Dear Kind Person:
Almost every morning I have a form of a migraine. Any tips? Here is one tip to share: I noticed one thing that has worked for me: When I wash my face with my hands, using Cetaphil to clean, and not use a facecloth, my skin is much better. Maybe, that will help someone. I am trying to always give one positive tip when I ask a question. Good day.
hi have same thing hope your well today
Yet another night up and down. Legs throbbing cannot get comfy. No matter which side I lay on it hurts. Really struggling with the broken sleep, my legs are so irritable find my self getting up just to ease it, so draining,
I've been using hylands leg cramp pills and they help some
My is low degree fever for a few hours then go away.
I am now in my 40s with Ulcerative Colitis with associative arthritis and Ankylosis Sponydlitis and Fibromyalgia. I relaize more then ever the importance of nutrition especially since Ulcerative Colitis and many physical activities (including the three letter one) demand so much more from the body. I find myself needing more Potassium and Magnesium after the three letter one. I find myself needing more Iron when I get cold. I know I need some level of B vitamins for associative essential… read more
Similar with me on vitamin D for immunity and probiotic to maintain gut flora since I have Ulcerative Colitis (UC).
For energy/CFS, I used to do B12 injections myself, but its risky so I switched to… read more
Hi everyone. I’ve ended up here in my 4 month search to try and find out what is wrong with me. I would greatly appreciate your advice! Doctors have tried to palm it off as anxiety and make me feel like a hypochondriac but there’s something wrong and I can’t figure out what it is. They want me to try 10mg amytriptiline but I don’t know if that’s a good idea.
MY SYMPTOMS
🤢 Severe nausea that lasts around 2 weeks. No vomiting. I can barely eat as feel too sick and I’m very weak.
👤 Ache in the… read more
Amitriptyline makes me feel like I have brain fog. It also causes pressure in my head. I don't take it anymore
I'm going through menopause right now and I'm curious as to the symptoms that you guys are having. Did your fibro get worse or are you experiencing new symptoms?
Monday and Wednesday. Chair Yogalates Tuesday. Very tough after 4 years of no formal exercise. I'll push through it.
How does everyone else cope with there pain, if there on other meds, as for when I go into pain my body locks up and I don't like a person of my age, but a much older person
Can I ask what that is?
I have tried it. Was excruciatingly painful. Like, lift me off the table, kind of pain! Never again, for me. Other people I know ( without Fibro) love it!
Yes and also I'll have fever blisters for no apparent reason