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Chronicmigraine Pictures
Chronicmigraine
Hey ihr lieben, heute möchte ich euch Mal meine Eindrücke erzählen & meine schmerztage zeigen wie & was ich mir da nochmal aufschreibe. (Ich führe Tabelle und schreibe es dann extra noch zusammengefasst ins Buch), seit ich einen Antikörper nehme.
Im Juni hat man tatsächlich eine gute Wirkung gemerkt. Vorallem der Grundschmerz wurde deutlichst besser und es ging Teils ein wenig mehr & auch besser.
Ich war froh über die 2 leichten Tage und das, dass meiste tatsächlich nur mittlere Tagen kamen, aber dann kamen leider Trigger dazu, die es schlimmer machten siehe Juli & August.
Ich habe immer öfter schlechtere Phasen, die gefühlt nicht aufhören möchten.
Immerhin gehen im August die starken schmerztage wieder ein klein wenig zurück & ich hoffe das auch in diesem Monat der zusätzliche Trigger sich zusammenreist und man sieht dass der Antikörper wirkt & es wieder ähnlich wie Juni wird.
PS. Habe im August noch vergessen, den zusatztrigger dazu zu schreiben. Hab's ergänzt.
#meinegeschichte
#meinegedanken
#meineerfahrungen #meineerfolgsgeschichte #schmerztagebuch #meinebilanz #migræne #migräne #chronicpain #chronicmigraine #chronischemigräne #chronische schmerzen #meineerzählung
#meineeindrücke
Chronicmigraine
A moment of oxytocin amidst the fatigue and high anxiety. 🐾💜🐾
Having fur friends is one of my joys in life.
What brings you joy?
I’ve been extremely low energy and also high alert (so weird).
Not sure if it’s new medication side effects or just me.
#ChronicMigraine #Preventatives #MedicationSideEffects #LabRat #Anxiety #MigraineSupport #MigraineDog #Cuddles
Chronicmigraine
I am no one’s best friend.
I feel very alone with this & I think it’s one of those things that no one will be able to relate to. The small amount of friends that I do have, I really appreciate & treasure them. I’m glad I have them in my life & I would consider them my best friend.
But I know that they all have someone that they are closer to than me. I am not their best friend.
I’ve always had difficulty making & keeping friends, & over the years i felt that its my fault as I don’t communicate in the right way, or I don’t open up enough & I’m not always up for going out. I’d be trying my best & giving my all to the friendship, but they always seem to fall through the cracks. Sometimes I don’t know what I’m doing wrong.
I guess there is no real point in this post, just something I had been thinking a lot recently & wonder if anyone else feels the same🤷🏼♀️
Chronicmigraine
Life can be challenging, and your resilience is truly inspiring. Keep pushing forward, and remember that there is a world of support and encouragement around you, even from those you've never met. You are not alone on this journey 🫶🏻💛
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#chronicpain #chronicillness #chronicpainwarrior #chronicpainawareness #fibromyalgia #fibromyalgiawarrior #pots #potssyndrome #chronicmigraine #chronicheadache #newdailypersistentheadache #chronicfatigue #chronicallyill #fibro #invisibleillness #invisibleillnessawareness #chronicfatiguesyndrome #spooniesupport #spoonielife #dysautonomia #spooniewarrior #spooniemom #chroniclife #chronicpainlife #chronicillnesswarrior #spoonieproblems #spooniesisterhood #spooniestrong #spooniefamily
Chronicmigraine
It's that time again where I do my pre-visit evaluation for my pain management clinic and get to fill out all the questionnaires about my pain levels and bubble in the pain map figurine. I call this time my "bodily imposter syndrome cha cha," where I start to question the severity all of the symptoms I'm having because they "can't be that bad," and I "shouldn't say it affects me that often," and I "can't bubble in that whole area. - no one would believe me." I do this to myself every time, and have to keep taking breaks and coming back to the questionnaire to give an accurate answer. Because yes, I do hurt that much, that often, and just about everywhere (save for the elbows, knees, and chest, for some reason), and the truth is, a lot of nurses and doctors don't believe me, but it doesn't make it any less true.
accessibility: A diagram of a figure with two views, front and back, with most of its body, save for the chest , elbows, and knees shaded in dark pink.
