Sweating

Sweating

Does anyone sweat with there fibromyalgia not just at night but during the day as well?

A MyFibroTeam Member said:

Hi to everyone. I used to sweat a lot too. Also I suffered migraines regularly and whatever I ate used to upset my stomach. I was recommended to have reflexology. I have been going once a week for four months. It has been my saviour. My body is now able to regulate it's own temperature. I have not had a migraine. It has decreased my pain levels considerably and I can now go out without being worried as to where the nearest toilet is. Personally my experience of reflexology has been life changing. If you are able to find a reflexologist, I highly recommend it. Reflexology is able to balance your body and hopefully maintain homeostasis.Hope that may help some of you, because this condition is so debilitating.

posted over 1 year ago
A MyFibroTeam Member said:

I have something interesting to add! Over the last 25 years of sweating I have asked my G.P., my Endocrinologist & my Rheumatologist for help with my Hyperhidrosis to no avail. Two weeks ago I asked a Dermatologist for help. She put me on Ditropan XI 5 Mg tabs. It is a med. for Incontinence...which I do not have. However, it has greatly reduced my sweating. Miracle!!! It gave me a headache at first which has eased. It also gives me a terrible dry mouth, which I prefer to suffer thru as apposed to being dripping wet all the time! Just thought I would share! 😊

posted about 1 month ago
A MyFibroTeam Member said:

I can sure sympathize with the facial sweating and my whole head sweats. At times my hair is dropping and if I put my head down in runs out of my hair and down my face. It's embarrassing when you want to get fixed up to go somewhere special. I actually bought an antiperspirant called Faces Only. It can't be healthy because it works for 24+ hours and is very hard to wash off. I bought it to use for my daughter's wedding.
I have a question. Does anyone else get vibrations it feeling of current on your extremities. Sometimes it feels like if you were to have your cell phone in your pocket but it's on my legs and behind my knees. I have a lot of spinal problems that cause similar issues but I'm sure this one isn't coming from my spinal nerves.

posted 10 months ago
A MyFibroTeam Member said:

CBDstillery.com is a great place to purchase good quality CBD products. I recommend isolate (you can just eat it since it's already decarboxylated and it has no taste) and vaporizing (they sell disposable vape pens, cartridges, and they just came out with vape juice). The vapes are just CBD and coconut oil. Nothing bad at all and legal in all 50 states. It really helps my pain and calms me down from panic attacks like nothing else.

posted over 1 year ago
A MyFibroTeam Member said:

So do I!! I sweat if I'm just sitting not doing anything! If I'm getting ready to go anywhere the sweating is really bad! Usually it's my head, face, neck and chest!! Also if you go anywhere and it happens it's very embarrassing!! And it makes my anxiety worse!!!

posted over 1 year ago
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