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MTHFR Mutation + Deplin
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Depression
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laurar
Veteran Member
Joined : Jan 2006
Posts : 743
Posted 5/6/2011 3:19 PM (GMT 0)
Hi Everyone,
I found out yesterday that I have two MTHFR mutations (C677T and A1298C), which my doctor says have kept my body from being able to process folate. He believes this has led to many of my health/mental health problems including depression, anxiety and ulcerative colitis.
I started on 15mg of Deplin last night. From what I understand, Deplin is basically just a mega-dose of folate. I'm very medication sensitive, and felt a jolt of energy within a few hours, but also slept more soundly than I have in years last night! I woke up once, but drifted back to sleep because I was able to quiet my anxious thoughts pretty easily. Today I feel pretty happy and energized, but also notice my anxiety is slightly more pronounced.
Have others had good results with it? Has anyone else had slight heightening of anxiety that eventually tapered off? I've had the slight heightening of anxiety in the past with other antidepressants, but it usually never went away. I'm really hopeful with this drug, though, because of the fact that I could also sleep really well on it.
I'm going to post this in the anxiety forum, too. Any insight would be much appreciated!
getting by
Forum Moderator
Joined : Sep 2007
Posts : 45296
Posted 5/6/2011 5:54 PM (GMT 0)
Laurar,
I don't have any experience with deplin, but just wanted to say how happy I am that you got a good nights sleep and that you are feeling good. I hope that this medication continues to help you. If the anxiety gets too bothersome, maybe the doc can give you something for that.
Best wishes, and thank you for posting.
Hugs, Karen
Sometimes i am me (HT)...
Elite Member
Joined : Mar 2009
Posts : 22619
Posted 5/7/2011 7:11 AM (GMT 0)
just wanted to wish you all the best with it. with much healing compassion to you, jamie. have not had this med.
laurar
Veteran Member
Joined : Jan 2006
Posts : 743
Posted 5/9/2011 12:43 PM (GMT 0)
Hi Everyone,
*Just posted this in the Anxiety forum too*
Thanks for the responses. I've been on Deplin now for 5 days. I have definitely been feeling better, close to "normal" I'd say. Last night i woke up in the middle of the night having what I think was a mild anxiety attack, but I took half a Xanax and it passed quickly. I was then able to sleep again fairly quickly. I think I'll have to be careful since it seems to mildly flare up my anxiety ever few days, but that's really a small issue considering how much better I feel all around. I'll keep everyone posted!
~Laura
Sometimes i am me (HT)...
Elite Member
Joined : Mar 2009
Posts : 22619
Posted 5/9/2011 1:34 PM (GMT 0)
good. good. glad you are feeling better. jamie
pollyb
New Member
Joined : Jul 2011
Posts : 1
Posted 7/30/2011 12:46 AM (GMT 0)
Hi, I'm new member. Wanted to reply to your post about
mthf mutation and deplin.
Glad you're doing well on it. I'm in australia and l-methylfolate has not been passed by our food and drug admin yet. I heard about
the mthf thing and depression thru my sister's naturopathy lecturers at local university. As deplin not available here, I found a 1mg l-methylfolate supplement on line and started taking 6 caps a day, to get close to the dose provided by deplin. Have done this in consultation with my doctor who was keen to work with me on this. This is almost unheard of here as yet.
I have been taking Effexor for anxiety/ depression last few years, zoloft before that. My anxiety had become extreme in last two years. Effexor and daily mindfulness meditation were helping but I was still anxious all the time and really having to work hard to avoid becoming depressed.
After 2 weeks taking the l-methylfolate supplement, I had started to feel alot better, less anxious, sleeping better. Three weeks later I managed to take a trip to a family party in another part of the country and actually had a good time, rather than just managing to hang together by threads - which is how it has been. After 2 months now, I feel so much better. My mind no longer feels like a hollow, shattered mess. I am keeping in touch with friends and family more and handling my chronic pain better as well. I feel like I have my mind back.
The supplement is costing me 60 aus $ for every 20 days supply. Makes me sad and angry that we are so behind here. Deplin or equivalent could be helping lots of people the way it has helped me. Hope it gets to us soon. I am lucky to have financial support from my family (haven't been able to work sev years now), so I can afford to keep buying the supplement. Most people here couldn't.
My advice to anyone thinking of checking it out would be - go ahead. I had zero side effect (am medication sensitive also). I also think that if its going to be something that helps you, you will know pretty quickly- within a few weeks.
Glad to hear someone else this research has helped. Hope there will be more successes for people who are suffering. Thanks also. Good to share my story.
getting by
Forum Moderator
Joined : Sep 2007
Posts : 45296
Posted 7/30/2011 2:12 AM (GMT 0)
Polly,
Thanks you for the post and welcome to the depression forum. I am glad that you are feeling well.
Hugs, Karen...
Pisces0312
New Member
Joined : Jun 2012
Posts : 4
Posted 6/13/2012 4:14 AM (GMT 0)
Hi! I am new to this forum.
My dr prescribed Vit D3 10,000 units and 15mg of Deplin for my chronic nerve pain, stinging, burning, numbing sensations, as well as cracking of all of my joints and ringing in the ear. I was diagnosed with B6 toxicity over 2 years ago and since stopping all B6 supplements, have made no improvement. This new dr noticed that I had low folate levels, allergic to sulfur drugs, skin
rashes, high homocystein levels, had pre clampsia and of Scottish descent. NO OTHER DR MADE THE CONNECTION. I live
with severe chronic nerve pain, most of it is limited to mouth (teeth, gums, tongue and facial areas), I also have burning and stinging in my hands and feet. My joints (all of them including my vertebrae crack with the slightest movement). And there is much more...
However, I am unclear about
how he feels Deplin can help with this. I hope someone here on the forum can help me understand what is going on.
Thank you Pisces0312
getting by
Forum Moderator
Joined : Sep 2007
Posts : 45296
Posted 6/13/2012 11:11 AM (GMT 0)
Hi Pisces,
Have you ever been tested for fibromyalgia? It sounds like you may have it. Consider it as an option.
Welcome to the forum. I sure do hope that you feel better soon.
Hugs, Karen
Missyouall
Regular Member
Joined : Apr 2012
Posts : 68
Posted 2/7/2013 9:51 PM (GMT 0)
Pisces 0312, I found your comments because my Lyme Literate Medical Doctor (LLMD) just prescribed 7.5 mg of Deplin for me and I was curious to hear about
other people's reactions to it.
In reading about
your symptoms, it struck me that all of them can be caused by Lyme Disease. I'm certainly not a doctor, and I don't even know if Lyme Disease exists in Australia, but if it does, I would seek out an LLMD and get tested. I say LLMD because a regular MD would most likely not test you correctly. Check out the Healing Well Lyme Forum and I think you'll find a lot of people with Lyme who sound a lot like you.
Good luck and God bless you. No matter what, just keep going.
C677T
New Member
Joined : Jan 2014
Posts : 1
Posted 1/16/2014 10:02 AM (GMT 0)
Hi All, I have just joined this forum, I too have mthfr, c677t from both parents, I am in Australia and cannot get your 1 methylfolate, my physician suggested neurolift and a zinc supplement. But also tested hormone levels at the same time. I am now on bio identical natural hormones and feeling more balanced. I also have the ringing in the ears and sinus infections all the time. It was so nice to read of the same symptoms and realise you are not alone. Wish you well on your journeys, would like to hear of anyone in the same position :)
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