#Disabled #Disability #ChronicIllness #ChronicIllnessAwareness #Spoonie #DisabilityActivism #DisabilityRights #DisabilityAdvocate #DisabilitySupport #DisabilityBlogger #Fibromyalgia #MECFS #ChronicFatigueSyndrome #MyalgicEncephalomyelitis #ChronicPain #Pain #PainManagement #ChronicMigraine #Gastroparesis #NDI #Syncope #Dysautonomia
Chronicmigraine
Comment “I’m ready” or shoot me a DM to learn more✨
#runcoach #runningphysio #strengthcoach #gentlecoaching #physicaltherapist #chronicillness #heds #eds #ehlersdanlossyndrome #pots #posturalorthostatictachycardiasyndrome #chronicmigraine #migraine #chronicillnessawareness #chronicillnesswarrior #chronicpain #runnersofinstagram #beginnerrunner #amateurrunner #run #runner #potsie
Chronicmigraine
It’s nice when we can help our patients reduce their chronic pain. We love to hear when our patients are living pain-free! 💙
⭐⭐⭐⭐⭐
“I really like the doctors at this location. I feel they really listened to me. This is the 1st time in over a year that I have been almost pain-free.” - A.D.
Ready to start living a pain-free life? We’re currently accepting new patients.
◇ Call (502) 253-0505 to schedule an appointment or visit our website, www.specialistsinpaincare.com
#specialistsinpaincare #chronicpain #chronicpainawareness #chronicmigraine #chronicpainsucks #chronicpainlife #chronicpainrelief #chronicbackpain #chronicpainmanagement #chronicpelvicpain
Chronicmigraine
Mending Minds Women's Support Group meets virtually the 1st and 3rd Wednesday of the month at 5 PM (Mountain) 🏔️
For more information please visit:
🧠 www.Litupmymymind com 🧠
(Link in bio)
This group is facilitated by Lit-Up My Mind, LLC and @pueblobraininjuryllc
#traumaticbraininjury #BI #BIadvocate #BIAwarness #whatsonyourmind #BI #TBISurvivor #postconcussionsyndrome #brainhealth #braininjury #brainwaves #chronicmigraine #migraine #braindamage #challengeyourmind #healthandwellness #braininjurymatters #brainmatters #brainsurgerysurvivor
#mindyourbrain MINDyourmigraine #aphasiaawareness #ChronicMigraine #womenwhosupportwomen #supportgroup
Chronicmigraine
Day 92: bees bees bees ✨️
Bonus pic of the reason I very often can't get up to switch a light on so end up blindly stabbing the fabric and hoping for the best 😅🐶
@100daysprojectscotland
#100daysprojectscotland2023 #100daysprojectscotland #100daysofstitching #100daysofglimmers #stitching #embroidery #journal #glimmers #chronicillness #creativity #chronicmigraine #chronicpain
Chronicmigraine
Because at some point we have all laid down in the middle of Target to catch ourselves 🤍 • You’re not your, page 4 🤦♀️ a #b
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📸 Via @alice.explores.wonderland
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Tag someone who needs to see this💙
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Follow 👉 @dysautonomialent for more content💓🌼🥰
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Follow 👉 @dysautonomialent for more content💓🌼🥰
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#chronicfatiguesyndrome #invisibledisability #spoonie #chronicmigraine #spoonies #mentalhealthawareness #fibromyalgiaawareness #chronicfatigue #fibromyalgiawarrior #migraine #mecfs #chronicallyill #chronicillnesswarrior #sjogrens #hypermobileehlersdanlossyndrome #invisibledisabilityawareness #mastcellactivationsyndrome #disabilityowned #dysautomnia #edswarrior #chronicillnessfighter #invisiblenotimaginary #autonomicdysfunction #autonomicnervoussystem #chronicillnesssupport #potsproblems
Chronicmigraine
Hard days are always better with kitties.
#catmom #catsofinstagram #harddays #chronicmigraine #chronicpain #treatmentday
Chronicmigraine
Hi there! My name is Theresa and I am an accounting major university student. I suffer daily from diagnosed chronic and vestibular migraines. This account is my “blog” for what life is like as a disabled student trying to work my way through my degree. There are ups and downs, but I always try to stay positive and not let my illness define me <3
#chronicmigraine #vestibularmigraine #university #chronicillness
Chronicmigraine
#ChronischeErkrankung ⚡ #UnsichtbareErkrankung 🧠
Repost vom letzten Jahr zum gestrigen nationalen Kopfschmerztag:
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Ich bin chronisch krank. Seit 18 Jahren leide ich an chronischer hemiplegischer Migräne. Das ist über die Hälfte meines Lebens.
