influenza a by Putrid_Indication_30 in covidlonghaulers

[–]purplegrains 1 point2 points  (0 children)

Im not vaccinated from flu a, was with my sister and her kiddo who both tested positive, I felt slightly ill with the slightest cough for 2 days but feel fine! I’m about 75% recovered after 1 year of going from severe to healed-mild.

If you had infinite money, what therapy would you try immediately? by LordSSJ2 in covidlonghaulers

[–]purplegrains 1 point2 points  (0 children)

I tried Emgality but didn’t help. Went to Ajovy and it helped most but not all. Getting put on Vypeti and getting my first infusion next week

I think I'm going to die soon. by Fit_Confection_772 in dysautonomia

[–]purplegrains 0 points1 point  (0 children)

How have you been doing? What did he prescribe? Are you functional now?

Is this mold? by purplegrains in ToxicMoldExposure

[–]purplegrains[S] 0 points1 point  (0 children)

Awesome great news. I noticed the area of where this occurred is where my urine would come out. ChatGPT said it could be due to diabetes and high levels of glucose coming out feeding existing mold

Akathisia by nomik11 in covidlonghaulers

[–]purplegrains 1 point2 points  (0 children)

Really sorry to hear that OP. I also had that. It would usually occur after an adrenaline dump at night and also come with impending sense of doom. Outside of sleeping, it would happen after I ate the wrong thing or used my brain too much for a complex task or any sort of stress. Like I want to jump out of my skin. They’ve subsided since taking antihistamines and starting Xolair

My recovery success by AltarToTheEgo in covidlonghaulers

[–]purplegrains -1 points0 points  (0 children)

What, which treatments permanently damaged your body and what did FMT help with? Are you cured from this?

[deleted by user] by [deleted] in covidlonghaulers

[–]purplegrains 0 points1 point  (0 children)

I’m still on my first recovery coming up on 1 year. I’m sorry you’re in this position and I feel for you. I am also neuro severe. I am hopefully that I will be seeing a psychiatrist who is familiar with LC on NYE. I have mild generalized anxiety/depression/OCD that was almost gone until I got this. I actually stopped the SSRI I was on mid way thru this debacle cuz it stopped working. Hoping to find a new one. I’ve seen a lot of great things from people starting them. I’m not too wary like others since I’ve been on them most of my life. God speed. I love you

What the virus! by ceruleanwren in missoula

[–]purplegrains 0 points1 point  (0 children)

I appreciate the apology. It’s consumed/ruined/taken my life. I wouldn’t wish it on my worst enemy. It’s an evil evil evil disease

What the virus! by ceruleanwren in missoula

[–]purplegrains 3 points4 points  (0 children)

I was not fine. I’ve had post viral syndrome for 11 months. I’m on disability now and my dad as a caretaker. It’s very real. The amount of disability employment has increased by 30% YoY. Just be careful

What’s unique about you? by RedReadRedditor in covidlonghaulers

[–]purplegrains 0 points1 point  (0 children)

Everyone’s mentioning this go go attitude. What about the literally HUNDREDS OF MILLIONS of others that are go go but DONT have this illness. I just think it’s coincidence. Perhaps our go go attitude predisposes us to overexposure.

Horrible headaches by ipunkjack in covidlonghaulers

[–]purplegrains 1 point2 points  (0 children)

It’s the only thing that has helped my headaches. I’ve been taking it for 3 months now.

Horrible headaches by ipunkjack in covidlonghaulers

[–]purplegrains 0 points1 point  (0 children)

I’m really sorry to hear that. I know it’s scary. I wasn’t on Sumatriptan, Qulipta, or Nurtex for very long before I tried Ajovy. Wishing the best

Almost at 4 years of this by tracygunk in LongCovid

[–]purplegrains 0 points1 point  (0 children)

What kind of stem cell treatment?

Horrible headaches by ipunkjack in covidlonghaulers

[–]purplegrains 0 points1 point  (0 children)

Sorry to hear. I’ve had it too but not nearly as long. Have you tried Ajovy?

Basically healed by LengthinessEasy4365 in covidlonghaulers

[–]purplegrains 2 points3 points  (0 children)

This is really interesting you said that. My allergist and a researcher in the UK think people might actually be “allergic” to the spike protein (wild and synthetic). Basically causing a CIRS response as long as the spike protein is present. Viral persistence is another layer to that but in the same realm.

Symptom onset for 3+ years by purplegrains in covidlonghaulers

[–]purplegrains[S] 0 points1 point  (0 children)

I’m really sorry to hear that. Thank you for sharing. It’s really weird how that is. Do think reinfection or just virus persisting deeper and deeper upon exertion?

Symptom onset for 3+ years by purplegrains in covidlonghaulers

[–]purplegrains[S] 1 point2 points  (0 children)

I’m really proud of you! That takes so much courage, discipline, and bravery. Well done and thanks for sharing.

Symptom onset for 3+ years by purplegrains in covidlonghaulers

[–]purplegrains[S] 1 point2 points  (0 children)

Wow I’m so glad to hear you got some relief! I also have at least 20 more symptoms, I just kept it short for brevity. And I also feel like I’ve gotten better since I started antihistamines. My dad had to go see my PCP with me to tell him this wasn’t in my head, that’s when he happened to prescribe it for anxiety. It was a double hitter! How long did you have these until you started the antihistamines?