The (ugh) hug
 

I've been experiencing more and more trouble with the hug lately. It's always about the same, that tight constricting feeling in my chest, pressure on my diaphragm. But the last few days it's changed up on me. Sopmetimes I feel that same pressure much lower...I dont even know what part of my innerds is getting squished, but I feel squished somewhere below the diaphragm. I'm also getting sharp stabbing pains from the back and sides. But not a quick stab, a long slow constant stabbing, lasting a few minutes. Sometimes this comes on with the "usual" hug sensation, other times it is all by itself.

Is this just an additional MS Hug gift?

Dear Catch,
From my experience, though it probably is the hug, we can't always assume that. I had the ms hug but some time back I noticed it changing...to make a long story short...it was my gallbladder. Had it removed. You might need to check in with your PCP or neuro.

Hope you get some relief soon. :hug: ((((Gentle))))Hugs!

:rolleyes:hi pet:), dont worry u r not alone---I myself was having hugs and no reason, thought I was having a heart attack,:eek: went to emerg, dr said its your gallbladder-mmmmmm but I had it out anyways-there was a big stone caught way down in a duct-had to break my rib-its painful after but hey it beat the heart attack-then it happened again-well i only have 1 gallbladder and its gone lol:confused: so now what eh? so off to the dr I goes again, well its nothing I can think of-his final remark, so off I goes to my neuro-ohhhhhhhh my dear it's the MS Hug-mmmmm:confused:mm-really, took me along time but I sure know how u feel pet'and its no fun -and mine always comes early am or late night:p-naturally thats the panic times lol'cuz the hospitals and clinics r closed except for a emerg-so u hang in there kiddo''I am-so lets fight them together ok? post me if you want to''let me know if u ever get the MS Itch'now theres a bummer:eek:-but if u do -use Gold Bond itch creame it says that on the bottle-its the best ever for any itch'so hugs:hug: for now, i didnt mean that litterally lol':D
Terry-Joy :hug:
aka-TJ

The "Ugh Hug", I like that. Much better name than the "MS Hug", which sounds so cozy and lovable. I've given it names such as the "Boa Constrictor" and the "Vice". It's been one of my worst and most constant problems that began soon after the onset of my first major MS attack in 2006. Didn't know what it was for the longest time, and had so many other major ailments to discuss with my neuro that I never seemed to get to that one on the list. But did discuss it in the early days with my PCP and GI doc, telling them it felt like a wide band of hardening cement just beneath the skin wrapping around my midriff, causing a great deal of discomfort and making it difficult to breath, as though it was constricting my lungs to the point where I couldn't expand them enough to get the oxygen I needed, and struggling to breath was only worsening my fatigue. It was a vicious cycle. Plus, the pressure and discomfort around my abdomen only exacerbated my bowel dysfunction.:eek: What fun! But after I came out with a clean colonoscopy (so to speak):winky:, my docs could only scratch their heads about what this sensation might be.:confused: They knew I had MS, but had never heard of the infamous MS Hug. After near two years, I learned what it was from reading about it on other MS forums--Eureka, I'm not alone--and THEN I finally brought it up at my next neuro appt. Well, duh... In addition to gabapentin, I take clonazepam, which takes a little bit of the edge off of it, but not much. Considering switching to baclofen or zanaflex to see if it is any more effective. Ironically, it was suggested to me by an MS Nurse just a few months ago to try wearing an abdominal binder, which I thought was a crazy suggestion. Why on earth would I want MORE pressure around my midriff? But ironically, it did help. Don't know the biological mechanics behind it, but the additional pressure somehow short-circuits or overrides the pain/discomfort you're feeling from the hug, at least temporarily. To use a poor analogy, it's like it's strangling the serpent that's wrapped around your middle and squeezing the guts out of you. I can only wear the binder for a couple of hours at a time before it begins to be counterproductive and I've got to take it off. But it's the best thing I've found yet that works for me, even if it's shortlived. I'm thankful for ANY relief from this Ugh Hug. So, it's something you might want to consider. Good luck.

catch -
I'm not dx'd with anythng, but in Aug I had exactly what you had - (sharp stabbing pains along with a tight band sensation) and ended up in emergency on heart monitors. (When I phoned 'nurse-on-call' they told me call an ambulance!)
I was fine after a few hours and Dr said it was just unexplained 'muscle spasms'.

It's happened only mildy since.
If I have MS I would say it's the 'hug'.