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Ich schreibe diesen Beitrag, weil ich darauf aufmerksam machen will, dass Migräne weit mehr als nur Kopfschmerz ist. Unerträgliche Kopfschmerzen sind nur ein Symptom dieser komplexen neurologischen Erkrankung. Mehr dazu lest ihr in den Slides. Die Bilder 2 bis 9 stammen von der Homepage der Schmerzklinik Kiel, die auf verschiedene Kopfschmerzerkrankungen spezialisiert ist. Meine Symptome habe ich am Ende aufgelistet. Andere Betroffene leiden zudem u.a. unter Ohnmacht, Fieberträumen und Halluzinationen.
Kurz gesagt: Migräne legt Menschen vollkommen lahm und macht sie (zeitweise) unfähig, ihrem Alltag oder auch nur "einfachen" Tätigkeiten nachzugehen. Die dem Schmerz vorangehende Aura-Phase gleicht einem schleichenden Schlaganfall und macht Kommunikation teils unmöglich.
Einige Betroffene haben mehr Schmerz- als schmerzfreie Tage und sind arbeitsunfähig. Ab einer gewissen Anzahl von Schmerztagen im Monat gilt man als #schwerbehindert.
Ich habe "Glück", weil ich im Schnitt "nur" fünf Schmerztage im Monat habe. Dennoch betrifft die Erkrankung mein ganzes Leben:
Ich muss einen geregelten Tagesablauf haben und stets ausreichend schlafen. Zu kurze Nächte rächen sich schnell.
Ich verzichte inzwischen fast vollkommen auf Alkohol, Koffein und bestimmte Lebensmittel.
Ich muss Reizüberflutung und lang andauernden Lärm meiden (sehr schwierig als Grundschullehrkraft).
Ich bin schneller erschöpft als Menschen in meiner Umgebung und benötige viel Zeit für mich alleine, um mich zu erholen.
Ich habe sehr oft Angst vor unerwarteten Attacken, insbesondere, wenn ich auf der Arbeit, unterwegs, auf Reisen oder bei wichtigen Events wie Hochzeiten bin.
Ich muss immer Schmerzmittel für den Notfall dabeihaben.
Ich nehme täglich Prophylaxemedikamente ein, die starke Nebenwirkungen haben können.
Als Migränepatientin habe ich ein erhöhtes Schlaganfallrisiko.
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⬇️ WEITER IN DEN KOMMENTAREN ⬇️
Chronicmigraine
BOTOX BENEFITS
Book Appointment Now !
Consult: Dr. Swapna Lingamallu M.D, DVL
Dermatologist, Cosmetologist,
Dermatosurgeon & Hair transplant surgeon
Call: +91 89194 64220
Address: 1/2 Ramannapeta,opp lane to Kortipadu park, Guntur & Mainroad, kothapet, Guntur.
#drswapnalingamallu #dermatologist #cosmetologist #botoxbenefits #reducewrinkles #excessivesweating #treatlazyeyes #chronicmigraine #easy #healthyskin #skincare #beautifullook #looksmoreyounger #contactus #bookappointment.
Chronicmigraine
If you were taught to "be good," you were probably taught to ignore your own emotional alarm bells — the signals from your gut saying "this doesn't feel right" or "this isn't okay with me."
And when we're conditioned to ignore those inner voice signals, we learn to live in a chronic state of distress, enduring that which our nervous system is not okay with.
When we're conditioned to ignore our own boundaries, we live in a state of chronic stress, enduring boundary violations left and right...
And we may be so conditioned to ignoring our boundaries, that we aren't even aware that we have boundaries! We may feel distressed and not know why, because we aren't aware that our boundaries are being crossed.
In order to reverse the cycle of chronic distress — which can manifest as chronic pain — we need to learn how to get back in touch with our gut signals, our feelings, our needs and our boundaries.
➡️ That's exactly what we practice in my 6-week online program 𝗪𝗿𝗶𝘁𝗶𝗻𝗴 𝘁𝗼 𝗥𝗲𝗹𝗲𝗮𝘀𝗲 𝗖𝗵𝗿𝗼𝗻𝗶𝗰 𝗣𝗮𝗶𝗻. Visit my link 🔗 in bio to learn more. 💖
Chronicmigraine
La migraña es muchísimo más que un dolor de cabeza. Aunque el dolor de cabeza sea el síntoma principal, este se acompaña de otra serie de síntomas que también son muy molestos y que aparecen como consecuencia de una hipersensibilidad a los estímulos externos. En este caso, hablaremos de la fotofobia y la sonofobia.
