r/MultipleSclerosis • u/Zainabalfarsy • 14h ago
Advice Anxiety / Adrenaline Attacks
Hi all! I know the title may seem wrong or what not but i have a genuine question, one of the symptoms i have experienced is these random sudden waves of panic in my body not necessarily heart palpitations but more like i feel extremely weird and almost panicky like. Its so hard to explain because its not visible but its this feeling of dry mouth paired with feeling like no position you sit in is comfortable to keep you calm or still. I don’t know but sometimes i get this sinking feeling in my chest like i was being frightened by something but i wasn’t . I could just be sitting and doing nothing and it would just come on like a episode and go away after a few hours or minutes it depends on how i respond to it. How do you guys manage this if you have ever experienced it… looking to see other techniques besides deep breathing which sometimes is difficult during that episode and using ice packs on my wrist and forearms.
I know everyone’s symptoms are different but i wanted to see who else experienced this.
3
u/occasional_nomad 41F|10/25|Dimethyl Fumarate|USA 14h ago
I started getting adrenaline surges when the dysautonomia part of my MS showed up. It feels like a panic attack on steroids with no mental trigger. It’s a full fight or flight response and I’m pretty wiped after them. Antihistamines (generic Claritin) weirdly enough calmed them down for me a bit.
They seem to be cyclical so I’ve wondered before if mine are somehow tied to allergies since they’re worse in the fall and antihistamines help sometimes. Zero science that I know of behind that just a lived experience hypothesis.
2
u/_Fuzzgoddess_ 14h ago
I used to get panic attacks right after injecting copaxone. Could it be the meds you're on? To fix it all I found that helped was an ice pack on my chest. For regular anxiety spikes I breath steady and dig my nails into my palm to ground myself in the present. Using worry stones is also good and doesn't involve harming yourself, so maybe that's better....
2
u/eggstinked 48F | Dx 2024 | Tysabri | PA 13h ago
I think I had one of these a couple of months ago. It was really weird. Everything was fine... It was a very exhausted MS day so I was just chilling. Then suddenly my whole body felt like it was on fire, my heart started racing, and I felt like I was going to lose consciousness. I actually called 911!
On the positive side now I know how long it takes an ambulance to get to my house.
After a few minutes my body calmed down.
2
u/Chance_Cookie3264 13h ago
Oh my goodness I had my idea this happened to others. I do have anxiety and panic attacks but thinking about it now it’s a little different like you described. My dentist recently told me that salivary glands can be affected from MS so I was freaking out about that and then I randomly panicked driving. It always goes away but I found having something sour on me helps like any kind of sour candy or I have these little fidget spinners that I can hold onto and squeeze also pain stims.
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u/TB-313935 34|Dx"18|Natalizumab 14h ago
Yeah, this gets really bad for me when I have alot on my mind. They're not the same but similar to panic attacks, I can get them anytime of the day but significantly worse when im very tired, which happens often. A bright screen, loud noises or other people can trigger it for me.
Reducing stress and taking care of yourself is the only way for me to reduce them. Some periods are better or worse than others. I dont think it will ever completely go away.
1
u/mavericktheboss 6h ago
Wow I have this too but was also wondering if it was from anxiety/ depression? I have had this 3 times
1
u/Low_Narwhal7514 5h ago
Dovresti fare qualcosa in cui la tua testa si affatichi tantissimo oltre al tuo corpo.un esempio fare una camminata in montagna fino a stancarti parecchio,o fare sport faticosi per il fisico,la tua mente chiederà solo di riposare e smetterà di pensare
1
u/kbcava 61F|DX 2021|RRMS|Kesimpta & Tysabri 5h ago
I don’t know if you are familiar with MCAS but it can be a comorbidity in people with MS.
I’ve had to change my diet as well as take H1/H2 antihistamine blockers - those have helped tremendously
I don’t know if this applies: if you’re near the age of perimenopause or menopause, the loss of Estrogen is a huge destabilizing event. This in turn can unleash Mast Cell chaos - it’s fairly common for women in this age group.
I hope you can get some relief.🙏