Search Tags for fibormyalgia

Comment from Casey Kemp:

1 Years ago

Comment from 🌹..Torill..🌹:

1 Years ago

Comment from Kenya White:

1 Years ago

Comment from healmylight:

This is my first post here. Today was like the others, pain, fear, and more pain. But I have no choice but to try not to be negative, although my mind is running horrible thoughts and my legs and chest aches. I ate quite well today though it feels like too much, soon I will post my meals as well, though I do warn you they are quite boring. I had my first bio feed back meeting, I just hope it will help.. I can't take it much longer, but positive thoughts!!!! Things to be thankful for: ❤️went to the movies with my mom ❤️ didn't feel so bad after a meal ❤️ had a good review in poetry class ❤️ was complimented my friends ❤️ - tomorrow is a new day, big hug to any one who feels suffering 🌻🌻🌻 #anxiety #anxietydisorder #stayingpositive #panicdisorder #ibs #fibormyalgia #chronicillness #chronicpain #gettingbetter #healing #tryingtoheal #depression #mentalillness #mentalhealth #tryingtobehappy

1 Years ago

Comment from Roxanne Rojas:

2 Years ago

This is the physical representation of Ehlers-Danlos Syndrome Hypermobility aka EDS just in case anyone didn't know this is what I have. It's a genetic condition that can range drastically in severity and unfortunately I can't move without most of my joints being out of place even by just a little and I'm never sure if I can get them back :( just how it goes for me but maybe not for you. But if you have your own list pains and problems, fatigue anything else listed up there or more look up the Joint Hypermobility Syndrome Paper written by Dr. Alan Pocinki if that describes you in most ways then you need to see a doctor about it. Even if you don't have chronic pain you may have the gene to pass on and should be aware of this since severity can range within one family as well. #hypermobile #doublejointed #tmj #eds #ehlersdanlossyndrome #geneticcinditions #hypermobility #strechyskin #wingedscapula #bendybody #chronicpain #chronicillness #chronicallyill #misdiagnoised #fibormyalgia #chronicfatiguesyndrome #MS #Lyme #lupus #connectivetissuedisorder #marfans #spoonie #spoonies #readthis #awareness #spreadtheword

2 Years ago

Comment from GP Carebear:

2 Years ago

Comment from GP Carebear:

I decide to go to a friends house and end up at this bar and people made faces because im not drinking, and its not like can say i have #gastroparesis and more #spoonie #healthproblems then another guys like yeah its harder to prove your case in #virginia (referring to the fact im on ssi) i wasnt even talking about that, i was sayin that im having issues getting a secondary insurance, and its just #annoying im just going to sit here & drink my #slushie after getting a whole beer on me & i know people are talking about me #drunkpeople #depressed #anxiety #fibormyalgia #gpawareness #chronicallyill #chronicallyfabulous #whatever #idontdeservethis😠💔😣

2 Years ago

Comment from Ashley Marie:

Do you need to cleanse your body? This product is absolutely amazing and has been helping me with my #fibormyalgia and can help you with you pains and aches, among other things and is all natural! Feel and be #healthy with me your Plexus Ambassador!

2 Years ago

Comment from GP Carebear:

~ I have a family who does not care ~ even my feelings they do not spare ~ they do not know how bad my sickness is ~ because they act like its none of their biz ~ I do not get it ~ but I need to move on ~ its just hard being sick and gone ~ #gastroparesis #gastroparesisawareness #gastroparesissucks #gpact #gastroparesishope #chronicillness #invisableillness #dehydrated #depressed #depression #anxiety #fightlikeagirl #fibormyalgia #spoonie #tubie #nocure #notfeelinggood #weneedacure #sad #sosickofit #piccline #pain

More Than 2 Years ago

Comment from GP Carebear:

It's #invisableillness week!! I may not look sick, but I am. I'm too sick to work, I lay in bed most of my days. People judge me because I'm so young and I don't look like anything is wrong with me. I have #gastroparesis and #fibormyalgia to name a few. Gastroparesis makes me so sick. I lose weight, food sits in my stomach for hours causing lots of pain, nausea, and vomiting. I lost so much weight, I have a #piccline to get fluids. There's many of us that can't even eat at all. I have to take the bus to my appointments and walk a lot too and it takes so much out of me. I don't really get much support from my family (they're on the east coast & I'm on the west) even they don't understand or know half of what I go through ...

More Than 2 Years ago