La fotofobia es el más frecuente pudiendo aparecer incluso fuera de la crisis, y básicamente consiste en que no toleramos los estímulos lumínicos. Por lo tanto, o bien buscaremos meternos en un cuarto a oscuras, o bien usaremos gafas de sol. Si ves a alguien en el metro con gafas de sol, hay altas probabilidades de que estés ante una migrañosa.
Por otro lado, tenemos la sonofobia, de tal manera que la paciente migrañosa se vuelve especialmente sensible a los estímulos sonoros durante la crisis. Por lo tanto, además de a oscuras buscaremos estar en un lugar libre de ruidos o bien haremos uso de tapones.
Tanto la fotofobia como en la sonofobia están relacionadas con la liberación del CGRP, un neuropéptido que se libera durante las crisis y que también está relacionado con la aparición del dolor.
Petición a personas que convivan con migrañosas: si estamos con una crisis, la televisión bajita (mejor apagada) y las persianas hasta abajo. Queremos que a las tres de la tarde parezcan las doce de la noche.
#migräne #dolorcrónico #sanidad #visibilizatumigraña #salud #iwillsurvive #convivirconmigraña #nevergiveup #pain #chronicmigraine #migraña #migraine #migrañacronica #dolor #workandmigraine #migrañaytrabajo #díasrobados #NoEsSoloUnDolorDeCabeza #migranya
Chronicmigraine
Not having a good time of it at the moment😔
Lots of appointments from tomorrow and over the next week. Trying to remain hopeful of those🤞🏼 but at the minute struggling with the effects post migraine and have a very much ‘I give up’ approach. Let’s see what tomorrow’s appointment brings…
#lotsoftears #chronicpain #neurology #neuronurse #gp #medical #hemiplegicmigraine #totallyfedup #giveup #losthope #chronicmigraine #pain #getmetobed
Chronicmigraine
A loving reality check: the way you nourish yourself impacts EVERY aspect of migraine management.
The food you eat and the way you eat it literally builds the foundation for your health. This can feel scary sometimes, because you don't want to mess it up! And it can feel overwhelming, because there's so much shopping/prepping/cooking/ENERGY required to eat a healthy diet.
Or at least, that's how it's been.
NeuroNourish is my brand new, 4-week program that teaches you how to nourish yourself as a migraineur without the stress and frustration.
Because my friend, you don't need another diet. You need the information and strategy to create your own way of eating that actually works for you!
You'll walk away from NeuroNourish feeling GOOD about how you eat, and you'll have an arsenal of tools and tips to help you stick with it.
And no - you won't have to spend a bunch of time at the store or in the kitchen! I don't want to do that either so I'm not going to make you do it 😆
If you want to head into the holidays feeling confident with food as a migraineur, I'd be honored to have you join us! Early bird pricing is available until this FRIDAY, September 8th.
Welcome materials will be available immediately, and the first week of modules will open September 24th.
➡️ Comment below with "I'm in!" if you want me to send you link so you can learn more about NeuroNourish and grab limited early bird pricing.
And if you have any questions, feel free to drop them here too!
#migraine #migraines #migrainediet #healyourheadache #whole30 #ketoformigraines #vestibularmigraine #chronicmigraine
Chronicmigraine
Why does it always feel like there’s a new ‘thing’ to deal with when you live with chronic illness? Or is it just me? 🤔
A new symptom, a new referral, another test, another surgery etc etc etc.
It’s a rollercoaster isn’t it 🎢
Hoping you are having a low stress and low symptom week so far 🤞.
📌 Follow @through.the.fibro.fog for more on daily life with chronic illness!
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#chronicillness #chronicpain #chronicfatigue #spoonie #spoonielife #spoonies #spooniecommunity #invisibleillness #fibro #fibromyalgia #fibrowarrior #pots #dysautonomia #eds #ehlerdanlossyndrome #ehlersdanlos #mcas #mastcellactivationsyndrome #lichensclerosus #chronicuti #migraine #chronicmigraine #vestibularmigraine #autoimmunedisease #butyoudontlooksick
Chronicmigraine
Some people who say things that should not be said to a person with chronic illness is out of innocent ignorance, and sometimes it’s out of pure cruel ignorance. However, whether it’s done out of innocence or cruel intentions it’s still very hurtful and invalidating to someone who lives with chronic illness.
