root cause of the fluid retention?
Because I'm constantly reducing my insulin inj units I'm at sometimes at a loss or gain on bg levels I must admit, at mo I'm a little higher than normal, normal for me.The amount of salt in soluble cocodomol. Been avoiding them quite successfully for a few months, but the pain (muscular spasms in back) just gets too much sometimes. I've been decorating and shifting furniture from pillar to post, not ideal for bad backs.
Soluble preferred to tablets although capsules OK I'm going to go without for the time being. The increase in weight is so rapid it has to be fluid especially the way my ankles look and the tightness in the skin in my shins.
I'm sort of alluding to a theory that the more water in the body, the more the glucose is "thinned out". Just wondering if anyone else has noticed anything similar.
If not normal to you get fluid retention checked out please.
I've had mine checked up to a limit as its not heart related.
I'm waiting for bariatric surgery pre-op endoscope to answer a few more of my whys!
It seems mine is either tramadol related but had it less on codeine but still had it.
GERD seems likely but I'd like an endoscope to rule out anything sinister as all my fluid retention is in the stomach area only. No legs only when bad bg control over the years. Arms swelled up on atorvastatin with numbness so stopped it immediately and told gp.
Is yours mainly in legs and feet?
How has your walking or sitting around more levels? Increased, decreased or same?
Often I had swollen feet if the office heating up too high in the winter on top of extra hours sitting at my desk!
Get it checked out regardless.
Bgs are irratic more for me in the winter, my diet changes and dark nights keep me indoors more.
Editted to also add.
Bgs need more insulin per weight to keep steady. I know you're not on insulin but your own insulin needs will change.
Also the only time I've had fantastic run of bgs is when I was losing weight without any effort in the summer. When I believe my tsh was perfect was when my body clicked into weight loss and excellent bgs.
I didn't get them to print it off nor have used their on-line blood test results but in front of dn at hospital on screen it was hugely improved. Endo stated that due to a much improved diet this has occured but I feel more due to a switch had just been switched on in my body at last.what is your ideal level of TSH...? I ask because it is one of my "why´s"
Is yours mainly in legs and feet?
How has your walking or sitting around more levels? Increased, decreased or same?
Yes elivated legs does reduce their swellings and then you pee the water out if your kidneys can do their job properly.Noticeable in legs and feet. I've been on my feet a lot more because of the decorating, carpet comes tomorrow and I'm all set to lock myself away where I don't have to listen to my wife and her mother talking over anything I might want to watch on the TV.
It's surprising how much the ankles go down just by having my feet up. The fluid goes somewhere else. I'd almost forgotten that the lymph nodes in my legs aren't 100%, I've even attended a lymphodema clinic several years ago.
I'm not taking soluble cocodomol now, so hopefully fluid retention should ease. It will be interesting to see if less fluid means BG becoming less stable.
Drink plenty of water to help kidneys do their job easier!
I recently took Furosemide for a short period. Raised bg is one of the side effects mentioned in the patient leaflet, and this did happen to me. I'm not sure whether it is because it reduces the amount of fluid in the blood, so making it more concentrated, or because it causes potassium to be lost, or some other reason. I got myself put onto Frumil, which contains a combination of the potassium-sparing drug Amiloride with Furosemide, but the raised bg continued, so I persuaded my GP to let me take Amiloride alone. When taking only Amiloride it is very important not to take in too much potassium, especially in the form of supplements or Lo-salt, as it could be dangerous. Amiloride is supposed to be less effective than Furosemide. Btw people usually prefer to take Furosemide only in the morning, to avoid having to get up in the night to pee. However at one point I was taking two pills in the morning and one at night and I still didn't have to get up, so you might like to experiment with a slightly higher dose.I started with furosemide
I asked gp to increase but said no as liver is a fatty liver. Still. Scan confirmed it recently again. Low carbing strictly helps but causes more palpatations if too low carb.I recently took Furosemide for a short period. Raised bg is one of the side effects mentioned in the patient leaflet, and this did happen to me. I'm not sure whether it is because it reduces the amount of fluid in the blood, so making it more concentrated, or because it causes potassium to be lost, or some other reason. I got myself put onto Frumil, which contains a combination of the potassium-sparing drug Amiloride with Furosemide, but the raised bg continued, so I persuaded my GP to let me take Amiloride alone. When taking only Amiloride it is very important not to take in too much potassium, especially in the form of supplements or Lo-salt, as it could be dangerous. Amiloride is supposed to be less effective than Furosemide. Btw people usually prefer to take Furosemide only in the morning, to avoid having to get up in the night to pee. However at one point I was taking two pills in the morning and one at night and I still didn't have to get up, so you might like to experiment with a slightly higher dose.
And Christmas presents for all your hard work!I have quite a thirst most of the time. Usually water, sometimes berocca, tea or coffee. HID doesn't do waiting on me, even now she's retired. She under cook the steamed vegetables last night, I'm beginning to think it's intentional LOL
The decorating is as a result of a realisation that the MIL has been with us every christmas since my wife's father died 35 years ago. A very nice man, how he got lumbered with . . . . . . . . . . you get the picture. I don't want to be stuck in the same room as
MIL for too long so I'm looking after number one this year.
You're dead right about pacing yourself. This decorating has taken several weeks but when you consider I have removed all the furniture on my own, dug up central heating pipes because new radiator is not the same size as old one, filled god knows how many cracks and holes, painted ceiling, walls and skirting (replacement knees are fine, just not as bendy as real ones). And installed a TV on the wall, dug holes for power sockets etc etc. I feel that I have accomplished something. I hope there's some decent TV over christmas! LOL
Indeed! I often feel I have far too many organs, all with their problems and their own separate hospital appointments and sometimes incompatible drugs. Sigh! How anyone over a certain age can find time to work is a mystery to me.Still trying to please all organs needs regarding liver and palpatations pressure on the heart.
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