Pelvic Congestion Syndrome Community Group
Pelvic venous congestion syndrome PCS or Pelvic Venous Insufficiency / Incompetence is similar to the condition of varicose veins in the legs. In both cases, the valves in the veins that help blood flow toward the heart do not work properly. As a result, blood pools in the veins, and the veins in the affected body part stretch and bulge. In pelvic venous congestion...
thank you :)
our bodies DO notice when not all of it makes it back up and when something is 'out of order' ! and legs must firstly go through the pelvis before making it back up to the heart !
i have read many articles stating that extreeme varicose veins cause hypotension (low blood pressure).-- and inturn our hearts beat faster trying to keep up the flow.
whilst i do not need proof.. that is not the point of me posting these, the point is... how can they still be so ignorant to things that are just complete common sense!!!!
here are two other great ones, you definitely need to read the first one:
http://www.pediatricnetwork.org/medical/OI/johnshopkins.htm identical to what i feel. it even states that people with this thing do this: -''Many patients have adopted these postures without knowing why. ie: squatting etc.it also mentions pelvic congestion.
here is the second: http://en.wikipedia.org/wiki/Postural_orthostatic_tachycardia_syndrome
it mentions shaking/tremor. and here is what it says near the bottom:- ''Reduced venous return is one of the main mechanisms that causes POTS symptoms. Venous return can be reduced due to conditions such as low plasma volume (hypovolemia), venous pooling and denervation. A hyperadrenergic state may result as the body attempts to compensate for these abnormalities.''
and one of the first things to enter my mind in hospital when they said they couldnt help was because valves not damaged there was only pooling was- medication to help restrict the veins/ compress them together. now i am not saying this is a good or healthy idea... but this is what i thought of out of desperation when i was thinking ahead already after being wheeled out of 'surgery'.
and funny enough the first article also mentions that.. here is a snippet:- For those with more frequent or more severe symptoms, Step 1 may need to be supplemented by medications. Most of the drugs in common use for NMH and POTS help to improve the ability of the vessels to constrict and return blood to the heart when we stand.
THERE YOU GO !!!!!!!!!!!!!!!!!! how was that for an argument ?
now i am not saying i have POTS or hypotension or synascope or or or all the rest of these postural or what ever things. but it is the same kind of thing! get it?!
here is the link of the discussion of PCS and that lady!
http://www.pelvicpain.org.uk/forum/viewtopic.php?t=350
http://dinet.ipbhost.com/index.php?showtopic=14921&pid=136766&st=0&#entry136766
http://www.pediatricnetwork.org/medical/OI/johnshopkins.htm
c. Treat contributing medical conditions
Attention to other medical conditions is crucial to ensuring that the NMH or POTS treatments are as effective as they can be. In particular, preventing activation of even mild asthma and allergies has been important in keeping our patients from developing a worsening of symptoms. In patients with asthma, we usually try to reduce reliance on albuterol and other beta-agonist inhalers, as these medications can mimic the effect of too much epinephrine, and can aggravate NMH in particular. Endometriosis and other painful conditions may aggravate symptoms, and ovarian vein varices in women with pelvic pain are associated with fatigue and worse orthostatic intolerance. Sinusitis, anxiety disorders, depression, and infections of any sort are examples of other conditions that need appropriate medical attention when present.
its all common sense to me really. i wish they had it too, to have a little intuition.