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@aser3337n08: #سيد_نجم

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Region: EG
Tuesday 20 October 2026 15:46:10 GMT
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bosahmad598
❤️ خيال الروح ❤️ :
والله صح
2026-10-20 17:30:01
1
mzbetteporter3
MoUnA❤️RoNa🔥 :
صح
2026-10-20 21:06:14
0
hussn7696
المهندس خيري الشربيني :
@انت ابنتي وحبيبتي احبك Aع
2026-10-20 21:59:29
0
amira36968
amira369 :
كلام جميل 😍
2026-10-20 18:56:15
0
lamisyasser276
Lamis yasser :
2026-10-20 20:48:35
0
aylatouline08
Ayla Touline :
❣️❣️❣️
2026-10-20 21:39:02
0
_sara_aa_1
🌹🌹 :
🌹🌹🌹
2026-10-20 21:06:25
0
ziad.mohamed1335
Ziad Mohamed :
💔💔💔
2026-10-20 17:02:04
0
ws.sh37
محمود مغربي :
🥰🥰🥰
2026-10-20 22:20:12
0
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My treatment plan is for me, please respect that I cannot, handle or respond to everyone who is suffering and looking for help who has Mecfs. I am also severely sick. I had to wait YEARS to be seen by this specialist. my MEcfs is from double walking pneumonia as well. I'm not going to be on Mecfs medications because I have personal history of issues with addiction. everyone's body's are different. I hope you all well but all I can say and recommend is. SPEAK too your doctors, if you PCP doesn't HEAR your concerned then try for a new PCP. I found this MEcfs specialist online with a recommendation from my old psychiatrist. please remember, I will not be able to respond to every person, and most people with MEcfs typically are placed on medications that they do not feel would be safe for me to use. please respect, I will not be sharing my treatment information or my doctors name I will tell y'all I went through delta neuro health in Ohio and got set up with a doctor who specializes in Mecfs with Pots and dysautonomia. y'all have a good day, again please stay respectful. I am not your doctor I cannot share my treatment plan with people in fear it could make y'all worse I have been warned that my treatment plan WILL make me worse before I feel better.
My treatment plan is for me, please respect that I cannot, handle or respond to everyone who is suffering and looking for help who has Mecfs. I am also severely sick. I had to wait YEARS to be seen by this specialist. my MEcfs is from double walking pneumonia as well. I'm not going to be on Mecfs medications because I have personal history of issues with addiction. everyone's body's are different. I hope you all well but all I can say and recommend is. SPEAK too your doctors, if you PCP doesn't HEAR your concerned then try for a new PCP. I found this MEcfs specialist online with a recommendation from my old psychiatrist. please remember, I will not be able to respond to every person, and most people with MEcfs typically are placed on medications that they do not feel would be safe for me to use. please respect, I will not be sharing my treatment information or my doctors name I will tell y'all I went through delta neuro health in Ohio and got set up with a doctor who specializes in Mecfs with Pots and dysautonomia. y'all have a good day, again please stay respectful. I am not your doctor I cannot share my treatment plan with people in fear it could make y'all worse I have been warned that my treatment plan WILL make me worse before I feel better.

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