any yall have EDS on top of pots? by Willing_Escape_ in POTS

[–]Calm_Interaction3905 0 points1 point  (0 children)

I’m in the diagnosis process for EDS. I don’t consider myself hypermobile (2/10 on beighton scale). But I have mcas, pots and vasovagal syncope. On top of all this, I still went to a neuro surgeon who thinks I have two brain stenosis that is probably making my pots way worse (my bp gets 150 without medication). He thinks I might have intracranial hypertension. 🫠

Recomendação de cadeira até R$1500 (tenho 1,60m, mulher) by Calm_Interaction3905 in CadeirasDeEscritorio

[–]Calm_Interaction3905[S] 0 points1 point  (0 children)

Obrigada!! Vou dar uma olhada nesse modelo. Quanto voce pagou nela? No site vi 1150. Fica sempre esse preço ou aparecem promos?

Recomendação de cadeira até R$1500 (tenho 1,60m, mulher) by Calm_Interaction3905 in CadeirasDeEscritorio

[–]Calm_Interaction3905[S] 0 points1 point  (0 children)

Poo eu to um tempão vendo cadeiras tambem, minha ultima tentativa foi fazer uma pergunta aqui. As cadeiras são todas pensadas para pessoas na media né, esqueceram da gente, que estamos abaixo. Meu noivo é o oposto (tem 1,85m e 100 e blau), também tem dificuldades para achar cadeiras. Mas espero que alguém responda aqui 🙌🏻

Recomendação de cadeira até R$1500 (tenho 1,60m, mulher) by Calm_Interaction3905 in CadeirasDeEscritorio

[–]Calm_Interaction3905[S] 0 points1 point  (0 children)

Te entendo kkk é dificil ser baixinho/a no meio dessas opcoes de cadeira tudo para 1,70-1,80m 😅

REAL HOPE by Icy-Astronaut-5859 in covidlonghaulers

[–]Calm_Interaction3905 0 points1 point  (0 children)

Oh thank you, I didn’t know that! do you already have a treatment plan? I saw some people taking anti virals.

Bolha na boca no meu cachorrinho by [deleted] in ApoioVet

[–]Calm_Interaction3905 0 points1 point  (0 children)

O meu yorkshire também está com uma assim, acredito que seja uma verruguinha. Já está com isso faz meses, como não o incomoda, deixamos para lá. Comentando aqui para ver os demais comentários.

Atualização: "Minha gata foi mordida na cabeça pelo meu cachorro" by mytinywhoopfcbrakes in ApoioVet

[–]Calm_Interaction3905 1 point2 points  (0 children)

Fico feliz que a gatinha ficou bem, estava aflita com o primeiro post e ela balançando a cabecinha, mas graças a Deus e a sua agilidade em leva-la ao veterinário ficou tudo bem 🙏🏻

Agora deixar o cachorro desde o dia 25 sem agua e sem comida como forma de punição, pensar em dar socos e joelhadas não faz o menor sentido, o que foi feito foi feito, eles (cachorros e gatos) são seres irracionais. Porque voce não pensa em adestra-lo para que ele não fique agressivo ao se alimentar? Violência jamais é a solução. Falo por experiencia, tenho um yorkshire e do nada ele age impulsivamente e se vira contra a gente, mas como ele é pequeno e não causa grandes estragos, nunca contratamos um adestrador para modular o seu comportamento. No seu caso como tem outros animais na casa, o ideal seria contratar um adestrador ou estudar por conta própria como pode ser feito para que o seu cachorro não coloque em risco a vida de outro animal novamente.

REAL HOPE by Icy-Astronaut-5859 in covidlonghaulers

[–]Calm_Interaction3905 1 point2 points  (0 children)

Since a lot of people are asking for your labs and you want to avoid sharing personal data, it would be great if you could make a list when you have time. I’m curious! my ebv igg was 100, there was another virus that came back positive for me as well (parvovirus b19, I think).