Have you had someone say 1 or more of these 10 things to you? What would you add to this list?
#chronicillness #10thingsnottosaytosomeonewithchronicillness #invisibledisease #validatedontinvalidate #chronicpainwarrior #fibro #pots #chronicmigraine #chronicillnesswarrior
Chronicmigraine
I had a breakdown/breakthrough! I finally hit enough of rock bottom for the shite to push past the shame. I spoke to a friend at work and cried. Then I called my auntie and cried some more. Someone is finally going to come past my front door and see (and help) with the state of my flat. Give me some love and peace that I have been sorely missing recently, and hopefully help make a plan for the next steps that is actually realistic for where I am right now. (Mine have been far too ambitious). Feeling extremely emotional and deflated, but with a hint of hope. #chronicpain #invisibledisability #spoonieclub #fatiguesucks #unseensideofdisability #disabilityawareness #chronicfatigue #ehlersdanlossyndrome #chronicmigraine #crapcollagenclub #rockbottom #onewayforward #onestepatatime #letpeoplehelpyou
Chronicmigraine
Got put on Paxlovid (can't take it due to the amount of lactose in it! That surprised me) Thankful the husband is home this week and can care for me. I had a good run... #covid #chronicillness #chronicpain #chronicmigraine #tmjd #trigeminalneuralgia #pots
Chronicmigraine
Making some long-awaited progress on the frame of my #universalmonstersal
The blackwork is surprisingly soothing to stitch when I'm battling light sensitivity during a migraine attack. I ❤️❤️❤️ this project, but once it gets put in the WIP stash, I struggle to pull it back out instead of a new start. I'm determined to make progress on it this season, though!
Pattern: Universal Monster SAL
Designer: @thewitchystitcher
Fabric: #16ctaida #picturethisplus #ptphaunted
Floss: #dmcfloss
#universalmonsters #teamsparkleandshine #stitchyforwitchy #moderncrossstitch #crossstitch #xstitch #chronicmigraine
Chronicmigraine
CMA's CEO & Founder, Cat, manning the CHAMP (Coalition for Headache & Migraine Patients) Table at the PAINweek conference, at the Cosmopolitan of Las Vegas.
#CMAware
#PainWeek
#PAM2023
#Migraine
#ChronicMigraine
#Pain
#ChronicPain
Chronicmigraine
Org restock makeup, aku restock minyak angin...seminggu sebotol .macam jajan pulak eh .tapi dlm banyak banyak minyak angin ni paling best .migrain ke sakit pinggang ke sapu jr .cepat lega.aku tak jual aku pengguna je.dlm handbag aku segala minyak ada.minyak angin.minyak gamat minyak wangi.minyak dagu je takde.hahahahaha..
#chronicmigraine
#gerd
#gallbladderstone
#hiatalhernia
Chronicmigraine
I have this thing where I lie to myself for a while about not having a migraine, like I will have this persistent headache but I will always first do the self blame thing ”oh I just haven’t exercised as much as I need to, I’m on my phone too much, I watch too much TV, I’m a bad ugly person who has a headache because she does everything wrong!” And then it gets worse the next day and I have to acknowledge that nope, not everything is my fault and I gotta work on that self-talk and it is the multi-day migraine season!
Facebook did remind me that it always happens this time of the year but I did not take it seriously and now I have to suffer. I should have upped my preventitive med earlier but I did not because I always think maybe this time it won’t happen. I don’t want to keep upping it because I never feel good enough in between that I could lower the dosage and I don’t want it to go up and up and up but what are you gonna do?
Still keep thinking there’s gotta be better meds for this, even if I have tried so many. It just feels ridiculous that we have a guy who has so much money that he can try to get people in space like pretty often and then can buy entire social media platforms but we do not have a working medicine for migraine.
Well, here are cats being cute and Mischa once again being surprised by how there is something behind the glass when she is on the balcony. You’ve lived here for four years now girl!
