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What really unlocked eating for me when i was sick was using a heavy duty numbing throat spray about ten minutes before trying to swallow anything, works wonders. Also maybe sounds weird but switch from ice cold to warm liquids. Cold was making my throat muscles spasm and feel tighter, whereas lukewarm chicken broth or warm tea with a massive spoon full of honey smoothed things over enough to coat the raw lining. How was the recovery? Hopefully you are feeling better now, since it’s been 2 months.

Interesting that the cramps stopped after changing your diet. It could be related to changes in electrolytes, hydration or other dietary factors, but I’d still wait for the blood tests and MRI before assuming the diet has fixed the underlying cause. The tingling and spasms are worth mentioning to your doctor as well, especially since they were happening before the cramps stopped. I’d also keep an eye on your hydration and electrolyte intake rather than relying only on the multivitamin. If you’re wondering about Wi-Fi or the router, I wouldn’t put that high on the list of likely causes. There isn’t good evidence that normal home Wi-Fi exposure causes muscle cramps or this type of tingling. If you notice the symptoms only when using a particular room or device, though, it could be worth tracking that pattern alongside your diet and other triggers.

Be very cautious about having the rod removed just because of this. wifi signals aren’t known to cause migraines by interacting with spinal metalwork, so I wouldn’t assume the rod is the cause. That said, if the headaches reliably start when he’s in a certain environment, it’s worth discussing with his doctor. Things like lighting, heat, smells, stress or even being somewhere different could be triggering the headaches. Try changing one thing at a time and keep track of when the headaches happen. I definitely wouldn’t go through major surgery unless his doctors have a clear medical reason for removing the hardware.

I know, but I got my heart checked, ct scans, abdomen and thyroid scans. All good. I have had dizziness for 5 years now. I was told it’s PPPD.

Really exhausting. Menopause can cause a lot of these symptoms but with the dizziness, headaches, BP changes and thyroid results, don’t assume that everything is from menopause. I would suggest to talk to your doctor and mention all of the symptoms together rather than one at a time.

what you’re going through sounds like a classic, awful snowball effect rather than something catastrophic. When your period hits, the sudden drop in estrogen is a massive trigger for chronic migraines which already drains your nervous system. Catching a fluey cold right on top of that is a total double hit because your immune system was already run down. That hot and cold, shaky, nauseous feeling is extremely common when your body is dealing with post viral inflammation, and migraines themselves frequently cause dysautonomia like symptoms like chills, severe nausea, and muscle tremors.

I had to get it too, it was because of skin bridges everywhere. They gave me stitches that dissolved on their own. It turned out well though, 6 weeks or more does sound about right too, to heal. You should be good as long as no signs of infection.

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I and 50 year old without period for 2 months now. Every time I miss my period, my weight goes up. I am getting these symptoms on and off Dizziness Water retention Melasma Hair thinning Gerd Anxiety Headache Fluctuating thyroid panel Fluctuating bp an so on. I am sick and tired of always dealing with some symptom or the other. Menopause has robbed me of my life. I miss the fun and motivation in my life.

Hi all. I’ve been on sertraline for probably two years now. I started sertraline 50mg a few years ago, came off for 6 months as felt better, then went back on after my anxiety skyrocketed. Went to therapy and have been feeling a lot better. I reduced my dose to 25mg a day and have been on this dose for about a year. I wanted to keep reducing and try coming off the tablets, but went through some more personal trauma as I was just taking 25mg every other day in July and had to up my dose back to 25 mg every day in August. Since then I’ve noticed worsening intrusive thoughts (particularly around death and worrying about those emergency phone alerts going off!). Could this be lingering effects from going down and then up a dose? Is it like starting the medication again? I want to try reducing my dose again to just 25mg every other day, but I’m a bit worried I’m making myself worse! The intrusive thoughts are just very upsetting at the moment and wondered if anyone else had gone through something similar. Maybe the dose is too low for me and I need to go back to 50mg every day to be able to live life again? Or maybe I need to stick with 25mg a bit longer, or just take the plunge and try and come off completely again?

Hi all, I’m hoping to find anyone who has experienced anything similar to me, particularly severe digestive slowing/dysmotility without the typical nausea or vomiting associated with gastroparesis. My problems started around 18 months ago and gradually became quite debilitating. My digestion seemed to slow down dramatically. I completely lost my appetite and could feel full after only a few mouthfuls. My lower digestive tract would feel very distended and uncomfortable, and I went from previously normal bowel habits to only opening my bowels every 3–5 days. What has always been unusual is that I never really suffered with nausea and I wasn’t vomiting. Food wasn’t making me feel sick — I simply had almost no hunger and felt as though my digestive system wasn’t moving properly. Because I could eat so little, I lost around 3 stone (19 kg) over approximately 10 months. The weight loss wasn’t unexplained in the sense that I knew why I was losing weight — I was barely able to eat enough. At the same time, I became extremely unwell in other ways. I experienced overwhelming fatigue that could leave me feeling almost bed-bound, pins and needles in my face and hands, crawling sensations over my arms, burning/sunburn-like sensations in my thighs, chest tightness, palpitations/racing heart and generally felt very unwell. B12 then became a major part of the picture. My B12 had historically been low/borderline — around 175–210 on previous testing — and my folate had also been towards the l