Home Actress Dianna Cowern HD Instagram Photos and Wallpapers July 2023 Dianna Cowern Instagram - (A more real/raw update from Dianna, posted by Kyle) It’s been nearly 5 months of being completely bedridden. I’ve made very little progress. I can still barely move, or think or talk. I want to be out in the world living a life. My body hurts. But my heart hurts more. I wish I had a more positive update, but this is the reality of my #longcovid #mecfs #mcas

Dianna Cowern Instagram – (A more real/raw update from Dianna, posted by Kyle) It’s been nearly 5 months of being completely bedridden. I’ve made very little progress. I can still barely move, or think or talk. I want to be out in the world living a life. My body hurts. But my heart hurts more. I wish I had a more positive update, but this is the reality of my #longcovid #mecfs #mcas

Dianna Cowern Instagram - (A more real/raw update from Dianna, posted by Kyle) It’s been nearly 5 months of being completely bedridden. I’ve made very little progress. I can still barely move, or think or talk. I want to be out in the world living a life. My body hurts. But my heart hurts more. I wish I had a more positive update, but this is the reality of my #longcovid #mecfs #mcas

Dianna Cowern Instagram – (A more real/raw update from Dianna, posted by Kyle)

It’s been nearly 5 months of being completely bedridden. I’ve made very little progress. I can still barely move, or think or talk.

I want to be out in the world living a life. My body hurts. But my heart hurts more.

I wish I had a more positive update, but this is the reality of my #longcovid
#mecfs #mcas | Posted on 03/Jun/2023 02:17:30

Dianna Cowern Instagram – Kyle here – we wanted to share this (Dianna writes me notes when talking is too hard). For context, when she says she “cant do something” it means there’s often an energy or symptom cost to trying. For the last 5 months, tiny amounts of activity trigger awful symptoms.

The symptoms can come unpredictably, either immediately or delayed for a day. For her, that’s the hardest part of MECFS and long covid – not knowing when or how sick she’ll become if she tries to be herself. #longcovid #MECFS
Dianna Cowern Instagram – Health Update from Dianna (posted by Kyle)

Thank you everyone so much for the kind messages and checking in. The support and love is overwhelming. 

I just don’t know how to respond. I am…very sick. 

My brain works at 20% capacity a few minutes a day. I can barely move or talk. The rest of the time, I lie here with my eyes closed in a quiet dark room, no music, no reading, no phone. I count breaths, meditate, repeat mantras to soothe my fears. Sometimes I succeed. 

I have severe MCAS. (And severe MECFS, POTS, SIBO, and a lower gut infection, that have been diagnosed so far.) 

The MCAS is brutal. I get dizziness, nausea, and chest pain from everything. Every food I eat, fragrance I smell, organic cotton sheets that have been boiled with no detergent, all my meds (that are supposed to help MCAS). I can’t wear clothes, I can’t use toothpaste, Kyle has to boil hypoallergenic baby wipes so I can “bathe” without getting rashes. This disease is truly horrible. 

But we’re still trying treatments. And I promise, I am hanging in there. I have the best support system I could imagine, you all included. ❤ D

#longcovid #mecfs #mcas

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