for spouse depressive symptoms. Spouses’ depressive symptoms may be more a function of their own interpretations of events. Future research will determine whether these processes are at work. [Citations omitted; emphasis added.]That said, I can't endorse traditional "cognitive behavoral therapy," in which the issue of pain catastrophizing is central, where that behavior is itself addressed in an aversive context rather through an approached grounded in love of self and other. See, Changes after multidisciplinary pain treatment in patient pain beliefs and coping are associated with concurrent changes in patient functioning, Jensen MP, Turner JA, Romano JM, Pain 2007 Sep; 131(1-2): 38-47, PubMed Central FULL TEXT @ http://www.ncbi.nlm.nih.gov/pmc/arti...ihms-29341.pdf : Treatment was focused on (1) increasing strength, flexibility, endurance, and sitting and standing times; (2) assisting the patient in returning to customary work, household, and avocational activities; (3) instruction in and practice of specific pain coping strategies thought to be adaptive (use of regular exercise, pacing, coping self-statements, and task persistence); (4) decreasing use of coping strategies and responses thought to be maladaptive (guarding, resting, asking for assistance, catastrophizing); (5) medication management, with a focus on decreasing and eliminating the use of sedative and opioid medications; and (6) encouraging a shift in cognitions from those thought to be maladaptive (e.g., that one is necessarily disabled by pain, that hurt necessarily means that damage is occurring and that activities associated with increased pain should be avoided) towards cognitions thought to be adaptive (e.g., that one can control pain and its impact). Patients’ family members (usually spouses) were asked to participate with the patient during the last two days of treatment in order to (1) observe patient functioning and how program staff encouraged patient functioning and (2) meet with the program psychologist to discuss how they can best support the treatment gains made by the patient. [Page 4 of PMC copy.]In fact, and I after running various PubMed searches, I am unaware of any evidence that strengthening exercise unless combined with the use blocks or other medical treatments, was ever proved useful for a patient with CRPS. My personal experience was certainly to the contrary: for days after a session my legs felt like they were packed with broken glass, even to the PT who discharged me! Nevertheless, not only would I agree with the proposition that chronic pain will almost always make a bad marriage worse, there is evidence to suggest that a bad marriage (along with other chronic stress factors) could lay the foundation for RSD in the first place! Check this out: Hostile Marital Interactions, Proinflammatory Cytokine Production, and Wound Healing, Janice K. Kiecolt-Glaser, PhD; Timothy J. Loving, PhD; Jeffrey R. Stowell, PhD; William B. Malarkey, MD; Stanley Lemeshow, PhD; Stephanie L. Dickinson, MAS; Ronald Glaser, PhD, Arch Gen Psychiatry. 2005;62:1377-1384 FULL TEXT @ http://archpsyc.ama-assn.org/cgi/reprint/62/12/1377.pdf Abstracthttp://www.ncbi.nlm.nih.gov/pubmed/16330726 take care, Mike Last edited by fmichael; 07-31-2010 at 05:17 PM. Reason: a couple of more thoughts . . . |
|||
![]() |
![]() |
Reply |
|
|
![]() |
||||
Thread | Forum | |||
No top, no bottom. | Computers and Technology | |||
Bottom row of teeth | Dentistry & Dental Issues | |||
For all parents (Read to the bottom) | Social Chat | |||
The Thank you's at the bottom | Community & Forum Feedback |