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It's cuuute!!! Why did you chop it and may I repost?

I love your hair, its as long as Lorroakan's

I think you did a great job. Probably better than a salon. I kept wanting you to stop before going to far. LOL

Shout out to the SD shirt

Great depiction of the situation. Wild that it has been 7 weeks and some parts still look pretty devastated. Great video thank you

I hope Asheville returns to normal soon! Sending all my deepest prayers ❤

I love to tour

🎉

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We can't find our homeless community it's crazy they're all gone😢

This

I had to “evacuate” due to hurricane Helene

It took 3 years before they diagnosed. Nerve block injections have not worked. Also can not take Gabba. What state are you in?

Thanks for sharing your story, good to hear from others who are also suffering. I developed this after Covid as part of my Long Covid. It really sucks. When it is flaring up it is impossible to look at a computer screen. It is such a sharp awful burning, searing pain. I agree ice and just resting seems to help but it is frustrating to deal with on an ongoing basis. I wish there was some topical treatment we could use, like a cream or gel that has a freezing/numbing effect. That ice mask you have looks good I need to get one! I just got a TENS machine to see if it helps.

I really appreciate your explanation

I'm 24 years old only. I'm also having supraorbital neulargia. Today just went to see doctor.

S

Thanks for sharing! What a cool facility. Will need to visit one day :)

Oh im suffering from same problem...does it put pressure on your eyes too

RUclips

M literally crying now..feeling anxious..plz reply me the pain will go away or not...!and how long the pain will last?

Can anyone suddenly develop this, i mean without any head injury??

Hi thank you for this! Question: do you have this pain on one side or both? I have had pain in both Supraorbital notches now for a couple of years, but it seems consistent with sinus issues (it gets much worse as soon as allergy season arrives and it’s not bad during winter). Also, Whenever I don’t get enough sleep, I usually have a headache the next day stemming from this area

LOL

emikly

msuca

Does it have to be an MRI or will a CT scan detect it?

Hey if I may ask what test determined this diagnosis? I feel like I’m experiencing the same thing but I’m not sure which test(s) would be appropriate to determine that it is? Thank you in advance!

San Francisco the only part of the planet where churches shouldn't be there !

I just found out to today i might have this.. I thought iam having a some migraines.. but this actually sucks.. Doc just prescribed me with painkillers amd if it doesn't go away than have to go back for diagnosis

𝔗𝔥𝔢 𝔞𝔣𝔱𝔢𝔯 𝔥𝔬𝔲𝔯𝔰 𝔱𝔥𝔞𝔫𝔨 𝔶𝔬𝔲 𝔣𝔬𝔯 𝔭𝔲𝔯𝔠𝔥𝔞𝔰𝔢. 𝔗𝔥𝔢 𝔱𝔯𝔦𝔭 𝔶𝔬𝔲 𝔴𝔦𝔩𝔩 𝔟𝔢 𝔴𝔢𝔩𝔠𝔬𝔪𝔢 𝔱𝔬 𝔖𝔞𝔫 𝔉𝔯𝔞𝔫𝔠𝔦𝔰𝔠𝔬 𝔣𝔬𝔯 𝔞𝔪𝔟𝔞𝔰𝔰𝔞𝔡𝔬𝔯 𝔬𝔣 𝔱𝔥𝔢 𝔠𝔦𝔱𝔶 𝔱𝔬 𝔰𝔢𝔢 𝔩𝔞𝔫𝔡 𝔶𝔬𝔲 𝔴𝔦𝔩𝔩 𝔳𝔦𝔰𝔦𝔱. 𝔓𝔩𝔢𝔞𝔰𝔢 𝔫𝔬𝔱𝔢, 𝔫𝔬 𝔯𝔢𝔡𝔢𝔢𝔪𝔞𝔟𝔩𝔢 𝔭𝔬𝔦𝔫𝔱𝔰 𝔣𝔯𝔬𝔪 ℑ𝔫𝔤𝔩𝔢𝔰 𝔭𝔞𝔯𝔨𝔦𝔫𝔤 𝔩𝔬𝔱 𝔰𝔥𝔢𝔫𝔞𝔫𝔦𝔤𝔞𝔫𝔰. 𝔱𝔥𝔞𝔫𝔨 𝔶𝔬𝔲 𝔣𝔬𝔯 𝔞𝔰𝔰𝔢𝔪𝔟𝔩𝔢

𝖈𝖆𝖗𝖈𝖍𝖚𝖓𝖌𝖚𝖘

🦄🦄🦄🦄🦄🦄🦄🦄🦄🦄

I think I have this. I had the flu and it came with a massive headache. Now my forehead and the top of my head is numb. If I apply pressure on the nerve I can feel a pressure relief like a massage. Raising my eye brows no longer feels weird. Hopefully it goes

I want my mommy

Show me my gift

Think of the victims every-time u go shopping. U can eat all grains, seeds, legumes, vegetables etc. beans and rice and oats are stables of vegan diet. Watch dominion on RUclips to give u motivation.

