Things that have helped my Ehlers Danlos Syndrome
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6:30
Journey of Connective Tissue, Autoimmune disease, steroid treatment updates.by Michellemlm14,781 views- 5:47
Ehlers Danlos Syndromeby LivingWithEDS5,689 views
- 8:48
Real Life Living with Ehlers-Danlos Syndrome episode 7by angelEDSer1,416 views
- 5:42
My life with Ehlers Danlos Syndome-Type 3by jkweirich4,665 views
- 5:29
Update on Ehlers-Danlos Hypermobile Spineby Elfins1,851 views
- 3:27
Ways and Means on coping with EDS on a day to day basisby kandinsky51842 views
- 1:18
Treat Yourself for tendonitis / tendinitis of the wristby willowsyster2,013 views
- 5:10
411 on Ehlers Danlos Syndromeby owlsdragonsstuff996 views
- 3:39
Complications of EDSby DarkWaterfall3,659 views
- 4:58
Living with Ehlers Danlos Syndromeby tcscott171,943 views
- 0:59
My Life with Ehlers Danlos Syndromeby vegandanielle9,821 views
- 7:17
Ehlers Danlos Syndrome and my symptomsby telephonoscope2,371 views
- 3:38
Ehlers Danlos Syndrome - Dying to Liveby rarediseaseday8,096 views
- 10:00
Real Life Living with Ehlers-Danlos Syndrome episode 1by angelEDSer2,543 views
- 8:30
Real Life Living with Ehlers-Danlos Syndrome episode 2by angelEDSer1,957 views
- 1:24
Child with Hypermobility, bendy, stretchy double joints, Ehlers Danlos Syndrome.by dyfcheer5,325 views
- 7:09
Physical Therapy: Ehlers-Danlos Syndromeby vivisonga11111,210 views
- 3:11
Ehlers-Danlos Syndrome.... Nothing Hurts in my World.by Elfins29,748 views
- 5:28
Finger Splints - Ehlers-Danlos Syndromeby ufo8mykat2,852 views
@MuslimBrezz dude seriously id like to how you handle it! it effing hurts everyday! the only reason im still able to move is because i walk and i have the tea!
Takoda666 1 month ago
@Takoda666 Tracie can't evensuck a cock now
MuslimBrezz 1 month ago
@HunkerInTheBunker rockerchik76 died RIP.
danthehempsmog 2 months ago
My 11 yr old daughter has EDS type 3 - her major complaint is leg/ankle pain. She has to use a wheel chair when we have to walk long distances. We live in Michigan and are looking for someone experienced in treating EDS... do you know where I can find a good doctor in Michigan for her?
HunkerInTheBunker 2 months ago
I'm 17 I've had ehlers danlos my whole life and never known it. I would fall all the time as a kid and my ankles would hurt so bad. Its only recently that the pain got much worse and spread throughout my whole body. My legs and chest are the worse and sometimes my limbs go numb. But my dad found this tea that really helps and it reduces the pain a lot its called horsetail tea. For those who want the little help I can offer.
Takoda666 2 months ago
rockerchik76, hope hubby makes you a nice cumnog for the holidays.
danthehempsmog 2 months ago
I have the same fingers as you!! I'm super hypermobile, only thing that helps me is narcotics which I need to take a ton of since I'm becoming tolerant. I don't personally know anyone like me, so thank you for posting this!
jennadrums 9 months ago
@mystery8881 yes, because i have type 3 and i have never had a full blown dislocation, but my knee pops out (so it's just loose within the socket, instead of being a snug fit likes it's suppose to be), and it happened to my hip once in my sleep. i have slightly stretchy skin, but nothing too abnormal. i also have the racing heart and i always feels weak and tired.
xoDressage 11 months ago
Very good video. I was just recently diagnosed and we both have very similar circumstances with our mother. I am in so much pain and feel like i am holding myself constantly together. Im falling apart and have no suport. I would love some people with the disease to speak to. God bless Lindsey
Linzor1126 1 year ago
Can you still have EDS without having stretchy skin and being hypermobile all over? I have fibromyalgia but now that I think about it I have this feeling of some "loose, popping joints"... plus I have some heart issues such as a racing heart and a general feeling of weakness.
mystery8881 1 year ago