See Alike in...

Alike App

Browser

Mimi_Jewell

655d

Chiari is so weird it comes up randomly where I feel like passing out... Can anyone tell me what they do to get through it... Talk to family, deal with it alone, take medicine etc.. It's like it's ok for a while and then bam it's like "hey I'm still here" sucks

Top reply
    • Maryoochki

      639d

      How can chiari type 1 get worse

    • Maryoochki

      639d

      How can chiari type 1 get worse

    • dees

      653d

      sometimes I feel alone cause no one understands what it's like. I thank you for listening to my rant. You also let me know how your doing or if you just need want to chat. I'll be here 😊

    • dees

      654d

      I tried to get disability but they said no because I didn't make enough money for the quarter. I used to be a lab tech for magnetite but because of COVID I didn't work as much as I used to. I talked with the lady that was reviewing my case and I told her" so if you have a disability you can't get disability cause you didn't make enough money" she said" basically". Everything is about money. I'm going to appeal it let's see. What have you been doing to get through your day? Do you have to take medicine?

      • Mimi_Jewell

        653d

        @dees I don't take meds everyday no.... Head isn't bad anymore to where meds wouldnt even work.. ibuprofen 800 mg every now and then gets me through it

        • dees

          653d

          @Mimi_Jewell I'm glad you are doing ok. I got some good insurance this week. Now I can find a better doctor. 🙏

    • MountainRoamer

      655d

      I have chiari as well as EDS and POTS. There's a definite overlap. Just throwing it out there for something to look into.

    • dees

      655d

      I have been dealing with chairi for a year now. Mine hit me all of the sudden. I have every symptom you can think of. I take 3 amitriptyline ( 75 mg) and 6 gabapentin a total of 1800mg. I hear ringing and noise in my brain like how a noisy refrigerator sounds ( that's how I explain the noise 😅) it gets louder throughout the day and if I walk too much talk too much laugh, cry, angry or sad I literally feel it in my brain. I have to lay down a lot!!! I can't work anymore and house cleaning takes all day when before I could get it done fast. Before I could do that,clean the yard, give haircuts,fix my car and go to my mother's and do the same. My doctor has never seen the really bad episodes I was having and still do whatever I do too much tries to tell me I'm not that bad but yet puts me on meds. Its very fustrating! It's hard not to be depressed 😔 but I'm trying to be optimistic and trying to find a better doctor. Sorry I vented😅coffee really helps with the pain. I also drink soda a lot now cause the caffeine helps to get through the day.

      • Mimi_Jewell

        655d

        @dees are you able to get disability for it? Or you have to suffer through it. I hate that it takes everything away from us... are you able to get benefits? Yours sounds worse than mine you have the spina bifida right... either way you've got more than I

☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision

Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.

Want to chat or share? Download the Alike app now and get complete access to Alike.health's unique features.

Find people who are
experiencing a similar
medical reality

100% Free
100%
Free

Download Alike for the full experience

JOIN

View All

Bupropion

night sweats

paranoid

Valium

sertraline

palpitations

Anxiety (Including GAD)

Depression

palpitations

Depression

Valium

Bupropion