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Bookmark or Share- Does anybody with Chiari have these symptoms? Urgent need of help ...I know some surgeons downplay Chiari if there’s no syrinx present, without giving too much consideration to your quality of life. It’s so hard missing work and personal events due to an “invisible” condition that few people can empathize with. Frankly, it sucks, and Chiari can be a lonely place.
- Just found out I have Chiari 1 malformation-I'm very scared ... - RedditI know it probably seems overwhelming, but a chiari doesn't mean a lifetime of illness. A few years ago, before I was diagnosed and started taking control, my symptoms were debilitating. Now, they are an occasional annoyance in my otherwise chiari-free existence. Typically my symptoms are worse when I'm not taking good care of myself.
- Chiari Decompression Surgery - Experience & Recovery : r/chiari - RedditAbout 10 days ago I had chiari decompression surgery. I was back up on my feet in 48 hours and well ahead of where I expected to be. Slowly working through my neck exercises and taking very short walks each day. The problem.... the last few days my head aches are pretty constant and worse than the week following surgery.
- Would you please share what Chiari surgery recovery was like ... - RedditAt 2 weeks I was able to drive again. I felt drastically better somewhere around 4-5 weeks. Also, if you’re nervous the days leading up to the surgery, you could ask you doctor for Ativan or another anti-anxiety medication. It’s been a year now and all of my chiari complications are gone, and my syrinx has shrinked considerably.
- Arnold Chiari Malformation Support Group - RedditI have Chiari Malformation Type I (8mm herniation) and scoliosis/degenerative disc disease. I recently had a major flare 3 weeks ago (vertigo, panic, neck/occipital pain and pressure) and had to quit my job (which is giving me too much time to panic inside of my house alone all day oof).
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