ramakentesh

Hi my cousin hit 27 and suddenly developed gastroparesis. anyone here know the kinds of treatments that work?

The acute times i rest, the in betweens i try tk stabilise with exercise and diet but it does what it does.

It changes and sometimes more often than not there is no trigger. I crash for a while zlowly improve then it comes again. Cycle.

If it works enjoy it. Signs of too much would be throat numbness and diaherra.

As you exercise your body becomes less reliant on veinous return and alpha receptor activity to maintain blood flow to the brain - your movement does the work. If you move 24 hours a day you'd be fine

The brain fog is cerebral hypoxia. Anything that helps your pots will help brainfog. For me low starch and low inflammatory diet and no solanines helps.

Well said - i get bad relapses but i always improve

The problem with making conclusions about plasma levels of dopamine or norepinephrine is that high levels in plasma may not correlate with high levels in the synapses where they are active via alpha adrenergic and dopamine post ganglionic receptors. Too much in plasma may suggest faulty reuptake which can result in paradoxical low synaptic levels and over release which can flood and down regulate post ganglionic receptors. in cfs and some pots there can be signs of low ne and dopamine activity parafoxically with very high plasma levels.

Its funny. Before i was on florinef i could not tolerate midodrine. Now i am i tolerate it fine. phenylephrene/ neo synephrine works i a similar way to midodrine.

Northera does not cause supine hypertension and is now also being trialldd in pots. Its a norepinephrine prodrug.

Clonidine is best tolerated. Losartan is being tested

Hi anyone with abnormal QSART results get extreme all body itching?

Oh I see. The nerves and receptors implicated in some pots are also Intimately involved in intestinal processes

Yes hypoperfusion can cause depression and anxiety as can reduced cerebral sodium reception and co2 changes in pots. . I was assume that depression would not normally follow a similar pattern to pots symptoms and resolve in the evening each day. Consider that pots and all oi conditions involve neurotransmitter(s) that are also involved in central mood and cognitive regulation. Consider also that if a pots patient had reduced ne reception the symptoms would be similar to low norepinephrine rather than high. medications that deplete norepinephrine in pre synaptic vesicles cause severe depression. Can you tolerate caffeine? As a one off it would be hypothetically interesting to see how your mood responded to a mild stimulant. My guess is it may help.

I have this problem that waking like I'm dead feeling

I personally think its good stuff for POTS. Why it works is very confusing but for me its the best POTS med ive been prescribed.

Its a good question. Studies suggest people with POTs can have successful pregnancies with it without significant worsening of symptoms, but if yours arrived postpart. then it might be worth treading with caution.

Once you realise that POTs and OI comprises of probably 40+ different disease processes you realise that works for some may not for others.

I dont see the signs of parasympathetic activation? Mestinon which boosts both sympathetic and parasympathetic activity does not cause a worsening in symptoms. In many sympathetic activity is an ineffectual response to sudden fluctuations in circulatory return to the heart and brain.

sorry just read through the whole thread. I wonder if the depression is actually related to the POTS. As in being caused by it. Its a tough one man.

sorry to hear about this. SNRIs are controversial but one of the most hyper patients on these forums reported success with SNRIs when it would be presumed the opposite would be the case. MAOIs seem better for depression in CFS i remember reading.

This is quite common - in fact for me medications I have tried int he past and didnt work have later for some reason. Or vice versa. Talk to your doctor as now days there are many options available according to peer reviewed papers: Other vasoconstrictors include Phenylephrene, dihydroergotamine, synephrene, pseudoephedrene have all been prescribed for OI and POTS. Some docs prescribe Modafinil, Ritalin and other stimulants for vasoconstriction and central stimulant effects. Mestinon is another option. There are papers on its efficacy in POTS. Losartan has been reported to be beneficial in select patients. Licorice kept me employed for six years LOL

It is weird however because most POTSies who take a beta blocker to block sympathetic excess can feel more dizzy - whereas alcohol doesnt do that

Ive always reported this although it doesnt always work - sometimes a beer can actually bring on POTS if it is already looking for an excuse to play up. Ive had many theories over the years - just cold volume loading constricting stomach veins while mildly suppressing sympathetic symptoms? immuno suppression? ( i met a lady with RA who sadly used alcohol to keep her pain under control ) The other interesting thing is that alcohol causes an excessive post alcohol sympathetic rebound response which means you may feel better the next day at well if your sympathetically mediated vasoconstriction is already messed up. Also alcohol reduces clotting factors and there was a recent study that associated POTS with autoimmune clotting disorders like APS. When they work out the cause(s) one day they may explain why this happens for some but not all.

My POTS fluctuates totally independent of volume status or all sorts of other variables. it is just a fluctuating illness at least for me and my volume status may help me cope with the symptoms but the underlying problem is not down purely to volume status or we would all be 100% cured by florinef.