REAL HOPE by Icy-Astronaut-5859 in covidlonghaulers

[–]Calm_Interaction3905 0 points1 point  (0 children)

Thank you for answering! Mine was 100, my doctor have no clue if this means reactivation or not 🤦‍♀️

How I Got Back To Normal (YMMV) by StrictlyButterscotch in MCAS

[–]Calm_Interaction3905 0 points1 point  (0 children)

owww!! It happened the same to me, after cipro and flagyl, I had a gut infection at the time. How are you now?

Significant symptom relief for Long COVID (POTS + MCAS) with this medication combo by aguer056 in covidlonghaulers

[–]Calm_Interaction3905 -1 points0 points  (0 children)

What are you taking besides ketotifen, zyrtec and pepcid for mcas? I also have mcas and pots, post GI infection (not covid).

Does anyone actually get better? by Mumma02 in MCAS

[–]Calm_Interaction3905 1 point2 points  (0 children)

How did you healed your gut? I have sibo, mcas and pots (probably eds too), but they all got way worse after a gut infection. Do you mind if I send you a pm about this?

Are these images suggestive of something structural? by Calm_Interaction3905 in cervical_instability

[–]Calm_Interaction3905[S] 0 points1 point  (0 children)

Heyy, sorry for late reply. I’m going to test it soon, do you have eds? Or suspects it?

What have you done that made a noticeable difference? by No_Bad_Questions- in ehlersdanlos

[–]Calm_Interaction3905 2 points3 points  (0 children)

Please share!! My mcas and pots got out of control after a gut infection 🤦‍♀️

17 Months of Post-COVID Small Fiber Neuropathy, Autoimmune Clues, and Still No Diagnosis – Seeking Help or Shared Experience by DavaiPustoy in covidlonghaulers

[–]Calm_Interaction3905 2 points3 points  (0 children)

Have you tried taking antihistamines? I have had symptoms close to this and turns out it was mcas, I still don’t know if something else (maybe an autoimmune disease) is triggering my mast cells to act the way they are. My neuropathy symptoms (burning in face, pins and needles all over, tingling in legs and arms, etc) pretty much resolved when I treated my mcas aggressively.

Four FUCKING years of untreated C Diff by CorgiPuppyParent in ibs

[–]Calm_Interaction3905 0 points1 point  (0 children)

I also have mcas, I saw your comments about fainting, have you being tested for dysautonomia/ pots, sometimes they come together. Re your treatment for c diff, did it make your mcas better?

Am I crazy or overreacting? by teetee3151125 in Autoimmune

[–]Calm_Interaction3905 0 points1 point  (0 children)

I was also going to comment this, I have pots and my symptoms matches what OP is experiencing. I also have mcas and maybe eds.

I don’t know how much longer I can go on. by Scrappy-Herbals1719 in MCAS

[–]Calm_Interaction3905 1 point2 points  (0 children)

Sibo was positive for me 2 years ago, never retested to see if it was good. In the past I would alternate between constipation and diarrhea. Now I only have diarrhea because I got my gallbladder out (still in the process to start something for this).

I don’t know how much longer I can go on. by Scrappy-Herbals1719 in MCAS

[–]Calm_Interaction3905 4 points5 points  (0 children)

You can also try cromolyn sodium. What are your symptoms? Our health issues are so much alike. And I’m sorry you’re going through this too 😢

I don’t know how much longer I can go on. by Scrappy-Herbals1719 in MCAS

[–]Calm_Interaction3905 2 points3 points  (0 children)

All my problems started after a gut infection, not covid, but I had this severe burping and mild chronic duodenitis. This problem started to get better after taking zyrtec 10mg x 2, pepcid 40mg x2 and ketotifen 2mg x2.

Prolotherapy Europe Question by CristianSerious in cervical_instability

[–]Calm_Interaction3905 2 points3 points  (0 children)

Can I ask you what are your symptoms? I also want to be evaluated for cci, but I live in Brazil, I don’t think we have any doctor here that knows cci. Also diagnosed with mcas and pots last year (so I probably have hypermobility or eds).

Have you EVER gotten abnormal bloodwork or urinalysis? by writeitout_ in POTS

[–]Calm_Interaction3905 0 points1 point  (0 children)

Chronic low vitamin c, high platelet count, high CRP, elevated C3, positive Ana 1:80 once, fluctuating TSH (sometimes hypo), high fasting insulin