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- Anyone here have a weak immune system? I do
Anyone here have a weak immune system? I do
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@Amariez10585 tysm, same for you and your family. The seasons almost over we got this! lol
wrote 24 days ago last edited by@Zeonder lol I hope so bc these winter months are killing me
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@Zeonder lol I hope so bc these winter months are killing me
wrote 24 days ago last edited by@Amariez10585 yesss dude, the dryness from heaters is what gets me legit had the change JOBS lol
Boy Mystic raised from the Wilkins baby
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@GabbyW0205 I don’t think being pregnant can ruin your immune system but this year I’ve been sick 3 times already and the 2nd and 3rd time was awful. It felt like I was dying.
wrote 24 days ago last edited by@Amariez10585 It does in a way! Body is working overtime to protect baby.
beautiful mind
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@Amariez10585 It does in a way! Body is working overtime to protect baby.
wrote 24 days ago last edited by@GabbyW0205 oh wow I didn’t know that
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Anyone here have a weak immune system? I do. Ever since I got sick a couple weeks ago I haven’t been able to get rid of this cough and runny nose. It’s driving me nuts.
wrote 23 days ago last edited by@Amariez10585 I have a very rare blood cancer called aHus (Atypical Hemolytic Uremic Syndrome) and it first attacked my kidneys in 2015. I was in kidney failure from 2016 to 2024. And just got my transplant December 2023. Being immunosuppressed has been a very weird struggle. Some days I’ll have all the energy in the world, somedays I’ll have none. Some days I’ll be able to work out and eat properly, somedays I’ll fast for 3 weeks and never get a hunger pain. I found out that there’s ever only 100 people worldwide with my disease alive on earth at any given time (it was first discovered in 1937) and there’s very few medications and chemotherapy treatments that work effectively. One day, unfortunately, it will take my life because it will continue to reduce my red blood cell count until my blood basically coagulates inside my veins. There’s currently no cure but I am prayerful and hopefully for one someday, for all those that may have it in the future. I work closely with one of the leading specialists in the world on it, get weekly blood tests and talk with him every 3ish months on a progress report for new medicine for the disease. I’m what he’s dubbed Patient Black, and no it’s not cuz I’m African American
although that what I thought. But it’s because as long as the treatment is working, my life is in the black (clear). So his hope is to find and produce a cure before my life is over. Lord God, have your way!
In my beautiful mind, is a recipe, check your set degrees before you check for me, freezing cold electively
Electrically fire on the ground as i rest in peace
The Memory of Testing the limits of what your Yes can B
-Gambit tha Aternal -
@Amariez10585 I have a very rare blood cancer called aHus (Atypical Hemolytic Uremic Syndrome) and it first attacked my kidneys in 2015. I was in kidney failure from 2016 to 2024. And just got my transplant December 2023. Being immunosuppressed has been a very weird struggle. Some days I’ll have all the energy in the world, somedays I’ll have none. Some days I’ll be able to work out and eat properly, somedays I’ll fast for 3 weeks and never get a hunger pain. I found out that there’s ever only 100 people worldwide with my disease alive on earth at any given time (it was first discovered in 1937) and there’s very few medications and chemotherapy treatments that work effectively. One day, unfortunately, it will take my life because it will continue to reduce my red blood cell count until my blood basically coagulates inside my veins. There’s currently no cure but I am prayerful and hopefully for one someday, for all those that may have it in the future. I work closely with one of the leading specialists in the world on it, get weekly blood tests and talk with him every 3ish months on a progress report for new medicine for the disease. I’m what he’s dubbed Patient Black, and no it’s not cuz I’m African American
although that what I thought. But it’s because as long as the treatment is working, my life is in the black (clear). So his hope is to find and produce a cure before my life is over. Lord God, have your way!
wrote 23 days ago last edited by@HandOFGod777 aww, I’m so sorry that u have to go through that. I pray that u do find a cure for it. 🥺
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@HandOFGod777 aww, I’m so sorry that u have to go through that. I pray that u do find a cure for it. 🥺
wrote 23 days ago last edited by@Amariez10585 thank you
In my beautiful mind, is a recipe, check your set degrees before you check for me, freezing cold electively
Electrically fire on the ground as i rest in peace
The Memory of Testing the limits of what your Yes can B
-Gambit tha Aternal -
@Amariez10585 thank you
wrote 23 days ago last edited by@HandOFGod777 your welcome
🩵
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wrote 22 days ago last edited by
EDS and POTS here. I've flatlined twice from viruses lol.
(PLEASE wear a mask in crowded spaces, folks! It protects people like me!)"I know the demons in the room is gonna say it's more that I can chew, BUT NOW ALL I HEAR IS THE DINNER BELL."
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wrote 22 days ago last edited by
I have Crohn’s disease. It’s much better handled now because after 5 years of fighting for my life I got surgery done and I have a colostomy. However, the biological therapy I’m on means I gotta be extra careful with my immune system because the slightest thing might take me out
Although I guess if I knew tomorrow
I guess I wouldn't need faith
I guess if I never fell, I guess I wouldn't need grace
I guess if I knew His plans, I guess He wouldn't be God, God, God -
EDS and POTS here. I've flatlined twice from viruses lol.
(PLEASE wear a mask in crowded spaces, folks! It protects people like me!)wrote 22 days ago last edited by@Forest oh wow I didn’t know that
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I have Crohn’s disease. It’s much better handled now because after 5 years of fighting for my life I got surgery done and I have a colostomy. However, the biological therapy I’m on means I gotta be extra careful with my immune system because the slightest thing might take me out
wrote 22 days ago last edited by@tiachante_ I’m so sorry that u suffer from that