Nice tree. CNice lights. It livened up the tree and the room.

1st

You have beautiful healthy looking hair! Before AND after! Thanks for showing how you cut your hair.

Ｐｒⓞм𝕠𝕤𝐌 🤘

I LOVE your Poppy kitty!!! Did you know that she's a Bombay kitty?!? I've been trying hard to find one because my cat is 17 years old now and I would like to get a little friend for her so she doesn't die alone and has a friend to play with, ya know? I have subscribed to your channel. My name is Elizabeth and I am from Albany Georgia. So HI!!! 🐈‍⬛♥️🙏🎃🍁

You look gorgeous and in my opinion you did a great job cutting your hair. Also you could got a few inches shorter and still look gorgeous.

Thanks for the video. It is really super helpful. I have just started getting symptoms. Hard to get a neuro appointment. May I know how long it took for the symptoms to progress? Did it develop over a period of time? or was it just one fine day ?

Finallllly!! I've found someone else who presents with symptoms like mine!! I went to my GP about 8 years ago after I started getting these weird sensations around my eyebrows, bridge of my nose, & forehead. The only way I could describe it was it's like having a bruise for no reason like something hit me.... but it doesn't go away. It's not really painful, just super annoying! Some days are worse than others. I work night shifts, & I definitely notice it more when I'm tired or if it's really cold. After coming up clueless, my GP referred me to a Neurologist who carried out a thorough examination as well as an MRI, which thankfully all came up clear... & was conclusive proof for my twin brother, that I did in fact have a brain.... I was just selective on it's use 🤷‍♂ The notes were sent back to my GP who interpreted my symptoms as Trigeminal Neuralgia, but when I looked up the symptoms for this, it didn't really fit what I was experiencing, but they prescribed Amitriptyline tablets, which does dull the sensation into the background... However the downside is that they make me feel really sleepy & groggy when I've woken up. For the first time in 8 years, I feel like I've found a diagnosis that better fits my symptoms. I'm not sure if I should speak to my GP to see if there is a better suited treatment, or at least to see what they think, with this new info. But with it being quite rare... They probably wouldn't have a clue anyway lol. Anyway thanks for your video & I hope you're doing well. Much love, Kev

Thanks, was looking for personal experiences of supra-orbital neuralgia, like you I've found very few, still working out if it is related to what I have. There is a suggestion it is sometimes related to Thyroid Eye Disease, asked for personal experiences in big FB group with TED sufferers and it was like watching tumbleweed in the desert. Beginning to wonder if the paper linking the two was made up....

Thank you, thank you, thank you, for sharing this video. I just found it today. I have been in tears this afternoon. I have this same struggle and can relate to everything you say. Emotions trigger this same pain in the exact area you mentioned. I have managed to give up caffeine but not sugar. I do see a Neurologist and get botox and supra-orbital injections. The botox gives me 50% relief the Supra Orbital only a day or two. I hate taking medications as well but have also been offered medications which I have finally given into because I can no longer take the horrible pain I have been having. Wow! I can not believe I have finally found someone who has this same struggle. I don't post video's. I am in my 50's but thank you for being willing to do this one. I appreciate it. (Gail)

I have this also and I thank you for for sharing. I am going to have a Supraorbital Abrasion in a couple of weeks to hopefully stop the pain. TPI's I receive to my supraorbital nerve only lasts 6 weeks and it is suppose to last months. So this is my next option.

Hi! So I’m getting a brain and orbital MRI next week, and my neurologist didn’t say any possibilities out loud, because she said she wanted to look at MRIs before doing anything else. In the mean time she put me on gabepetin. Which has taken my pain from a 9 to a 6. My pain has been when ever my upper eyelid is touched it shoots pain to my forehead/scalp area. I was looking at a nerve map of the face yesterday and saw that the supraorbital nerve is almost the exact line of the shooting pain. However, I can touch my forehead and brow ok, it’s just when I touch my eyelid it’s horribly painful. They’ve already ruled out anything wrong with my eye. I was wondering if you’ve experienced any eyelid issues with your neuralgia?

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