#kilithekid #mischakissa #kissakaverit #catfriends #popopet #fosterfail #fosteringsaveslives #calico #greytuxedocat #greytuxie #migraine #killme #chronicmigraine
Chronicmigraine
🇧🇻 • og det handler ikke om at jeg ikke er glad på andres vegne, for deg er jeg så absolutt! Det gjør bare så vondt å føle at alle andre lever, mens du selv bare eksisterer. Har du følt på dette? Vit i så fall at du ikke er alene ❤️
🇨🇦 • And it's not that I'm not happy for other people, because I absolutely am! It just hurts so much to feel that everyone else is living, while I'm just existing.
#chronicillness
#kronisksykdom #utmattelse #fatigue #chronicmigraine #kroniskmigrene #vestibularmigraine #vestibulærmigrene
Chronicmigraine
I've talked about this world of comparisons before
Yes, sharing stories can help us to feel more supported
Just don't compare...it's not a competition
We spend so much time feeling like imposters or frauds in our own failing bodies
Let's support one another in Advocacy and with kindness and compassion
Let's share stories and not compare lives
We are all so different and unique that even if a person had the exact same medical diagnosis as another, their lives would look very different based on environment
Let's build up, not tear down
This world encourages fighting, separation and segregation
Being alone keeps us vulnerable, even those with good health
We were built differently so we could collectively survive
We have each been given our own unique abilities
Let them shine through 💞
If you or someone you know might benefit from this information, tag them and follow me @cssrecovery
To learn more. Don't forget to turn on notifications!
Like, share, comment and save this video to help me raise awareness by telling my story
#chronicillness #chronicillnesadvocate #chronicillnesswarrior #ehlersdanlosawareness #ehlersdanlossyndrome #chronicmigraine #Endometriosis #Fibromyalgia #myalgicencephalomyelitis #chronicfatiguesyndrome #posturalorthostatictachycardiasyndrome #potssyndrome #connectivetissuedisorder #dontcompare #beuniquelyyou
Chronicmigraine
This is how I spent my Wednesday afternoon and night.
The migraine was due to a combination of things; the heat (almost 40 C), the humidity (89%), I'm at the end of my botox cycle, and I slept less that 5 hours and night for 3 nights.
It was a doozy!!! Vision loss, nausea, massive anxiety, and of course pain.
I'm feeling better today, and this afternoon, I have my migraine botox.
#chronicpain #chronicmigraine #humiditymigraine #heatmigraine #ontarioheatwave
Chronicmigraine
Wusstest du, dass weltweit 10-15 % der Erwachsenen an Migräne leiden?
Für einige ist Migräne eine Art Kopfschmerz, für andere der pure Horror. Denn Migräneattacken bringen eine Reihe an schlimmen Begleiterscheinungen mit. Was genau eine Migräne ist, erfährst du im heutigen Post.
Du hast Fragen zum Thema? Dann stelle sie uns in den Kommentaren.
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#kopfschmerzen #migräne #migraine #headacherelief #migraineawareness #migrainelife #chronicmigraine #migrainewarrior #migrainesupport #chronicillness #migrainerelief #hormonimbalance #exhaustion #migraineproblems #reduceinflammation #headache #sleepdeprived #painmanagement #headaches #clusterheadache #stressabbau #kopf #lebensqualität #ruhe #achtsamkeit #achtsamkeitstraining #krafttanken #preventative #zufriedenheit #naturheilkunde
Chronicmigraine
What are the benefits of the CEFALY Rewards program?
As a member, you earn reward points every time you make a purchase on the site. You also may receive exclusive offers, such as free shipping and special event invitations.
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#CEFALY #CEFALYDevice #Migraine #MigraineTreatment #migrainerelief #migraineawareness #health #migrainesupport #headaches #tradein #affirm #chronicpain #chronicillness #migrainessuck #invisibleillness #pain #chronicmigraine #anxiety #migrainelife #migrainewarrior #health #migrainesupport #vestibularmigraine #vertigo #headacherelief #neckpain #wellness #depression #migraineproblems #migraineur
Chronicmigraine
Link im Profil gf.me/u/4fquth
Mein Zustand hat sich weiter verschlechtert und es scheint als ob die Spendensumme nicht zusammen kommt. Ich bitte euch den Beitrag zu teilen - an Familie - Freunde. Jeder € hilft mir nicht für für die Behandlungen sondern auch jeden Monat aufs Neue finanziell zu überleben.
Heute kommt die Rhein-Zeitung zu mir und wird über mich berichten , ich halte euch auf dem laufenden so gut ich kann.
#mecfs #schwerkrank #gofundme #help #vira #jesus #god #christian #chronicpain #chronicmigraine