Heat Intolerance: Symptom of Neuropathy?
So I am waiting to get my diagnosis, but does anyone else feel odd after being out in the heat for a period of time? I love gardening this weekend was watering for about 20 minutes in the sun. I just felt weird afterwards, symptoms I can't explain. Sweat will just roll down my face, this never happened with me before.I love to take hot showers and one time I felt somewhat ill afterwards. I just feel I can't be out in the heat anymore.
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I would look into happy , mood lifting supplements, or medicinal marihuana, whatever you can use, after consultation with your doctor. And I will wear all the time , some scarves dipped in cold water, or even keep some in freezer and rotate them. I would use soft towel ones for gym, and some beautiful for going out or work.
Cotton, cashmere, in zip lock bag and freeze them, not damp, just dry scarves and keep changing them.
You can keep some in work fridge or freezer, or in the car in freeze bag or picnic box with ice? Just suggesting, what I would try.
I'm sure you've tried lots of things, and yes, it's annoying, especially we're not that old, as to say, getting old suck, but it really does.
I've got my diagnosis at 54 years of age, but it started earlier.
I feel bad for you. You sound so down. Don't give up on meeting some one. Maybe join some clubs or activities connected with your church or house of worship. I have friends that volunteer in the churches food pantry and have meet some nice people. One friend of mine has a son with many health challenges in a wheelchair but has managed to get out and about and just recently announced his engagement.
On a another note , don't let the house temp. go below 55 because the pipes might freeze.
I hope in some small way I've helped...good luck.
Thank you so much.
Hi Brooklyn . As everyone has said don’t give up little lady God has a plan for us just believe in him . We’ve all been through something traumatic I just turned 52 myself and since 2020 Ive not been able to Walk and in a wheelchair I still fight every day this dang disease ain’t whooping me 🙏🏻 I do pull-ups 3 days a week and use bands to stretch my leg muscles I also have a contraction machine to stimulate my leg , calf, Quads, hamstrings etc
I have pain 24/7 it never shuts off mind of matter . I know all to well about the HEAT I sleep with gel ice packs 3 of them I made little pillowcases for the ones I have so I can wash them . This helps me tremendously I thought I would share this little thing I do any gel pack will work I bought mine at CVS pharmacy through the drive thru as it very difficult me to go places even though I have drive controls in my truck try this method I think you’ll like it . Hang in there I’ll say a prayer for you every day as do with everyone on this board . God Bless Everyone today lord as we need blessings and guidance thank you for not judging
me and helping me through difficult times Amen !!! 🙏🏻
Thank you. I really appreciate it.
I would love to know what it gave it to us. So very odd.
Thank you all so much. You helped me. I been watching the group for awhile but, I never wrote. You know that feeling in your stomach when you have to try to explain it to people and they don't get it? I bring a fan in my purse...everywhere I go. I think I had to just do the holiday. My first one alone. But I made a turkey with all the trimmings. It was wonderful!! You know when you cook something so well, you're proud? I was. And I was happy I cooked so well. I haven't cooked since February. I just buy whatever. Anyway, I feel better. I just didn't know what to expect for being alone the holidays.
I go a few places sometimes. I loved this Italian restaurant, I went once a week. But, now that it's winter...even though it's still hot....I went recently several times. Now they don't have the ac running because it's not summer. So, that sucked. Believe it or not it is easier to live somewhere hot, even though I'm not crazy about extreme heat. Because in the summer, everywhere has good ac running. Because I thought about this years ago. I thought of moving somewhere cold. It's worse. If it's cold....then the heat is on everywhere. Like the grocery store, and restaurants. So, no way. Living somewhere where the heat was on.....no way. I went to Vail last year...OMG it was like 7 degrees. I LOVED IT. I was out in a tee shirt. I hope to write more. Well, look at that. I wrote a positive message. Maybe being able to talk to people helped too. You guys were my therapy...and still are. Send me the bill.
Have a good night you all. Attached is a pic of my Winnie. I love animals. I've had collies over 25 years. This is Winnie at a few months old. Thank you all. Please don't leave me. I get lonely. And just to talk to people who understand what a "small fiber neuropathy" is. No one believes it is even a thing...lol...people just look at me like...what? Enjoy this puppy picture of Winne.
He is so cute!
The first time I had a EMG test it came back normal, but the next time it came back I had Neuropathy. Didn't make sense. My symptoms started after I took the double dose Shingrix Vaccine in November 2019 and been messed up off and on since then. I had all kinds of xrays, scans, mri's EEG, EMG, and couldn't find anything, then they found neuropathy the second time around. Doesn't make sense, never did. I had only 1 doctor state it was vaccine related. So how do you "undo" a vaccine related injury?
If there was an undo option, there would definitely be a lot of happy campers in the world. The best you can do is find something that provides relief for the symptoms, hopefully something that doesn't require drugs (in my humble opinion).