BrainTalk Communities - Forums https://www.braintalkforums.org/ BrainTalk Commuity Forums en Wed, 14 Oct 2026 07:47:14 GMT vBulletin 60 images/misc/rss.png BrainTalk Communities - Forums https://www.braintalkforums.org/ October Keep On Moving thread https://www.braintalkforums.org/forum/neurological-disorders-and-injury/multiple-sclerosis/274349-october-keep-on-moving-thread Tue, 06 Oct 2026 00:13:03 GMT Here is the original message Sunshine 2 (BBS1951) always used to start this monthly thread: Better late than never--here it is the 5th of the...
MS creates some real challenges to keep on moving. It helps to inspire each other on how to find ways to move.

Did you stretch in your bed, swing your arms, roll side to side today? Or perhaps you did housework? Or exercised in a pool? Tracked your count of steps? Chased your cat around the home? Pushed the wheelchair wheels with your arms at the store? Post them here and we can support and egg each other on.

REMEMBER: This is a keep on moving thread, not keep on exercising! Any moving is important it doesn't have to be exercise! Even Science proves that.
Better late than never--here it is the 5th of the month already, and I'd like to say I've been so busy exercising that the time has flown by but in reality I'm just slow.

The world has been waiting for my September average step count. So here at long last it is: 1,039 steps/day (based on 26 days)

Not a stellar record but I did have 2 falls in September. Of course those falls might not have happened if I'd been walking more.

Others here will chime in about what kind of exertions or even exercise you've been doing, I hope.]]> Multiple Sclerosis agate https://www.braintalkforums.org/forum/neurological-disorders-and-injury/multiple-sclerosis/274349-october-keep-on-moving-thread Complex Neurological Symptoms https://www.braintalkforums.org/forum/neurological-disorders-and-injury/general-neurology-rare-disorders/274341-complex-neurological-symptoms Fri, 02 Oct 2026 16:59:45 GMT I am a 24-year-old pre-medical graduate who has unfortunately been out of work on medical leave for the past 5 months after a sustained 7-week period... I ended up in the ER twice in April with what my PCP described as “catecholamine storms,” where my heart rate and blood pressure were extremely high and I demonstrated other symptoms indicative of severe over-activation of my sympathetic nervous system (including an inability to defecate despite the urge and urinating clear water throughout the whole crisis, and loss of sensation across my entire body).
Since the ER, I have been having extreme symptoms of autonomic nervous system blunting. Most of the symptoms from the crisis phase have resolved, but my main symptoms now are that my blood pressure and heart rate, although normal, do not appear to be adjusting properly to my physical or emotional activity, like they once did.
I have been having intense, constant brain fog that makes it almost impossible to focus on any tasks, I have felt extremely low in energy and emotionally flat without improvement, and I have almost constant head and chest pain and nausea. None of these issues respond to typical interventions that I used to utilize before this crisis to manage depression and anxiety.
In short, it is very difficult to function on a daily basis.
I have consulted multiple neurologists, but have not received any advice except for managing my OCD and anxiety and a diagnosis of “somatic symptom disorder.” Most neurologists don’t know how to deal with post-stress nervous system conditions, and psychiatry has been inadequate.
However, despite working on my OCD, anxiety, and depression from a psychiatric standpoint for the past several months, I have not really had any improvement in my bodily, cognitive, or energy symptoms.
I contracted COVID for the first time around 3 months before all of this occurred and had not felt right ever since.
I had a normal head CT scan, neurological exam, and cognitive evaluation despite a substantial subjective decline in functioning.
I had extremely nuanced emotions, social intelligence, and high intellect before all of this, and my quality of life has become very poor in such a short amount of time (I am literally unable to connect with others emotionally and have not even been able to smile or genuinely laugh for months behind the pain and head pressure). Nothing at all is able to distract me from how I am feeling physically.
My relationships now feel very shallow compared to the past, and I fear that I will never be able to feel love or romantic or sexual attraction again.
My internal clock is completely messed up, and I cannot even feel the normal cues that alert you to time of day or year, my energy level’s just a constant low flatline, no matter how much I sleep.
Close to the 6-month mark after all of this occurred, I am starting to become very discouraged and am desperate to return to some semblance of normalcy after these very difficult months.
At this point, I can’t imagine ever feeling the same again.
I live in the Boston area and am wondering if anyone has any suggestions or knows of any specialists experienced in such complex cases.]]> njf2001 https://www.braintalkforums.org/forum/neurological-disorders-and-injury/general-neurology-rare-disorders/274341-complex-neurological-symptoms Diagnostic Performance Of CSF Protein 14-3-3 For Prion Disease In The Modern Era https://www.braintalkforums.org/forum/neurological-disorders-and-injury/creutzfeldt-jakobs-disease-cjd/274331-diagnostic-performance-of-csf-protein-14-3-3-for-prion-disease-in-the-modern-era Thu, 24 Sep 2026 16:24:10 GMT THURSDAY, SEPTEMBER 24, 2026 Diagnostic Performance Of CSF Protein 14-3-3 For Prion Disease In The Modern Era, Singeltary Review ...
Diagnostic Performance Of CSF Protein 14-3-3 For Prion Disease In The Modern Era, Singeltary Review

https://prpsc.proboards.com/thread/2...-protein-prion

https://madcowtesting.blogspot.com/2...f-protein.html

terry]]> Creutzfeldt Jakobs Disease (CJD) flatfish https://www.braintalkforums.org/forum/neurological-disorders-and-injury/creutzfeldt-jakobs-disease-cjd/274331-diagnostic-performance-of-csf-protein-14-3-3-for-prion-disease-in-the-modern-era Pocket dialing https://www.braintalkforums.org/forum/neurological-disorders-and-injury/multiple-sclerosis/274328-pocket-dialing Wed, 23 Sep 2026 18:02:14 GMT The people who keep track of words at the Oxford English Dictionary are listing pocket dial and pocket dialing as terms that have recently entered... pocket dial and pocket dialing as terms that have recently entered the language to the point where the OED sees fit to include them.

To make sure I had the meaning right, I asked (who else?) AI and was told:

A pocket dial is an accidental phone call made when a mobile phone in a pocket, purse, or bag registers unintended touches against its screen or buttons
I get a lot of wrong-number calls and this is probably one reason why. I don't know about other people but I don't like the idea that I might be interrupting someone's day by having a phone that accidentally makes calls.

Growl.]]> Multiple Sclerosis agate https://www.braintalkforums.org/forum/neurological-disorders-and-injury/multiple-sclerosis/274328-pocket-dialing Oh snap, now the bacon, CWD, TSE, PrP, the Singeltary Files, Confidential https://www.braintalkforums.org/forum/neurological-disorders-and-injury/creutzfeldt-jakobs-disease-cjd/274327-oh-snap-now-the-bacon-cwd-tse-prp-the-singeltary-files-confidential Tue, 22 Sep 2026 16:44:01 GMT TUESDAY, SEPTEMBER 22, 2026 Oh snap, now the bacon, CWD, TSE, PrP, the Singeltary Files, Confidential, In Confidence ...
Oh snap, now the bacon, CWD, TSE, PrP, the Singeltary Files, Confidential, In Confidence

https://chronic-wasting-disease.blog...d-tse-prp.html

https://prpsc.proboards.com/thread/2...ngeltary-files]]> Creutzfeldt Jakobs Disease (CJD) flatfish https://www.braintalkforums.org/forum/neurological-disorders-and-injury/creutzfeldt-jakobs-disease-cjd/274327-oh-snap-now-the-bacon-cwd-tse-prp-the-singeltary-files-confidential