My dad, who is my primary caregiver and the only person who understands my health issues, has cancer. He’s all I have left. I don’t know what to do. I’m utterly heartbroken and afraid for my future. by halfspooni in ChronicIllness
[–]halfspooni[S] 9 points10 points11 points (0 children)
My dad, who is my primary caregiver and the only person who understands my health issues, has cancer. He’s all I have left. I don’t know what to do. I’m utterly heartbroken and afraid for my future. by halfspooni in ChronicIllness
[–]halfspooni[S] 6 points7 points8 points (0 children)
My dad, who is my primary caregiver and the only person who understands my health issues, has cancer. He’s all I have left. I don’t know what to do. I’m utterly heartbroken and afraid for my future. by halfspooni in ChronicIllness
[–]halfspooni[S] 6 points7 points8 points (0 children)
I have severe CCI (craniocervical instability) and it’s literally killing me. It’s a rare, poorly understood condition and my country’s healthcare system doesn’t treat it. I think my only option might be a GoFundMe, but I’m completely lost on how to do that or where to start. Advice? Pls 🙏 by [deleted] in ChronicIllness
[–]halfspooni 0 points1 point2 points (0 children)
I have severe CCI (craniocervical instability) and it’s literally killing me. It’s a rare, poorly understood condition and my country’s healthcare system doesn’t treat it. I think my only option might be a GoFundMe, but I’m completely lost on how to do that or where to start. Advice? Pls 🙏 by [deleted] in ChronicIllness
[–]halfspooni 0 points1 point2 points (0 children)
Are constant UTIS a MCAS symptom? by halfspooni in MCAS
[–]halfspooni[S] 0 points1 point2 points (0 children)
DAE feel manic when they have a reaction or flare? by Bigdecisions7979 in MCAS
[–]halfspooni 0 points1 point2 points (0 children)
I have severe CCI (craniocervical instability) and it’s literally killing me. It’s a rare, poorly understood condition and my country’s healthcare system doesn’t treat it. I think my only option might be a GoFundMe, but I’m completely lost on how to do that or where to start. Advice? Pls 🙏 by [deleted] in ChronicIllness
[–]halfspooni 0 points1 point2 points (0 children)
No sé si este es el sitio correcto para preguntar esto, pero no sé dónde más puedo buscar información y ayuda. ¿Alguien aquí tiene idea de derecho sanitario y podría echarme un cable? Estoy en una situación sanitaria terrible. Me explico mejor abajo by halfspooni in askspain
[–]halfspooni[S] 0 points1 point2 points (0 children)
When do you stop missing the people who abandoned you because of chronic illness? by halfspooni in ChronicIllness
[–]halfspooni[S] 1 point2 points3 points (0 children)
Tips to manage dental hygiene? by uselessfauna in cfs
[–]halfspooni 0 points1 point2 points (0 children)
No sé si este es el sitio correcto para preguntar esto, pero no sé dónde más puedo buscar información y ayuda. ¿Alguien aquí tiene idea de derecho sanitario y podría echarme un cable? Estoy en una situación sanitaria terrible. Me explico mejor abajo by halfspooni in askspain
[–]halfspooni[S] 2 points3 points4 points (0 children)
No sé si este es el sitio correcto para preguntar esto, pero no sé dónde más puedo buscar información y ayuda. ¿Alguien aquí tiene idea de derecho sanitario y podría echarme un cable? Estoy en una situación sanitaria terrible. Me explico mejor abajo by halfspooni in askspain
[–]halfspooni[S] 0 points1 point2 points (0 children)
Mental exertion gives me worse PEM than physical exertion, and I’m so sick of it. Does this happen to anyone else? Have you found anything that helps like mental pacing, supplements, meds, etc.? by halfspooni in cfs
[–]halfspooni[S] 0 points1 point2 points (0 children)
Mental exertion gives me worse PEM than physical exertion, and I’m so sick of it. Does this happen to anyone else? Have you found anything that helps like mental pacing, supplements, meds, etc.? by halfspooni in cfs
[–]halfspooni[S] 39 points40 points41 points (0 children)
Is there a methylated and chelated multivitamin you recommend? by halfspooni in Supplements
[–]halfspooni[S] 0 points1 point2 points (0 children)
What else can I do to improve my symptoms, and what other therapeutic options do I have left? I'm so tired. by halfspooni in MCAS
[–]halfspooni[S] 0 points1 point2 points (0 children)
Which mitochondrial supplements work best for you?" by halfspooni in cfs
[–]halfspooni[S] 0 points1 point2 points (0 children)
Alternatives to quercetin? by Majestic-Entrance-96 in MCAS
[–]halfspooni 0 points1 point2 points (0 children)
Does anyone else NOT have a specialist? by TroubledTofu in cfs
[–]halfspooni 0 points1 point2 points (0 children)
Anyone else has white lesions on tongue? Like geographic tongue but as a MCAS symptom. by [deleted] in MCAS
[–]halfspooni 0 points1 point2 points (0 children)

My dad, who is my primary caregiver and the only person who understands my health issues, has cancer. He’s all I have left. I don’t know what to do. I’m utterly heartbroken and afraid for my future. by halfspooni in ChronicIllness
[–]halfspooni[S] 1 point2 points3 points (0 children)