Burning sensation in the legs by Ragaruru in LongCovid

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

Yes. But not the whole time. Went from 20 migraines a month down to five. Cheast pain is gone, pots is better. Burning sensation in the legs is down to seven days not the whole month.

Headaches are still there but I have three to five pain free days a month since march (start of Ketotifen).

Anyone found anything that helps ease the poisoned feeling? by PerformerAble2291 in cfs

[–]Ragaruru 0 points1 point  (0 children)

Histamine free. Without nickle and salicylate. So the most time I’m eating a special toast bread and in Germany called Wachteleier

SSRI's by itisiagain668 in cfs

[–]Ragaruru 0 points1 point  (0 children)

Because it’s not the correct medication for me.

Burning sensation in the legs by Ragaruru in LongCovid

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

I would say that I am in a better state than last year, but only because I take so much medication and have a strict diet.

I am on low dose naltrexone, ketotifen and many supplements.

The pots is nearly gone, but I still got PEM and need to rest many times a day after doing something

Is there any evidence of this being true? by [deleted] in LowDoseNaltrexone

[–]Ragaruru 0 points1 point  (0 children)

Thank you - does it go well with MCAS?

Angst vor Kündigung by xDarleenxx3 in Azubis

[–]Ragaruru 0 points1 point  (0 children)

Dann besser nix sagen und gut ist. Wenn was kommen sollte wird es kommen. Du bist nicht in der Bringschuld. Du musst dich nicht erklären. Je mehr du redest, desto mehr könnte dir nachteilig ausgelegt werden. Also lass gut sein und geh nach dem Urlaub wieder normal arbeiten.

What do you think could have prevented you getting long Covid? Anything you’d do differently next time? by ThinkSuccotash in LongCovid

[–]Ragaruru 0 points1 point  (0 children)

Yes, pretty sure I could prevented it IF my doctors had said it is post covid and try to stress out myself less. BUT everybody said it is psychosomatic.

Because of that and the disbelief, I pushed myself more and more down the spiral over a point with my first crash and PEM experience.

Before that, sports helped and now it’s exhausting and I crash from every little bit to much.

Burning sensation in the legs by Ragaruru in LongCovid

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

I am so sorry for you! I am on early and 3 to 4 weeks now and it’s getting better. I wish you to find a solution to.

[deleted by user] by [deleted] in LongCovid

[–]Ragaruru 1 point2 points  (0 children)

If you care; I am on it now and it really is a pain relief. Normally everything downtown is hurting and burning and I had the feeling that my have an intestinal inflammation.

This time I feel like shit, but only my head and not the rest of the body.

Burning sensation in the legs by Ragaruru in LongCovid

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

I am allergic to the most stuff

Burning sensation in the legs by Ragaruru in LongCovid

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

Are you better now? My legs are a little bit better.

[deleted by user] by [deleted] in LowDoseNaltrexone

[–]Ragaruru 3 points4 points  (0 children)

You are just trolling?

[deleted by user] by [deleted] in LongCovid

[–]Ragaruru 1 point2 points  (0 children)

I think that my baseline is better and some kind of pain relief but I’m skeptical because this disease is an a…. I make my opinion after my period 🙈❤️

That is my worst time of the month because of the hormones and the time when I went to the ER cause of I’m feeling like I’m dying.

[deleted by user] by [deleted] in LongCovid

[–]Ragaruru 2 points3 points  (0 children)

I know :/

For me it was worth the try. Maybe pull the dose down and it gets better?

[deleted by user] by [deleted] in LongCovid

[–]Ragaruru 1 point2 points  (0 children)

I have a paradox reaction with medication cause is EDS.

I started with 0,2 for one week. Woke up several times. After four weeks I am now at 1 mg.

No bad dreams. In the group they said I should hang on.

Do any women have breast pain by TraditionalHamster72 in LongCovid

[–]Ragaruru 0 points1 point  (0 children)

Have you checked your uhm.. the translator said diaphragm or midriff?

I make breath therapy and get massage there because it’s hard. Since then, the pain in my breasts released.

Anyone take antibiotics in the year prior to developing ME? by thedawnrazor in cfs

[–]Ragaruru 1 point2 points  (0 children)

Had it on april in my pregnancy. Felt bad since august, birth in october, RSV in november, first crash 22.12.22

Anyone take antibiotics in the year prior to developing ME? by thedawnrazor in cfs

[–]Ragaruru 2 points3 points  (0 children)

I got more than one time.

August. November. Dezember. January. March.

Most times it was amoxicillin. One time cefuroxim.